GE XR6000 X-Ray - Service Manual

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PioneerSM_ENG.book

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GE Healthcare gehealthcare.com

Technical  Publication Direction 5275601-100 Revision 12

Copyright © 2007~2008 by General Electric Company, Inc. All Rights Reserved

[email protected]

GE Healthcare Medical Diagnostic Radiography XR 6000 Service Manual

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 XR 6000 SERVICE MANUAL

[email protected]

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Legal Notes TRADEMARKS All other products and their name brands are the trademarks of their respective holders.

COPYRIGHTS All Material, Copyright © 2007~2008 by General Electric Company, Inc. All rights reserved. The material presented and contained herein may not be reproduced in any form or manner, without the written permission of General Electric Company, Inc.

[email protected]

Legal Notes

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[email protected]

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Legal Notes

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Important Precautions LANGUAGE

ПРЕДУПРЕЖДЕНИЕ (BG)

 ТОВА УПЪТВАНЕ ЗА РАБОТА Е НАЛИЧНО САМО НА АНГЛИЙСКИ ЕЗИК.  АКО ДОСТАВЧИКЪТ НА УСЛУГАТА НА КЛИЕНТА ИЗИСКА ЕЗИК, РАЗЛИЧЕН ОТ АНГЛИЙСКИ, ЗАДЪЛЖЕНИЕ НА КЛИЕНТА Е ДА ОСИГУРИ ПРЕВОД.  НЕ ИЗПОЛЗВАЙТЕ ОБОРУДВАНЕТО ПРЕДИ ДА СТЕ СЕ КОНСУЛТИРАЛИ И РАЗБРАЛИ УПЪТВАНЕТО ЗА РАБОТА.  НЕСПАЗВАНЕТО НА ТОВА ПРЕДУПРЕЖДЕНИЕ МОЖЕ ДА ДОВЕДЕ ДО НАРАНЯВАНЕ НА ДОСТАВЧИКА НА УСЛУГАТА, ОПЕРАТОРА ИЛИ ПАЦИЕНТ В РЕЗУЛТАТ НА ТОКОВ УДАР ИЛИ МЕХАНИЧНА ИЛИ ДРУГА ОПАСНОСТ.

(ZH-CN)

 本维修手册仅提供英文版本。  如果维修服务提供商需要非英文版本,客户需自行提供翻译服务。  未详细阅读和完全理解本维修手册之前,不得进行维修。  忽略本警告可能对维修人员,操作员或患者造成触电、机械伤害或其他形式的伤害。

VÝSTRAHA (CS)

 TENTO PROVOZNÍ NÁVOD EXISTUJE POUZE V ANGLICKÉM JAZYCE.  V PŘÍPADĚ, ŽE EXTERNÍ SLUŽBA ZÁKAZNÍKŮM POTŘEBUJE NÁVOD V JINÉM JAZYCE, JE ZAJIŠTĚNÍ PŘEKLADU DO ODPOVÍDAJÍCÍHO JAZYKA ÚKOLEM ZÁKAZNÍKA.  NESNAŽTE SE O ÚDRŽBU TOHOTO ZAŘÍZENÍ, ANIŽ BYSTE SI PŘEČETLI TENTO PROVOZNÍ NÁVOD A POCHOPILI JEHO OBSAH.  V PŘÍPADĚ NEDODRŽOVÁNÍ TÉTO VÝSTRAHY MŮŽE DOJÍT K PORANĚNÍ PRACOVNÍKA PRODEJNÍHO SERVISU, OBSLUŽNÉHO PERSONÁLU NEBO PACIENTŮ VLIVEM ELEKTRICKÉHOP PROUDU, RESPEKTIVE VLIVEM MECHANICKÝCH ČI JINÝCH RIZIK.

ADVARSEL (DA)

 DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.  HVIS EN KUNDES TEKNIKER HAR BRUG FOR ET ANDET SPROG END ENGELSK, ER DET KUNDENS ANSVAR AT SØRGE FOR OVERSÆTTELSE.  FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE DENNE SERVICEMANUAL HAR VÆRET KONSULTERET OG ER FORSTÅET.  MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDFØRE SKADE PÅ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR TEKNIKEREN, OPERATØREN ELLER PATIENTEN.

Important Precautions

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[email protected]

警告

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WAARSCHUWING (NL)

 DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS VERKRIJGBAAR.  ALS HET ONDERHOUDSPERSONEEL EEN ANDERE TAAL VEREIST, DAN IS DE KLANT VERANTWOORDELIJK VOOR DE VERTALING ERVAN.  PROBEER DE APPARATUUR NIET TE ONDERHOUDEN VOORDAT DEZE ONDERHOUDSHANDLEIDING WERD GERAADPLEEGD EN BEGREPEN IS.  INDIEN DEZE WAARSCHUWING NIET WORDT OPGEVOLGD, ZOU HET ONDERHOUDSPERSONEEL, DE OPERATOR OF EEN PATIËNT GEWOND KUNNEN RAKEN ALS GEVOLG VAN EEN ELEKTRISCHE SCHOK, MECHANISCHE OF ANDERE GEVAREN.

WARNING (EN)

• •

• •

(ET)

 KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.  KUI KLIENDITEENINDUSE OSUTAJA NÕUAB JUHENDIT INGLISE KEELEST ERINEVAS KEELES, VASTUTAB KLIENT TÕLKETEENUSE OSUTAMISE EEST.  ÄRGE ÜRITAGE SEADMEID TEENINDADA ENNE EELNEVALT KÄESOLEVA TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU SAAMIST.  KÄESOLEVA HOIATUSE EIRAMINE VÕIB PÕHJUSTADA TEENUSEOSUTAJA, OPERAATORI VÕI PATSIENDI VIGASTAMIST ELEKTRILÖÖGI, MEHAANILISE VÕI MUU OHU TAGAJÄRJEL.

VAROITUS (FI)

 TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.  JOS ASIAKKAAN HUOLTOHENKILÖSTÖ VAATII MUUTA KUIN ENGLANNINKIELISTÄ MATERIAALIA, TARVITTAVAN KÄÄNNÖKSEN HANKKIMINEN ON ASIAKKAAN VASTUULLA.  ÄLÄ YRITÄ KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT JA YMMÄRTÄNYT TÄMÄN HUOLTO-OHJEEN.  MIKÄLI TÄTÄ VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA HUOLTOHENKILÖSTÖN, LAITTEISTON KÄYTTÄJÄN TAI POTILAAN VAHINGOITTUMINEN SÄHKÖISKUN, MEKAANISEN VIAN TAI MUUN VAARATILANTEEN VUOKSI.

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Important Precautions

[email protected]

HOIATUS

THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY. IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE TRANSLATION SERVICES. DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD. FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, MECHANICAL OR OTHER HAZARDS.

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ATTENTION (FR)

• •

• •

WARNUNG (DE)

CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS. SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE AUTRE LANGUE QUE L’ANGLAIS, C’EST AU CLIENT QU’IL INCOMBE DE LE FAIRE TRADUIRE. NE PAS TENTER D’INTERVENTION SUR LES ÉQUIPEMENTS TANT QUE LE MANUEL SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS. LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAÎNER CHEZ LE TECHNICIEN, L’OPÉRATEUR OU LE PATIENT DES BLESSURES DUES À DES DANGERS ÉLECTRIQUES, MÉCANIQUES OU AUTRES.

 DIESE SERVICEANLEITUNG EXISTIERT NUR IN ENGLISCHER SPRACHE.  FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENÖTIGT, IST ES AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE ÜBERSETZUNG ZU SORGEN.  VERSUCHEN SIE NICHT DIESE ANLAGE ZU WARTEN, OHNE DIESE SERVICEANLEITUNG GELESEN UND VERSTANDEN ZU HABEN.

ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ (EL)

 ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ ∆ΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.  ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙ∆ΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ, ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ.  ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ ΕΚΤΟΣ ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ.  ΕΑΝ ∆Ε ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝ∆ΕΧΕΤΑΙ ΝΑ ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝ∆ΥΝΟΥΣ.

FIGYELMEZTETÉS (HU)

 EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHETŐ EL.  HA A VEVŐ SZOLGÁLTATÓJA ANGOLTÓL ELTÉRŐ NYELVRE TART IGÉNYT, AKKOR A VEVŐ FELELŐSSÉGE A FORDÍTÁS ELKÉSZÍTTETÉSE.  NE PRÓBÁLJA ELKEZDENI HASZNÁLNI A BERENDEZÉST, AMÍG A KARBANTARTÁSI KÉZIKÖNYVBEN LEÍRTAKAT NEM ÉRTELMEZTÉK.  EZEN FIGYELMEZTETÉS FIGYELMEN KÍVÜL HAGYÁSA A SZOLGÁLTATÓ, MŰKÖDTETŐ VAGY A BETEG ÁRAMÜTÉS, MECHANIKAI VAGY EGYÉB VESZÉLYHELYZET MIATTI SÉRÜLÉSÉT EREDMÉNYEZHETI.

Important Precautions

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[email protected]

 WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN DURCH STROMSCHLÄGE, MECHANISCHE ODER SONSTIGE GEFAHREN KOMMEN.

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AÐVÖRUN (IS)

 ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.  EF AÐ ÞJÓNUSTUVEITANDI VIÐSKIPTAMANNS ÞARFNAST ANNAS TUNGUMÁLS EN ENSKU, ER ÞAÐ SKYLDA VIÐSKIPTAMANNS AÐ SKAFFA TUNGUMÁLAÞJÓNUSTU.  REYNIÐ EKKI AÐ AFGREIÐA TÆKIÐ NEMA AÐ ÞESSI ÞJÓNUSTUHANDBÓK HEFUR VERIÐ SKOÐUÐ OG SKILIN.  BROT Á SINNA ÞESSARI AÐVÖRUN GETUR LEITT TIL MEIÐSLA Á ÞJÓNUSTUVEITANDA, STJÓRNANDA EÐA SJÚKLINGS FRÁ RAFLOSTI, VÉLRÆNU EÐA ÖÐRUM ÁHÆTTUM.

AVVERTENZA



(IT)





 このサービスマニュアルには英語版しかありません。 (JA)

 サービスを担当される業者が英語以外の言語を要求される場合、翻訳作業はその業 者の責任で行うものとさせていただきます。  このサービスマニュアルを熟読し理解せずに、装置のサービスを行わないでくださ い。  この警告に従わない場合、サービスを担当される方、操作員あるいは患者さんが、 感電や機械的又はその他の危険により負傷する可能性があります。

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Important Precautions

[email protected]



IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE SOLTANTO IN INGLESE. SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEMS RICHIEDE IL MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE È TENUTO A PROVVEDERE DIRETTAMENTE ALLA TRADUZIONE. SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL CONTENUTO. IL NON RISPETTO DELLA PRESENTE AVVERTENZA POTREBBE FAR COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI ALL’ADDETTO ALLA MANUTENZIONE, ALL’UTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE ELETTRICA, PER URTI MECCANICI OD ALTRI RISCHI.

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경고 (KO)

 본 서비스 지침서는 영어로만 이용하실 수 있습니다.  고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우, 번역 서비스를 제공하는 것

은 고객의 책임입니다.  본 서비스 지침서를 참고했고 이해하지 않는 한은 해당 장비를 수리하려고 시도하지

마십시오.  이 경고에 유의하지 않으면 전기 쇼크, 기계상의 혹은 다른 위험으로부터 서비스 제공

자, 운영자 혹은 환자에게 위해를 가할 수 있습니다.

BRĪDINĀJUMS (LV)

 ŠĪ APKALPES ROKASGRĀMATA IR PIEEJAMA TIKAI ANGĻU VALODĀ.  JA KLIENTA APKALPES SNIEDZĒJAM NEPIECIEŠAMA INFORMĀCIJA CITĀ VALODĀ, NEVIS ANGĻU, KLIENTA PIENĀKUMS IR NODROŠINĀT TULKOŠANU.  NEVEICIET APRĪKOJUMA APKALPI BEZ APKALPES ROKASGRĀMATAS IZLASĪŠANAS UN SAPRAŠANAS.

ĮSPĖJIMAS (LT)

 ŠIS EKSPLOATAVIMO VADOVAS YRA PRIEINAMAS TIK ANGLŲ KALBA.  JEI KLIENTO PASLAUGŲ TIEKĖJAS REIKALAUJA VADOVO KITA KALBA – NE ANGLŲ, NUMATYTI VERTIMO PASLAUGAS YRA KLIENTO ATSAKOMYBĖ.  NEMĖGINKITE ATLIKTI ĮRANGOS TECHNINĖS PRIEŽIŪROS, NEBENT ATSIŽVELGĖTE Į ŠĮ EKSPLOATAVIMO VADOVĄ IR JĮ SUPRATOTE.  JEI NEATKREIPSITE DĖMESIO Į ŠĮ PERSPĖJIMĄ, GALIMI SUŽALOJIMAI DĖL ELEKTROS ŠOKO.  MECHANINIŲ AR KITŲ PAVOJŲ PASLAUGŲ TIEKĖJUI, OPERATORIUI AR PACIENTUI.

ADVARSEL (NO)

 DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.  HVIS KUNDENS SERVICELEVERANDØR TRENGER ET ANNET SPRÅK, ER DET KUNDENS ANSVAR Å SØRGE FOR OVERSETTELSE.  IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE SERVICEHÅNDBOKEN ER LEST OG FORSTÅTT.  MANGLENDE HENSYN TIL DENNE ADVARSELEN KAN FØRE TIL AT SERVICELEVERANDØREN, OPERATØREN ELLER PASIENTEN SKADES PÅ GRUNN AV ELEKTRISK STØT, MEKANISKE ELLER ANDRE FARER.

Important Precautions

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[email protected]

 ŠĪ BRĪDINĀJUMA NEIEVĒROŠANA VAR RADĪT ELEKTRISKĀS STRĀVAS TRIECIENA, MEHĀNISKU VAI CITU RISKU IZRAISĪTU TRAUMU APKALPES SNIEDZĒJAM, OPERATORAM VAI PACIENTAM.

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OSTRZEŻENIE (PL)

 NINIEJSZY PODRĘCZNIK SERWISOWY DOSTĘPNY JEST JEDYNIE W JĘZYKU ANGIELSKIM.  JEŚLI DOSTAWCA USŁUG KLIENTA WYMAGA JĘZYKA INNEGO NIŻ ANGIELSKI, ZAPEWNIENIE USŁUGI TŁUMACZENIA JEST OBOWIĄZKIEM KLIENTA.  NIE PRÓBOWAĆ SERWISOWAĆ WYPOSAŻENIA BEZ ZAPOZNANIA SIĘ I ZROZUMIENIA NINIEJSZEGO PODRĘCZNIKA SERWISOWEGO.  NIEZASTOSOWANIE SIĘ DO TEGO OSTRZEŻENIA MOŻE SPOWODOWAĆ URAZY DOSTAWCY USŁUG, OPERATORA LUB PACJENTA W WYNIKU PORAŻENIA ELEKTRYCZNEGO, ZAGROŻENIA MECHANICZNEGO BĄDŹ INNEGO.

ATENÇÃO (PT)

 ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL EM INGLÊS.  SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A GEMS, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.

 O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A CHOQUES ELÉTRICOS, MECÂNICOS OU OUTROS.

ATENŢIE (RO)

 ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZĂ.  DACĂ UN FURNIZOR DE SERVICII PENTRU CLIENŢI NECESITĂ O ALTĂ LIMBĂ DECÂT CEA ENGLEZĂ, ESTE DE DATORIA CLIENTULUI SĂ FURNIZEZE O TRADUCERE.  NU ÎNCERCAŢI SĂ REPARAŢI ECHIPAMENTUL DECÂT ULTERIOR CONSULTĂRII ŞI ÎNŢELEGERII ACESTUI MANUAL DE SERVICE.  IGNORAREA ACESTUI AVERTISMENT AR PUTEA DUCE LA RĂNIREA DEPANATORULUI, OPERATORULUI SAU PACIENTULUI ÎN URMA PERICOLELOR DE ELECTROCUTARE, MECANICE SAU DE ALTĂ NATURĂ.

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Important Precautions

[email protected]

 NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E COMPREENDIDO ESTE MANUAL DE ASSISTÉNCIA TÉCNICA

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

ОСТОРОЖНО! (RU)

 ДАННОЕ РУКОВОДСТВО ПО ОБСЛУЖИВАНИЮ ПРЕДЛАГАЕТСЯ ТОЛЬКО НА АНГЛИЙСКОМ ЯЗЫКЕ.  ЕСЛИ СЕРВИСНОМУ ПЕРСОНАЛУ КЛИЕНТА НЕОБХОДИМО РУКОВОДСТВО НЕ НА АНГЛИЙСКОМ, А НА КАКОМ-ТО ДРУГОМ ЯЗЫКЕ, КЛИЕНТУ СЛЕДУЕТ САМОСТОЯТЕЛЬНО ОБЕСПЕЧИТЬ ПЕРЕВОД.  ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО ОБРАТИТЕСЬ К ДАННОМУ РУКОВОДСТВУ И ПОЙМИТЕ ИЗЛОЖЕННЫЕ В НЕМ СВЕДЕНИЯ.  НЕСОБЛЮДЕНИЕ ТРЕБОВАНИЙ ДАННОГО ПРЕДУПРЕЖДЕНИЯ МОЖЕТ ПРИВЕСТИ К ТОМУ, ЧТО СПЕЦИАЛИСТ ПО ОБСЛУЖИВАНИЮ, ОПЕРАТОР ИЛИ ПАЦИЕНТ ПОЛУЧАТ УДАР ЭЛЕКТРИЧЕСКИМ ТОКОМ, МЕХАНИЧЕСКУЮ ТРАВМУ ИЛИ ДРУГОЕ ПОВРЕЖДЕНИЕ.

UPOZORNENIE (SK)

 TENTO NÁVOD NA OBSLUHU JE K DISPOZÍCII LEN V ANGLIČTINE.  AK ZÁKAZNÍKOV POSKYTOVATEĽ SLUŽIEB VYŽADUJE INÝ JAZYK AKO ANGLIČTINU, POSKYTNUTIE PREKLADATEĽSKÝCH SLUŽIEB JE ZODPOVEDNOSŤOU ZÁKAZNÍKA.  NEPOKÚŠAJTE SA O OBSLUHU ZARIADENIA SKÔR, AKO SI NEPREČÍTATE NÁVOD NA OBLUHU A NEPOROZUMIETE MU.

ATENCION (ES)

 ESTE MANUAL DE SERVICIO SOLO EXISTE EN INGLES.  SI ALGUN PROVEEDOR DE SERVICIOS AJENO A GEMS SOLICITA UN IDIOMA QUE NO SEA EL INGLES, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN SERVICIO DE TRADUCCION.  NO SE DEBERA DAR SERVICIO TECNICO AL EQUIPO, SIN HABER CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.  LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN LESIONES PROVOCADAS POR CAUSAS ELÉCTRICAS, MECÁNICAS O DE OTRA NATURALEZA.

Important Precautions

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 ZANEDBANIE TOHTO UPOZORNENIA MÔŽE VYÚSTIŤ DO ZRANENIA POSKYTOVATEĽA SLUŽIEB, OBSLUHUJÚCEJ OSOBY ALEBO PACIENTA ELEKTRICKÝM PRÚDOM, DO MECHANICKÉHO ALEBO INÉHO NEBEZPEČENSTVA.

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

VARNING (SV)

 DEN HÄR SERVICEHANDBOKEN FINNS BARA TILLGÄNGLIG PÅ ENGELSKA.  OM EN KUNDS SERVICETEKNIKER HAR BEHOV AV ETT ANNAT SPRÅK ÄN ENGELSKA ANSVARAR KUNDEN FÖR ATT TILLHANDAHÅLLA ÖVERSÄTTNINGSTJÄNSTER.  FÖRSÖK INTE UTFÖRA SERVICE PÅ UTRUSTNINGEN OM DU INTE HAR LÄST OCH FÖRSTÅR DEN HÄR SERVICEHANDBOKEN.  OM DU INTE TAR HÄNSYN TILL DEN HÄR VARNINGEN KAN DET RESULTERA I SKADOR PÅ SERVICETEKNIKERN, OPERATÖREN ELLER PATIENTEN TILL FÖLJD AV ELEKTRISKA STÖTAR, MEKANISKA FAROR ELLER ANDRA FAROR.

DİKKAT (TR)

 BU SERVİS KILAVUZUNUN SADECE İNGİLİZCESİ MEVCUTTUR.  EĞER MÜŞTERİ TEKNİSYENİ BU KILAVUZU İNGİLİZCE DIŞINDA BİR BAŞKA LİSANDAN TALEP EDERSE, BUNU TERCÜME ETTİRMEK MÜŞTERİYE DÜŞER.  SERVİS KILAVUZUNU OKUYUP ANLAMADAN EKİPMANLARA MÜDAHALE ETMEYİNİZ.

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Important Precautions

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 BU UYARIYA UYULMAMASI, ELEKTRİK, MEKANİK VEYA DİĞER TEHLİKELERDEN DOLAYI TEKNİSYEN, OPERATÖR VEYA HASTANIN YARALANMASINA YOL AÇABİLİR.

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

DAMAGE IN TRANSPORTATION All packages should be closely examined at time of delivery. If damage is apparent write “Damage In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for” by a GE representative or hospital receiving agent. Whether noted or concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier. A transportation company will not pay a claim for damage if an inspection is not requested within this 14 day period. Call GEHC Global Parts 1-800-548-3366 and select option 8, immediately after damage is found. At this time be ready to supply name of carrier, delivery date, consignee name, freight or express bill number, item damaged and extent of damage. Complete instructions regarding claim procedure are found in Section S of the Policy And Procedures Bulletins. 14 July 1993

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT

IMPORTANT...X-RAY PROTECTION X-ray equipment, if not properly used, may cause injury. Accordingly, the instructions herein contained should be thoroughly read and understood by everyone who will use the equipment before you attempt to place this equipment in operation. The General Electric Company, Healthcare Group, will be glad to assist and cooperate in placing this equipment in use. Although this apparatus incorporates a high degree of protection against x-radiation other than the useful beam, no practical design of equipment can provide complete protection. Nor can any practical design compel the operator to take adequate precautions to prevent the possibility of any persons carelessly exposing themselves or others to radiation. It is important that anyone having anything to do with x-radiation be properly trained and fully acquainted with the recommendations of the National Council on Radiation Protection and Measurements as published in NCRP Reports available from NCRP Publications, 7910 Woodmont Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission on Radiation Protection, and of any other local authorities, and take adequate steps to protect against injury. The equipment is sold with the understanding that the General Electric Company, Healthcare Group, its agents, and representatives have no responsibility for injury or damage which may result from improper use of the equipment. Various protective materials and devices are available. It is urged that such materials or devices be used.

Important Precautions

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All electrical Installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. In addition, electrical feeds into the Power Distribution Unit shall be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE Healthcare personnel. The products involved (and the accompanying electrical installations) are highly sophisticated, and special engineering competence is required. In performing all electrical work on these products, GE will use its own specially trained field engineers. All of GE’s electrical work on these products will comply with the requirements of the applicable electrical codes. The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers, personnel of third-party service companies with equivalent training, or licensed electricians) to perform electrical servicing on the equipment.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

OMISSIONS & ERRORS Customers, please contact your GE Sales or Service representatives. GE personnel, please use the GEHC Complaint Record Process to report all omissions, errors, and defects in this publication. WARNINGS Do not modify this equipment without authorization of the manufacturer. Upon request, MANUFACTURER will provide circuit diagrams, component part lists, descriptions, calibration instructions, or other information to assist service personnel to repair parts

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Important Precautions

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Preface Publication Conventions

 XR 6000 SERVICE MANUAL

Standardized conventions for representing information is a uniform way of communicating information to a reader in a consistent manner. Conventions are used so that the reader can easily recognize the actions or decisions that must be made. There are a number of character and paragraph styles used in this publication to accomplish this task. Please become familiar with them before proceeding forward. It’s important that you read and understand hazard statements, and not just ignore them.

Section 1.0 Safety & Hazard Information Proper product safety labeling allows a person to safely use or service a product. The format and style for safety communications reflected in this publication represents the harmonization of IEC/ ISO 3864 and ANSI Z535 standards.

1.1

Hazard Messages Any action that will, could or potentially cause personal injury will be preceded by the safety alert symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation mark within it. It’s always used next to the signal word to indicate the severity of the hazard. Together, they are used to indicate a hazard exists. Signal words describe the severity of possible human injures that may be encountered. The alert symbol and signal word are placed immediately before any paragraph they affect. Safety information includes: 1.) Signal Word - The seriousness level of the hazard. 2.) Symbol or Pictorial - The consequence of interaction with the hazard. 3.) Word Message: a.) The nature of the hazard (i.e. the type of hazard) b.) How to avoid the hazard. The safety alert symbol is not used when an action can only cause equipment damage.

1.2

Text Format of Signal Words DANGER - INDICATES AN IMMINENTLY HAZARDOUS SITUATION WHICH, IF NOT AVOIDED, WILL RESULT IN DEATH OR SERIOUS INJURY. THIS SIGNAL WORD IS LIMITED TO THE MOST EXTREME SITUATIONS. WARNING - INDICATES A POTENTIALLY HAZARDOUS SITUATION WHICH, IF NOT AVOIDED, COULD RESULT IN DEATH OR SERIOUS INJURY. Caution - Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury. It may also be used to alert against unsafe practices. Preface - Publication Conventions

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Within this publication, different paragraph and character styles are used to indicated potential hazards. Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify important safety information. Text (Hazard) styles are applied to the paragraph contents that are applicable to each specific safety statement.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

NOTICE - Indicates information or a company policy that relates directly or indirectly to the safety of personnel or protection of property. This signal word is associated directly with a hazard or hazardous situation and is used in place of 'DANGER,' 'WARNING,' or 'CAUTION.' It can include:

1.3



Destruction of a disk drive



Potential for internal mechanical damage, such as to a X-ray tube

Symbols and Pictorials Used The following Symbols and Pictorials are be used in this publication. These graphical icons (symbols) may be used to make you aware of specific types of hazards that could possibly cause harm.

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magnetic

biohazard

compressgas

ppe-hearing

fragile

impact

corrosive

heavyobject

ppe-2people

static_elec

heat

general

laser

ppe-respitory

keep_dry

pinch

radiation

poisongas

ppe-loto

general

explosive

electrical

flammable

ppe-eye

torque

crush/mechanical

tipping

Read Manual

ppe-gloves

ce

instuction

poisonmatl

entanglement

instuction

SPECIAL NOTICES

Section 1.0 - Safety & Hazard Information

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1.3.1

keep_up

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Dangerous Voltage. Indicates an avoidable dangerous high voltage hazard. This symbol on the equipment means that the operating instructions should be consulted to assure safe operation. This symbol indicates that waste electrical and electronic equipment must not be disposed of as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment. Follow instructions for use.

1.3.2

X-ray Tube X-ray emission. X-ray tube head is emitting X-rays. Take adequate precautions to prevent the possibility of any persons carelessly, unwisely, or unknowingly exposing themselves or others to radiation. Identifies controls or indicators associated with the selection of a small focal spot or the connection for the corresponding filament.

1.3.3

Power ON and OFF Power ON switch or switch position that applies mains voltage. Indicated connection to the mains for all mains switches or their positions. This symbol is used in all cases where safety is involved. Power OFF switch or switch positions that removes mains voltage. Indicated disconnection from the mains for all mains switches or their positions. This symbol is used in all cases where safety is involved.

1.3.4

Electrical Type Type B Equipment. Equipment providing a particular degree of protection again electrical shock regarding leakage current and protective grounding per IEC 60601-1.

1.3.5

Electrical Current Alternating Current. Indicates equipment that is suitable for alternating current only. Direct Current. Indicates equipment that is suitable for direct current only.

1.3.6

Collimator Control for indicating radiation field by using light. Preface - Publication Conventions

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Identifies controls or indicators associated with the selection of a large focal spot or the connection for the corresponding filament.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

1.3.7

Ground Functional Earth (ground) Terminal. Terminal directly connected to a point of a measuring supply or control circuit or to a screening part which is intended to be earthen for functional purposes. Protective Earth (ground). Identifies any terminal that is intended for connection of an external protective conductor to protect against electrical shock in case of a fault.

Section 2.0 Publication Conventions 2.1

General Paragraph and Character Styles Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such as Purpose, Example, Comment or Note) are used to identify important but non-safety related information. Text styles are also applied to text within each paragraph modified by the specific prefix.

EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:

Note: Example: Comment:

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Conveys information that should be considered important to the reader. Used to make the reader aware that the paragraph(s) that follow are examples of information possibly stated previously. Represents “additional” information that may or may not be relevant to your situation.

Section 2.0 - Publication Conventions

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Purpose: Introduces and provides meaning as to the information contained within the chapter, section or subsection (such as used at the beginning this chapter, for example).

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

2.2

Page Layout Publication Part Number & Revision Number

The current section and its title are always shown in the footer of the left (even) page.

Paragraphs preceeded by Alphanumeric characters (e.g. numbers) contain information that must be followed in a specific order.

The current chapter and its title are always shown in the footer of the right (odd) page. Paragraphs preceeded by a symbol (e.g. bullets) contain information that has no specific order.

Headers and footers in this publication are designed to allow you to quickly identify your location. The document part number and revision number appears in every header on every page. Odd numbered page footers indicate the current chapter, its title and current page number. Even page footers show the current section and its title, as well as the current page number.

2.3

Computer Screen Output/Input Text Character Styles Within this publication, mono-spaced character styles (fonts) are used to indicate computer text that’s either screen input and output. Mono-spaced fonts, such courier, are used to indicated text direction. When you type at your keyboard, you are generating computer input. Occasionally you will see the math operator “greater-than” and “less-than” symbols used to indicate the start and finish of variable output. When reading text generated by the computer, you are reading it as computer generated output. In addition to direction, characters are italicized (e.g. italics) to indicate information specific to your system or site.

Example: Fixed Output

This paragraph’s font represents computer generated screen “fixed” output. Its output is fixed from the sense that it does not vary from application to application. It’s the most commonly used style used to indicate filenames, paths and text that do not change from system to system. The character style used is a fixed width such as courier.

Example: Variable Output

This paragraph’s font represents computer screen output that is “variable”. It’s used to represent output that varies from application to application or system to system. Variable output is sometimes found placed between greater-than and less-than operators for clarification. For example: or . In both cases, the < and > operators are not part of the actual input. Preface - Publication Conventions

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An exclamation point in a triangle is used to indicate important information to the user.

Publication Title

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Example: Fixed Input

This paragraph’s font represents fixed input. It’s computer input that is typed-in via the keyboard. Typed input that does not vary from application to application or system to system. Fixed text the user is required to supply as input. For example: cd /usr/3p

Example: Variable Input

This paragraph’s font represents computer input that can vary from application to application or system to system. With variable text, the user is required to supply system dependent input or information. Variable input sometimes is placed between greater-than and less-than operators. For example: . In these cases, the () operators would be dropped prior to input. For example: ypcat hosts | grep would be typed into the computer as: ypcat hosts | grep 3.45.120.3 without the greater-than and less-than operators.

2.4

Buttons, Switches and Keyboard Inputs (Hard & Soft Keys) Different character styles are used to indicate actions requiring the reader to press either a hard or soft button, switch or key. Physical hardware, such as buttons and switches, are called hard keys because they are hard wired or mechanical in nature. A keyboard or on/off switch would be a hard key. Software or computer generated buttons are called soft keys because they are software generated. Software driven menu buttons are an example of such keys. Soft and hard keys are represented differently in this publication. A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style that uses both over and under-lined bold text that is bold. This is a hard key.

Example: Soft Keys

Whereas the computer MENU button that you would click with your mouse or touch with your hand uses over and under-lined regular text. This is a soft key.

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Section 2.0 - Publication Conventions

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Example: Hard Keys

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Table of Contents 3 5 Preface Publication Conventions ...................................................................................... 15 Section 1.0 Safety & Hazard Information ........................................................................... 15 1.1 1.2 1.3

15 15 16 16 17 17 17 17 17 18

Section 2.0 Publication Conventions ................................................................................. 18 2.1 2.2 2.3 2.4

General Paragraph and Character Styles........................................................................ Page Layout..................................................................................................................... Computer Screen Output/Input Text Character Styles .................................................... Buttons, Switches and Keyboard Inputs (Hard & Soft Keys) ...........................................

18 19 19 20

Chapter 1 - Before You Begin............................................................................... 37 Section 1.0 Introduction ...................................................................................................... 37 Section 2.0 Objective and Scope of this Manual............................................................... 37 2.1 2.2 2.3 2.4

Pre-Installation Check...................................................................................................... Installation Plan ............................................................................................................... Interconnection ................................................................................................................ Presentation.....................................................................................................................

37 37 37 38

Section 3.0 On-Site Requirements...................................................................................... 38 3.1 3.2 3.3 3.4

EMC Requirements ......................................................................................................... Tools and Test Equipment............................................................................................... Documentation................................................................................................................. Audio and Visual..............................................................................................................

38 38 38 39

Section 4.0 Description of System ..................................................................................... 39 Table of Contents

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Hazard Messages............................................................................................................ Text Format of Signal Words ........................................................................................... Symbols and Pictorials Used ........................................................................................... 1.3.1 SPECIAL NOTICES............................................................................................ 1.3.2 X-ray Tube .......................................................................................................... 1.3.3 Power ON and OFF ............................................................................................ 1.3.4 Electrical Type .................................................................................................... 1.3.5 Electrical Current ................................................................................................ 1.3.6 Collimator............................................................................................................ 1.3.7 Ground................................................................................................................

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Chapter 2 - Physical Installation .......................................................................... 41 Section 1.0 System Installation Guide................................................................................ 41 Section 2.0 Installation Checklist........................................................................................ 44 Section 3.0 Before You Begin.............................................................................................. 48 Section 4.0 Integrated Table ................................................................................................ 49 4.1

4.2

4.3 4.4 4.5 4.6 4.7

49 49 57 62 62 64 69 72 82 83 84 85 88 89 94 97 98

Section 5.0 System Console................................................................................................ 99 5.1 5.2

Without Console Stand ................................................................................................... 99 With Console Stand ........................................................................................................ 99

Section 6.0 Collimator Alignment ..................................................................................... 101 Section 7.0DAP Meter Installation................................................................. 102 Section 8.0 Standard Wall Stand....................................................................................... 105 8.1 8.2 8.3 8.4

8.5

Unpacking ..................................................................................................................... Installation ..................................................................................................................... Cassette Tray................................................................................................................ Ion Chamber and Grid (Optional).................................................................................. 8.4.1 Install both Ion Chamber and Grid for standard wall stand .............................. 8.4.2 Install the Grid Only for standard wall stand .................................................... 8.4.3 Install both Ion chamber and grid..................................................................... Counterweight ...............................................................................................................

105 108 111 111 112 115 116 120

Section 9.0 Final Cover Installation .................................................................................. 121 9.1 Page 22

Install Standard Tube Stand Covers ............................................................................. 121 Table of Contents

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4.8 4.9 4.10

Radiography Table.......................................................................................................... 4.1.1 Unpacking and Positioning................................................................................. 4.1.2 Installation .......................................................................................................... Tube Stand...................................................................................................................... 4.2.1 Unpacking .......................................................................................................... 4.2.2 Installation .......................................................................................................... X-Ray Tube ..................................................................................................................... Control Box and Collimator ............................................................................................. Counterweight ................................................................................................................. Cassette Tray.................................................................................................................. Ion Chamber and Grid (Optional).................................................................................... 4.7.1 Install both Ion Chamber and Grid for system with standard Integrated table ... 4.7.2 Install the Grid Only for system with standard Integrated table.......................... 4.7.3 Install the Ion Chamber and Grid for system with advanced Integrated table.... Electrical Connections..................................................................................................... Install Cabinet Tray ......................................................................................................... Table Top Installation and Leveling ................................................................................

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 9.2 9.3

Install Table Front Cover ............................................................................................... 124 Install Standard Wall Stand Covers ............................................................................... 124

Section 10.0 Labels and Rating Plates............................................................................... 125 10.1 10.2 10.3 10.4

System Console............................................................................................................. Integrated Table............................................................................................................. Cabinet .......................................................................................................................... Wall Stand .....................................................................................................................

125 125 126 126

Section 11.0 Installation Checklist ..................................................................................... 128 Section 12.0 Regulatory Tests and Final Steps................................................................. 130 12.1

130 130 130 130 130 130 130 131 131 131 132 132

Chapter 3 - Configuraton & Calibration ............................................................. 135 Section 1.0 Configuration & Calibration List ................................................................... 135 Section 2.0 Configuration & Calibration Contents.......................................................... 135 2.1 2.2

2.3

2.4

System Configuration .................................................................................................... X-Ray Tube Seasoning.................................................................................................. 2.2.1 Requirements ................................................................................................... 2.2.2 Procedure ......................................................................................................... Service Software User Guide ........................................................................................ 2.3.1 Supplies ............................................................................................................ 2.3.2 Tools ................................................................................................................. 2.3.3 Safety Precautions............................................................................................ 2.3.4 Prerequisites..................................................................................................... 2.3.5 Personnel.......................................................................................................... 2.3.6 Time.................................................................................................................. 2.3.7 Procedure ......................................................................................................... 2.3.7.1 Loading service software on service laptop .................................. 2.3.7.2 Using service software .................................................................. 2.3.7.3 Typical screen description............................................................. Tube Configuration ........................................................................................................ 2.4.1 Supplies ............................................................................................................ 2.4.2 Tools ................................................................................................................. Table of Contents

135 136 136 136 139 139 139 139 139 139 139 139 139 139 141 145 145 146

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12.2

AEC Tests...................................................................................................................... 12.1.1 AEC Maximum MAS ......................................................................................... 12.1.1.1 Overview ....................................................................................... 12.1.1.2 Procedure (50kV) .......................................................................... 12.1.2 AEC Minimum Exposure Time.......................................................................... 12.1.2.1 Overview ....................................................................................... 12.1.2.2 Procedure...................................................................................... 12.1.3 Reproducibility Of Exposure ............................................................................. 12.1.3.1 Overview ....................................................................................... 12.1.3.2 Procedure...................................................................................... > Calculation for Coefficient of Variation (C.V.):............................... Final Installation and Admin Tasks ................................................................................

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 2.4.3 2.4.4 2.4.5 2.4.6 2.4.7

2.5

2.6

2.8

2.9 Page 24

Table of Contents

146 146 146 146 146 146 146 146 146 146 146 147 147 147 147 147 147 147 149 149 151 151 151 151 151 151 151 151 151 152 152 153 158 158 158 159 159 160 160 160 160 160 160 160 160 160 160 160 161 161 161 162

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2.7

Safety Precautions ........................................................................................... Prerequisites .................................................................................................... Personnel ......................................................................................................... Time ................................................................................................................. Procedure......................................................................................................... 2.4.7.1 Load software according to tube present in the installation.......... 2.4.7.2 Verify............................................................................................. Receptor Programming ................................................................................................. 2.5.1 Supplies ........................................................................................................... 2.5.2 Tools ................................................................................................................ 2.5.3 Safety Precautions ........................................................................................... 2.5.4 Prerequisites .................................................................................................... 2.5.5 Personnel ......................................................................................................... 2.5.6 Time ................................................................................................................. 2.5.7 Procedure......................................................................................................... 2.5.7.1 Introduction ................................................................................... 2.5.7.2 Calling the subroutine ................................................................... 2.5.7.3 Parameter selection...................................................................... 2.5.7.4 Renard or normal scale for kv selection ....................................... 2.5.7.5 Date & Time.................................................................................. Automatic AEC Calibration............................................................................................ 2.6.1 Supplies ........................................................................................................... 2.6.2 Tools ................................................................................................................ 2.6.3 Safety precautions ........................................................................................... 2.6.4 Personnel ......................................................................................................... 2.6.5 Time ................................................................................................................. 2.6.6 Prerequisites .................................................................................................... 2.6.7 PROCEDURE .................................................................................................. 2.6.7.1 Development equipment............................................................... 2.6.7.2 Preliminary Remarks .................................................................... 2.6.7.3 Principle ........................................................................................ 2.6.7.4 KVEF Adjustment ......................................................................... CR AEC Calibration ...................................................................................................... 2.7.1 Systems with CR Filming Only ......................................................................... 2.7.1.1 Program Generator with Default CR Parameters ......................... 2.7.1.2 CR Dose Adjustment .................................................................... 2.7.2 System with Film and CR Filming Combined ................................................... 2.7.3 Final Adjustment .............................................................................................. 2.7.3.1 Disable Unused Film-Screen ........................................................ 2.7.3.2 Perform Checksum ....................................................................... 2.7.3.3 Save Memory................................................................................ Checksum Validation .................................................................................................... 2.8.1 Supplies ........................................................................................................... 2.8.2 Tools ................................................................................................................ 2.8.3 Safety Precautions ........................................................................................... 2.8.4 Prerequisites .................................................................................................... 2.8.5 Personnel ......................................................................................................... 2.8.6 Time ................................................................................................................. 2.8.7 PROCEDURE .................................................................................................. 2.8.7.1 Preliminary Remarks .................................................................... 2.8.7.2 Checksum Validation .................................................................... Backup and Restore Database Parameters..................................................................

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 2.9.1 2.9.2 2.9.3 2.9.4 2.9.5 2.9.6 2.9.7 2.9.8

2.10

Supplies ............................................................................................................ Tools ................................................................................................................. Safety Precautions............................................................................................ Prerequisites..................................................................................................... Personnel.......................................................................................................... Time.................................................................................................................. Applicability....................................................................................................... Procedure ......................................................................................................... 2.9.8.1 CPU memory backup .................................................................... 2.9.8.2 CPU memory restore..................................................................... 2.9.8.3 Error messages ............................................................................. Dosimetric Calibration.................................................................................................... 2.10.1 Dose/DAP accuracy check procedure .............................................................. 2.10.2 Dose/DAP accuracy maintenance ....................................................................

162 162 162 162 162 162 162 162 162 163 163 163 163 164

Chapter 4 - Functional Checks........................................................................... 165 Section 1.0 Introduction .................................................................................................... 165 Section 2.0 Tools and Test Equipment ............................................................................ 166

3.1 3.2

System Power Up .......................................................................................................... Tube Assembly Operation ............................................................................................. 3.2.1 Tube Stand Longitudinal Movement ................................................................. 3.2.2 Tube Stand Rotation......................................................................................... 3.2.3 Tube Arm Vertical Movement ........................................................................... 3.2.4 X-Ray Tube Angulation..................................................................................... 3.2.5 X-Ray Tube Tilting ............................................................................................ 3.2.6 Table Top Movement Checks........................................................................... 3.2.7 Cassette Tray Movement.................................................................................. 3.2.8 Collimator Rotation ........................................................................................... 3.2.9 Collimator Light Timer....................................................................................... 3.2.10 Wall Stand Carriage Vertical Movement...........................................................

167 167 168 168 168 168 169 169 169 169 169 169

Section 4.0 Performance Checks...................................................................................... 169 4.1 4.2

4.3

4.4 4.5

Console.......................................................................................................................... Accuracy of X-Ray Field and Light Field Alignment....................................................... 4.2.1 Requirements ................................................................................................... 4.2.2 Test Method...................................................................................................... Alignment of Centers of X-Ray Field and Image Receptor............................................ 4.3.1 Requirements ................................................................................................... 4.3.2 Test Method...................................................................................................... Image Quality................................................................................................................. 4.4.1 Test Method...................................................................................................... Tube Voltage Accuracy.................................................................................................. 4.5.1 Tools ................................................................................................................. 4.5.2 Requirements ................................................................................................... 4.5.3 Procedure ......................................................................................................... Table of Contents

169 170 170 170 173 173 173 174 174 175 175 175 175

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Section 3.0 Operational Checks........................................................................................ 167

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 4.6

4.7

4.8

4.9

4.10

Tube Current ................................................................................................................. 4.6.1 Requirements ................................................................................................... 4.6.2 Procedure......................................................................................................... Exposure Time .............................................................................................................. 4.7.1 Requirements ................................................................................................... 4.7.2 Procedure......................................................................................................... Exposure mAs............................................................................................................... 4.8.1 Requirements ................................................................................................... 4.8.2 Procedure......................................................................................................... Automatic Exposure Control (AEC) - Optional .............................................................. 4.9.1 Table AEC........................................................................................................ 4.9.2 Wall Stand AEC ............................................................................................... Collimator Light Timer ...................................................................................................

175 175 175 176 176 176 176 176 176 177 177 177 177

Section 5.0 HHS Test.......................................................................................................... 178

Chapter 5 - JEDI GENERATOR THEORY AND FUNCTIONAL DESCRIPTION 179 Section 1.0 Theory.............................................................................................................. 179 1.1 1.2

Glossary ........................................................................................................................ 179 JEDI HIGH LEVEL BLOCK DIAGRAM ......................................................................... 180

2.1 2.2 2.3 2.4

2.5

Introduction ................................................................................................................... Standard Features ........................................................................................................ Applications................................................................................................................... Architecture ................................................................................................................... 2.4.1 A Kernel ........................................................................................................... 2.4.2 Options Depending on the Application............................................................. A Packaging Architecture.............................................................................................. 2.5.1 Auxiliaries Box.................................................................................................. 2.5.2 Power Box........................................................................................................ 2.5.3 AC/DC Box ....................................................................................................... 2.5.4 System Interface Box ....................................................................................... 2.5.5 Optional Boxes .................................................................................................

181 181 181 182 182 182 184 184 184 184 184 184

Section 3.0 Technique Factors Measurement Criteria .................................................... 186 3.1 3.2 3.3 3.4

kV Accuracies ............................................................................................................... mA Accuracies .............................................................................................................. mAs Accuracies ............................................................................................................ Exposure Time Accuracies ...........................................................................................

186 186 186 186

Chapter 6 - Exception Handling And Error Codes ........................................... 187 Section 1.0 Exception Handling ........................................................................................ 187 1.1 1.2 Page 26

Diagnostics.................................................................................................................... 187 Power-On Diagnostic .................................................................................................... 187 Table of Contents

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Section 2.0 Theory Presentation ....................................................................................... 181

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 1.3 1.4 1.5 1.6 1.7 1.8 1.9 1.10 1.11

Live Diagnostics............................................................................................................. Error Code Structure...................................................................................................... Simplified Error Code Definition..................................................................................... Generator Phase Definition ........................................................................................... Error Class Definition..................................................................................................... Error Code Definition ..................................................................................................... Data Associated With The Error Code........................................................................... Number Of Occurrences................................................................................................ Date & Time...................................................................................................................

187 187 188 188 188 189 190 190 190

Section 2.0 Error Codes, Diagnostics & Troubleshooting ............................................. 190 2.1 2.2 2.3 2.4 2.5 2.6

190 190 191 195 195 195 197 197 197 199 201 203 203 205 205 205 206 206 207 209 210 210 213 213 214

Section 3.0 Console Troubleshooting & Error Codes .................................................... 216 3.1 3.2

Error Codes ................................................................ Console Troubleshooting............................................................................................... 3.2.1 System Error (C01-0001).................................................................................. 3.2.2 Memory Error on Console Control Board (C02-0001) ...................................... 3.2.3 Membrane Button Error (C02-1000) ................................................................. 3.2.4 JEDI Communication Error (C03-0001)............................................................ 3.2.5 APR Random or All (C04-0001) ....................................................................... 3.2.6 No AEC Config (C04-0002) .............................................................................. 3.2.7 Overlimit (C04-0003) ........................................................................................ 3.2.8 Phase Missing (C04-0004) ............................................................................... 3.2.9 Generator Error (C05-0001) ............................................................................. 3.2.10 Other Troubleshooting ...................................................................................... Table of Contents

216 216 216 217 218 219 219 219 219 220 220 220

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2.7 2.8 2.9 2.10 2.11 2.12 2.13 2.14

Introduction .................................................................................................................... Power On Diagnostics ................................................................................................... Error Code List............................................................................................................... Error Reporting .............................................................................................................. Diagnostics .................................................................................................................... Detailed Error Description & Troubleshooting Guide..................................................... 2.6.1 Errors ................................................................................................................ 2.6.1.1 Tube spits detection Errors (Code 30) .......................................... 2.6.1.2 Anode Rotation errors (Code 40) .................................................. 2.6.1.3 Filament Heater errors (Code 50) ................................................. 2.6.1.4 Exposure errors (Code 60) ................................. 2.6.1.5 Power supply (Code 70) ................................... 2.6.1.6 Hardware errors (Code 80) ................................. 2.6.1.7 Application errors (Code 90) ......................................................... 2.6.1.8 Communication errors (code 100)................................................. 2.6.1.9 Thermal errors (code 110) ................................. 2.6.1.10 Manipulation errors (code 120) ............................. Warning Errors............................................................................................................... Other Failures ................................................................................................................ Heating Function diagnostics......................................................................................... Rotation Function diagnostics........................................................................................ Inverter in Short Circuit Function diagnostics ................................................................ AEC diagnostics ............................................................................................................ No Load HV diagnostics ................................................................................................ Inverter Gate Command diagnostics .............................................................................

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 3.2.10.1 3.2.10.2 3.2.10.3 3.2.10.4 3.2.10.5

LED Unlit Failure........................................................................... Buzzer Failure............................................................................... LCD Display Failure...................................................................... LCD Display Faintness ................................................................. Power Un failure ...........................................................................

220 220 220 220 221

Section 4.0 PDU Troubleshooting ............................................................................................. 221 4.1

PDU Troubleshooting.................................................................................................... 4.1.1 No Console Power ........................................................................................... 4.1.2 No EM Lock Power or No Collimator Power .................................................... 4.1.3 No Generator Power ........................................................................................

221 221 222 223

Chapter 7 - Planned Maintenance...................................................................... 225 Section 1.0 Preventive Maintenance Action List ............................................................. 225 Section 2.0 Preventive Maintenance................................................................................. 227 2.1

2.3

2.4

Page 28

Table of Contents

227 227 227 227 227 227 227 227 227 227 228 228 228 228 228 228 228 228 228 228 228 228 228 229 229 229 229 229 229 229 229 229

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2.2

General Cleaning and Painting ..................................................................................... 2.1.1 Supplies ........................................................................................................... 2.1.2 Tools ................................................................................................................ 2.1.3 Safety Precautions ........................................................................................... 2.1.4 prerequisites..................................................................................................... 2.1.5 Personnel ......................................................................................................... 2.1.6 Time ................................................................................................................. 2.1.7 Procedure......................................................................................................... Visual Inspection ........................................................................................................... 2.2.1 Supplies ........................................................................................................... 2.2.2 Tools ................................................................................................................ 2.2.3 Safety Precautions ........................................................................................... 2.2.4 Prerequisites .................................................................................................... 2.2.5 Personnel ......................................................................................................... 2.2.6 Time ................................................................................................................. 2.2.7 Procedure......................................................................................................... Functional Checks......................................................................................................... 2.3.1 Supplies ........................................................................................................... 2.3.2 Tools ................................................................................................................ 2.3.3 Safety Precautions ........................................................................................... 2.3.4 Prerequisites .................................................................................................... 2.3.5 Personnel ......................................................................................................... 2.3.6 Time ................................................................................................................. 2.3.7 Procedure......................................................................................................... Table Base Maintenance .............................................................................................. 2.4.1 Supplies ........................................................................................................... 2.4.2 Tools ................................................................................................................ 2.4.3 Safety Precautions ........................................................................................... 2.4.4 Prerequisites .................................................................................................... 2.4.5 Personnel ......................................................................................................... 2.4.6 Time ................................................................................................................. 2.4.7 Procedure.........................................................................................................

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2.6

2.7

2.9

2.10

Table of Contents

230 230 230 230 230 230 230 230 230 230 230 230 231 231 231 231 231 231 231 231 231 231 231 232 232 232 232 232 232 232 232 232 232 232 233 233 233 234 235 235 235 235 235 235 235 235 235 235 235 235 236 236

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2.8

Patient Support Maintenance ........................................................................................ 2.5.1 Supplies ............................................................................................................ 2.5.2 Tools ................................................................................................................. 2.5.3 Safety Precautions............................................................................................ 2.5.4 Prerequisites..................................................................................................... 2.5.5 Personnel.......................................................................................................... 2.5.6 Time.................................................................................................................. 2.5.7 Procedure ......................................................................................................... Cassette Tray Carriage Maintenance ............................................................................ 2.6.1 Supplies ............................................................................................................ 2.6.2 Tools ................................................................................................................. 2.6.3 Safety Precautions............................................................................................ 2.6.4 Prerequisites..................................................................................................... 2.6.5 Personnel.......................................................................................................... 2.6.6 Time.................................................................................................................. 2.6.7 Procedure ......................................................................................................... Tube Stand and Wall Stand Maintenance ..................................................................... 2.7.1 Supplies ............................................................................................................ 2.7.2 Tools ................................................................................................................. 2.7.3 Safety Precautions............................................................................................ 2.7.4 Prerequisites..................................................................................................... 2.7.5 Personnel.......................................................................................................... 2.7.6 Time.................................................................................................................. 2.7.7 Procedure ......................................................................................................... Generator Functional Checks ........................................................................................ 2.8.1 Supplies ............................................................................................................ 2.8.2 Tools ................................................................................................................. 2.8.3 Safety Precautions............................................................................................ 2.8.4 Prerequisites..................................................................................................... 2.8.5 Personnel.......................................................................................................... 2.8.6 Time.................................................................................................................. 2.8.7 Procedure ......................................................................................................... 2.8.7.1 Test exposure................................................................................ > Post display initialization: .............................................................. > mA accuracy.................................................................................. > AEC functionality check (if existing) .............................................. 2.8.7.2 Record last error codes ................................................................. 2.8.7.3 Record results on counters ........................................................... 2.8.7.4 Check technique factors................................................................ 2.8.7.5 Tighten terminals and remove dust ............................................... HV Cable and Sockets Regreasing ............................................................................... 2.9.1 Supplies ............................................................................................................ 2.9.2 Tools ................................................................................................................. 2.9.3 Safety Precautions............................................................................................ 2.9.4 Prerequisites..................................................................................................... 2.9.5 Personnel.......................................................................................................... 2.9.6 Time.................................................................................................................. 2.9.7 Procedure ......................................................................................................... Replace Generator NonVolatile Parameters RAM ........................................................ 2.10.1 Supplies ............................................................................................................ 2.10.2 Tools ................................................................................................................. 2.10.3 Safety Precautions............................................................................................

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 2.10.4 2.10.5 2.10.6 2.10.7

Prerequisites .................................................................................................... Personnel ......................................................................................................... Time ................................................................................................................. Procedure......................................................................................................... 2.10.7.1 Remove and Replace the RAM .................................................... 2.10.7.2 Download Database .....................................................................

236 236 236 236 236 236

Chapter 8 - Renewal Parts .................................................................................. 237 Section 1.0 Renewal Parts List.......................................................................................... 237 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 1.10

Bearing kit 5196543, 5196544 ...................................................................................... X-Ray Tube (5192454) / Collimator (5189248) Replacement....................................... Collimator Lamp (5136302) Replacement .................................................................... Rotundity Electricity Brake Assembly (5184986) Replacement .................................... Wall Stand Cassette Tray Spring Kit (5196542) Replacement ..................................... Console Replacement................................................................................................... Console Main Board Replacement ............................................................................... Hand Switch Replacement............................................................................................ TAV Board Replacement .............................................................................................. Table Top IF Board (5335073) Replacement................................................................

247 248 248 250 252 253 254 255 255 257

2.1 2.2 2.3 2.4 2.5 2.6

Introduction ................................................................................................................... JEDI Generator Renewal Parts List .............................................................................. FRU Information............................................................................................................ Jedi 50 R 1T Structure .................................................................................................. Renewal Parts............................................................................................................... Cables ...........................................................................................................................

257 257 258 259 260 263

Section 3.0 JEDI Generator Disassembly/Reassembly................................................... 264 3.1 3.2 3.3

3.4

Page 30

Introduction ................................................................................................................... Tools ............................................................................................................................. HV Tank, 1 Tube, 1-3 Phase......................................................................................... 3.3.1 Supplies ........................................................................................................... 3.3.2 Tools ................................................................................................................ 3.3.3 Safety Precautions ........................................................................................... 3.3.4 Prerequisites .................................................................................................... 3.3.5 Personnel ......................................................................................................... 3.3.6 Time ................................................................................................................. 3.3.7 Disassembly..................................................................................................... 3.3.8 Reassembly ..................................................................................................... 3.3.9 Verify ................................................................................................................ Inverter Mid-Power Assembly ....................................................................................... 3.4.1 Supplies ........................................................................................................... 3.4.2 Tools ................................................................................................................ 3.4.3 Safety Precautions ........................................................................................... 3.4.4 Prerequisites .................................................................................................... 3.4.5 Personnel ......................................................................................................... 3.4.6 Time ................................................................................................................. Table of Contents

264 264 265 265 265 265 265 266 266 266 268 269 269 269 270 270 270 270 270

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Section 2.0 JEDI Generator Renewal Parts ...................................................................... 257

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 3.4.7

3.5

3.6

3.8

Table of Contents

271 272 272 273 274 276 278 278 278 279 279 279 279 279 279 279 280 280 280 280 280 280 281 282 282 282 282 282 282 282 283 283 283 283 283 283 283 284 284 285 285 285 285 285 285 286 286 286 286 287 287 287

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3.7

Disassembly ..................................................................................................... 3.4.7.1 Remove the Auxiliary Unit ............................................................. 3.4.7.2 Remove the Interface Unit............................................................. 3.4.7.3 Remove the AC/DC Unit and the support plate............................. 3.4.7.4 Remove the Inverter Mid Power Assembly ................................... 3.4.8 Reassembly ...................................................................................................... 3.4.9 Verify................................................................................................................. I/F Board RAD ............................................................................................................... 3.5.1 Supplies ............................................................................................................ 3.5.2 Tools ................................................................................................................. 3.5.3 Safety Precautions............................................................................................ 3.5.4 Prerequisites..................................................................................................... 3.5.5 Personnel.......................................................................................................... 3.5.6 Time.................................................................................................................. 3.5.7 Disassembly ..................................................................................................... 3.5.7.1 Remove the I/F Board Rad............................................................ 3.5.8 Reassembly ...................................................................................................... KV Board RAD............................................................................................................... 3.6.1 Supplies ............................................................................................................ 3.6.2 Tools ................................................................................................................. 3.6.3 Safety Precautions............................................................................................ 3.6.4 Prerequisites..................................................................................................... 3.6.5 Personnel.......................................................................................................... 3.6.6 Time.................................................................................................................. 3.6.7 Disassembly ..................................................................................................... 3.6.7.1 Remove the Auxiliary Unit ............................................................. 3.6.7.2 Remove the Interface Unit............................................................. 3.6.7.3 Remove the kV Control Board....................................................... 3.6.8 Reassembly ...................................................................................................... 3.6.9 Verify................................................................................................................. EMC Board 3 Phases .................................................................................................... 3.7.1 Supplies ............................................................................................................ 3.7.2 Tools ................................................................................................................. 3.7.3 Safety Precautions............................................................................................ 3.7.4 Prerequisites..................................................................................................... 3.7.5 Personnel.......................................................................................................... 3.7.6 Time.................................................................................................................. 3.7.7 Disassembly ..................................................................................................... 3.7.7.1 Remove the AC/DC Unit ............................................................... 3.7.7.2 Remove the EMC Board ............................................................... 3.7.8 Reassembly ...................................................................................................... 3.7.9 Verify................................................................................................................. AC/DC 3 PH Mid Power Assembly ................................................................................ 3.8.1 Supplies ............................................................................................................ 3.8.2 Tools ................................................................................................................. 3.8.3 Safety Precautions............................................................................................ 3.8.4 Prerequisites..................................................................................................... 3.8.5 Disassembly ..................................................................................................... 3.8.5.1 Remove the AC/DC Unit ............................................................... 3.8.5.2 Remove the AC/DC Board ............................................................ 3.8.5.3 Remove the Rectifier Block ........................................................... 3.8.6 Reassembly ......................................................................................................

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3.10

3.12

3.13 Page 32

Table of Contents

288 288 288 288 288 288 288 289 289 289 289 289 290 292 292 292 292 292 292 292 292 292 292 292 293 294 297 297 297 297 297 297 297 297 298 298 299 299 299 300 300 300 300 300 300 300 301 301 302 302 302 302

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3.11

3.8.7 Verify ................................................................................................................ Inverter Coil Mid Power Assembly ................................................................................ 3.9.1 Supplies ........................................................................................................... 3.9.2 Tools ................................................................................................................ 3.9.3 Safety Precautions ........................................................................................... 3.9.4 Prerequisites .................................................................................................... 3.9.5 Personnel ......................................................................................................... 3.9.6 Time ................................................................................................................. 3.9.7 Disassembly..................................................................................................... 3.9.7.1 Remove the Auxiliary Unit and the Interface Unit ......................... 3.9.7.2 Remove the AC/DC Unit and the support plate ............................ 3.9.7.3 Remove the Inverter Coil Mid Power Assembly ........................... 3.9.8 Reassembly ..................................................................................................... 3.9.9 Verify ................................................................................................................ Capacitor Inverter Assembly ......................................................................................... 3.10.1 Supplies ........................................................................................................... 3.10.2 Tools ................................................................................................................ 3.10.3 Safety Precautions ........................................................................................... 3.10.4 Prerequisites .................................................................................................... 3.10.5 Personnel ......................................................................................................... 3.10.6 Time ................................................................................................................. 3.10.7 Disassembly..................................................................................................... 3.10.7.1 Remove the Auxiliary Unit and the Interface Unit ......................... 3.10.7.2 Remove the AC/DC Unit and the Support Plate ........................... 3.10.7.3 Remove the Capacitor Inverter Assembly .................................... 3.10.8 Reassembly ..................................................................................................... 3.10.9 Verify ................................................................................................................ LV Power Supply 3 Phase Board.................................................................................. 3.11.1 Supplies ........................................................................................................... 3.11.2 Tools ................................................................................................................ 3.11.3 Safety Precautions ........................................................................................... 3.11.4 Prerequisites .................................................................................................... 3.11.5 Personnel ......................................................................................................... 3.11.6 Time ................................................................................................................. 3.11.7 Disassembly..................................................................................................... 3.11.7.1 Remove the Auxiliary Unit ............................................................ 3.11.7.2 Remove the LV Power Supply Board ........................................... 3.11.8 Reassembly ..................................................................................................... 3.11.9 Verify ................................................................................................................ Filament Board 1 INV.................................................................................................... 3.12.1 Supplies ........................................................................................................... 3.12.2 Tools ................................................................................................................ 3.12.3 Safety Precautions ........................................................................................... 3.12.4 Prerequisites .................................................................................................... 3.12.5 Personnel ......................................................................................................... 3.12.6 Time ................................................................................................................. 3.12.7 Disassembly..................................................................................................... 3.12.7.1 Remove the Auxiliary Unit ............................................................ 3.12.7.2 Remove the Filament Board ......................................................... 3.12.8 Reassembly ..................................................................................................... 3.12.9 Verify ................................................................................................................ Rotor Board High Speed ...............................................................................................

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3.14

302 303 303 303 303 303 303 303 304 304 305 305 305 305 305 305 305 305 306 306 306 307 307

Chapter 9 - Service Tool Job Cards................................................................... 309 Section 1.0 Software Download / Upgrade ...................................................................... 309 1.1 1.2 1.3 1.4 1.5 1.6 1.7

Supplies ......................................................................................................................... Tools .............................................................................................................................. Safety Precautions......................................................................................................... Prerequisites.................................................................................................................. Personnel....................................................................................................................... Time............................................................................................................................... Procedure ...................................................................................................................... 1.7.1 Load Software File on Service Laptop.............................................................. 1.7.2 Unzip software file ............................................................................................ 1.7.3 Software download ...........................................................................................

309 309 309 309 309 309 309 309 309 310

Section 2.0 Tube Replacement Software Procedure ...................................................... 311 2.1 2.2 2.3 2.4 2.5 2.6 2.7

Supplies ......................................................................................................................... Tools .............................................................................................................................. Safety Precautions......................................................................................................... Prerequisites.................................................................................................................. Personnel....................................................................................................................... Time............................................................................................................................... Procedure ...................................................................................................................... 2.7.1 Perform a Database backup ............................................................................. 2.7.2 Reset Tube Data tracking counter and error log............................................... 2.7.3 Verify new tube operation, clear error log......................................................... 2.7.4 Generator Counter Reading Record................................................................. Table of Contents

311 311 311 311 311 312 312 312 312 314 314

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3.13.1 Supplies ............................................................................................................ 3.13.1.1 Tools.............................................................................................. 3.13.2 Safety Precautions............................................................................................ 3.13.3 Prerequisites..................................................................................................... 3.13.4 Personnel.......................................................................................................... 3.13.5 Time.................................................................................................................. 3.13.6 Disassembly ..................................................................................................... 3.13.6.1 Remove the Auxiliary Unit ............................................................. 3.13.6.2 Remove the Rotor Board............................................................... 3.13.7 Reassembly ...................................................................................................... 3.13.8 Verify................................................................................................................. AEC Board..................................................................................................................... 3.14.1 Supplies ............................................................................................................ 3.14.2 Tools ................................................................................................................. 3.14.3 Safety Precautions............................................................................................ 3.14.4 Prerequisites..................................................................................................... 3.14.5 Personnel.......................................................................................................... 3.14.6 Time.................................................................................................................. 3.14.7 Disassembly ..................................................................................................... 3.14.7.1 Remove the Auxiliary Unit ............................................................. 3.14.7.2 Remove the AEC Board ................................................................ 3.14.8 Reassembly ...................................................................................................... 3.14.9 Verify.................................................................................................................

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 2.7.5

Tube Database Download................................................................................ 315

Chapter 10 - Schematics .................................................................................... 317 Section 1.0 MIS Map ........................................................................................................... 317 1.1

Jedi 50 R 1T Cabling..................................................................................................... 321

Section 2.0 Central Listings............................................................................................... 323 2.1 2.2 2.3

2.4 2.5 2.6 2.7

2.12 2.13

323 324 325 326 326 327 328 329 330 331 331 331 332 333 334 335 335 336 336

Section 3.0 Schematics...................................................................................................... 337 3.1 3.2 3.3 3.4 3.5 3.6 3.7 3.8 3.9 3.10 3.11 3.12 3.13 3.14 3.15

PDU Connection Diagram............................................................................................. Table Electrical Schematics .......................................................................................... A61001C Console Control Board Circuit Diagram ........................................................ Jedi Generator TAV Interface Board............................................................................. I/F Board RAD Electrical ............................................................................................... I/F Board RAD V2 Electrical.......................................................................................... Rotor board ................................................................................................................... Heater board ................................................................................................................. LVPS board................................................................................................................... Inverter .......................................................................................................................... Gate cmd....................................................................................................................... Dual snub ...................................................................................................................... AC/DC board................................................................................................................. AEC board..................................................................................................................... Rad IF ...........................................................................................................................

337 338 341 355 359 363 367 378 385 387 388 391 392 393 397

Chapter 11 - MIS Chart........................................................................................ 401 Section 1.0 Scope ............................................................................................................... 401 Page 34

Table of Contents

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2.8 2.9 2.10 2.11

kV Measure Board ........................................................................................................ Filament Board 1 Inv. .................................................................................................... Rotation Board High Speed .......................................................................................... 2.3.1 Indicators.......................................................................................................... 2.3.2 J2 Wiring .......................................................................................................... LV Power Supply 3 PH Board ....................................................................................... Gate Command Board .................................................................................................. Dual Snub Board........................................................................................................... kV Control Board........................................................................................................... 2.7.1 Switches and Jumpers ..................................................................................... 2.7.2 Indicators.......................................................................................................... 2.7.3 Non Volatile RAM............................................................................................. AC/DC 3 Phase board................................................................................................... I/F Board RAD V1 ......................................................................................................... I/F Board RAD V2 ......................................................................................................... AEC Board .................................................................................................................... 2.11.1 Test Points ....................................................................................................... AEC Board V2............................................................................................................... Test Points ....................................................................................................................

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Section 2.0 How to Use...................................................................................................... 401 Section 3.0 MIS Charts....................................................................................................... 402 3.1

3.2

3.3

System Console............................................................................................................. 3.1.1 J1 Handswitch Interface, 5184620 ................................................................... 3.1.2 J2 FW Download Serial Port, 5194292............................................................. 3.1.3 J3 Power and RTL Interface, 5183903 ............................................................. 3.1.4 J4 Generator Interface, 5182354...................................................................... Generator....................................................................................................................... 3.2.1 Generator Power Cable, 5196454 .................................................................... 3.2.2 Generator Grounding Cable, 5196643 ............................................................. Table.............................................................................................................................. 3.3.1 TM1-XS105 Cable, 5193103 ............................................................................ 3.3.2 Table Grounding Cable 1, 5193105.................................................................. 3.3.3 Table Grounding Cable 2, 5193106.................................................................. 3.3.4 Table Grounding Cable 3, 5193107.................................................................. 3.3.5 Table Grounding Cable 5, 5193109.................................................................. 3.3.6 Table Power Cable, 5193607 ........................................................................... 3.3.6.1 Table MC7 Cable, 5197242 .......................................................... 3.3.7 Table Cable No1, 5197244...............................................................................

402 402 402 403 404 406 406 406 406 406 407 407 407 407 408 408 409

Section 1.0 Compliance Statement................................................................................... 411 Section 2.0 Compatibility Tables ...................................................................................... 412 2.1 2.2

Electromagnetic Emission ............................................................................................. 412 Electromagnetic Immunity ............................................................................................. 413

Section 3.0 Use Recommendations.................................................................................. 416 Section 4.0 Installation Recommendations ..................................................................... 416 4.1 4.2 4.3 4.4 4.5

Cable Shielding & Grounding ........................................................................................ Subsystem & Accessories Power Supply Distribution .................................................. Stacked Components & Equipment............................................................................... Low Frequency Magnetic Field...................................................................................... Electrostatic Discharge Environment & Recommendations ..........................................

416 416 416 417 417

Chapter B - Revision History.............................................................................. 419

Table of Contents

Page 35

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Chapter A - Electromagnetic Compatibility (EMC) ........................................... 411

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[email protected]

Page 36

Table of Contents

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Chapter 1 - Before You Begin Section 1.0 Introduction The goal of this document is to guide the service representative through an entire X-ray room installation and to provide Diagnostic and Calibration information for troubleshooting and repair. The following On-site Requirements must be accounted for prior to beginning installation of the system.

Section 2.0 Objective and Scope of this Manual This direction will lead you in a correct sequence through the manuals needed to install the equipment. Following the suggested sequence will result in an orderly installation. However, extenuating circumstances may dictate a deviation from the recommended sequence. Feel free to deviate, but keep track of your progress by checking off the tasks in the flowchart as you complete them.

2.1

Pre-Installation Check Pre-installation planning should be complete. Inspect the pre-installation “checklist”, found in GEHC document 5275600-100 (XR 6000 System Pre-Installation Manual), and verify that the tasks specified have been completed. Immediately arrange for completion of any tasks still not completed.

2.2

Installation Plan The main steps in the installation plan are easily seen by referring to the Table of Contents of this document. The plan objectives are to: Give a logical installation order which recognizes mechanical and electrical interface areas. Test and adjust each subsystem independently. To obtain a good overall view of how these objectives are to be achieved review the Table of Contents for this document before beginning the installation work. Then, if it is necessary to deviate from the stated plan, you will be aware of the essential interface area. This document will give you the information required to make another effective plan that applies to particular situations.

2.3

Interconnection Interconnection of products by furnished cables or contractor supplied wiring is indicated by numbered MIS runs in the installation sections. Run interconnect charts are available, which describe the connection and function of each wire. For XR 6000 System, refer to the following: •

XR 6000 System Schematics (Chapter 10)



XR 6000 System MIS Chart (Chapter 11) Chapter 1 - Before You Begin

Page 37

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Check equipment according to the packing list for your system against the main catalog numbers in the FDO (Field Delivery Order). Also, verify that all the manuals are present in the binders according to the Table of Contents.

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2.4

Presentation The procedures in this steering manual are presented in jobcard forms.

Section 3.0 On-Site Requirements 3.1

EMC Requirements If electromagnetic compliance is mandatory for the local country where this system is installed, this equipment is allowed to be installed only in X-ray protected rooms, which provide an attenuation of at least 12 dB for radio disturbances from 30 MHz to 1 GHz.

3.2

Tools and Test Equipment There are no additional tools and test equipment besides the standard service representative tool kit which must be available before installing the XR 6000 System as below.

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3.3



Electric hammer drill with bits



Digital multimeter



4 Ft. Level (or two standard levels)



Torque wrench



HV cable removal spanner



Push-pull Gauge



Common service tools



Resolution Pattern



Dose Meter



Loctite 242

Documentation Directions are necessary for correct installation of the XR 6000 System. Procedures from each document will be used and reflect the latest information available at this time. Not all procedures in this manual apply to all sites. Before you begin installation, cross out the procedures that do not apply to your site.

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Section 3.0 - On-Site Requirements

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3.4

Audio and Visual It is the User’s responsibility to provide the means for audio and visual communication between the Operator and the patient.

Section 4.0 Description of System

5 6

2 Standard / Advanced [email protected]

3

1

Cabinet

4 WLS Standard / Advanced

Operator Console

The XR 6000 is divided into basic components: 1. 2. 3. 4. 5. 6.

Operator Console (Console Stand - Optional) Integrated Table Standard / Advanced Cabinet Wall Stand Standard / Advanced (Optional) 50kW X-ray Tube - Toshiba E7843X Collimator

Figure 1-1 XR 6000 System Component Identification

Chapter 1 - Before You Begin

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Item

Component

Model Number

1a

Console

5194507

1b

Console Pedestal

5192392

2

Standard Integrated Table

5180891

2

Advanced Integrated Table

5316772

2a

Standard Integrated Tube Stand

5183392

2a

Advanced Integrated Tube Stand

5183392-2

3a

Generator (VR Jedi 50 R1T)

2212259-2

3b

PDU

5220653

4

Standard Wall Stand

5194508

4

Advanced Wall Stand

5316773

5

50kW X-ray Tube - Toshiba E7843X

5192454

6

Manual Collimator

5189248

Table 1-1 XR 6000 System Component Identification

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Section 4.0 - Description of System

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Chapter 2 - Physical Installation Installation is broken into two primary tasks: mechanical and electrical. Mechanical tasks focus on the physical aspects of hardware assembly, equipment positioning, and cabling. Electrical tasks are performed when system power is applied. The primary tasks are designed to be performed in sequence. Follow the sequence of tasks describe for each primary task in Section 1.0 that follow.

Section 1.0 System Installation Guide 1

Complete Pre-Installation Checklist People Required: 1 Minutes to Complete: 10 Fill out the Pre-Installation Checklist to confirm completion of pre-install activities before beginning the installation process.

2

Receive and Inventory System

People Required: 1

Minutes to Complete: 10

Inventory equipment & report discrepancies immediately. Plan route and transport equipment to room. 3

Install Table

People Required: 2

Minutes to Complete: 140

Remove table from shipping container. Position and install table according to site plans & drawings, and secure. Remove tube stand from shipping container. Install tube stand. Install X-ray tube. Install control box and collimator. Counterweight balance. Install cassette tray(Not needed for advanced Integrate table). Install ion chamber and grid (optional). Electrical connections. Install cabinet tray. Table top installation and leveling. 4

Install System Console

People Required: 1

Minutes to Complete: 15

Position and install system console according to site plans & drawings, and secure. 5

Collimator Alignment

People Required: 1

Minutes to Complete: 30

Power up system. Collimator alignment.

Chapter 2 - Physical Installation

Page 41

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Collect Product Locator Cards and store in a secure location.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 (Continued)

6

Install Wall Stand

People Required: 2

Minutes to Complete: 50

Remove wall stand from shipping container. Position and install wall stand according to site plans & drawings, and secure. Install cassette tray. Install ion chamber and grid (optional). Counterweight balance. 7

Equipment and Personnel Readiness

People Required: 1

Minutes to Complete: 10

Verify equipment is configured per the site plans and drawings. Verify that the resistance between subsystems grounds is less than 0.1 ohms. Fix and/or report any discrepancies. 8

Configure and Calibrate System

People Required: 1

Minutes to Complete: 215

People Required: 1

Minutes to Complete: 30

Tube seasoning. Software installation. Tube configuration. Receptor parameter. Checksum validation. Backup database. 9

Install Subsystem Protective Covers Tube stand covers. Table cover. Wall stand covers.

10

System Checks

People Required: 1

Minutes to Complete: 30

11

Attach Warning Labels and Rating Plates

People Required: 1

Minutes to Complete: 15

Attach all the warning labels and detent marks. If your country requires the product rating plate to be in the language of that country, follow the instructions on document #45474336. Paste the appropriate language label over the English rating plate.

12

Cleanup Site

People Required: 1

Minutes to Complete: 20

Remove and dispose of shipping materials and tools properly. 13

Customer Turnover

People Required: 1

Complete & Return Product (i.e; Locator) Cards. Perform general house keeping tasks and turn system over to user.

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Section 1.0 - System Installation Guide

Minutes to Complete: 10

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AEC calibration.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 14

Complete Installation Checklist

(Continued) People Required: 1

Minutes to Complete: 10

Field Engineer to fill out installation checklist at completion of installation.

Lead is used in this system to provide required radiation shielding, such as in tube, collimator, please pay attention and do not touch it directly.

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Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 2.0 Installation Checklist Pre-Installation Checklist Delivery Date:

Sales Person:

Customer:

FDO No.:

Room #

Equipment: Physical Requirements of Site

Completed

1.) Room size adequate for intended equipment configuration? 2.) Floor is strong enough for intended equipment and mounting methods approved? 3.) Delivery route accommodates all intended equipment? 4.) Radiation physicist consulted? 5.) Necessary alterations made to circumvent obstructions? 6.) Modifications to room finished? [email protected]

7.) Supports, platforms materials been provided? 8.) Support structures installed for floor and wall mounted equipment? 9.) Has floor been modified for cable ducts? 10.) Electrical service in place – at the ratings specified in pre-installation documentation? 11.) Power available to operate power tools? 12.) All non-electrical lines (air, water, oxygen, vacuum) installed? Interconnections

Completed

1.) Signal cable, power and grounding plans produced? 2.) Necessary interconnection hardware, such as junction boxes, conduit or raceways, and fittings provided? 3.) Interconnection hardware installed? 4.) Flexible, stranded wire provided for System input power connection? 5.) System “feeder” power cables pulled and sufficient length available at disconnect box for connections? 6.) Interconnecting cables continuity checked, and labeled? 7.) All high voltage cable lengths verified? 8.) Interface information available for equipment?

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Section 2.0 - Installation Checklist

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 General

Completed

1.) Walls and floor clear of all obstructions? 2.) Walls finished? 3.) Finished floor installed? 4.) Room lights installed? 5.) Dust-creating work completed? 6.) Old equipment within room removed? 7.) Component positions clearly marked on floor? 8.) Space available to store equipment? 9.) Lock on door, or locked room available? 10.) Have all fire/safety inspections for occupancy been completed? 11.) Send completed checklist to the GE Healthcare installation team.

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Comments:

Inspection Date(s):

Installation Project Manager Signature

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Installation Checklist Purpose:

Installation checklist to confirm that all critical installation steps have been completed.

Item # 1.)

Item

Sign Off

Power and ground cables connected and tightened: Power cables (how many?, where?) Ground cables (how many?, where?) All signal cables connected and tightened.

3.)

Cable shield clamps installed and tightened (how many?, where?).

4.)

All mounting bolts installed and tightened (floor and wall).

5.)

Control room cables properly dressed.

6.)

All covers installed.

7.)

Room cleaned.

8.)

Product locator cards collected.

9.)

Missing components and/or options:

10.)

List of any installation drawing deviations (all deviations should be signed by customer and reviewed by the installation specialist).

11.)

Packing materials disposed of.

12.)

Dollies and crates returned: Positioner table / Standard Wall Stand dolly

13.)

Have all calibrations been completed?

14.)

Have purchased options been installed/enabled/configured?

15.)

All appropriate regulatory labels installed: X-ray tube focal spot Warning labels Rating plates

16.)

InSite checkout completed?

17.)

Have functional checks been completed?

18.)

Are all covers installed?

19.)

Have all protective tape/coverings been removed?

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Section 2.0 - Installation Checklist

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2.)

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Item #

Item

20.)

Are there any cosmetic issues?

21.)

Are there any system issues?

22.)

Are there any functional limitations?

23.)

Has system documentation (paper and CDROM) been given to the customer?

24.)

Has local physics inspection been completed. Some states/sites may not allow use of system for patients until this is done.

25.)

Has backup of pristine system been performed? (Patient Data Base as well as total system backup)

26.)

Has Field Engineer completed all checklists:

Sign Off

Pre-Installation Installation checklist

Field Engineer Signature:

____________________________________ [email protected]

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 3.0 Before You Begin Check all the crates appearances, preventive collision labels and preventive tilting labels. If the center of the preventive collision label is GREEN, it means the system is OK without any collision during shippment. If the center of the preventive collision label is RED, it means the system is not OK with collision during shippment. Please open the crates to check system carefully.

Green

Red

Figure 2-1 Preventive Collision Label

If the center of the preventive tilting label is RED, it means the system is not OK with tilting during shippment. Please open the crates to check system carefully.

Green

Red

Figure 2-2 Preventive Tilting Label

Page 48

Section 3.0 - Before You Begin

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If the center of the preventive tilting label is GREEN, it means the system is OK without any tilting during shippment.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 4.0 Integrated Table 4.1

Radiography Table

4.1.1

Unpacking and Positioning Be careful of injured by the nails.

Note:



Do not discard any packing materials such as envelopes, boxes, bags until all parts are accounted for against the packing list.



Check the mechanical conditions and external appearances of all parts for possible damages or missing items.



The distribution center or factory must be notified immediately of any damage or shortage of parts.

Unpacking OPEN ME FIRST box (Pink Box) in Crate #1 at first. Take out the Documents: Pre-Installation Manual (5275600-100), Service Manual (5275601-100), Operator Manual (5275602-100), and Quick Start (5275603-100). Read Pre-Installation Manual and Service Manual carefully before system installation and calibration. [email protected]

Figure 2-3 OPEN ME FIRST 1.) Loosen the 12 fibulaes on the side of shipping container.

Figure 2-4 Loosen Fibulaes Chapter 2 - Physical Installation

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Note:

To remove the side shipping container successfully, fix the fibulaes after loosen them.

2.) Remove the side shipping container, and table top is bound on it. See Figure 2-5. Side Shipping Container with Table Top

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Figure 2-5 Table Crate with Side Removed 3.) Loosen the remaining fibulaes, and remove the top and other sides of shipping containers together. See Figure 2-6 and Figure 2-7.

Figure 2-6 Loosen Remaining Fibulaes

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Section 4.0 - Integrated Table

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-7 Remove Crate Top and Sides 4.) Remove the protective covering.

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Figure 2-8 Remove the Protective Covering 5.) Take out all the boxes from the crate.

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-9 Take Out All the Boxes 6.) Unpack the ramps and dolly.

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Figure 2-10 Unpack Ramps and Dolly 7.) Place the ramps.

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Section 4.0 - Integrated Table

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Ramps

Figure 2-11 Place Ramps 8.) Install the dolly to the table. [email protected]

Figure 2-12 Install Dolly to Table 9.) Demount the two fixed screws, and remove the table front cover. Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-13 Remove Table Front Cover 10.) Demount the four bolts which fixed the table to the crate base.

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Figure 2-14 Demount Table Fixed Bolts_Front

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Section 4.0 - Integrated Table

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Figure 2-15 Demount Table Fixed Bolts_Rear 11.) Adjust caster bolts to lower the casters down the table base level. See Figure 2-16.

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Figure 2-16 Lower Casters 12.) Pull the table down the ramp and to the field. DO NOT put your feet under the table base. Be careful of being injured by integrated table because of the heavy weight.

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-17 Pull Table Down the Ramps

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Figure 2-18 Pull Table to Field 13.) Unpack the table top, and take it into the field.

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Section 4.0 - Integrated Table

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-19 Cut Belts

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Figure 2-20 Remove Protective Covering

Figure 2-21 Take to Field

4.1.2

Installation 1.) Refer to the room layout in Pre-Installation Manual (5275600-100), confirm the location of the table with the operator, make marks and move the table away. 2.) Drill four holes at the marks, and then clean the holes of all dust and chips. Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Note:

Please use  10 drill.

Figure 2-22 Drill Holes 3.) Move the table, let the mounting holes on the table align the holes in the floor, and adjust caster bolts to upper the casters above the table base level.

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Figure 2-23 Upper Casters 4.) Demount the casters. 5.) Insert the supplied four M10 anchors and washers, and hammer the anchors into the holes. 6.) Level the table base as necessary with shims, and place the shims close to the anchors.

Figure 2-24 Table Base Level Page 58

Section 4.0 - Integrated Table

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 7.) Tighten the anchors to fix the table to the floor.

8.) Demount the three table stop plates (RED color) in the table frame.

Figure 2-25 Demount Table Stop Plates 9.) Take out all the cables inside the tube stand rail, and route the cables. Note:

Suggest to route the cables from the table food end.

Table Head End

Figure 2-26 Route Cables 10.) Demount the cabinet tray with two screws each side and pull it out. Be careful! DO NOT damage the cables.

Chapter 2 - Physical Installation

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Table Foot End

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-27 Demount Cabinet Tray Note:

Pull the center of the foot pedal. [email protected]

Pull Here Figure 2-28 Pull Out Cabinet Tray 11.) Demount generator cover with four screws and PDU cover with two screws, and put them aside.

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Section 4.0 - Integrated Table

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-29 Demount Covers

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Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

4.2 4.2.1

Tube Stand Unpacking Be careful of injured by the nails. •

Do not discard any packing materials such as envelopes, boxes, bags until all parts are accounted for against the packing list.



Check the mechanical conditions and external appearances of all parts for possible damages or missing items.



The distribution center or factory must be notified immediately of any damage or shortage of parts.

1.) Loosen all the 6 fibulaes, and remove the top and sides of shipping containers together. See Figure 2-30.

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Figure 2-30 Loosen Fibulaes and Remove Crate

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Section 4.0 - Integrated Table

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 2.) Take out the covers. 3.) Remove the two fixed plates with two bolts each.

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Figure 2-31 Remove Fixed Plates 4.) Remove the protective covering.

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-32 Remove Protective Covering

4.2.2

Installation 1.) Demount the rubber bumper and leveling bolt on one side of the tube stand rail. Suggest to install the tube stand from the table head end (if the cables are routed from the table food end).

Table Head End

2.) Raise the tube stand.

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Section 4.0 - Integrated Table

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Note:

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Figure 2-33 Raise the Tube Stand 3.) Slide the tube stand into the rail.

Figure 2-34 Install the Tube Stand 4.) Install the rubber bumper and screw back. 5.) Demount the RED counterweight lock screw on the back of tube stand.

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-35 Demount Lock Screw 6.) Demount tube stand back cover, connect the tube stand cables (TM1-XS105 cable 5193103, No1 cable 5197244, and Grouding cables 5193106 / 5193107), and remount the back cover. Part No.

Part Name

5193103

TM1-XS105 Cable

END1 Label XP105

From

END2 label

5197244’s XS105

To Table TM1 1

TM1-2

Table TM1 2

TM1-3

Table TM1 3

TM1-4

Table TM1 4

XS106

5220569’s XP106

5139106

Table Grounding Cable 2

PE1

PE1

PE2

PE2

5193107

Table Grounding Cable 3

PE2

PE2

PE3

PE3

5139106/5139107

5139103 - XP105

5139103 - XS106

Figure 2-36 Connect Tube Stand Cables

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Section 4.0 - Integrated Table

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TM1-1

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-37 Mount Back Cover 7.) Mount the cable routing plate to the tube stand.

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Figure 2-38 Cable Routing in Plate Note:

DO NOT twist the cables when mounting the plate.

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-39 Mount Cable Routing Plate 8.) Press the tube arm to the appropriate position that are easy to install the tube and collimator, and insert the carriage fixed bolt again to fix the carriage.

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Figure 2-40 Fix the Carriage

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4.3

X-Ray Tube Note:

For tube instruction, refer to related contents contained in the related specifications. Check calibration due date of Torque wrench and shelf-life of Loctite before usage. In order to ensure to meet the security needs, apply Loctite 242(or 243) to the three screws and tighten these 3 screws to 24 N-m (17.7 lbs-ft) with the torque wrench is the step must be performed, while installation and FRU replace. 1.) Loosen the three bolts on the tube arm, put the tube forks into the tube stand arm. 2.) Apply Loctite 242(or 243) to the three screws assembling the tube fork with tube stand arm 3.) Tighten these three bolts to 24 N-m (17.7 lbs-ft) with the torque wrench 4.) Mount the cable supporting plate

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Figure 2-41 Install Tube Fork and Supporting Plate Note:

Insert the tube fork by referring to the mark.

Figure 2-42 Mark 5.) Loosen the four screws of the upper clamp of tube fork, and remove the upper clamp of tube fork. To prevent the clamps from any impact. In case impact occurred, it should be verified that the clamp has enough strength before installation.

Chapter 2 - Physical Installation

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Upper Clamps

Lower Clamps

6.) Take out X-ray tube from the box. 7.) Put the X-ray tube on the lower support of tube fork. Notice the tube installation direction. If the direction is wrong, the tube focal spot will be inaccurate, and the tube may be falling down if the clamps are loose. Hold the tube to prevent it falling down. Check calibration due date of Torque wrench and shelf-life of Loctite before usage. In order to ensure to meet the security needs, apply Loctite 242(or 243) to the screws and tighten screws to 9.9 N-m (7.3 lbs-ft) with the torque wrench is the step must be performed, while installation and FRU replace. 8.) Reinstall the upper clamp of the tube fork. a.) Apply Loctite 242(or 243) to the four screws assembling the upper clamp with lower support before mounting. b.) Tighten these four screws to 9.9 N-m (7.3 lbs-ft) with the torque wrench. Note:

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After installation of the tube, balance the tube arm again.

Section 4.0 - Integrated Table

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Figure 2-43 Remove Upper Clamps

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Figure 2-44 Install X-ray Tube 9.) Adjust the tube to align the RED indication label with 0 degree, and lock the tube.

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Locks Figure 2-45 Tighten the Tube 10.) Rotate the tube 180 degrees.

Figure 2-46 Rotate Tube 180 Degrees

Chapter 2 - Physical Installation

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4.4

Control Box and Collimator Control Box Handle

Control Box Cover

Spacer Collimator 1.) Demount the two stop plates and take out the collimator flange.

Stop Plates [email protected]

Collimator Flange

Figure 2-47 Demount Stop Plates and Take Out Flange

Suggest to demount the two stop plates totally, but NOT only loosen them. Or the stop plates will crash the glass window during collimator installation.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Glass Window

Figure 2-48 Wrong Way

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Figure 2-49 Correct Way 2.) Demount the four mounting screws on the tube.

Figure 2-50 Demount Mounting Screws

Chapter 2 - Physical Installation

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Check calibration due date of Torque wrench and shelf-life of Loctite before usage. In order to ensure to meet the security needs, apply Loctite 242(or 243) to the screws and tighten bolts to 9.9 N-m (7.3 lbs-ft) with the torque wrench is the step must be performed, while installation and FRU replace. 3.) Put the spacer and control box handle between the collimator flange and the tube, apply Loctite 242 (or 243) to the four screws, tighten to 9.9 N-m (7.3lbs-ft) with the torque wrench. Note:

Please install the collimator flange according to the marks on the x-ray tube.

Figure 2-51 Mark

Drop into the hole

Collimator Flange

Spacer

Control Handle

Figure 2-52 Mount Control Box Handle

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Section 4.0 - Integrated Table

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Daub to the screw thread

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Check calibration due date of Torque wrench and shelf-life of Loctite before usage. In order to ensure to meet the security needs, The Loctite 242(or 243) to the bolts and tighten bolts to 9.9 N-m (7.3 lbs-ft) with the torque wrench is the step must be performed, while installation and FRU replace. 4.) Mount collimator onto the collimator adapter using the two stop plates, apply Loctite 242 (or 243) to the four screws, tighten to 9.9 N-m (7.3lbs-ft) with the torque wrench.

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Figure 2-53 Mount Collimator 5.) Rotate tube back.

Figure 2-54 Rotate Tube Back 6.) Route the cable through cable supporting bracket to the tube side. Note:

DO NOT fix the cables on supporting bracket or plate before the cable connections on tube side. 7.) Prior to the connection of the high-voltage cables, remove the old silicone compound on the plug surfaces with clean dry cloth and check to verify there are as cracks, flaws, or traces of creeping discharge on the surfaces.

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Note:

When the traces of creeping discharge are found, be sure to replace the defective parts. Grinding off the traces only will not be effective. 8.) Coat the tip of the cable plugs with the silicone compound about five to seven grams, that is, to the extent the tip is hidden under the heaped up compound. At this time, the side of the cable plug should be greased.

Figure 2-55 Coating with Silicone Compound

10.) Connect the anode and cathode HV cables (2269002-5) to the X-ray tube. HV Cable Socket

HV Cable

+ (ANODE)

+

- (CATHODE)

-

Check the polarity of HV cables carefully, and DO NOT connect the two HV cables reversely. Connect the HV cables in the correct polarity with sufficient care not to produce clearance between the cable plug flange and the cable socket at the insertion of the plugs. Presence of such clearance or incomplete silicone compound coating will cause creeping discharge and normal operation of tube will be disturbed.

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Section 4.0 - Integrated Table

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9.) Remove the cap covered the socket of the tube housing and wipe the inside softly with a clean dry cloth. DO NOT use any chlorinated solvents to clean any parts.

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Figure 2-56 Inserting Cable Plug 11.) Tighten the high-voltage cables solidly to the sockets of the tube housing by the threaded cable flange. 12.) Demount the tube cover on Anode side. [email protected]

Figure 2-57 Demount Tube Cover 13.) Connect the anode rotation cable (5195936). Note:

Fix the cable with clamp.

Chapter 2 - Physical Installation

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Figure 2-58 Anode Rotation Cable Conections HV Tank

Color

1

C

White

2

M

Black

3

A

Red

SW

SW

Brown

SW

SW

Yellow

E

E

Green

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Tube

14.) Remount the tube cover.

Figure 2-59 Remount Tube Cover 15.) Connect the control box cables to the connecting plate, fix the plate onto control box, ty-rap the cables and fix with a cupule, and mount the control box cover. Part No. 5197242

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Part Name MC7 Cable

END1 Label XP102

From Tube Fork 5197245's XS102

Section 4.0 - Integrated Table

END2 Label

To

MC7+

MC7+

MC7-

MC7-

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Part No. 5197244

5193107

Part Name

END1 Label

No1 Cable

Table Grounding Cable 3

From

END2 Label

To

XS105

5197103's XP105

XP104

Collimator 5135895-1's XS104

XS101

5193101's XP101

XP103

Control Box 5197245's XS103

PE2

PE2

PE3

PE3

5193107 5197244-E

XS103 XP103 5197244

5135895-1 XS104 XP104 5197244 5197242

XP102 XS102 5197245

Figure 2-60 Connect Control Box Cables

Chapter 2 - Physical Installation

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[email protected]

5197245

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 a. Loosen the handles.

b. Install the control box cover.

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c. Tighten the handles. Figure 2-61 Install Control Box Cover 16.) Install the cable supporting plate, route and ty-rap the cables, and fix them onto the plate. Be careful of the cable moving range, and make sure the cable will not be damaged during tube movement.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Fix

Supporting Plate Figure 2-62 Fix Cables onto Supporting Plate 17.) Mount the cable supporting bracket onto the back of the tube stand, put the cables onto the supporting bracket, but DO NOT fix the cables.

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Figure 2-63 Mount Cable Supporting Bracket 18.) Connect the No1 cable (5197244). Part No. 5197244

5193101

Part Name No1 Cable

MC6 Cable

END1 Label

From

END2 Label

To

XS105

5197103's XP105

XP104

Collimator 5135895-1's XS104

XS101

5193101's XP101

XP103

Control Box 5197245's XS103

MC6

MC6

XP101

5197244’s XS101

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5193101 XP101 XS101 5197244

DO NOT FIX

19.) Fix the cables.

4.5

Counterweight Adjust the counterweight by adding or removing couterweight blocks until the up/down operation force is balanced.

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Section 4.0 - Integrated Table

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Figure 2-64 Connect No1 Cable

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Figure 2-65 Adjust Counterweight

4.6

Cassette Tray For the systems which used advanced Integrated Table, the Cassette was installed before and you can jump to the next step directly. Unpack and take out the cassette tray, slide it into the table, and connect the cassette tray grounding cable.

Figure 2-66 Insert Cassette Tray

Chapter 2 - Physical Installation

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[email protected]

Note:

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Figure 2-67 Connect Cassette Tray Grounding Cable

4.7

Ion Chamber and Grid (Optional) DO NOT put anything onto the ion chamber or grid. And pay attention to the Ion Chamber and Grid's orientation. Note:

The fixers installation method is different with different options.

[email protected]

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Section 4.0 - Integrated Table

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

4.7.1

Install both Ion Chamber and Grid for system with standard Integrated table 1.) Demount the cassette tray side cover and two of the four fixers, and loosen the other two.

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Limit Position

Fixer

Cassette Tray Side Cover

Figure 2-68 Demount the Cover and Fixers 2.) Install the ion chamber and grid, connect table ion chamber (5167409) and 4 m cable (5166493), and install the cassette tray side cover back.

Chapter 2 - Physical Installation

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Block is in the lower place

Note: Cassette Tray handle direction.

Grid

Note: Ion Chamber direction. Ion Chamber

Cassette Tray Side Cover

Connect to JEDI

Cable Routing 5166493

Figure 2-69 Install Ion Chamber and Grid

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Section 4.0 - Integrated Table

[email protected]

Cable Routing 5167409

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

AEC1

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Figure 2-70 Table Ion Chamber to JEDI

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

4.7.2

Install the Grid Only for system with standard Integrated table 1.) Demount the four fixers.

Fixer

Figure 2-71 Demount the Fixers 2.) Install the grid.

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Section 4.0 - Integrated Table

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Limit Position

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Block is in the upper place

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Figure 2-72 Install Grid

4.7.3

Install the Ion Chamber and Grid for system with advanced Integrated table For the system with advanced integrated table, the grid was oscillate grid. The installatation should be done as steps below:

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 1.) Remove the cover A by remove the five screws as fig 2-73 shown.

screw used to Cover A mount the cover

2.) Loosen the four screws marked with circle in Fig 2-74 which were used to tighten the ion chamber.

the four screws used to tighten the ion chamber. The ion chamber was used to help to show the screw’s position.

Figure 2-74 Loosen the four screws 3.) Insert the ionion chamber to the holder as Fig 2-75 shown. Please be care for the orientation

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Section 4.0 - Integrated Table

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Figure 2-73 Remove the cover A

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 of the grid.

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Figure 2-75 Insert the ion Chamber to the holder 4.) Adjust the position of the ion chamber as these steps: 1.) Make the rod perpendicular.

Make the rod perpendicular

Figure 2-76 Make the rod perpendicular 2.) Use the cover A dismounted before as ruler to mark the center of the rectangle used to hold the grid, then adjust the position of ion chamber to make the center of the ion

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

chamber superpose with the center line marked by the cover A. See fig 2-77.

Superpose the center of ion chamber and the center of the rectangle.

Figure 2-77 Superpose the center of ion chamber and the center of the rectangle

5.) Route the ion chamber cable as Fig 2-78 shown.

Figure 2-78 Route the ion chamber cable as Fig 2-78 arrow shown

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Section 4.0 - Integrated Table

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3.) Tighten the four screws removed in step 2 as Fig 2-74 shown.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 6.) Connect the ion chamber cable as Fig 2-79 circle shown.

Figure 2-79 Connect the ion chamber cable 7.) Insert the cable connections into the holder and mount the cover A.

Figure 2-80 Install the grid

Chapter 2 - Physical Installation

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8.) Put the grid on the ion chamber surface with their center superposed as Fig 2-80 shown. Note the orientation of the grid.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 9.) Fix the grid with four fixers.

Fixer

Figure 2-81 Fix the grid with four fixers

4.8

Electrical Connections

1.) Connect and route System Power Cable (hospital provide).

Figure 2-82 Connect and Route System Power Cable 2.) Connect and Xray-on Light (pin 4, 6) and Room Door interlock (pin 1, 2) Cables (hospital Page 94

Section 4.0 - Integrated Table

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For details, please refer to Chapter 10 - Schematics, Chapter 11 - MIS Chart, and Pre-Installation Manual (5275600-100).

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

provide). For details, please refer to Room Power Supply in Chapter 4 of Pre-Installation Manual (5275600-100).

9 8 7 6 5 4 3 2 1

3.) If wall stand ion chamber is ordered, connect and route the ion chamber 24 m cable (5166654) and grounding cable (5193110) to JEDI.

Chapter 2 - Physical Installation

Page 95

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Figure 2-83 Connect Xray-on light and Room Door interlock Cables

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Service Laptop

System Console

AEC1 - Table AEC2 - Standard Wall Stand

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Figure 2-84 Wall Stand Ion Chamber Cables

Cable Routing 5166654/5193110

Connect to Wall Stand Ion chamber Figure 2-85 Cable Routing

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Section 4.0 - Integrated Table

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

4.9

Install Cabinet Tray 1.) Install generator and PDU covers, and push cabinet tray to under the table.

Push Here

Figure 2-86 Install Generator and PDU Covers [email protected]

2.) Fix the cabinet tray to the table base with two screws.

Figure 2-87 Install Cabinet Tray

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

4.10

Table Top Installation and Leveling 1.) Demount the stopper on one side of the table top, slide the table top onto the table base, and remount the stopper.

2.) Check the table top leveling. If it is not level, loosen the mounting anchors, and adjust the leveling bolts, then fix them with washers.

Figure 2-89 Adjust Leveling Bolts

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Section 4.0 - Integrated Table

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Figure 2-88 Install the Table Top

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 5.0 System Console Route the console cables to the control room.

5.1

Without Console Stand Connect and ty-rap the console cables. Position the system console to the location where the operator can observe the patients conveniently.

Figure 2-90 Console Cable Connections Part Name

System Console

The Other End

5184620

Handswitch

J1

Handswitch

J2

Service Laptop

5194292/5241079 RS232 Service Cable / ISP Download Cable

5.2

5183903

Console Power Cable

J3

PDU - TM3

5182354

JEDI Generator Communication Cable

J4

PDU - J1

With Console Stand 1.) Assemble the console onto the console stand, and demount the rear cover.

Figure 2-91 Console Installation Chapter 2 - Physical Installation

Page 99

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Part No.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 2.) Connect and ty-rap the console cables.

Figure 2-92 Console Cable Connections Part No.

Part Name

System Console

The Other End

5184620

Handswitch

J1

Handswitch

J2

Service Laptop

5194292/5241079 RS232 Service Cable / ISP Download Cable Console Power Cable

J3

PDU - TM3

5182354

JEDI Generator Communication Cable

J4

PDU - J1

3.) Demount console stand bottom cover with two screws. Confirm the location of the console with the operator, make marks and move the console away.

Figure 2-93 Demount Bottom Cover 4.) Drill two holes at the marks, and then clean the holes of all dust and chips. Note:

Please use  7 drill. 5.) Move the console, and let the mounting holes on the console foot panel align the holes in the floor. 6.) Insert the supplied two M6 anchors and washers, and hammer the anchors into the holes. 7.) Tighten the anchors. 8.) Mount the bottom cover back.

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Section 5.0 - System Console

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5183903

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 6.0 Collimator Alignment 1.) Power up the system. Check LEDs status. Refer to Chapter 4 - Functional Checks - 3.1 System Power Up. 2.) Move the tube to the lowest position above the table top, open collimator light, confirm the center of the light field projected by the collimator with an article, such as a screw.

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Figure 2-94 Lowest SID 3.) Move the tube up to the highest position.

Figure 2-95 Highest SID 4.) Make sure the bias of the center is less than 3 mm, and make sure the collimator beam can align the center point of the cassette tray handle.

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Bias in less than 3 mm

Collimator beam

Handle Center Figure 2-96 Collimator Beam Align Cassette Tray Handle Center Point 5.) If the requirements above cannot be met, adjust the three screws on the tube fork to align the collimator.

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Figure 2-97 Align Collimator

Section 7.0DAP Meter Installation Note:

Do not touch the active area of the ionization chamber (1) with bared finger. It may degrade the light transparency of the DAP meter.

Figure 2-98 DAP Meter Procedures: Page 102

Section 7.0 - DAP Meter Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Note:

Fix the cable inside the tube cover for the system which does not include the DAP meter. 1.) Installing the Chamber in the X-ray Unit Slide the chamber into the middle level of accessory rails of the collimator till the detent is reached.

Figure 2-99 Insert DAP Meter into the middle level of the collimator rail 2.) Connect the Chamber with system The back side of the DAP meter includes a short cable with a round plastic plug connector (ODU: MediSnap, 4-pin). This includes the connections for the power supply. Note:

Please be aware that the connector cable from tube stand side is only for the use of connecting the DAP meter. [email protected]

Figure 2-100 Connect the DAP Meter to the 24V Power Supply 3.) Connect the other end of the connector to the 24V power supply of the PDU. Connection diagram as below:

TURN OFF THE POWER BEFORE CONNECT/DISCONNECT THE CHAMBERDo not connect/disconnect the chamber to/from the system when the power is turned on. It may damage the electronics. Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

DO NOT PUT THE ADDITIONAL FILTER ABOVE THE CHAMBER Do not put any filtration between chamber and the patient in the exam. It may cause the wrong indication of DAP value. 4.) Switching the device on/ DAP meter ready for using After DAP meter is well mounted to collimator and connected to system power supply, the meter is switched on when system is powered on. The display unit responds with a brief signal tone and the following labels: VACUDAP Vx.xx 11111111 22222222 : WAITING 0.00 The firmware version (Vx.xx) of the display unit is output first. The Power-On test in the measuring chamber is then started and a display test is executed simultaneously. The display unit waits for the result of the TEST function when the WAITING label is displayed. After the successful conclusion of the power-on test, the meter is either in the Measuring function or an error message is output. The measuring readiness is displayed by the measured value zero (display: 0.00 or 0.0). [email protected]

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Section 7.0 - DAP Meter Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 8.0 Standard Wall Stand 8.1

Unpacking Be careful of injured by the nails. •

Do not discard any packing materials such as envelopes, boxes, bags until all parts are accounted for against the packing list.



Check the mechanical conditions and external appearances of all parts for possible damages or missing items.



The distribution center or factory must be notified immediately of any damage or shortage of parts.

1.) Loosen all the 6 fibulaes, and remove the top and sides of shipping containers together. See Figure 2-101.

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Figure 2-101 Loosen Fibulaes and Remove Crate

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 2.) Take out the covers. 3.) Remove the two fixed plates with two bolts each.

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Figure 2-102 Remove Fixed Plates 4.) Remove the protective covering.

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Section 8.0 - Standard Wall Stand

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-103 Remove Protective Covering 5.) Raise the wall stand. [email protected]

Be careful of being injured by wall stand because of the heavy weight.

Figure 2-104 Raise Wall Stand

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 6.) Install dolly (5241044).

Rear

Front

Figure 2-105 Dolly 7.) Adjust caster bolts to lower the casters down the wall stand base level. See Figure 2-106. Pull wall stand into the field.

Rear

Figure 2-106 Lower Casters

8.2

Installation 1.) Refer to the room layout in Pre-Installation Manual (5275600-100), and confirm the location of the wall stand with the operator. Move wall stand and its template to the location, adjust caster

Page 108

Section 8.0 - Standard Wall Stand

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Front

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

bolts to upper the casters above the wall stand base level, and let wall stand stand on the template. 2.) Demount the casters. 3.) Adjust the four leveling bolts to level the wall stand top frame and front panel in longitudinal level and vertical level.

Figure 2-107 Wall Stand Leveling 4.) Rotate the tube facing to the wall stand front panel. [email protected]

Figure 2-108 Rotate Tube 5.) Open the collimator light, move the tube from SID 1.5 m to 1.8 m, and make sure that the bias between the cross hair projected by the collimator and the cross hair in the wall stand front panel is less than 3 mm in two orthogonal directions. Note:

When the collimator blades are closed to one line, it should be overlapped with the wall stand cross hair. Measure the rectangle’s length and width at 1.5 SID and 1.8 SID to make sure the bias is less than 3 mm.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-109 SID 1.5 m ~ 1.8 m

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Figure 2-110 Alignment 6.) If the requirements above cannot be met, adjust wall stand location or the four leveling bolts. 7.) Drill two holes through the two holes on wall stand base, and clean holes of all dust and chips. Note:

Please use  10 drill. 8.) Insert the supplied two M10 anchors and washers, and hammer the anchors into the holes. 9.) Tighten the anchors to fix the wall stand to the floor.

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Section 8.0 - Standard Wall Stand

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-111 Fix the Wall Stand

8.3

Cassette Tray Unpack and take out the cassette tray, and slide it into the wall stand.

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Figure 2-112 Insert Cassette Tray

8.4

Ion Chamber and Grid (Optional) Note:

The fixers installation method is different with different options. For details, please refer to section 4.7 Ion Chamber and Grid (Optional) in table installation.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

8.4.1

Install both Ion Chamber and Grid for standard wall stand 1.) Demount the wall stand front panel.

Figure 2-113 Demount Front Panel 2.) Install ion chamber and grid. Note: Note:

The side of grid marked as "tube side" should be on the tube side. During the installation of grid, be careful not colliding the Ion chamber cable connection. If 40 line grid is ordered, use the wide edge of the fixers. [email protected]

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Section 8.0 - Standard Wall Stand

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Note:

If 60 line or 78 line grid is ordered, use the wide edge of the fixers to the bottom and narrow edge to the top.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 3.) Connect and route the wall stand ion chamber cable.

Cable Routing

From JEDI Figure 2-114 Routing Ion Chamber Cables Note:

Ion Chamber direction.

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Cable Routing

From back of Wall Stand

Ion Chamber Cable Connection (5167409/5166654) Ion Chamber Grounding Cable (5193110) Figure 2-115 Connect Ion Chamber Cables 4.) Remount the front panel.

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Section 8.0 - Standard Wall Stand

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

8.4.2

Install the Grid Only for standard wall stand 1.) Demount the wall stand front panel. 2.) Install the grid.

Note:

The side marked as "tube side" should be on the tube side. If 40 line grid is ordered, use the wide edge of the fixers.

Note:

If 60 line or 78 line grid is ordered, use the wide edge of the fixers to the bottom and narrow edge to the top.

3.) Remount the front panel.

Chapter 2 - Physical Installation

Page 115

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Note:

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

8.4.3

Install both Ion chamber and grid 1.) Demount the wall stand front panel 2.) Demount the cassette holder with the four screws marked with circle as the Fig below shown.

four screws fix the cassette holder

3.) Pull the the cassette holder out carefully and put it standing on ground. 4.) Demount the top cover of the cassette holder.

Figure 2-117 Remove the top cover of cassette holder

Page 116

Section 8.0 - Standard Wall Stand

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Figure 2-116 Demount the cassette holder

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 5.) Loosen the four screws used to fix the ion chamber.

Loosen the four screws used to fix the ion chamber.

Figure 2-118 Loosen the four screws used to fix the ion chamber 6.) Demount the cover at the bottom of the front surface of the cassette holder. 7.) Insert the ion chamber in from the right side of the cassette hold at the orientation as the fig shown below and route the cable according to the path the arrown shown.

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Figure 2-119 Insert the ion chamber into the cassette holder and route the ion chamber cable according to the path the arrow shown 8.) Lie down the cassette holder. 9.) Adjust the position of ion chamber to make sure that its center can superpose the center of FOV as these steps:

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 1.) Make the rod perpendicular.

Make the rod perpendicular

Figure 2-120 Make the rod perpendicular 2.) There is a screw hole on the center of the top side and bottom side of the rectangle used to hold grid. Suppose the line across the two hole point was the FOV center and we can use the cover dismounted at step 6 as a ruler to mark the line. Adjust the position of ion chamber to make its center superpose the FOV’s center. [email protected]

the two screw holes can used to mark the FOV’s center line

Figure 2-121 Make the center of ion chamber superpose the FOV’s center 10.) Tighten the four screws loosened at step 5 as Fig 2-115 to fix the ion chamber. 11.) Remount the top cover of the cassette holder. 12.) Remount the cassette holder to wall stand.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

13.) Connect the Ion chamber cable and ground cable as below Fig shown.

Connect the ground cable here

Connect the ion chamber cable here

[email protected]

Figure 2-122 Connect the Ion chamber cable and ground cable 14.) Remount the cover at the bottom of the front surface of the cassette holder. 15.) Remount the wall stand front panel.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

8.5

Counterweight Note:

Load a cassette onto cassette tray before adjust the counterweight. Adjust the counterweight by adding or removing couterweight blocks until the up/down operation force is balanced.

[email protected]

Figure 2-123 Adjust Counterweight

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Section 8.0 - Standard Wall Stand

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 9.0 Final Cover Installation After system configuration and calibration, ty-rap all the cables, and install the protective covers.

9.1

Install Standard Tube Stand Covers

3 1 2 [email protected]

Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 1.) Loosen the screw on the tube arm protective cover.

Figure 2-124 Loosen the Protective Cover 2.) Insert SID ruler through the cover, and install the ruler. [email protected]

Figure 2-125 Install SID Ruler 3.) Install tube stand side covers, and tighten the tube arm protective cover. Note:

Notice the side covers directions. The No1 Cable (5197244) should be routed inside the right side cover.

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Section 9.0 - Final Cover Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-126 Route Cable Inside Right Side Cover

[email protected]

Figure 2-127 Tighten the Screw 4.) Install tube stand top cover.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

9.2

Install Table Front Cover

Figure 2-128 Install Table Front Cover

9.3

Install Standard Wall Stand Covers

2 Figure 2-129 Wall Stand

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Section 9.0 - Final Cover Installation

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1

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 10.0 Labels and Rating Plates Attach English/multilingual labels to overlay the English/Chinese labels attached in factory.

10.1

System Console

Label

Description

References

5194330

System Console Rating Plate

See Figure 2-130

[email protected]

Figure 2-130 5194330, System Console Rating Plate

10.2

Integrated Table

Label

Description

References

5180891

Standard Integrated Table Rating Plate

See Figure 2-131

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-131 Integrated Table Rating Plate

10.3

Cabinet

Description

References

5220653

PDU Rating Plate

See Figure 2-132

Figure 2-132 PDU Rating Plate

10.4

Page 126

Wall Stand

Label

Description

References

5183492

Standard Wall Stand Rating Plate

See Figure 2-133

Section 10.0 - Labels and Rating Plates

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Label

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Figure 2-133 5183492, Wall Stand Rating Plate

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 11.0 Installation Checklist Purpose:

Installation checklist to confirm that all critical installation steps have been completed. Item # 1.)

Item Power and ground cables connected and tightened: •

Power cables (how many, where)



Ground cables (how many, where)

All signal cables connected and tightened.

3.)

Cable shield clamps installed and tightened (how many, where).

4.)

All mounting bolts installed and tightened (floor and wall).

5.)

Mechanical alignments done.

6.)

Control room cables properly dressed.

7.)

All covers installed.

8.)

Room cleaned.

9.)

Product locator cards collected.

10.)

Missing components and/or options:

11.)

List of any installation drawing deviations (all deviations should be signed by customer).

12.)

Packing materials disposed of.

13.)

Dollies and crates returned: Positioner Table / Standard Wall Stand dolly

14.)

Have all calibrations been completed?

15.)

Have the sample images been installed on the system?

16.)

Have purchased options been installed/enabled/configured?

17.)

All appropriate regulatory labels installed: •

X-ray tube focal spot

18.)

HHS testing completed?

19.)

Have functional checks been completed?

20.)

Are all covers installed?

21.)

Have all protective tape/coverings been removed?

Table 2-1 Installation Checklist Section 11.0 - Installation Checklist

[email protected]

2.)



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Sign Off

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Item #

Item

22.)

Are there any cosmetic issues?

23.)

Are there any system issues?

24.)

Are there any functional limitations?

25.)

Has system documentation (paper) been given to the customer?

26.)

Has local physics inspection been completed? (some states/sites may not allow use of system for patients until this is done)

27.)

Has backup of pristine system been performed? (Patient Data Base as well as total system backup)

28.)

Field engineer has completed all checklists: •

Pre-Installation



Installation checklist

Sign Off

Table 2-1 Installation Checklist

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

 XR 6000 SERVICE MANUAL

Section 12.0 Regulatory Tests and Final Steps 12.1

AEC Tests

12.1.1

AEC Maximum MAS

12.1.1.1

Overview At 50kV or more, exposures shall not exceed 600mAs per exposure.

12.1.1.2

Procedure (50kV) 1.) Select 50 kV, AEC (all three areas selected) and an mA that selects 600mAs. 2.) Position the X-ray tube away from the Ion chamber selected, close collimator blades. 3.) Perform an exposure. 4.) Record the selected mAs and actual mAs. After exposure, mAs will be displayed on the LCD screen. Selected mAs ________________ Measured mAs _______________ 5.) Verify that the AEC exposure is less than 600 mAs.

AEC Minimum Exposure Time

12.1.2.1

Overview At 50 kV or more, minimum exposures must be less than 16 msec.or less than the time to deliver 5 mAs, whichever time is greater.

12.1.2.2

Procedure 1.) Align the tube with the image receptor. Lateral Detent ON. Select 50kV, AEC (area 1 selected). 2.) Set the SID to 100 cm. 3.) Remove all phantoms. 4.) Acquire an AEC exposure. 5.) Record the exposure time: Ion Chamber Area 1 _____________ msec Ion Chamber Area 2 _____________ msec Ion Chamber Area 3 _____________ msec 6.) Verify that the exposure time is less than 16 msec, or less than 5 mAs. 7.) Repeat the above procedure for each detector in the system. Record the exposure time: Ion Chamber Area 1 _____________ msec Ion Chamber Area 2 _____________ msec Ion Chamber Area 3 _____________ msec 8.) Verify that the exposure time is less than 16 msec, or less than 5 mAs.

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Section 12.0 - Regulatory Tests and Final Steps

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12.1.2

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

12.1.3

Reproducibility Of Exposure

12.1.3.1

12.1.3.2

Overview •

For any specific combination of selected technique factors, the estimated coefficient of variation (CV) of radiation exposures shall be no greater than 0.05. HHS rejection limit is 0.045.



Test Equipment: Radiation meter with integrate mode, 3.8 cm thickness of Aluminum.

Procedure 1.) Align the tube with the image receptor. Lateral Detent ON. 2.) SID = 100 cm. 3.) For Digital table place 3.8 cm aluminum on the table, center in the collimator light. 4.) Center radiation probe 30 cm above the table top. 5.) Collimate to a field size of 13 cm square. 6.) Select 80 kV, AEC mode and mA such that the exposure will be at least 0.1 second long. 7.) Measure the exposure in mR for each of the 10 exposures. After each exposure, recycle the technique (switch to other values and then return them to the original values). Also vary the time between exposures to record any filament heating variations. Test Results: kV

mA

Time

mR

1

_______

_______

_______

_______

2

_______

_______

_______

_______

3

_______

_______

_______

_______

4

_______

_______

_______

_______

5

_______

_______

_______

_______

6

_______

_______

_______

_______

7

_______

_______

_______

_______

8

_______

_______

_______

_______

9

_______

_______

_______

_______

10

_______

_______

_______

_______

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Exposure #

Coefficient of Variation = ______________ (see formula at the end of this section) 8.) Verify that the coefficient of variation is < 0.045 for AEC exposures. 9.) Repeat the above procedure for each detector on system. Test Results Exposure #

kV

mA

Time

mR

1

_______

_______

_______

_______

2

_______

_______

_______

_______

3

_______

_______

_______

_______

4

_______

_______

_______

_______

5

_______

_______

_______

_______

6

_______

_______

_______

_______

7

_______

_______

_______

_______

8

_______

_______

_______

_______

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 9

_______

_______

_______

_______

10

_______

_______

_______

_______

Coefficient of Variation = ______________ (see formula at the end of this section) 10.) Verify that the coefficient of variation is < 0.045 for AEC exposures.

Calculation for Coefficient of Variation (C.V.): Formula:

C.V. = s / X(avg.)

where s = sample standard deviation (n-1)

Sample standard deviation (s) can be calculated on a calculator with statistics functions (such as the TI36Y) as follows:

12.2

*

Clear the stat register, press (CSR).

*

Enter the first reading and then press (+). Repeat this step for all readings.

*

Press (mean) to get X(avg.).

*

Press sample standard deviation key (n-1).

*

Enter the results in the formula above.

Final Installation and Admin Tasks 2.) Install all covers on system equipment. (Refer to above for procedure.) 3.) Remove trash, remove installation equipment and tools, clean up room and store service manuals. 4.) Fill out Product Locator Cards and return them. Part No.

Page 132

Part Name

5183178

Pioneer console assembly

5180891

Standard integrated table assembly

5183392

Standard integrated tube stand assembly

5189248

Manual collimator

5192454

50kW Tube: Toshiba E7843X

2212259-2

Generator (VR Jedi 50 R1T)

5220653

Platform PDU

5213401

78l 10:1 180cm grid

080-1004

60l 10:1 180cm grid

5198785

40l 10:1 180cm grid

5167409-1

Table ion chamber

5167409-2

Wall stand ion chamber

Section 12.0 - Regulatory Tests and Final Steps

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1.) Ready system for normal customer operation.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Part No. 5176556

Part Name Pioneer system console control board

5.) Record installation time in Service database.

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Chapter 2 - Physical Installation

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 This page is intentionally left blank.

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Section 12.0 - Regulatory Tests and Final Steps

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Chapter 3 - Configuraton & Calibration Section 1.0 Configuration & Calibration List

Section

Content

Page

System Configuration

123

2.2

X-ray Tube Seasoning

124

2.3

Service Software User Guide

139

2.4

Tube Configuration

145

2.5

Receptor Programming

146

2.6

Automated AEC Calibration

151

2.7

CR AEC Calibration

158

2.8

Checksum Validation

160

2.9

Backup and Restore Database Parameters

162

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2.1

Section 2.0 Configuration & Calibration Contents 2.1

System Configuration During the Application screen, press these two buttons for more than 5sec to switch from Application screen to Configuration screen. If system is at configuration screen, press these two buttons to switch from Configuration screen to Application screen. At the configuration screen, operator can configure the Type of Generator, System Power, Table AEC, Wall Stand, Wall Stand AEC. 1.) Configure the Generator Press the Patient View button

to configure that the generator is Jedi or Djinn.

2.) Configure the System Power Press Receptor button

to configure the system power is 50kW.

3.) Configure Table AEC

Chapter 3 - Configuraton & Calibration

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Press the Patient Size button

to configure that system is with Table AEC or not.

4.) Configure Wallstand Press the Focus Spot button

to configure if there is Wall-stand.

5.) Configure the Wall-stand AEC Press the Previous Exp Recall button

to configure if there is Wall-stand AEC.

6.) Configure Dose Display Press this button

2.2

to configure if console will display the Dose or not.

X-Ray Tube Seasoning

NO EXPOSURES SHALL BE ALLOWED WITHOUT TUBE CURRENT AT A TUBE VOLTAGE OF MORE THAN 50KV.

2.2.1

Requirements 1.) Use the larger focal spot of the tube, and the seasoning will be done with the circuit specified in technical data. 2.) The operating tube voltage and current should be monitored all exposures during this seasoning operation. 3.) The anode rotation should be utilized at normal speed (3000 or 3600 min-1). 4.) Do not exceed either the generator or the tube ratings. ALL RADIATION SAFETY RULES MUST BE OBSERVED. IN ORDER TO PROTECT HUMANBODY FROM HARMFUL X-RAY, CLOSE THE COLLIMATOR OR BLOCK THE TUBE ASSEMBLY RADIATION PORT WITH AT LEAST A SIX (6) MM THICK PIECE OF LEAD. NO PATIENT OR PERSONNEL IS ALLOWED IN THE ROOM.

2.2.2

Procedure Effecting exposure at near peak potential and current without prior tube warm up will damage the tube. To maximize tube life, perform the following tube seasoning procedure. 1.) Provide continuous input of small tube current (Approx.1 mA) and increase the tube voltage stepwise according to the time of the Seasoning Schedule at installation (See Figure 3-1).

Page 136

Section 2.0 Configuration & Calibration Contents

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When warming up the tube, always take the precautionary measures to protect personnel from Xray radiation. When a new x-ray tube is put into operation for the first time or when it has not been in operation for more than one month, the seasoning procedures Seasoning Schedule at installation (See Figure 3-1) shall be carried out to assure subsequent trouble-free operation. This procedure establishes the proper relation to its new environment with the equipment in used. The action establishes a favorable distribution of the electrical charges and Electrostatic stresses in the insulation system of the tube and the associated equipment.

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

For any X-ray equipment without the fluoroscopy circuit, perform seasoning of short-time input from 50 kV. 2.) Use the larger focus, rotate the anode, set the tube current to 50% of the maximum permissible tube current at maximum tube voltage, apply short-time input once a minute with exposure time of 0.1s, and increase the tube voltage stepwise. When unstable, states of the tube current are observed in the course of increasing tube voltage, reduce the tube voltage to the extent that no variation occurs, and then increase it more slowly than previously. 3.) Stain like impact traces might appear on the X-ray tube target surface by the slight discharge in the course of the seasoning. The phenomena are one process to recover the withstanding voltage performance at that time, Even if unstable states appear in the course of the seasoning, the stable operation is obtained at the maximum tube voltage of succeeding seasoning, the tube unit can be used without any interference to its electrical performance. (The maximum tube testing voltage must be strictly limited to the maximum rated tube voltage of the tube unit.) 4.) When the X-ray tube unit is used after a dormant period of a week or more, use the tube unit after performing the Seasoning Schedule at Starting (See Figure 3-1). 5.) Every day morning, when you start to use X-ray tube, you are requested to warm-up the tube to your necessary high voltage condition for stabilized equipment operation. a.) At least 80kV (Step 1) is requested for all operation. b.) Need voltage up to your necessary daily voltage (Step 2 or higher step). If discharge happened, re-warm up again under the previous condition.

Steps (condition)

Voltage [kV]

Current [mA]

Focus

Expose Time [sec.]

Cooling Time after Exposure [sec.]

Number of cycle

1

80

160

Large

0.05

20

1

2

100

160

Large

0.05

20

1

3

110

160

Large

0.05

20

1

4

120

160

Large

0.05

20

1

5

over 120 kV (Note 1)

160

Large

0.05

20

1

Note 1: If you use over 120 kV, up voltage by 5 kV to your necessary voltage. 6.) After these seasoning operations are completed, the X-ray tube unit can be used in the usual way.

Chapter 3 - Configuraton & Calibration

Page 137

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c.)

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

 XR 6000 SERVICE MANUAL

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Figure 3-1 Seasoning Schedule

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Section 2.0 Configuration & Calibration Contents

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Note:

2.3 2.3.1

Please press

and

together to get into HUB Mode.

Service Software User Guide Supplies None.

2.3.2

Tools • • •

2.3.3

JEDI service software (the software is a DOS application) Console R232 cable (5194292) Computer with floppy or CD drive

Safety Precautions Not applicable.

2.3.4

Prerequisites Basic knowledge of PC based computer laptop, DOS and usage of Microsoft WINDOWS.

Personnel

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2.3.5

1 person.

2.3.6

Time 15 minutes.

2.3.7

Procedure

2.3.7.1

Loading service software on service laptop The Service software is a DOS application. It can operate under DOS or Windows; but for software download or database backup, it is required to run ASIAN.exe under DOS to avoid communication problem (with the mouse, click on START, SHUTDOWN, RESTART COMPUTER UNDER DOS MODE; see Chapter 9 - - Service Tool Job Cards - Section 1.0 Software Download / Upgrade). To load the software on to the hard drive: • Power ON Service laptop. Under Windows, run the File Manager (Explorer)) • Create a new directory (e.g.: JEDISVC) under C:\ • Insert the "Service Software" CD delivered with the equipment in the Service Tool set into the CD drive. • Copy all the files from the CD to your hard drive. (Double click on A:\, drag and drop on C:\ JEDISVC or whatever name of your directory.) • Double click the file JEDP424B expanding the software to your hard drive. The service software is installed and ready for use.

2.3.7.2

Using service software Connect Service terminal as follows: • Use the 9 pin Service cable, Part No 2207478, to connect serial line of Service terminal to system console. Chapter 3 - Configuraton & Calibration

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 XR 6000 SERVICE MANUAL

• Switch on the Service terminal. • To run the program: Under Windows: Exit Windows. Restart computer in MS-DOS mode. Select Disk Drive from where you want to run the program: C: [enter] Change to the new directory Type: "ASIAN" [enter] to run the program The following screen appears:

Power ON the generator. Press function key F1. The following screen appears:

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• •

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

The software will load the help screen information contained in Asiane .msg file. •

Wait or press space bar to jump to screen. The Application screen will appear: "English text Version 1.2" is displayed 5 sec., then display shows the last used parameters.

2.3.7.3

If the serial line to the generator is not operating (e.g.: cable not correctly connected, I/F or kV Control board down, Generator not ready or powered OFF), further screens will not be displayed and no function keys will operate. Correct this problem before continuing.

Typical screen description 1 2 3

4

1 : Area for Parameters, Error codes. Controlled by JEDI Software. Display of exposure parameters setup in Application mode, depending on technique selection: kV, mAs, mA, Exposure time. (max. number of exposure in sequence, not used on Rad product.) Specific display in Maintenance Mode (Alt S or Alt D). Chapter 3 - Configuraton & Calibration

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Note:

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

2 : Status area. Displayed by Service Software, Enlighten or blinking key controlled by JEDI Software. Display of function keys usable with menu displayed. Commands are remembered in help area: Right arrow: Increase kV

Left arrow: Reduce kV

F1: Set 2 points mode F2: Set 3 points mode F3: Increase mA or mAs (3 points or 2 points)

F4: Decrease mA or mAs (3 points or 2 points)

F5: Increase Exposure Time

F6: Decrease Exposure Time

F9: Darkness correction + (w/t AEC Cell)

F0 (F10): Darkness correction - (w/t AEC Cell)

Lit when thermal limit is reached

Lit when ready for exposure

Error or impossible selection Lit during exposure Lit during exposure

3 : Select Technique, Screen film pairs, AEC cell, ...

1...4: Select workstation, whenever programmed in service menu TECH. 0: select Large focus

9: select Small focus

A, B, C: Select screen film pair (Whenever programmed) A: Slow speed

B: Medium speed

C: High speed

D, E, F: Select cell in AEC (Whenever programmed) D: Left cell

E: Central cell

F: Right cell

R: to Reset whenever error occurs

U: Toggle fast or normal kV change.

Z: to display in area (1) the measured exposure parameters when "DISP" in menu 5 is set ON. APR valid: enlighten when the display in area (1) is valid for recording in Customized protocols. (Not used in RAD) 4 : Area for Static Help, related to screen in Service Mode. Displayed by Service Software.

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Keys always displayed, but will be active depending on configuration and technique selection. Includes help command.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

SELECTING MAINTENANCE AND APPLICATION MODE; MAJOR KEYS FROM

PROCEDURE

TO

APPLICATION MODE

Type - (Together)

SETUP/MAINTENANCE MODEMENU 3

APPLICATION MODE

Type - (Together)

SETUP/MAINTENANCE MODELAST MENU OR SUB-MENU selected.

SETUP/MAINTENANCE MODE

From any menu, type (several times if necessary) or

APPLICATION MODE

[Q]

Return to application mode

[R]

Return to a higher level menu

[W]

Validate

[ALT] & [S] (Together)

Calibration mode (Menu 3)

[ALT] & [D]

Calibration mode (Last menu called)

[

] and [

]

In maintenance mode, to move through menus

[F1] to [F0]

Function keys with action based on context.

Other keys

Based on context. Main function recalled in the screen and also in sections wherever used.



Type [ALT] & [S] (Together) to go to Maintenance Menus (MENU 3)



Type [



Figure 3-2 shows the relationship between the Maintenance Mode menus and the function keys used to access those menus. To return to a higher level, key in [R]



] and [

] keys to select a menu.

The darkened menus are used for Generator and room setup (Configuration and Calibration): menu 3, 4, 5. Menu 3 is used to Configure the system Menu 4 is used to calibrate AEC mode (Automatic Exposure Control) Menu 5 is used to perform Checksum Menu 1 is used to perform generator test and diagnostics. Menu 2 is used to enter Date and Time, view/clear error log, and view/clear tube and generator recorded tracking Data.

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SERVICE MENU TREE BREAKDOWN

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

MENU 1

[F1]

[F3]

HEAT

[F5] HIGH

ANOD

AUTO, 3,4,5

[F3]

GATE CD Tst

ShC INV Tst

[F5]

LIST

MENU 3

AEC

AUTO, 3k, 9k NoLD

MENU 2

[F7]

[F7]

NEXP

DATE

[F1]

[F5]

TECH

MODE

[F7]

[F5] AEC

[F1]

MENU 5

[F3] KG

KVEF

CAL

[F5] KTIME

[F1]

CKS

KF

[F7]

RAMS

[F1]

[F9]

Vx Px.x

DSPL

[F3] MCL

Figure 3-2 Service Menu Tree Breakdown SUB-MENU SUMMARY DESCRIPTION 1.) Configuration - MENU3 TECH: programming workstation, technique parameters. MODE: Select Renard or Normal scale for kV selection. Calibration - MENU4 AEC: To set parameters if known, or modify them manually. CAL: To calibrate Automatic Exposure Control, for each AEC chamber and Screen-film combination. Page 144

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MENU 4

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 (See 2.6 - Automatic AEC Calibration) 2.) Ram - MENU5 RAMS: NVRAm operation & display: Note:

CKSM: To update Checksum after configuration, calibration, parameter change. (See 2.8 - Checksum Validation) MCLR: Clear NVRam memory. Normally not to be used, unless specifically instructed. Do not use if Data Base backup has not been performed previously. Vx Px.x: Display generator software version (e.g. P3.3)

DSPL: In Maintenance Mode, to display parameter after exposure using key [Z] 3.) Utilities - MENU2 LIST: To display last recorded error codes (up to 64) -

Last error is viewed with Date and Time Function keys allow to scroll down and up [Z] to get back to the last recorded error Same consecutive error are counted Up in the same line [^H ], and [W] to clear error log

NEXP: To view/clear tube and generator recorded tracking Data. Clear must be performed only when replacing X-Ray tube. Meaning of each parameter is found in Chapter 9 - - Service Tool Job Cards - Section 2.0 - Tube Replacement Software Procedure. DATE: To enter / modify the date and time. 4.) Diagnostics - MENU1 -

Auto: run fixed current on both filament (if 2 filaments) in sequence on selected tube (If more than 1). L or S: run 3, 4, or 5 Amps on Large or Small Focus.

ANOD: To exercise Rotor function. -

Auto: run rotation cycle in Low Speed then High Speed (If allowed by configuration) on selected tube. (If more than 1) 3k: run one cycle acceleration, hold, break in Low Speed on selected tube (If more than 1) 9k: run one cycle acceleration, hold, break in High Speed (If allowed by configuration) on selected tube (If more than 1)

HIGH: To exercise High Voltage function. Note: Note:

NoLD: To troubleshoot HV problem, without mA nor rotation with or without X-Ray tube. Test is run from 80 to max. kV, adjustable from 1 to 60 sec. Gate CD Test: to verify operation of the gate command board on the Inverter. Test is run during 10 sec. At 0 kV. Requires manual set up. Read related information in diagnostics section. ShC INV Tst: To verify operation of inverter with inverter in short circuit. Test is run during 100 msec. At 0 kV. Requires manual set up. Read related information in diagnostics section.

AEC: To verify operation of AEC board. Refer to diagnostics section.

2.4 2.4.1

Tube Configuration Supplies None.

Chapter 3 - Configuraton & Calibration

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HEAT: To exercise Heater/filament function.

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2.4.2

Tools • • •

2.4.3

 XR 6000 SERVICE MANUAL

JEDI service software (the software is a DOS application) Console R232 cable (5194292) Computer with floppy or CD drive

Safety Precautions Not applicable.

2.4.4

Prerequisites The service terminal must be configured and software installed (refer to 2.3 - Service Software User Guide).

2.4.5

Personnel 1 person.

2.4.6

Time 15 minutes.

2.4.7

Procedure Load software according to tube present in the installation A database is available on the JEDI Service Software supplied in Service Tools: • for 50 kW tube: Type E7843X File = E7843_R?.mx (? means the current revision) Load the file corresponding to the tube present in the installation from Service Terminal. Refer to 2.9 - Backup and Restore Database Parameters.

2.4.7.2

Verify According to the tube used in the installation, verify if 50 kW database loaded for tube E7843X • The maximum mA displayed on the console must be 630 mA for 80 kV. The word "Workstation" is incorrectly used and displayed in the JEDI software screens. "Workstation" actually refers to the word "Receptor".

2.5 2.5.1

Receptor Programming Supplies None.

2.5.2

Tools • • •

2.5.3

JEDI service software (the software is a DOS application) Console R232 cable (5194292) Computer with floppy or CD drive

Safety Precautions The JEDI is factory preprogrammed. Therefore, even if the data appears to correspond to the preprogramming, it must be confirmed. For example, AEC enable, wall bucky enable must be confirmed.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

2.5.4

Prerequisites Service terminal must be configured and software installed. Refer to 2.3 - Service Software User Guide.

2.5.5

Personnel 1 person.

2.5.6

Time 15 minutes.

2.5.7

Procedure

2.5.7.1

Introduction Receptor programming uses function keys indicated on screen for the following : • receptor select, • tube select, • define nominal number of exposures for 2-point mode operation, • AEC : types of chamber and number of pickup fields in each, • Screen-film combination select, (if only one Select A).

Calling the subroutine

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2.5.7.2

Call TECH (setup mode, menu 3, function key [F1]).

MENU3 TECH ->

MODE F5

F1

mAs at 80 kV for AEC1 found during Autocalibration Page 156

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AEC2

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 SID = new SID Example:

mAs0 = 5mAs SID = 1.4 mAs = 5 * (!.4)2 = 10 mAs Set mAs to 16 for backup. • Run exposure in AEC • Develop the film and measure the density • If the density is not equal to 1, go to MENU 4 AEC (F5) • Select KG (Key F3) • Select Grille 2 (Key F5/F6) • Enter a KG parameter : If density is greater than 1, decrease KG value If density is smaller than 1, increase KG value • Redo the same exposure and correct KG if density is not equal to 1. CHECKSUM VALIDATION The checksum must be validated at the end of the calibration. See 2.8 - Checksum Validation. AEC REPETITION TEST Make a series of 10 exposures in 2-point AEC (exposure time : aproximatively 10ms) and check mAs accuracy (+/-10%) for each exposure. [email protected]

SET KVEF, KT, KG Call the AEC menu (setup mode, menu4, function key [F5]).

AEC

KVEF KG KTIME

KF

SET KVEF •

Use the function key F1 to select sub-routine KVEF.

AECV 40KV 1 KV step

• • • • •

a.bc

screen-film combination 1,2 or 3

KVEF

Select screen-film combination with A, B or C keys. Select kV step 40, 60, 80, 100, or kVmax with F3/F4 keys. Set KVEF to known value with key pad. Validate each new setting with W key. Press the R key when settings have been completed.

SET KT •

Use function key F5 to select sub-routine KG.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

AEC T N = 0 T = 0.5 1 a.bc Time step #



• • • • •

Time

screen-film combination 1,2 or 3

KTIME

Use the following keys to select the screen-film combination : A for combination 1, B for combination 2, C for combination3. The screen-film combination selected is displayed in reverse video. Select time step number with F1/F2 keys. (N = 0 T = 10ms, N = 1 T = 100ms, N = 2 T = 500, N = 3 T = 1s, N = 4 T = 2s, N = 5 T = 3.2s). If necessary, select time with F3/F4 keys. Set KTIME to the known value with F9/F10 keys. Validate each new setting with the W key. Press the R key when the settings have been completed.

SET KG •

Use the function key F3 to select sub-routine KG.

AEC G GRILLE 1 KG = a.b

• • •

KG 0.8 to 2

Use the function keys F5/F6 to scroll grid (grid number corresponds to the ionization chamber number). Set KG to the known value using F9/F10 keys Validate each new setting with the W key Press the R key when settings have been completed.

CHECKSUM VALIDATION The checksum must be validated after settings have been completed; refer to 2.8 - Checksum Validation.

2.7 2.7.1

CR AEC Calibration Systems with CR Filming Only Usually, a CR system does not require any compensation, so you can set all the values to 1.

2.7.1.1

Program Generator with Default CR Parameters 1.) Enter Generator service mode. Select MENU 4, AEC. 2.) Select the proper film - screen to calibrate.

Example: A: SCR1

B: SCR2

C: SCR3

3.) Program the generator with the following default values for KVEF, KG, KTIME, and KF.

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grid no (from 1 to 4)

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Menu 4

F1 KVEF

Default KVEF Values

40 kV

60 kV

80 kV

100 kV

125 kV

Max kV

(how the film responds to kV)

1

1

1

1

1

1

Menu 4

F5 AEC

F3 KG

Default KG Values

Grille 1

Grille 2

Grille 3

Grille 4

(overall density adjustments)

1

1

1

1

(table)

(chestand)

Menu 4

F5 AEC

F5 KTIME

Default KVEF Values

N0

N1

N2

N3

N4

N5

(how the film respoonds to Time)

10

100

500

1000

2000

3200

1.00

1.00

1.00

1.00

1.00

1.00

F5 AEC

F9 KF

Default KVEF Values

0

1

2

3 thru 16

(collimator size compensation)

1

1

1

1

4.) 5.) 6.) 7.)

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Menu 4

2.7.1.2

F5 AEC

Go to MENU 5, select F7 and turn display ON using F1. Go to MENU 5 and run CHECKSUM. Exit service mode into applications by pressing "R" on the laptop several times. Perform the "CR Dose Adjustment" procedure below.

CR Dose Adjustment Refer to the specific CR service manuals for specific details. 1.) Set up the system to measure dose to the CR cassette. 2.) Make an exposure and record the dose. 3.) Adjust the KG parameter to get the desired dose (the desired dose may need determined by Operators or CR supplier).

2.7.2

System with Film and CR Filming Combined If the system will be used with both Film and CR at the same time, then please keep the AEC calibration data for Film. If the dose for CR is not proper, the "+" and "-" button on the console can be used to increase or decrease the dose.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

2.7.3

Final Adjustment

2.7.3.1

Disable Unused Film-Screen Program the generator to disable all unused film-screen combinations. Menu 3 F1 TECH

Example:

If you calibrated SCREEN 2 only, disable SCREEN 1 and SCREEN 3. If you calibrated Film and CR, disable the unused screen.

2.7.3.2

Perform Checksum Refer to 2.8 - Checksum Validation: Menu 5 F1 RAMS

2.7.3.3

F1 and V at the same time

Save Memory Back up the generator database. First service screen F6 Save Memory The file can be named, but it must be in the DOS format. Default name:

SV_VAR.MX

Acceptable name:

xxxxxxxx.MX (8 characters max.MX)

Save the file on the laptop hard drive. Copy the file to the site floppy.

2.8.1

Checksum Validation Supplies None.

2.8.2

Tools • • •

2.8.3

JEDI service software (the software is a DOS application) Console R232 cable (5194292) Computer with floppy or CD drive

Safety Precautions Not applicable.

2.8.4

Prerequisites Service terminal must be configured and software installed (refer to 2.3 - Service Software User Guide.

2.8.5

Personnel 1 person.

2.8.6

Time 5 minutes.

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2.8

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2.8.7

PROCEDURE

2.8.7.1

Note: Note:

2.8.7.2

Preliminary Remarks Checksums must be validated at end of generator setup or whenever a parameter is changed. In the checksum validation process, the processor computes a number which is a function of all the setup parameters. When the generator is powered up, this number is computed, i.e. the sum is "checked". If the two numbers differ, the generator displays an error code, indicating that one or more parameters have been changed since the last time the sums were checked, or that a RAM-related fault has occurred. X-ray generation is inhibited if there is a checksum error. The display Va.b on menu 5 is for the software version in the CPU board EPROMS.

Checksum Validation Call RAMS (setup mode, menu 5, function key [F1].

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Resulting display:

RAMS

CKSM

MCLR

Enter function key [F1] and [V] simultaneously. A buzzer will sound, indicating that the sums have been checked and OK on display screen. MCLR is used to erase all setup parameters. Function key [F3] corresponding to this function should not be used.

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2.9 2.9.1

 XR 6000 SERVICE MANUAL

Backup and Restore Database Parameters Supplies None.

2.9.2

Tools • • •

2.9.3

JEDI service software (the software is a DOS application) Console R232 cable (5194292) Computer with floppy or CD drive

Safety Precautions Not applicable.

2.9.4

Prerequisites 1.) The service terminal must be configured and the software installed (refer to 2.3 - Service Software User Guide). 2.) All calibrations must have been completed.

2.9.5

Personnel 1 person.

Time 15 minutes.

2.9.7

Applicability Setup parameters must be logged after the setup procedure has been completed, or whenever these parameters are changed. This enables service engineers to key in parameters rapidly, i.e. when changing the KV Control Board in the event of a battery outage.

2.9.8

Procedure

2.9.8.1

CPU memory backup The generator must be in application mode. The control console push buttons will be inactive during the transfer. • Connect service terminal to system console. • Power up. • Insert the calibration CD disk with write protection off. • From Laptop Dos, A: (It can also be run from Service Laptop Hard Disk Drive but in DOS mode). • Type JEDI on the terminal. • Hit [F6] to save memory. The system asks for a file name. Default file name is A:\sv_var.mx. • Type a file name or hit [ENTER]. During transfer, the number of frames sent is displayed. When transfer ends, the message "Transfer successful" is displayed. If any error is detected, the transfer stops and an error message is displayed. See list of error messages in this section.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

2.9.8.2

Note:

2.9.8.3

CPU memory restore All parameters stored in CPU NVRAM memory must have been saved previously on calibration CD disk. The procedure is the same as "Memory backup" except: Hit [F7] to restore memory. This procedure is also used to down load new software (File type for Database or Software is automaticaly recognised). Errors during memory restore may cause unpredictable results. A new transfer is required. If generator is locked, cycle power and repeat the entire memory restore procedure.

Error messages

MESSAGE

2.10.1

Cannot open file

- No CD disk. - CD write protected during attempt to backup.

File contains data. Delete old (y,n):

The file already exists (backup). If you answer "y", the existing file will be erased.

Error time out

- Generator OFF. - Terminal not connected to generator..

Error communication

Error during transfer. Try a new transfer from the beginning. Note: Ensure ASIAN.exe software running under DOS and not under WINDOWS.

Dosimetric Calibration Dose/DAP accuracy check procedure Before conducting this procedure, make sure following items have been calibrated: - Generator - Tube - HVL - Collimator - Positioner - mR/mAs Procedure: 1.) Set the dosimeter probe with the small ion chamber sensor at 25 cm above the Tabletop/ Wallstand where the prediction algorithm is performed. Ensure the center of the probe is at the center of x-ray beam. 2.) Cover the detector with lead or other material, or move it out of the FOV if possible, so that the detector will not be damaged from over exposure. 3.) Set Exposure technique: FIXED (NON-AEC) mode Table or Wallstand mode Chapter 3 - Configuraton & Calibration

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2.10

ERROR

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 XR 6000 SERVICE MANUAL

100kV, 50mA, 3.2mAs 20×20 cm FOV 100cm SID 4.) Take exposure. 5.) Read and take note of the results on dosimeter DoseRef. (unit in mR or μGy), the DAP value on the DAP meter DAPviewer (μGy *m2). 6.) Convert dose unit if needed: 1 mR = 8.76μGy, 1μGy = 0.001 mGy 7.) Determine the reference field size (convert unit to m2 if needed) at the dosimeter position Reference Field size = collimated FOV * (SOD/SID)2 where SOD is distance from tube focal spot to dosimeter upper surface. 8.) Calculate the Reference Dose Area Product DAPRef. = DoseRef. * Reference Field size. 9.) Compare the DAPRef. with DAPviewer as following: (DAPRef. - DAPviewer) / DAPRef.*100% The acceptable error is less than ±30% when DAP ≥ 5μGy*m2

2.10.2

Dose/DAP accuracy maintenance 4.2In case the DAP error is larger than ±30% when DAP ≥ 5μGy*m2, check if the SID, FOV calibration is good. If there is no problem, run Dose Prediction (mR/mAs) calibration then redo the accuracy check.

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Chapter 4 - Functional Checks Section 1.0 Introduction Functional Checks describes the procedures necessary to determine whether the XR 6000 system (Refer to Figure 4-1) is operating correctly and performing within specifications. All the XR 6000 system functions should conform to safety regulations, local codes or other applicable standards. •

Operational Checks



Performance Checks

Operational Checks may be performed by the customer or trained personnel. These checks only indicate that the unit is functioning correctly at an operational level. They do not indicate that the unit is performing within specifications.

Before performing Functional Checks all System Configuration and Calibrations must be completed. Refer to Chapter 3 - - Configuraton & Calibration.

Chapter 4 - Functional Checks

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Performance Checks must be performed by trained personnel only. These checks verify that the unit is performing to specification. It is recommended to complete these checks during and after installation, during periodic maintenance, and when the equipment is replaced or modified.

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

1

3 2

10 9

4

8

5 [email protected]

7

6

Figure 4-1 XR 6000 System 1.) Tube Stand

2.) Tube Arm

3.) X-ray Tube

4.) Table Top

5.) Longitudinal Support

6.) Table Base

7.) Foot Pedal

8.) Cassette Tray

9.) Collimator

10.) Control Box

Section 2.0 Tools and Test Equipment In addition to the standard service tool kit the following tools and test equipment will be necessary to perform the functional checks described in this chapter:

Page 166



DVM



Metric Tape Measure



KEITHLEY 35080A kV peak meter (or equivalent)



RADCAL MDH2025 dosimeter (or equivalent) with 20x5-60 probe Section 2.0 Tools and Test Equipment

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 3.0 Operational Checks 3.1

System Power Up Power up the XR 6000 system, check that all the corresponding LEDs are displaying correctly.

Green

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Red

Figure 4-2 LEDs

3.2

Tube Assembly Operation This section is used to perform mechanical movement checks.

Chapter 4 - Functional Checks

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

5

6

1.) 2.) 3.) 4.) 5.) 6.)

2

3

4

6

Vertical Travel Control Switch. Longitudinal Travel Control Switch. Angulation Rotating Control Switch. All Moving Function Control Switch. Angular Indicator. Handle.

Tube Stand Longitudinal Movement Pressing the longitudinal movement button moving the tube stand.

3.2.2



Check the tube stand movement is operating smoothly and uniformly.



Check that the operation of the tube stand along with the cassette tray moves smoothly all the way to the end of the table.

Tube Stand Rotation Hold the operation handle to drive the tube arm to the left or to the right for rotation, and check that the tube stand can be rotated +/- 180 degree and can be stopped in anywhere.

3.2.3

Tube Arm Vertical Movement 1.) Press and hold the vertical button on the control box and check the tube arm can move smoothly up and down. 2.) Release the button, it will stop in any position. 3.) Press the collimator lamp button. 4.) Move the tube from the lowest position to the highest position. 5.) Check the variance of the cross line, and make sure that it will be less than 5 mm, otherwise, adjust the tube position.

3.2.4

X-Ray Tube Angulation Press and hold the angulation button and check that the X-ray tube angulation range is from -120 degree to +120 degree. The detents are at 0, +/-90 and +/-120 degree, and 0 degree detent position is the tube arm's horizontal axis.

Page 168

Section 3.0 Operational Checks

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3.2.1

1

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

3.2.5

X-Ray Tube Tilting Release the machine lock (two), and check the tube can be tilting from forward 20 degree to backward 30 degree.

3.2.6

Table Top Movement Checks 1.) Double press the table foot pedals, check the tabletop is free for both Longitudinal and transverse movement. 2.) Check that all movements are smooth. 3.) Release the table foot pedal, the table top will automatically lock at any position.

3.2.7

Cassette Tray Movement The Cassette Tray is normally coupled with the tube stand.. 1.) In coupled state: The Cassette Tray should move together with the Tube Stand. 2.) Uncoupled state: a.) Press the push button on the carriage. Check that the Cassette Tray can be moved longitudinally without the tube stand. b.) Release the push button, the Cassette Tray is locked in the position.

3.2.8

Collimator Rotation

3.2.9

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1.) 2.) 3.) 4.)

Loosen set screw. Rotate the collimator. Check the collimator can be rotated. Secure the set screw.

Collimator Light Timer Press the collimator light button and check the light will be power off in more than 30 seconds.

3.2.10

Wall Stand Carriage Vertical Movement Check that the carriage can be moved smoothly up and down and can be locked in any position.

Section 4.0 Performance Checks 4.1

Console 1.) Check the buttons functions. a.) Power up. b.) Press every button except power up and off button, a beep sound will be heard. 2.) Check the APR Save function. a.) Change any parameter of the factory default APR database. b.) Press the APR Save button

for more than 3 seconds, and the system console will

give a beep sound to inform the operators. Chapter 4 - Functional Checks

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 c.)

Power off.

d.) Power up. e.) Check the technique parameters be saved. 3.) Check the APR Restore factory default function. a.) Press the buttons

together for more than 10 seconds. System console will

retrieve the factory default APR database. After the retrieve is done, system console will give a beep sound to inform the operators. b.) Power off. c.)

Power up.

d.) Check the technique parameters.

4.2 4.2.1

Accuracy of X-Ray Field and Light Field Alignment Requirements The following image is gotten in a plane that is perpendicular to x-ray field. Verify below requirements are met. |a1| + |a2| 75% of the operator selection). Note: mAs measure is also called postdisplayed. Radiography, manual mode: exposures shorter than 40ms (=mA loop setting time): +/- 5%+/-0.1mAs exposures longer than 40ms (=mA loop setting time): +/- 5%+/-0.1mAs

3.4

Exposure Time Accuracies JEDI emperor: Generator 50kW Time accuracy (3 point Mode) Definition: accuracy between operator selection and real exposure time (characterized by real kV>75% of the operator selection). Radiography: +/- 5%+/-0.5ms

Page 186

Section 3.0 Technique Factors Measurement Criteria

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JEDI emperor: Generator 50kW Two accuracies have to be defined: one in 3 point Mode, one in 2 point Mode.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

XR 6000 SERVICE MANUAL

Chapter 6 - Exception Handling And Error Codes Section 1.0 Exception Handling JEDI software performs auto-test at power up and continuously monitors the correct operation of its functions during application. Any malfunction is stored in the JEDI error log. Errors found can only be reported if the generator is powered on and functional.

1.1

Diagnostics There are different levels of diagnostics.

1.2

Power-On Diagnostic

1.3

Live Diagnostics 1.) Under application faults will be reported through an error code on the Service Laptop. Some are straightforward and convey the root cause. Refer to the recommended action in the error list. 2.) Diagnostics run separately: -

heating function

-

rotation function

-

inverter gate command diagnostic

-

inverter in short circuit diagnostic

-

no load HV fucntion diagnostics

3.) Manual Diagnostics Through a troubleshooting guide based on an error message or when the generator does not reply.

1.4

Error Code Structure The error code structure described in this chapter applies to JEDI error detection and logging. The JEDI error log file can be accessed from the system through the system console or a laptop (JEDI error log upload functionality).

Chapter 6 - Exception Handling And Error Codes

Page 187

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At power-up the kV control performs its own initialisation, checks its memory integrity (checksum of program and NVRAM) and starts the communication with its peripherals as well as the system. Communication is permanently checked afterwards. It then initialises the Rotation board and Heater board with their respective database parameters and loads kV control FPGA. Eight LEDs (S7..S0) on the kV control board show the software status. During power-on, the Heater board and the Rotation board CPUs are initialised and check their memory integrity and hardware. If a problem is encountered, a PRD error is reported to the kV control.

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

When an error is detected, it is logged in the JEDI error log file. The file contains a maximum of sixty four error logs. Each log shows the following structure: Simplified Generator Error Error Data associated Number of Date & error code Phase Class Code with the error code occurrences time The fields are described in the following paragraphs.

1.5

Simplified Error Code Definition

1.6

Generator Phase Definition The generator phase field contains the state of the generator when the error occurred. Generator Description Phase 0 idle: entered in diagnostic mode 1 powered up; waiting for configuration 2 Stand by: configuration completed, waiting for a preparation command 3 Preparation in progress: JEDI gets ready to take X-rays 4 Ready for exposures (rotation at speed; filament; HV inverter drive ready; no errors): waiting for an exposure command 5 High voltage on 6 Error detected and not yet cleared

1.7

Class Page 188

Error Class Definition There are five classes of errors that correspond to different levels of impact to the system. The class of errors correspond to the seriousness of the errors. Description Section 1.0 Exception Handling

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The simplified error code is a grouping of the JEDI error codes. This field gives a rapid understanding of which part of JEDI is faulty. Simplified Description Error Code 30 Tube spits errors 40 Rotation errors 50 Heater errors 60 Exposure errors (HV inverter + mA measure + exposure control 70 Power supply errors (low voltage + DC bus)Hardware errors (internal communications + cables) 80 Hardware errors (internal communications + cables) 90 Application errors (saved RAM + software) 100 External communication errors 110 Thermal errors 120 Manipulation error 10 Rotation warnings (engineering use) 20 Heater warnings (engineering use) 25 LVPS warnings (engineering use) 27 Application warnings (mainly saved RAM battery change)

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GE HEALTHCARE

1.8

Error Code Definition Each error code comprises two fields (which cannot be generated and used separately); • the first field describes the JEDI function which is faulty (referred to as the function code) • the second field describes the error detected. Example: error code 0306 means: • 03: high voltage generation function; • 06: no kV feedback on anode. Function Codes List Function Code 01 02 03 04 05 06 07 08 09

Description Rotation heater High voltage generation mA control Power supplies System interface Software Application Tube control

Chapter 6 - Exception Handling And Error Codes

Page 189

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DIRECTION 5275601-100, REVISION 12 XR 6000 SERVICE MANUAL 1 Errors which have no impact on the system operation. Errors detected in background diagnostics during application. They are referred as "Warning" errors, to monitor drifts and used for engineering tracking. The generator phase remains unchanged. Errors are stored in the JEDI error log. 2 Errors which are detected by JEDI and that are recoverable automatically without noticeable effect on the system, such as error related to recovered tube spits. The generator phase remains unchanged. Errors which usually occur during exposure. 3 Errors detected by JEDI during exposure. They stop the exposure and revert the generator into a safe state. Error will be reset on Exposure Command release. It will require another Exposure Command to restart the sequence. The generator phase is set to "error" until the error is cleared. 4 Errors which are related to any hardware failures, software application or communication errors. JEDI will revert to a safe state. If preparation is in progress, it is stopped. Errors are cleared either by a reset error action from the system (for system having a reset error mechanism) or by a prep release or by a new prep command. The generator phase is set to "error" until ther error is cleared. Application cannot work if errors are persistent. 5 These codes may appear when the generator or tube temperature limits are reached. The application waits until the thermal information disappears. The error information is temporary. The generator phase is set to "error" until the error is cleared.

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 10 11 12 13 14

1.9

Tube management Grid Bias AEC Hardware

Data Associated With The Error Code The field "data associated with the error code" shows detailed information over the state of the generator when the error occurred.

Example:

1.10

Rotation high speed acceleration state, small focus preheat, tube number 1 selected.

Number Of Occurrences The field "number of occurrences" is used to log the same error occurring several times consecutively. Instead of filling the error log file with the same error which has occurred consecutively several times, the first error is logged and successive errors are recorded through increasing the "number of occurrences" field.

1.11

Date & Time

Section 2.0 Error Codes, Diagnostics & Troubleshooting 2.1

Introduction This diagnostics section is to introduce the JEDI generator with the following information: • Power-On diagnostics LED indication. • List all the potential error codes that can be issued by JEDI Generator. • Provide error code explanation, potential cause and recommended action. • List of diagnostics aids and explanation of diagnostics.

2.2

Power On Diagnostics Refer to theory of operation for power-on sequence. This paragraph in this section is to provide meaning of boards' LED status. The LED display status is offering useful information at a glance to proceed to error code based troubleshooting. Whenever in doubt, a simple step is to watch the LED status display on the kV control board, then the Rotation and Heater. kV control LED status: • During Power On Diagnostics

Page 190

Section 2.0 Error Codes, Diagnostics & Troubleshooting

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The field "date & time" stores the date and time when the error occurred. This is the JEDI internal date and time which may be different from the system date and time. In the case of logging the same error the date/time is of the most recent entry.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

XR 6000 SERVICE MANUAL

kV control board S0..................S7 _

 

oooo

S0.........................S7

The 8 LED's (S0...S7) are lit successively in both directions (Scrolling as indicated by the arrows): the power up diagnostics are completed, kV control board is up and running.

S0.....................S7 o

o

o

o

One out of two is lit: Data base checksum problem. An error code is logged. Refer to error code description.



o oo

S7, S6, S5 are lit along with either S0 or S1 or S2 (depending of the type of FPGA downOne out of two is lit: Data base checksum problem. An error code is logged. Refer to error code description. •

When an application error occurs (Not PRD)

 

e.g: No communication

The simplified error code is displayed on the Leds. They blink; when the error is cleared (by a return to the standby mode for example), the 8 LEDs are lit successively.

Heater board LED status: (See central listing) After the power on diagnostics, heater board LEDs DS1 and DS2 are lit successively. Any different status correspond to an abnormal situation. An error code is logged. Refer to error code description.

Rotation board LED status: (See central listing) After the power on diagnostics, rotation board LED DS5 is blinking. Any different status correspond to an abnormal situation. An error code is logged. Refer to error code description.

2.3

Error Code List

Simplified Error Code 30

The error code list and associated short description is presented below. Description ErrorClass ErrorCode Description Tube Spits

2 2

0301H 0302H

Tube spit (kV+ and kV- dropped) Tube spit (kV+ has dropped)

Chapter 6 - Exception Handling And Error Codes

Page 191

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S0.....................S7

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Simplified Error Code

40

50

Description

Rotation Error

Heater Error

ErrorCode

Description

2 2 2 4

0303H 0304H 0305H 0101H

Tube spit (kV- has dropped) Tube spit (kV regulation error) FPGA problem (restarting safety signal) No CAN message received within 5 secs

4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4 4

Database not correct Rotation current overload Rotation Openload Rotation Phases unbalanced Rotation Phases error Rotation Inverter permanent overcurrent Rotation command error MAINS_DROP has failed PRD error F0 main frequency problem Unknown Rotation error No CAN message received within 5 secs Heater inverter permanent overcurrent Filament permanent open circuit Heater Inverter permanent short circuit Filament too high for Pre-heat Filament too high for Pre-heat Filament too high for Heat Heater command error Current under estimated fork Current over estimated fork MAINS_DROP detected PRD error Stay too long in Boost Filament selection error Measured current while inverter OFF Filament Database not correct

3

0102H 0103H 0104H 0105H 0106H 0107H 0108H 0109H 0110H 0111H 0149H 0201H 0203H 0204H 0205H 0206H 0207H 0208H 0209H 0210H 0211H 0212H 0213H 0214H 0215H 0216H 0221H 0222H 0223H 0224H 0248H 0249H 0306H

3 3 3 3 3 3

0307H 0308H 0309H 0310H 0311H 0312H

No kV Feedback on cathode No kV Feedback on anode and cathode kV detected during kV diag kV max detected ILP current not OK ILR current not OK

4 60

Page 192

Exposure errors

Unknown Heater error No kV Feedback on anode

Section 2.0 Error Codes, Diagnostics & Troubleshooting

[email protected]

ErrorClass

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GE HEALTHCARE 0313H 0314H 0316H 0317H 0318H 0319H 0320H 0323H 0401H 0402H 0403H 0504H 0801H 0802H 0803H 1406H 1407H 1408H 1409H 1410H 0501H

XR 6000 SERVICE MANUAL ILR max current detected ILR current timeout Spit Max error Spit Ratio error kV did not reach 75% after 20ms kV unbalanced detected FPGA problem (safety signal) ILP and ILR currents not OK No mA feedback mA scale error mA accuracy exceeded 5% Inverter Gate Power Supply failed Exposure backup mAs exceeded Exposure backup time exceeded Exp cmd while gene not ready time counter error mAs counter error AEC counter error mAs meter saturated FPGA Locked DC bus out of range

0503H 0505H 0506H 0507H 0549H 0553H 0557H 0563H 0567H 0573H 0577H 0180H

Inverter Gate Power Supply error Mains power supply has dropped during exposure DC bus 1 phase precharge error DC bus 1 phase discharge error Unknown LVPS error Detected +160V too high Detected +160V too low Detected +15V too high Detected +15V too low Detected -15V too strong Detected -15V too weak Rotor board communication problem

0181H 0280H 0281H 0321H 0322H 0601H 0602H 0902H 1402H 1403H 1404H

Rotor board has reset Heater board communication problem Heater board has reset kV conversion error kV ref ADC / DAC failed RTL error External CAN bus off tube Fan supply error Internal CAN bus off Connectic Fault FPGA configuration problem

Chapter 6 - Exception Handling And Error Codes

Page 193

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DIRECTION 5275601-100, REVISION 12 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 70 Power 4 Supply errors 4 4 4 4 4 4 4 4 4 4 4 80 Hardware 4 error 4 4 4 4 4 4 4 4 4 4 4

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 90

100

110

120

10

Page 194

Communica tion errors

Thermal error Manipulatio n error

Rotor Warning

Heater Warning

1405H 0701H

Tank sensor problem Saved RAM checksum pb

4 4 4 4

0702H 0703H 0704H 0603H

Software problem Watchdog reset has just occurred Rotor/Heater hold too long Debug screen com error

4 4 4 4 5

0604H 0605H 0606H 1301H 0804H

Database download error TAV communication error MPC/Madrid communication error AEC communication error Tank Thermal Error

5 5

0903H 1500H

Tube exceeded 70degC Tomo brightness error

5 5 1

1501H 1502H 0151H

Exposure switch released during exposure AEC cut off error CAN Domain command number error

1 1 1 1 1 1 1 1 1 1 1 1 1 1 1

0152H 0153H 0154H 0155H 0156H 0157H 0158H 0159H 0160H 0161H 0162H 0163H 0164H 0199H 0251H

CAN Domain request with no transfer init CAN Domain Toggle bit error CAN Domain : less than 2 data to download CAN Domain Abort received & applied Bad index in config upload Tube switch while rotor not off Acceleration cmd while no tube selected Acceleration cmd while database not OK Database download while rotor speeding Acceleration command not OK Rotor acceleration while in error No CAN message received within 4 secs Rotation Inverter overcurrent (< 3 times) Unknown rotation warning Received command is not OK

1 1 1

0252H 0253H 0254H

1 1 1 1 1 1

0255H 0256H 0257H 0258H 0259H 0260H

Heater command not OK No CAN message received within 4 secs Heater inverter overcurrent (inverter1) (

12

1

50

EXP

2007

OHM

BLM31P500S

FL4

PREP

TERLOCK 1

13:53:07

7C7>

7C7>

DOORIN

PDUGND

SMBJ5.0 6.7V

CR2

PDUGND

SMBJ5.0 6.7V

CR1

ON/OFF_KEY

0

1

2

12V

12V

2

4.99K 0.125W 1%

R38

1%

0.125W

15K

R37

4.99K 0.125W 1%

R36

1%

0.125W

15K

R42

1%

0.125W

15K

R43

1%

0.125W

15K

12V

11D3

R39

B

B Q1 MMBT3904

2

1%

GND

GND

0.125W

15K

R44

0.1U 50V 10%

C34

0.1U 50V 10%

C33

4

10

13

0.1U 50V 10%

C35

MMBT3904

Q2

PDUGND

E

C

PDUGND

E

C

2

U14

IN

3

GND

19

OPEN2 CLOSED2

4 5

Y1 Y2 Y3 Y4

3 6

8 1

9 7 5 3

3V3

OPEN1 CLOSED1

COILP COILN

11

O

VCC=VCC;GND=GND

RESP_CTRL

6 O

VCC=VCC;GND=GND

RESP_CTRL

8 O

A1 A2 A3 A4

10B1

VCC=3V3;GND=GND

11C8

11 13 15 17

OE_N

74LVC_LCX244

4

9B3

IO

CPLD_IO

4 5

CPLD_EXP

CPLD_PREP

Path

7A8<

9B3<

X_RAY_LIGHT

R45 10K 0.125W 1%

5

5

CPLD_INTERLOCK

VCC

PSW

interface

Block

3

1 2

CPLD_IO

CPLD_IO

0

CPLD_IO CPLD_IO

GND

OPEN2 CLOSED2

K3 G6B_2114P_US24VDC

0.1U 50V 10%

OPEN1 CLOSED1

3 6

8

6

5

3

24V_IN

C37

COILP COILN

U8

CLOSED OPEN CLOSED OPEN

K2 G6B_2114P_US24VDC

COM

COM

8 1

7

4

COIL1 COIL2

0.1U 50V 10%

VCC=VCC;GND=GND

MC1489A

U14

IN

1 2

K1 AZ742-2C-24D

4

C36

RESP_CTRL

MC1489A

U14

IN

MC1489A

GND

VCC

LSM340J 40V

D2

LSM340J 40V

D1

PDU24V

3

3

O

10D4<

IN

1

VCC=VCC;GND=GND

RESP_CTRL

OVER_CURRENT

U14 MC1489A

GND

6

6

0.1U 50V 10%

C38

R46

GND

R47 50

3 4

PIN

50

1 2

OHM

BLM31P500S

FL7

MH1

2

WIRE_TO_BOARD

RIGHT_ANGLE

J4

1

MHP4_50TB10_00

MH2

MHP4_50TB10_00

MH3

SHIELD

EXP

4

3

2

1

2A

1

J7

3

2

MHP4_50TB10_00

MH7

MH8

1 of

5

7

5176556SCH

Dwg No

PIN

C39

GND

22N 250V 20%

PDU24V

Rev

2

Company

8

7B5> 7C1<

15

R48 1MEG 0.125W 1%

7 of

Sheet

Restricted

GE Healthcare

CONNECTOR

WIRE_TO_BOARD

MHP4_50TB10_00

MH6

1 2 3 4

200V

8

SHIELD

TERLOCK

MURS320T3

D3

DOORIN

PSW

RIGHT_ANGLE

MHP4_50TB10_00

MH5

HANDLE

PREP

7D1<

F1

7D1<

2

PIN

1 2 3

RIGHT_ANGLE

4 5 6

WIRE_TO_BOARD

J6

MHP4_50TB10_00

2

1

GND

6

5

4

POWER CONNECTOR

MHP4_50TB10_00

MH4

7

XRAY_ON_LIGHT

MHP4_50TB10_00

4

3

Sheet

OHM

BLM31P500S

FL5

Block

1

PDUGND

1%

0.125W

15K

12V

10C6>

20K 0.125W 1%

R33

20K 0.125W 1%

2

3

R40

R41

1

20K 0.125W 1%

20K 0.125W 1%

12

9 5

1 1 1

1 1

Section 2.0 Central Listings 1

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

1

Thursday, October 30, 2014

[email protected]

Page 346

Page 346

1

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 XR 6000 SERVICE MANUAL B Size

Chapter 10 - Schematics

D

C

B

Fri

Dec

15

1

15:41:33

9C8<

IN

2006

GND

1 2

28 26 27

GND

3V3

5V

C41 0.1U 50V 10%

20K 0.125W 1%

R49

SYNCIN 0VIN1 0VIN2

VS1 VS2

3V3

ARM_RESET

C40 0.47U 16V 10%

U2 DCR010505U

2

VOUT ERROR_N VREC ENABLE 0VOUT

GND

17 12 16 13

14

R51 10K 0.125W 1%

R50 10K 0.125W 1%

1U 16V 10%

C42

CAN_GND

TIN

VCC

TP1

A

2

R52 0 0.125W 0%

9 10 11

6 7

3

CAN1_TX CAN1_RX

Q Q_N

26 25

YELLOW

1

DS1 HSMY-C650

12

5

CAN_VCC

C45 0.47U 16V 10%

VCC=3V3;GND=GND

A_N B RD

CEXT REXT_CEXT

C44 47U 10V 10%

R54 1K 0.125W 1%

TIN

U12 74VHC123A

C43 1U 16V 10%

R53 10K 0.125W 1%

TP2

3

2

3V3

4

R55 332 0.125W 1%

4

25

26

C47 0.1U 50V 10%

Path

GND

VCC

GND

C46 0.1U 50V 10%

interface

Block

CAN1_RX

CAN1_TX

VCC

5

6

8

4

2

1

5

5

VDD2

GND2

VO

GND2

GND1

VI

VDD1

U4

VO

VDD2

HCPL0720-060

GND1

VI

VDD1

U3 HCPL0720-060

ARM_IO

4

2

1

5

6

8

C48 0.1U 50V 10%

6

R56 332 0.125W 1%

CAN_GND

C49 0.1U 50V 10%

CAN_VCC

9B1

CAN_GND

IO

6

Block

RXD

TXD

VREF S

CANL

CANH

6

7

2 of

Sheet

5

CAN_L

7

5176556SCH

Dwg No

GND

VCC

CAN_H

VCC=CAN_VCC;GND=CAN_GND

4

1

5 8

U5 TJA1050

7

C50 0.1U 50V 10%

10C8

10C6

Rev

2

Company

8

8 of

Sheet

Restricted

GE Healthcare

8

15

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Page 347

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1

R57

Thursday, October 30, 2014

121 0.125W 1%

Page 347

B Size

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 XR 6000 SERVICE MANUAL

D

C

8B6

B

A

Mon Mar

12

1

13:22:15

ARM_IO

2007

GND

C51 0.1U 50V 10%

DATA_OUT 9 PO9_RXD1

24

Y1 Y2 Y3 Y4

A1 A2 A3 A4

OE_N

U8 74LVC_LCX244

C54 0.1U 50V 10%

2

0

PO8_TXD1 DATA_IN

T1IN T2IN R1IN R2IN

C1P C1M C2P C2M

1 3 4 5 11 10 13 8

VCC VP VN

16 2 6

U17 MAX3232C

8

3

GND

15

GND

R58 4.99K 0.125W 1%

PO1_RXD0

C56 1U 16V 10%

RS485_RX-

RS485_RX+

DATA_OUT

VCC

11C8

10C8>

14 7 12 9

10B1

7A5>

10C6>

T1OUT T2OUT R1OUT R2OUT

7D4

OVER_CURRENT

GND

PO0_TXD0

2 4 6 8

1

1 ISP_RXD

C55 0.1U 50V 10%

3V3

CPLD_IO

VCC=3V3;GND=GND

18 16 14 12

C53 0.1U 50V 10%

C52 0.1U 50V 10%

GND

3V3

1

4

14

ISP_TXD

R59 110 0.1W 0.1%

VCC

4

7

8

3

1

0

B

A

DI

VCC

U18 MAX488E

4

2

6

5

interface

Block

Path

GND

C57 0.1U 50V 10%

PO14_DCD1

GND

RO

Z

Y

GND

VCC

GND

5

RTS

D4 PMBD914 85V

0 0.125W +0.05

R63

DATA_IN

RS485_TX-

R60 110 0.1W 0.1%

RS485_TX+

5

B

10C6<

10C8<

3V3

Q3 MMBT3904

15K 0.125W 1% GND

E

C

R62 20K 0.125W 1%

3

R64 20K 0.125W 1%

6

ISP_ENTER

3V3

6

3

2

DTR

OUT

GND

R67 10K 0.125W 1%

R65 10K 0.125W 1%

1U 16V 10%

C58

Block

Sheet

3 of

GND

GND

E

C Q4 MMBT3904

5

7

4

C60 0.1U 50V 10%

R71

1

2

3V3

R72 332 0.125W 1%

8

Rev

2

Company

8

9 of

Sheet

Restricted

GE Healthcare

ARM_RESET

YELLOW

0 0.125W +0.05

11D6

C59 0.1U 50V 10%

GND

3V3

DS5 13 HSMY-C650

D6 PMBD914 85V

5176556SCH

Dwg No

RS232

D5 PMBD914 85V

B

3V3

PO9_RXD1

Q Q_N

VCC=3V3;GND=GND

A_N B RD

CEXT REXT_CEXT

PO8_TXD1

R69 0 0.125W 0%

1 2 3

14 15

U12 74VHC123A

7

15

8C1<

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

2

R68

1

R66

Section 2.0 Central Listings R61

20K 0.125W 1%

Thursday, October 30, 2014

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Page 348

20K 0.125W 1%

PioneerSM_ENG.book 1:28 PM

 XR 6000 SERVICE MANUAL

D

C

B

Mon Mar

11

1

2007

CPLD_IO

BUZ_CMD

10A6>

CPLD_IO

13:26:28

10C8<

12

11C8 7D4 9B3

GND

EXPOSURE_ENABLE

0.1U 50V 10%

C61

12V

9

8

7

6

5

4

DI

A

B

8

7

GND

RO

Z

Y

R75

C62

2

0.1U 50V 10%

A1 A2 A3 A4

OE_N

0.1U 50V 10%

C64

Y1 Y2 Y3 Y4

GND

VCC

7C5>

CPLD_IO

X_RAY_LIGHT

R79 10K 0.125W 1%

10

R82 10K 0.125W 1%

GND

R81 110 0.1W 0.1%

R80 4.99K 0.125W 1%

VCC

7

8

3

1

BUZ

B

A

DI

R77 10K 0.125W 1%

3

4

18PIN

5

4

3

2

1

1

Path

2

interface

Block

8

I1 I2 I3 I4 I5 I6 I7 I8

ULN2803

Q6

RO

Z

Y

GND

2111738

24V

VCC

MAX488E

U21

7

12

14

16

18

R78 10K 0.125W 1%

XRAY_ON/OFF-

XRAY_ON/OFF+

RESET

GND

0.1U 50V 10%

C65

6 VCC=3V3;GND=GND

8

6

4

2

1

RESET XRAY_CMD

3V3

10C6>

EXPOSURE_ENABLE

0.1U 50V 10%

C63

74LVC_LCX244

U7

GND

3V3

10C6< 10C8>

10C8<

VCC

4

3

GND

3

5

7

9

3

R83

O

10

RESP_CTRL

MC1489A

IN VCC=VCC;GND=GND

1

U20

1%

GND

B

VCC=3V3;GND=GND

A

0.125W

15K

2

74LVC-LCX14

B

74LVC-LCX14

A

U13

VCC=3V3;GND=GND

1

Y1 Y2 Y3 Y4

VCC=3V3;GND=GND

A1 A2 A3 A4

OE_N

74LVC_LCX244

U7

EXPOSURE_ENABLE-

R76 110 0.1W 0.1%

EXPOSURE_ENABLE+

U13

CPLD_IO

CPLD_IO

11

17

PREPARE

15

CPLD_IO

13

CPLD_IO

11

19

GND

CPLD_IO

GND

4

2

6

5

XRAY_ON/OFF

EXPOSURE

VCC

MAX488E

U19

3

1

CPLD_IO

R74 110 0.1W 0.1%

R73 4.99K 0.125W 1%

VCC

2

VCC

20K 0.125W 1%

2

R84

A

1

O1 O2 O3 O4 O5 O6 O7 O8

GND

5

R85 110 0.1W 0.1%

9

10

11

12

13

14

15

16

17

18

RESET-

RESET+

GND

24V

BUZ

XRAY_ON_LIGHT

PREPARE_SW

EXPOSURE_SW

XRAY_ON/OFF

COMMON GND

BUZZER

I150

P1

4

2

6

5

5

10A8> 10A6> 9B3<

10C8< 10C6< 7A7<

10B3< 10A3> 9A5>

8B8 10C6>

10B2<

10C8<

10C6<

6

6

XRAY_CMD

GND

VCC

C66

7 9

15

PREPARE_SW

Block

4 of

Sheet

5

CAN_GND

7

8

3

1

PIN

J11

RO

Z

Y

2 4 6 8 10 12 14 16 18 20 22 24 26

GND

RIGHT_ANGLE

1 3 5 7 9 11 13 15 17 19 21 23 25

B

A

DI

VCC

MAX488E

U22

26

24

22

20

18

16

14

12

10

8

6

4

2

4

2

6

5

1

7

OHM

CAN_L

12V

8

2

Company

8

10

of

15

10A8> 10A6> 9B3< 8C8

10C6>

Restricted Sheet

10C8<

10C6<

10C1< 10A3< 10A3> 9A5>

GE Healthcare Rev

RS485_RX-

RESET-

XRAY_CMD-

EXPOSURE_SW

RS485_TX+

2

XRAY_CMD-

R89 110 0.1W 0.1%

XRAY_CMD+

EXPOSURE_ENABLE+

XRAY_ON/OFF+

BUZ_CMD

50

BLM31P500S

FL6

GND

5176556SCH

Dwg No

GENERATOR CONNECTOR

RIBBON_CABLE_STANDARD

25

23

21

EXPOSURE_ENABLERS485_TX-

19 XRAY_ON/OFF-

17

13

CAN_H

11

5 RS485_RX+

3

1

RESET+

GND

R87 110 0.1W 0.1%

R86 4.99K 0.125W 1%

VCC

XRAY_CMD+

0.1U 50V 10%

7

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Page 349

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Chapter 10 - Schematics

R70

332 0.125W 1%

Thursday, October 30, 2014

332 0.125W 1%

Page 349

B Size

PioneerSM_ENG.book 1:28 PM

 XR 6000 SERVICE MANUAL

D

C

B

Wed Feb

28

IN

16:00:42

1

332 0.125W 1%

R35

332 0.125W 1%

R34

2007

LED

VCC

2

2

YELLOW

1

DS4 HSMY-C650

GREEN

1

DS3 HSMG-C650

GND

CPLD_IO CPLD_IO CPLD_IO CPLD_IO

2

16 CPLD_IO 17 CPLD_IO

12 13 14 15

0.1U 50V 10%

9 7 5 3

18 16 14 12

C67

A1 A2 A3 A4

7B2

3

GND

R97

READY

150 0.125W 1% R93

R99

10K 0.125W 1%

DTR

1 3 5 7 9

3 1 3 5 7 9

J8

KEYBOARD CONNECTOR J12

2 4 6 8 10

1 3 5 7 9 11 13 15 17 19 21 23 25 27 29 31

GND

4

2 4 6 8 10 12 14 16 18 20 22 24 26 28 30 32

2 4 6 8 10 12 14 16 18 20 22 24 26 28 30 32

2 4 6 8 10

Path

interface

Block

RTS

ISP_RXD

PDUGND

PIN RIGHT_ANGLE DUAL_ROW_HEADER

1 3 5 7 9 11 13 15 17 19 21 23 25 27 29 31

PIN RIGHT_ANGLE RIBBON_CABLE_LOW_PROFILE

OFF

ON

ISP_TXD

0

1

2

3

332 0.125W 1%

332 0.125W 1% R96

1.21K 0.125W 1% WARM R95

INHIBIT

TUBE

R98

10K 0.125W 1%

150 PDU24V 0.125W 1% POWER ON R100

VCC

XRAY ON

10K 0.125W 1%

R94

10K 0.125W 1%

R92

10K 0.125W 1%

10K 0.125W 1%

GND

R102

R91

5

RS232

10K 0.125W 1%

R106

10K 0.125W 1%

R105

10K 0.125W 1%

R104

R103 10K 0.125W 1%

R101

5

10K 0.125W 1%

ON/OFF_KEY

GND

11 13 15 17

A1 A2 A3 A4

VCC=3V3;GND=GND

Y1 Y2 Y3 Y4

19

OE_N

VCC=3V3;GND=GND U26 74LVC_LCX244

Y1 Y2 Y3 Y4

1 2 4 6 8

OE_N

U26 74LVC_LCX244

6

3V3

5

R90

2

10K 0.125W 1%

4

9D7

6

6

100V

100V D12 MMSD4148

100V D11 MMSD4148

100V D10 MMSD4148

100V D9 MMSD4148

100V D8 MMSD4148

D7 MMSD4148

Block

Y1 Y2 Y3 Y4

A1 A2 A3 A4

Y1 Y2 Y3 Y4

A1 A2 A3 A4

OE_N

5 of

Sheet

5

GND

11 13 15 17

19

2 4 6 8

1

GND

VCC

0.1U 50V 10%

C68

CPLD_IO CPLD_IO

CPLD_IO CPLD_IO CPLD_IO CPLD_IO

7

5176556SCH

Dwg No

VCC=VCC;GND=GND

9 7 5 3

VCC=VCC;GND=GND U23 74ABT244

18 16 14 12

OE_N

U23 74ABT244

7

19 18

23 22 21 20

Rev

2

Company

8

11

Sheet

of

Restricted

GE Healthcare

CPLD_IO

8

15

9B3 7D4 10B1

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

3

A

3

4

2

0

Section 2.0 Central Listings 1

1

1

Thursday, October 30, 2014

[email protected]

Page 350

Page 350

2

PioneerSM_ENG.book 1:28 PM

 XR 6000 SERVICE MANUAL B Size

Chapter 10 - Schematics

D

C

B

A

Fri

Dec

15

1

15:41:36

PDUGND

24V_IN

1

CR3 SM6T27A 27V 2

PDUGND

24V_IN

2

1

TIN

OHM

2006

OHM

GND

12V

200

FL2 ZJYS51R5-2P

200

FL1 ZJYS51R5-2P

TIN

TP4

3

4

TP3

3

4

2

1

200

OHM

2

GND

C72 0.1U 50V 10%

GND

C71 0.1U 50V 10%

3

4

TIN

TP6

C73 4.7U 50V 10% C74 0.1U 50V 10%

2

1

1 3 4 8

10N 50V 10%

C75

3

4

OUTPUT

5

4

5

3

3

10N 50V 10%

HV

L1

J1 1 2

G1 G2

33U 20% D14 5A LSM340J 40V

G1 G2

PIN RIGHT_ANGLE WIRE_TO_BOARD

1 2

C85

L2

33U 20% D13 5A LSM340J 40V

C86

4

TWO PARTS AS CLOSE AS POSSIBLE

CXA-L10L

2

1

U25

C76

1 3 4 8

TO 12V

INPUT SWIT_OUT FEEDBACK BOOST ON_OFF GND TAB_GND

U10 LM2676

24V

TIN

TP5

INPUT SWIT_OUT FEEDBACK BOOST ON_OFF GND TAB_GND

U9 LM2676

TO 5V

TO LCD

2 6 7 R112 1K 0.125W 1%

R111 9.09K 0.1W 0.1%

R109 3.16K 0.1W 0.1% 2 6 7 R110 1K 0.125W 1%

12V

FL8 ZJYS51R5-2P

C70 100U 50V 20%

5.11K 0.125W 1%

R108

C69 100U 50V 20%

5.11K 0.125W 1%

R107

24V

22U 35V 10%

5

Path

R114 1K 0.125W 1%

5

DS7 HSMG-C650 GREEN

R113 499 0.125W 1%

DS6 HSMG-C650 GREEN

power

Block

CR5 P6SMB18A 18V

CR4 SMBJ5.0 6.7V

12V

VCC

SHIELD

22U 35V 10%

2 1

POWER SUPPLY

4

2 1

3

5 4

C77

0.1U 50V 10%

1K 0.125W 1%

R115

PDUGND

24V_IN

GND

VCC

3.3V

2

1

6

200

OHM

FL9 ZJYS51R5-2P

10U 16V +80%-20%

Block

3

4

1.21V

Sheet

1 of

3 6

1 2

1

4 5

GND

24V

1.4K 0.1W 1%

7

5176556SCH

C82 100U 50V 20%

2.87K 0.1W 1%

1K 0.125W 1%

R120 1K 0.125W 1%

R118

TP9

R117

TIN

GND

Dwg No

C81 0.1U 50V 10%

GND

VOUT SENSE_ADJ

75V

D16 BAS116

GND1 GND2

VOUT SENSE

TO 20V

VIN SHDN_N

VR1 LT1963EQ 2 1

75V

VIN SHDN_N

VR2 LT1529-3.3

D15 BAS116

5V TO 3.3V

5V TO 1.8V

GND

C80 0.1U 50V 10%

1K 0.125W 1%

R116

7

TIN

6

TP7

C78 10U 16V +80%-20%

VCC

TIN

C79

TP8

2

GND

3V3

TIN

TP10

10U 16V +80%-20%

Rev

2

Company

8

12

Sheet

of

Restricted

GE Healthcare

1V8

C83 100U 16V 10%

8

15

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Page 351

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R119

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C84

Page 351

B Size

PioneerSM_ENG.book 1:28 PM

 XR 6000 SERVICE MANUAL

Section 2.0 Central Listings

Fri

Dec

15

1

15:41:38

2006

2

2

IO

3

3

ARM_JTAG

IN

4

ARM_RESET

4

5 2 4 3 0 1

IO

0.1U 50V 10%

GND

GND

2 4 6 8 10

R123 10K 0.125W 1%

R122 10K 0.125W 1%

jtag

Block

Path

CPLD_JTAG

3V3

R121 10K 0.125W 1%

5

2 4 6 8 10

1 3 5 7 9

J2 1 3 5 7 9

R126 10K 0.125W 1%

3V3

R127 10K 0.125W 1%

3

6

1 0 2 CPLD_TDI

R129 10K 0.125W 1%

1 3 5 7 9 11 13 15 17 19

J5 1 3 5 7 9 11 13 15 17 19

2 4 6 8 10 12 14 16 18 20

2 4 6 8 10 12 14 16 18 20

R130 10K 0.125W 1%

Block

1 of

Sheet

R131 10K 0.125W 1%

PIN STRAIGHT DUAL_ROW_HEADER_BREAK

6

CPLD_TCK CPLD_TDO CPLD_TMS

3V3

ARM_TRST ARM_TDI ARM_TMS ARM_TCK ARM_RTCK ARM_TDO

R128 10K 0.125W 1%

PIN STRAIGHT DUAL_ROW_HEADER_BREAK

GND

R124 10K 0.125W 1%

5

1

GND

C88

0.1U 50V 10%

7

5176556SCH

Dwg No

7

Rev

2

Company

8

13

Sheet

of

Restricted

GE Healthcare

8

15

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

D

C

B

A

1

Thursday, October 30, 2014

[email protected]

Page 352

Page 352

C87

PioneerSM_ENG.book 1:28 PM

 XR 6000 SERVICE MANUAL B Size

D

C

B

A

Mon Mar

12

1

13:27:29

2007

3V3

600

OHM

FL10 BLM31A601S

C89 1U 16V 10%

1

2

2

C90 10N 50V 10%

GND

OUT

C91 0.1U 50V 10%

HCLK

R134

R132 1K 0.125W 1%

1

4

Y2

33.2 0.125W 1%

B

A

5

40MHZ

ENABLE

VCC

3

GND

VOUT

GND

2

3

VCC=3V3;GND=GND

6

U13 74LVC-LCX14

3

A

B

4

IN

IN

3V3

VCC=3V3;GND=GND

3

U13 74LVC-LCX14

TIN

ARM_CON

R135

TIN

4

10K 500MW 10%

R133 CW

TP_LCDV

GND

ADDR ADDR ADDR ADDR ADDR ADDR ADDR ADDR ADDR ADDR ADDR ADDR ADDR ADDR ADDR ADDR

lcd

14B7> 14B7> 14B7> 14B7>

Path

FPD FPD FPD FPD

GND

FRM LOAD CP DISP

Block

0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15

3 9 4

CS3 OE WE

14B7> 14B7> 14B7> 14B7>

ARM_RESET

ADDR

4

33.2 0.125W 1%

IN

TP_LCDGND

R125

2

10K 0.125W 1%

Chapter 10 - Schematics

Page 353

[email protected]

1

5

3V3

3V3

5

CNF0 CNF1 CNF2 CNF3 CNF4

SCANEN TSTEN

37 38

G1 G2

G1 G2

VSS

GND

SHIELD

6

Block

Sheet

1 of

1

C93 0.1U 50V 10%

14C4<

C92 0.1U 50V 10%

14C4< 14C4< DISP

C94 0.1U 50V 10%

C95 0.1U 50V 10%

INPUT

7

5176556SCH

Dwg No

GND

3V3

14C4< LOAD FRM

CP

23 24 29 26 30 27 31

TIME

FPSHIFT XECL YSCL FPLINE FPFRAME MOD_OUT YDIS

CYCLE

14D4< 14D4< FPSHIFT:CLOCK 14D4< 14D4<

IO

IO

FPD FPD FPD FPD

DATA

21 20 19 18

0 1 2 3 4 5 6 7

FPDAT0 FPDAT1 FPDAT2 FPDAT3

DATA DATA DATA DATA DATA DATA DATA DATA

ARM_IO

52 51 50 49 47 46 45 44

54 PO16_EINT0

7

D0 D1 D2 D3 D4 D5 D6 D7

WAIT_N

SOCKET RIGHT_ANGLE FLEX_CABLE_ZIF_BOTTOM

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20

J14

XCG1 XCD1

35 34

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20

RESET_N

36 56 57 58 59 60 CLKI

A0 A1 A2 A3 A4 A5 A6 A7 A8 A9 A10 A11 A12 A13 A14 A15

16 15 14 13 11 10 9 8 6 5 4 3 2 64 63 62

39

CS_N RD_N WR_N AS_N

43 41 42 61

COREVDD HIOVDD NIOVDD

U15 S1D13700F02

6

1

C96 0.1U 50V 10%

:

Rev

2

Company

8

14

Sheet

of

Restricted

GE Healthcare

= 16

8

15

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

R136

Thursday, October 30, 2014

15K 0.125W 1%

16

Page 353

B Size

PioneerSM_ENG.book 1:28 PM

 XR 6000 SERVICE MANUAL

Page 354

Section 2.0 Central Listings

Fri

Dec

15

1

15:41:41

2006

2

IO

ARM_IO

3

3

2

PO3_SDA

PO2_SCL

R137 10K 0.125W 1%

3V3

4

GND

4

7

1 2 3

6 SDA

5

Path

memory

Block

VCC=3V3;GND=GND

A0 A1 A2

SCL

WP

U11 24C256

5

R138 10K 0.125W 1%

5

GND

3V3

0.1U 50V 10%

C97

6

6

Block

1 of

Sheet

1

7

5176556SCH

Dwg No

7

Rev

2

Company

8

15

Sheet

of

Restricted

GE Healthcare

8

15

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

D

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3

Thursday, October 30, 2014

B

A

2

Page 354

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1

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 XR 6000 SERVICE MANUAL B Size

Chapter 10 - Schematics

D

C

B

A

Fri

Dec

29

1

16:04:03

2006

GND

VCC

C1 10U 35V 10%

P 12V_GND

12V_IN

1A 63V

2

C2 0.47U 16V 10%

F1 FAST_ACTION

200

OHM

3

4

12V

1 2 28 26 27

5V

SYNCIN 0VIN1 0VIN2

VS1 VS2

U1 DCR010505U

ISOLATED

2

1

FL1 ZJYS51R5-2P

POWER SUPPLY

2

17 12 16 13

3

14

VOUT

C4 0.1U 50V 10%

ERROR_N VREC ENABLE 0VOUT

5V

C3 100U 35V 20%

3

TP1

2 6 7

12V

C5 1U 25V 10%

4

GND

TIN

TP2

4 8

1 3

5

jedi_tav

Path

10N 50V 10%

C7

D1 LSM340J 40V

33U 20% 5A

L1

5

RS232_GND

C8 0.47U 16V 10%

RS232_VCC

TO 5V

Block

C6 47U 35V 10%

TIN

TP3

INPUT SWIT_OUT FEEDBACK BOOST ON_OFF GND TAB_GND

VARIOUS U2 LM2676

CHANGE TO 16V

R3 10K 0.125W 1%

R2 1K 0.125W 1%

R1 3.16K 0.125W 1%

TIN

4

TIN

TP4

C9 10U 35V 10%

6

6.8V

D2 MMSZ5235B

6

VCC

Block

1 of

Sheet

4

7

5182285SCH

Dwg No

OFF WANG ZY

WANG ZY

SIGN

8

Rev

1

Company

Sheet

8

1 of

Restricted

GE Healthcare

29-DEC-06

DATE 03-JULY-06 1

ECR/ECO A

REVISION

POWER GOOD

DS1 HLMP-1790 GREEN

R4 511 0.125W 1%

7

4

D

C

B

A

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

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Jedi Generator TAV Interface Board

Page 355

Section 2.0 Central Listings

D

C

B

A

Wed Sep

13

1

14:29:56

2

2006

C11 0.1U 50V 10%

-

VCC

2

R8 0 0.125W +0.05

2

20K 0.125W 1%

R7

RS232_GND

R6 20K 0.125W 1%

C13 0.1U 50V 10%

RS232_VCC

1U 16V 10%

C14

3

C1P C1N C2P C2N

2 4 5 6

1 12

3

Q_N

Q

VCC=VCC;GND=GND

A_N B RD

CEXT REXT_CEXT

U4 74HC123

1 2 3

14 15

RS232_GND

14

GND

13 4

13 RS232_TX 9 RXD 10 16

T1OUT R1OUT

EN_N INVALID_N FORCEON FORCEOFF_N

T1IN R1IN

VCC VP VN

15 3 7

U3 MAX3221E

CONVERTOR

TXD 11 RS232_RX 8

RS232

C12 0.1U 50V 10%

R5 1K 0.125W 1%

RS232_VCC

RS232_RX

C10 0.1U 50V 10%

RS232

RS485

1

1

2

4

GND1

VCC

GND1

VI

VDD1

5

4

R16 110 0.1W 0.1%

Block

1

5

VCC

R13 1K 0.125W 1%

GND

C31 0.1U 50V 10%

GND

R14

6

1U 16V 10%

C15

CONSOLE_TX-

20K 0.125W 1%

4

Sheet

9 10 11

6 7

Z

Y

RO GND

4

GND

Q_N

Q

4

12

5

CONSOLE_RX+

7

2

3

1

VCC

R18 511 0.125W 1%

8

Rev

1

Company

Sheet

8

2 of

Restricted

GE Healthcare

RX LED

YELLOW

1

DS3 HLMP-1719

RS485

CONSOLE_RX-

R17 110 0.1W 0.1%

5182285SCH

Dwg No

VCC=VCC;GND=GND

A_N B RD

7

2 RS485_RX

6

5

CEXT REXT_CEXT

U4 74HC123

B

A

DI

VCC

U7 MAX488E

2 of

7

3 CONSOLE_TX+

8

2

C32 0.1U 50V 10%

VCC

5

VCC

6

6 RS485_TX

8

2 RS485_RX

1

VCC

GND2

VO

VDD2

Path

jedi_tav

Block

R11 511 0.125W 1%

GND2

VO

TX LED

YELLOW

1

5

6

VDD2

RS232_GND

TXD

4

VDD1 VI

U6 HCPL0720-060

RS232_VCC

8

1 2

RS232_GND

RXD

U5 HCPL0720-060

RS232_VCC

C30 0.1U 50V 10%

DS2 HLMP-1719

C29 0.1U 50V 10%

4

4

D

C

B

A

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 REV 2 01July04

Thursday, October 30, 2014

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B Size

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 XR 6000 SERVICE MANUAL

D

C

B

A

Wed Sep

13

1

14:29:56

2006

GND

R19 20K 0.125W 1%

B

2

Y

3

2

GND

VCC

C16 0.1U 50V 10%

3

GND

VCC

C17 0.1U 50V 10%

RS485

GND

VCC

C18 0.1U 50V 10%

CONSOLE_JEDI

1 2

1 2

GND

VCC

4 7 5

1

AND CONNECTORS

VCC=VCC;GND=GND

A

1

U8 74ACT00

INTERFACE

3

EXT_CAN_H

C19 0.1U 50V 10%

4

GND

VCC

C20 0.1U 50V 10%

GND

G1 G2

G1 G2

C23 0.1U 50V 10%

Path

GND

VCC

5

GND

VCC

C24 0.1U 50V 10%

RS232_GND

SHIELD

14EXPOSURE_SW 15PREPARE_SW 16ON_SW 17CONSOLE_RX18CONSOLE_TX19EXT_CAN_L 20JEDI_TX21JEDI_RX22JEDI_EXP_SW 23 24 EXT_CAN_H 25 RS232_TX

14 15 16 17 18 19 20 21 22 23 24 25

5

SOCKET RIGHT_ANGLE STD_DENSITY

1 2 3 4 5 6 7 8 9 10 11 12 13

J1

jedi_tav

Block

C21 0.1U 50V 10%

RS232_GND

VCC

1 2 3 4 5 6 7 8 9 10 11 12 13

12V_GND

12V_IN

CONSOLE_RX+ CONSOLE_TX+

JEDI_TX+ JEDI_RX+ JEDI_ON_SW JEDI_PREP_SW EXT_CAN_L RS232_RX 2

4

1

6

5

2 3 4

3 4

3 4

Block

Sheet

6

3 of

4

GND

7

5182285SCH

Dwg No

MH4 MHP4_50TB10_00

MH3 MHP4_50TB10_00

7

MH2 MHP4_50TB10_00

MH1 MHP4_50TB10_00

RS232

6

1 1

2

1

1

1

C22 22N 250V 20%

Rev

1

Company

Sheet

8

3 of

Restricted

GE Healthcare

SHIELD

8

4

D

C

B

A

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Page 357

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 XR 6000 SERVICE MANUAL

D

C

B

VCC

Wed Sep

2

13

GND

1

14:29:56

1U 16V 10%

C25

2006

EXPOSURE_SW

VCC

R22

GND

C26 0.1U 50V 10%

D3 BAS116 75V

2

RS232_GND

Q

IN

13 4

1U 16V 10%

C27

GND

3

COM

2

3

COIL1 COIL2

1 5

9 10 11

6 7

B

13

Q_N

Q

11

12

5

6

4

3

5

4 Y

6

15K 0.125W 1%

R24

R25 20K 0.125W 1%

VCC=VCC;GND=GND

B

A

U8 74ACT00

PREPARE_SW

12V

5

GND

IN

B

10

Y

4

Path

jedi_tav

Block

5

6 O

2

1 5

8

RED

4 3

511 0.125W 1%

R26

JEDI_PREP_SW

7

7

6

Block

4 of

Sheet

4

7

5182285SCH

Dwg No

8

Rev

1

Company

Sheet

8

4 of

Restricted

GE Healthcare

VCC

CONSOLE_JEDI

AND INDICATOR

1

2

CLOSED OPN

DS4 HLMP-1700

COM

COIL1 COIL2

K2 G6RN_1_12VDC

RESP_CTRL VCC=VCC;GND=GND

VCC=VCC;GND=GND

A

U8 74ACT00

4

6

RS232_GND

U10 MC1489A

9

C28 0.1U 50V 10%

D4 BAS116 75V

PREPARE,EXPORSURE

VCC=VCC;GND=GND

A_N B RD

Y

VCC=VCC;GND=GND

A

U8 74ACT00

JEDI_EXP_SW

12

4 3

CEXT REXT_CEXT

U9 74HC123

CLOSED OPN

K1 G6RN_1_12VDC

RESP_CTRL VCC=VCC;GND=GND

3 O

U10 MC1489A

Q_N

1

VCC=VCC;GND=GND

A_N B RD

CEXT REXT_CEXT

U9 74HC123

1 2 3

14 15

R23

200K 0.125W 1%

R21 20K 0.125W 1%

15K 0.125W 1%

12V

2

2

A

R20

Section 2.0 Central Listings

392K 0.125W 1%

5

1

4

D

C

B

A

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 REV 2 01July04

Thursday, October 30, 2014

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

3.5

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D

C

B

State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process. See the GEMS ePDM System to determine the status of this document.

1

Tue

26

A1

L2 FILTER

2

1

14:10:18

DCBUSN_IN 0.25AMP

2005

3 4 ISLOCALPART=TRUE ISLOCALPART=TRUE

1

ISLOCALPART=TRUE

0.25AMP 2.5A DCBUSP_IN 2X3.3MH

A1

DCBUS_N 0.25AMP

2

150K 0.1W 1%

C20 0.1U 50V 10%

C28 2.2N 50V 10%

R29 10K 0.1W 1%

DCBUS_N 0.25AMP

R26

C24 100P 50V 5%

DCBUS_N 0.25AMP

R30 20K 0.1W 1%

R32 4.99K 0.1W 1%

-400V_LINE

R28 20K 0.1W 1%

DCBUS_N 0.25AMP

C5 2.2U 450V 5%

1%

R31 1MEG 0.1W

DCBUS_N 0.25AMP

C29 2.2N 50V 10%

7 4 2 3

DCBUS_N

5

8 6 1

2

DCBUS_N 0.25AMP

GND

VREF VOUT COMP

0.25AMP STARTUP_CHAIN

100 0.1W 1%

R27

VIN RT_CT VFB I_SENSE

3

0.25AMP

R20

STARTUP_CHAIN

R13

0.25AMP STARTUP_CHAIN

STARTUP_CHAIN

U5 UC3844A

0.25AMP

C25 0.1U 50V 10%

Approved Document - 2212166-5SCH_r1.pdf Page 2 of 3

Apr

PIN STRAIGHT TAB

CF1

1

CF2 PIN STRAIGHT TAB

DCBUS_P

0.25AMP

+400_LINE

VOLTAGE

R21

2 R10 1 2 1 2

FROM LINE

47K 1W 5% 47K 1W 5% 47K 1W 5% 2

NEON

NE1 N76530

100K 0.5W 5% R23 1 C23

1

HIGH

C27 2.2N 50V 10%

3

R25 22 0.5W 5%

4

1K 0.1W 1%

R35

DCBUS_N 0.5AMP

CR17 70V BAV99

0.1U 50V 10%

DCBUS_N 0.25AMP

ISLOCALPART=TRUE C7

1

4

CR9 SMCJ43A 50.3V

C19 0.47U 50V 10%

Block

R24 20K 0.1W 1%

E

C

75V

Path

A

CR15 SMCJ43A 50.3V

CR14 SMCJ43A 50.3V

CR16 SMCJ43A 50.3V

CR21 SMCJ43A 50.3V

CR20 SSTA206S 600V

CR19 SSTA206S 600V

DCBUS_N 0.25AMP

CR11 SSTA206S 600V

CR5 SSTA206S 600V

5

T1

V160AC 0.75AMP

19 19

5

5

9 1010

SNUB_CHAIN 0.25AMP

11

7

1

9

6

20

6

12

12

13 13

14 14

15 15

R34

100V

CR2 DSS10-01A

1 of

Sheet

1AMP

0.5AMP LOW_VOLTAGE

2

-5V

VIN

GND

7

2

1

R3 1 OHM 0.5MW 5% LOW_VOLTAGE 1.5AMP

2

1

TAB STRAIGHT PIN TURN CF3

1

2

2

1

1

M15V

ISLOCALPART=TRUE

0.5AMP LOW_VOLTAGE

R12 1 OHM POWER_M15V 0.5MW 5%

0.75AMP LOW_VOLTAGE

Rev

1

Company

Sheet

8

1 of

Restricted

GE Healthcare

0.75AMP LOW_VOLTAGE

2212166-5SCH

Dwg No

3 1

VOUT

1AMP

A1

1

TAB STRAIGHT PIN CF4

0.75AMP LOW_VOLTAGE

L4 1U 2.5

A1

160V

2

ISLOCALPART=TRUE ISLOCALPART=TRUE ISLOCALPART=TRUE ISLOCALPART=TRUE ISLOCALPART=TRUE ISLOCALPART=TRUE X2 X1 X3 X4 X5 X6 HOLE HOLE HOLE HOLEHOLEHOLE

1U 2.5 TURN

8

P15V ISLOCALPART=TRUE

2PIN ISLOCALPART=TRUE

CR18 SMCJ43A 100V

R33 CR22 SMCJ43A 47K 100V LOW_VOLTAGE 1W 0.75AMP 5%

V160DC 0.75AMP

POWER_P15V ISLOCALPART=TRUE LOW_VOLTAGE L1 LOW_VOLTAGE 10A

U1 LM7915 ISLOCALPART=TRUE 2

100V

CR1 MBR3100

C13 0.47U 50V 10%

C8

3.3U 250V 20%

0.75AMP LOW_VOLTAGE

3.3U 250V 20%

C6

1U 2.5 TURN

ISLOCALPART=TRUE

LOW_VOLTAGE

Block

7

ISLOCALPART=TRUE L3

V160DC 0.75AMP

C16 0.47U 50V LOW_VOLTAGE10% 1AMP

1KV 1N 20%

C30

11A

1200V

CR3 DSEI12-12A

330 1W 5% ISLOCALPART=TRUE

V160DC 0.75AMP

220P 2KV 10%

C26

ISLOCALPART=TRUE

6

18 18 3 3 LOW_VOLTAGE 17 17 0.25AMP 16 44 16

22

DCBUS_N 0.25AMP 88

0.25AMP SNUB_CHAIN

SNUB_CHAIN 0.25AMP

0.25AMP SW_SNUB

C31 220P 2KV 10%

ISLOCALPART=TRUE HS1 HEATSINK

Q1 IRG4PH10U 2198557

3

CR13 BAW56

0.25AMP ZENERS_CHAIN

0.25AMP ZENERS_CHAIN

0.25AMP ZENERS_CHAIN

0.25AMP ZENERS_CHAIN

0.25AMP MID_ZD

DCBUS_SW 0.25AMP

5

LVPS_TRI_V5

0.25AMP DCBUS_N

G

2 K2

1 K1

CR10 SMCJ43A 50.3V

ZENERS_CHAIN 0.25AMP

ZENERS_CHAIN 0.25AMP CR8 SMCJ43A 50.3V

CR4 SMCJ43A 50.3V

ZENERS_CHAIN 0.25AMP

0.5AMP DCBUS_N

100U 25V 20%

3

R14

A

F1

F2

C4 C3

100K 0.5W 5% K2 1 A

1500U 25V 20% C1

2

R38 R37 R36

1 7 11

330 1W 5% 330 1W 5% 330 1W 5%

1500U 25V 20% CR12 SMCJ16A 330U 25V 20% CR7 SMCJ16A 1

0.1 DCBUS_N 0.1 1W 1W 1% 0.25AMP 1%

0.1 1W 1%

[email protected]

1

1

330U 25V 20% C2

2 1 18V 1

R7 R5 R4

D

C

B

A

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

330 1W 5%

1

6 20

C12 C18 1

ISLOCALPART=TRUE

1

AK

Chapter 10 - Schematics FORWARD_MEASURE

0.47U 50V 10%

GREEN 18V

DS2 HLMP-1790

0.47U 50V 10%

Thursday, October 30, 2014

REV 2 01July04

3.9

Page 385

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LVPS board

Page 385

State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process. See the GEMS ePDM System to determine the status of this document.

Section 2.0 Central Listings

D

C

B

1

12:17:55

2005

75V

2

K2 2

LOW_VOLTAGE 0.25AMP

C10 0.47U 50V 10%

0.25AMP

LOW_VOLTAGE 0.25AMP

R19 1K 0.1W 1%

R17 1K 0.1W 1%

3

R1

C15 0.1U 50V 10%

P15V

100K 0.1W 1%

LOW_VOLTAGE 0.25AMP

R8

4

4

C22 0.47U 50V 10%

M15V

LOW_VOLTAGE

2 LOW_VOLTAGE 3 0.25AMP

R15 20K 0.1W 1%

FOR 100MA

10 1W 5%

0.25AMP LOW_VOLTAGE

10K LOW_VOLTAGE 0.1W 1% VCC 0.25AMP

LOW_VOLTAGE

1AMP

C17 0.1U 50V 10%

OPTIMIZE

P15V

LOW_VOLTAGE R16 2K 0.1W 1%

R18 2K 0.1W 1%

M15V

C14 0.1U 50V 10%

C11 0.1U 50V 10% LOW_VOLTAGE

P15V

LOW_VOLTAGE R11 0.25AMP

3

8

K1 1

Approved Document - 2212166-5SCH_r1.pdf Page 3 of 3

Mon May 16

CR6 BAW56 0.5AMP LOW_VOLTAGE FORWARD_MEASURE 3 A

2

VP 4 VN 1 GND BAL_STR 6 5 BAL 1

R6 10K 0.1W 1%

5V

VIN

Path

VCC

C21 0.1U 50V 10%

LVPS_TRI_V5

Block

4 GND

0.75AMP

_MAINS_DROP

RED

LOW_VOLTAGE 0.25AMP

3

5

5

0.25AMP 4 3 6 7 2 DI DE A B RE_N

RO

U2 MAX485 1

0.25AMP LOW_VOLTAGE

C9 0.1U 50V 10%

LOW_VOLTAGE VCC 0.25AMP

6

6

VCC=VCC;GND=GND_CHASSIS

VCC LOW_VOLTAGE

DS1 HLMP 1709 ISLOCALPART=TRUE

LOW_VOLTAGE 0.25AMP

R9 2K 0.1W 1%

VCC 0.25AMP

VOUT

U4 MC78M05CDT

7 VOUT

U3 LM311

VCC

LOW_VOLTAGE

0.25AMP

2 1

A

1

Block

Sheet

2 of

R2 1K 0.1W 1%

2

2 4 6 8 10 12 14 16 18 20 22 24 26

7

2212166-5SCH

Dwg No

POWER_M15V

1 3 5 7 9 11 13 15 17 19 21 23 25

2 4 6 8 10 12 14 16 18 20 22 24 26

8

Rev

1

Company

Sheet

8

2 of 2

Restricted

GE Healthcare

LOW_VOLTAGE

POWER_P15V

PIN STRAIGHT RIBBON_CABLE_STANDARD

1 3 5 7 9 11 13 15 17 19 21 23 25

J1

0.25AMP

LOW_VOLTAGE

7

D

C

B

A

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 REV 2 01July04

Thursday, October 30, 2014

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Page 386

B Size

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3.10

Inverter

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Chapter 10 - Schematics

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3.11

Gate cmd

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Section 2.0 Central Listings

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Chapter 10 - Schematics

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3.12

Dual snub

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Chapter 10 - Schematics

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3.13

AC/DC board

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Section 2.0 Central Listings

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3.14

AEC board

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Chapter 10 - Schematics

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Chapter 10 - Schematics

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Section 2.0 Central Listings

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3.15

Rad IF

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Chapter 10 - Schematics

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Chapter 10 - Schematics

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Chapter 11 - MIS Chart Section 1.0 Scope This section provides detailed information about each MIS run in the form of individual MIS cable charts. Each of the following charts defines a single interconnection in the system. The charts are arranged in the order, according to MIS numbers. In some cases, a particular MIS number is repeated, except for a letter added at the end. Such a set of charts use the same cable, and carry essentially the same signals, however the applications for each chart is different - the point of connection is different (at one or both ends) for each chart in the set.

Section 2.0 How to Use

Figure 11-1 MIS Chart Example

Chapter 11 - MIS Chart

Page 401

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Each MIS cable shown on the MIS map has its own MIS chart. Each chart identifies all signals present on the cable, and the specific pins associated with each signal. See Figure 11-1 for an example.

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 3.0 MIS Charts 3.1 3.1.1

System Console J1 Handswitch Interface, 5184620

Handswitch

System Console

Handswitch

J1 COM

1

PREP

2

COM

3

EXP

4

2 3 4

J2 FW Download Serial Port, 5194292

System Console

Service Laptop

J2

Serial Port

1 2 3

Receive Data Transmit Data

to console from console

4 5

Page 402

Signal Ground

Section 3.0 MIS Charts

GND

[email protected]

3.1.2

1

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

System Console

Download Tool

J2

Serial Port

1 2 3

Receive Data Transmit Data

to console from console

Data Terminal Ready 4

from console Signal Ground

5

GND

6 7

from console [email protected]

3.1.3

Request to Send

J3 Power and RTL Interface, 5183903

PDU

System Console

TM3

J3

1

DC24V

2

GND

2 Console Power Input

3

GND

3 Console Power Input

4

E

5

Power Issue A

6 7

Power Issue B PSW

Chapter 11 - MIS Chart

1 Console Power Input

4 5 6 7 RTL (0-DC24V; Active: 0V)

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

3.1.4

J4 Generator Interface, 5182354

System Console

TAV

J4

1

12V_GND

9

RS485_RX+

2

10

RS485_TX+

3

11

12V_GND

12

12V_IN

13 14

17

22

23

24

CAN_H Exposure_SW Prepare_SW

ON_SW

RS485_RX-

RS485_TX-

CAN_L

Section 3.0 MIS Charts

1

4 5 6 14 15

16

17

18

19

[email protected]

15

Page 404

J1

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

JEDI

TAV

J9

J1

11

RS232-GND

10

RS485_TX+

8

9

RS485_RX+

9

17

ON_SW

15

Prepare_SW

24 23

14

13

RS485_TXRS485_RX-

Exposure_SW

CAN_H

JEDI

11 12 20 21

22

24

TAV

J8

J1

3

TX

2

RX

5

10

[email protected]

22

CAN_L

7

RS232-GND

Chapter 11 - MIS Chart

25 13 23

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

3.2 3.2.1

Generator Generator Power Cable, 5196454 PDU

TM1 Un TM1 Vn TM1 Wn

3.2.2

Generator

380 VAC 380 VAC 380 VAC

Page 406

P3

Generator

E

G

Table TM1-XS105 Cable, 5193103 Table

Tube Stand

TM1

XP105

1

1

2

2

3

3

4

4

XP106 1

5

XP106 2

6

Section 3.0 MIS Charts

[email protected]

Grouding Bar

3.3.1

P2

Generator Grounding Cable, 5196643 PDU

3.3

P1

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

3.3.2

Table Grounding Cable 1, 5193105 PDU

Grouding Bar

3.3.3

Table

E

Table Grounding Cable 2, 5193106 Table

PE1

Tube Stand

E

Table Grounding Cable 3, 5193107 Tube Stand

PE2

3.3.5

PE2

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3.3.4

PE1

Tube Control Box

E

PE3

Table Grounding Cable 5, 5193109 Table Base

PE5

Table Cassette Tray

E

Chapter 11 - MIS Chart

PE6

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

3.3.6

Table Power Cable, 5193607 PDU TM2

5 6 7 8 9

3.3.6.1

24 V 0V foot-1 24 V 0V

3 4 8 2 1

Table MC7 Cable, 5197242

Tube Stand

XP102

MC7 Cable

2

24V 0V

Section 3.0 MIS Charts

1 2

[email protected]

Control Box

1

Page 408

Table TM1

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 XR 6000 SERVICE MANUAL

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3.3.7

Table Cable No1, 5197244 Control Box / Collimator

Tube Stand

Control Box XS103 1

XP101 1

Control Box XS103 2

XP101 2

Control Box XS103 3 Control Box XS103 4

XP105 1

Control Box XS103 5

XP105 2 XP105 3 XP105 4

Collimator Connector 2

XP105 5

Collimator Connector 3

XP105 6

[email protected]

Collimator Connector 1

Collimator Connector 4

Chapter 11 - MIS Chart

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

 XR 6000 SERVICE MANUAL

Appendix A - Electromagnetic Compatibility (EMC) Section 1.0 Compliance Statement This equipment complies with IEC 60601-1-2:2001+A1:2004 EMC standard for medical devices. This equipment generates, uses, and can radiate radio frequency energy. The equipment may cause radio frequency interference to other medical and non-medical devices and radio communications. To provide reasonable protection against such interference, this product complies the radiated emission as per CISPR11 Group1 Class A standard limits. However, there is no guarantee that interference will not occur in a particular installation. If this equipment is found to cause interference (which may be determined by turning the equipment on and off), the user (or qualified service personnel) should attempt to correct the problem by one or more of the following measure(s): Reorient or relocate the affected device(s)



Increase the separation between the equipment and the affected device (see recommended separation distances)



Power the equipment from a source different from that of the affected device



Consult the point of purchase or service representative for further suggestions

Use of accessories, transducers, cables and other parts other than those specified by the manufacturer of this equipment may result in increased emissions or decreased immunity of the equipment. The manufacturer is not responsible for any interference caused by using other than recommended interconnect cables or by unauthorized changes or modifications to this equipment. Unauthorized changes or modifications could void the users' authority to operate the equipment. All interconnect cables to peripheral devices must be shielded and properly grounded, except when technologically prohibited. Use of cables not properly shielded and grounded may result in the equipment causing radio frequency interference. The XR 6000 is predominantly intended for use in non-domestic environments, and not directly connected to the Public Mains Network that supplies buildings used for domestic purposes. The compatible accessories must be used within the recommended operating conditions outlined in the operation manuals. In addition to calibration and warm-up, other devices must be reset before and after use to ensure accurate dose measurements. Sustained exposure to electromagnetic fields (exceeding the test conditions) may cause false measurements. Failure to follow the recommended use may cause false measurements. The magnetic field environment from a MRI device located nearby is a risk of interference. All of the above are required to achieve the Electromagnetic Compatibility for a typical installation of the XR 6000. Further detailed data & requirements are described in the Use Recommendations and Installation Recommendations sections.

Appendix A - Electromagnetic Compatibility (EMC)

Page 411

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Section 2.0 Compatibility Tables This equipment complies with IEC 60601-1-2:2001+A1:2004 EMC standard for medical devices. The XR 6000 is suitable to be used in an electromagnetic environment, as per the limits & recommendations described in the tables hereafter: •

Emission Compliance level & limits (Table 1).



Immunity Compliance level & recommendations to maintain equipment clinical utility (see Table 2 and Table 3).

Note: This system complies with above mentioned EMC standard when used with supplied cables. If different cable lengths are required, contact a qualified service representative for advice.

2.1

Electromagnetic Emission Guidance and manufacturer’s declaration – Electromagnetic Emissions The XR 6000 is intended for use in the electromagnetic environment specified below. The customer or the user of the XR 6000 should assure that it is used in such an environment. Compliance

Electromagnetic Environment Guidance

RF emission, CISPR 11

Group 1

The XR 6000 uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

RF emissions, Class A CISPR 11

The XR 6000 is suitable for use in non-domestic environments, and not directly connected to the Public Mains Network. The XR 6000 is predominantly intended for use (e.g. in hospitals) with an appropriate power supply (see operation manual) and the recommended shielding for portable use.

Harmonic emissions, Not applicable IEC 61000-3-2 Voltage fluctuations/ Not applicable flicker emissions, IEC 61000-3-3

Table 1 XR 6000 Electromagnetic Emission

Page 412

Section 2.0 Compatibility Tables

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Emissions Test

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

2.2

Electromagnetic Immunity

Guidance and Manufacturer’s declaration – electromagnetic immunity. The XR 6000 is intended for use in the electromagnetic environment specified below. The customer or the user of the XR 6000 should assure that it is used in such an environment. Immunity Test

IEC 60601-1-2 Test Level Compliance Level

Electrostatic  6 kV contact. discharge (ESD),  8 kV air. IEC 61000-4-2

Electrical transient/burst, EC 61000-4-4

 6 kV contact.  8 kV air.

Electromagnetic Guidance

Environment

Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.

fast  2 kV for power supply  2 kV for power supply Mains power quality should be lines. lines. that of a typical commercial or  1 kV for input/output  1 kV for input/output hospital environment lines.

Surge, IEC 61000-4-5

 1 kV differential mode.  1 kV differential mode. Mains power quality should be  2 kV common mode.  2 kV common mode. that of a typical commercial or hospital environment. < 5% UT, (> 95% dip in UT) 0% UT for 5 sec. for 0.5 cycle. 40% UT (60% dip in UT) for 5 cycles. 70% UT (30% dip in UT) for 25 cycles. < 5% UT, (> 95% dip in UT) for 5 sec.

Power frequency (50/ 3 A/m 60 Hz) magnetic field, IEC 61000-4-8

3 A/m

Mains power quality should be that of a typical commercial or hospital environment. If the user of the XR 6000 requires continued operation during power mains interruptions, it is recommended that the XR 6000 be powered from an uninterruptible power supply or a battery. Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

Note: These are guidelines. Actual conditions may vary.

Table 2 XR 6000 Electromagnetic Immunity

Appendix A - Electromagnetic Compatibility (EMC)

Page 413

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Voltage dips, short interruptions and voltage variations on power supply input lines, IEC 61000-411

lines.

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Guidance and Manufacturer’s declaration - electromagnetic immunity. The XR 6000 is suitable for use in the specified electromagnetic environment. The customer or the user of the XR 6000 should assure that it is used in an electromagnetic environment as described below. Immunity Test

IEC 60601-1-2 Compliance Test Level Level

Conducted IEC 61000-4-6

RF, 3 Vrms, 150 kHz to V1 = 3Vrms 80 MHz

Radiated IEC 61000-4-3

RF 3 V/m, 80 MHz to E1 = 3V/m 2.5 GHz

Electromagnetic Environment Guidance Portable and mobile RF communications equipment should be used no closer to any part of the XR 6000, including cables, than the recommended separation distance calculated from the equation appropriate for the frequency of the transmitter.

Recommended Separation Distance

d = 1.2 d = 1.2 d = 2.3

80 MHz to 800 MHz 800 MHz to 2.5 GHz

Field strengths from fixed RF transmitters, as determined by an electromagnetic site surveya, should be less than the compliance level in each frequency rangeb. Interference may occur in the vicinity of equipment marked with the following symbol:

a

Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the XR 6000 is used exceeds the applicable RF compliance level above, the XR 6000 should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the XR 6000. b

Over the frequency range 150 kHz to 80 MHz, field strengths should be less than [V1] V/m.

These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.

Table 3 XR 6000 Electromagnetic Immunity (Continued)

Page 414

Section 2.0 Compatibility Tables

[email protected]

where, P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m).

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 XR 6000 SERVICE MANUAL

GE HEALTHCARE DIRECTION 5275601-100, REVISION 12

Recommended separation distances between portable and mobile RF communications equipment and the XR 6000 The XR 6000 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the XR 6000 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the XR 6000 as recommended below, according to the maximum output power of the communications equipment. Rated Maximum Output Power (P) of Transmitter Watts (W)

Separation distance according to frequency of transmitter 150 kHz to 80 MHz

80 MHz to 800 MHz

800 MHz to 2.5 GHz

d = 1.2

d = 1.2

d = 2.3

Separation meters

Distance

Separation meters

Distance

Separation meters

0.01 (10 mW)

0.12

0.12

0.23

0.1 (100 mW)

0.38

0.38

0.74

1

1.2

1.2

2.3

10

3.8

3.8

7.3

100

12

12

23

Distance

NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.

Table 4 Recommended Separation Distances

Level System

Name XR-6000 system

Fix exposure Subsystem AEC

Subsystem

Positioner movement

Subsystem System console

Subsystem

Power Distribution Unit

Component Bucky

Essential Performance Exposur; Exposure parameter display and set; Positioner movement.

Prob./Appl . Severity of Failure of Failure See below

See below

Test Req’d

Test Methord

Pass/Fail Criteria

Yes

See subsystems below See subsystems below

No unintended exposure; No Incorrect exposure (the exposure results is not meet product registration standard)

Acquire expectant dose

MEDIUM

MEDIUM

Yes

Monitor exposure parameter that displaied on system console.

Table electromagnetic lock (EMlock) function.

MEDIUM

LOW

Yes

Check EM-lock after immunity test.

The EM-lock function work as intended after immunity test.

Exposure parameter display Exposure parameter set .

MEDIUM

LOW

Yes

Observance Exposure parameter; Set exposure parameter after Immunity Test.

No exposure parameter change during immunity test; Exposure parameter set as intended after immunity test.

LOW

LOW

Yes

Turn on and boot up.

System able to turn on and boot up successfully after immunity test.

MEDIUM

LOW

Yes

Monitor grid Oscillating No grid Oscillating aborted during immunity test. during immunity test.

Provide power to sub-systems.

Oscillating Grid

Appendix A - Electromagnetic Compatibility (EMC)

Page 415

[email protected]

For transmitters rated at a maximum output power not listed above, the separation distance can be estimated using the equation in the corresponding column, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. V1 and V2 are the COMPLIANCE LEVELS for the IEC 610004-6 test and E1 is the COMPLIANCE LEVEL for the IEC 61000-4-3 test. V1 and V2 are in V and E1 is in V/m.

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GE HEALTHCARE DIRECTION 5275601-100, REVISION 12 Table 5 Product Essential Performance

 XR 6000 SERVICE MANUAL

Section 3.0 Use Recommendations This product complies with IEC 60601-1-2:2001+A1:2004 EMC standard for medical devices and with radio frequency emission requirements per CISPR11 Group1 Class A standard limits. The XR 6000 is predominantly intended for use in hospitals. Do not use devices which intentionally transmit RF Signals (Cellular Phones, Transceivers, or Radio Controlled Products) in the vicinity of this equipment as it may cause performance outside the published specifications. Keep the power to these types of devices turned off when near this equipment. Adhering to the distance separation recommended in Table 4, between 150 kHz & 2.5 GHz, will reduce disturbances recorded at the image level but may not eliminate all disturbances. However, when installed and operated as specified herein, the system will maintain its essential performance by continuing to safely acquire controlled radiological X-ray exposures in a mobile radiography environment. For example, a 1W mobile phone (800 MHz to 2.5 GHz carrier frequency) shall be put 2.3 meters apart from the XR 6000 (in order to avoid image interference risks). The use of accessories, transducers, and cables other than those specified may result in degraded ELECTROMAGNETIC COMPATIBILITY of the XR 6000.

Section 4.0 Installation Recommendations This system complies with above mentioned EMC standard when used with supplied cables. In order to minimize interference risks, the following requirements shall apply.

4.1

Cable Shielding & Grounding All interconnect cables to peripheral devices must be shielded and properly grounded. Use of cables not properly shielded and grounded may result in the equipment causing radio frequency interference.

4.2

Subsystem & Accessories Power Supply Distribution All components, accessories subsystems, systems which are electrically connected to the XR 6000, must have all AC power supplied by the same power distribution panel & line.

4.3

Stacked Components & Equipment The XR 6000 should not be used adjacent to or stacked with other equipment; if adjacent or stacked use is necessary, the XR 6000 should be tested and verified in order to ensure normal operation in the configuration in which it will be used. Consult qualified personnel regarding device/system configurations.

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The medical staff in charge of this equipment is required to instruct technicians, patients, and other people who may be around this equipment to comply fully with the above equipment requirements.

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4.4

 XR 6000 SERVICE MANUAL

Low Frequency Magnetic Field Not applicable.

4.5

Electrostatic Discharge Environment & Recommendations In order to reduce electrostatic discharge interference, install a charge dissipative floor material to avoid electrostatic charge buildup. The relative humidity shall be at least 30 percent. The dissipative material shall be connected to the system ground reference, if applicable.

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Appendix A - Electromagnetic Compatibility (EMC)

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Appendix B - Revision History Revision

Date

Reason for change

1

June 20, 2007 First Release

2

Nov. 08, 2007 Add cabinet tray pull/push location, silicone compound to HV cables, PDU troubleshootings, part replacement, Jedi schematics, and PM form Update table unpacking process, accuracy of x-ray field and light field alignment, table top part number

3

Feb. 15, 2008 Remove "LING LONG" Add door light and gate command pin direction Add Collimator PM

4

April 25, 2008 Add technique factors measurement criteria. Add CR AEC calibration process. Add tube stand bearing replacement instruction Add note to grid installation instruction. Add instruction to table leveling adjustment. Add system configuration instruction.

5

Aug 28,2008

6

Mar 09, 2011 Update tube voltage accuracy in chapter 4. Update FRU list

7

Aug 18, 2011 Revise EMC standard version

8

Jun 15,2012

Add Bucky Handle Assembly to FRU list.

9

Jun 29, 2012

Add requirement to meet the 3rd edition IEC60601 standards.

10

Jun 25, 2014

Remove CE Mark.

11

Aug 25, 2014 Add CE Mark. update Figure 2-55

12

Oct 30, 2014

Add installation instruction for oscillate grid for the system configured with advanced tube stand and advanced wall stand. Add HHS test instruction.

Appendix B - Revision History

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Add LOCTITE 242(or 243) requirements during the tube installation; Add FRU parts Item 63, item 64

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GE HEALTHCARE

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NO.1, YONGCHANG NORTH ROAD ECONOMIC & TECHNOLOGICAL DEVELOPMENT ZONE FAX: 86-10-67881850 TELE: 86-10-58068888 BEIJING, P. R. CHINA 100176

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