Tenoscop 2 6000 - 9000 C.C.D - M.D.A. Service Manual

 

 

Medical Systems

e

Stenoscop/MDA 826921P615 HOME

 

TOC Preinstallation Installation Functional Check

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Technical Publications 826 9212 P615 Revision

STENOSCOP 2 6000/90 6000/9000 00 C.C.D. – M.D.A. sm Service Manual

do not duplicate

Copyright 1998 GE Medical Systems February 1998

TOC Preinstallation Installation Functional Check  

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ATTENTION LES APPAREILS À RAYONS X SONT DANGEREUX À LA FOIS POUR LE PATIENT ET POUR LE MANIPULATEUR SI LES MESURES DE PROTECTION NE SONT PAS STRICTEMENT APPLIQUEES Bien que cet appareil soit construit selon les normes de sécurité les plus sévères, la source de rayonnement X représente un danger lorsque le manipulateur est non qualifié ou non averti. Une exposition excessive au rayonnement X entraîne des dommages à l’organisme. Par conséquent, toutes les précautions doivent être prises pour éviter évi ter que les personnes non autorisées ou non qualifiées utilisent cet appareil créant ainsi un danger pour les autres et pour elles–mêmes. Avant chaque manipulation, les personnes qualifiées et autorisées à se servir de cet appareil doivent se renseigner sur les mesures de protection établies par la Commission Internationale de la Protection Radiologique, Annales 26 : Recommandations de la Commission Internationale sur la Protection Radiologique et les normes nationales en vigueur.

WARNING X–RAY EQUIPMENT IS DANGEROUS TO BOTH PATIENT AND OPERATOR UNLESS MEASURES OF PROTECTION ARE STRICTLY OBSERVED Though this equipment is built to the highest standards of electrical and mechanical safety, the useful x–ray beam becomes a source of danger in the hands of the unauthorized or unqualified unqualified operator. Excessive exposure to x–radiation causes damage to human tissue. Therefore, adequate precautions must be taken to prevent unauthorized or unqualified persons from operating this equipment or exposing themselves or others to its radiation. Before operation, persons qualified and authorized to operate this equipment should be familiar with the Recommendations of the International Commission on Radiological Protection, contained in Annals Number 26 of the ICRP, and with applicable national standards.

ATENCION LOS APARATOS DE RAYOS X SON PELIGROSOS PARA EL PACIENTE Y EL MANIPULADOR CUANDO LAS NORMAS DE PROTECCION NO ESTAN OBSERVADAS Aunque este aparato está construido según las normas de seguridad más estrictas, la radiación X constituye un peligro al ser manipulado por personas no autorizadas o incompetentes. Una exposición excesiva a la radiación X puede causar daños al organismo.

Por consiguiente, se deberán tomar todas las precauciones necesarias para evitar que las personas incompetentes o no autorizadas utilicen este aparato, lo que sería un peligro para los demás y para sí mismas. Antes de efectuar las manipulaciones, las personas habilitadas y competentes en el uso de este aparato, deberán informarse sobre las normas de protección fijadas por la Comisión Internacional de la Protección Radiológica, Anales No 26: Recomendaciónes de la Comisión Internacional sobre la Protección Radiológica y normas nacionales.

ACHTUNG RÖNTGENAPPARATE SIND EINE GEFAHR FÜR PATIENTEN SOWIE BEDIENUNGSPERSONAL, WENN DIE GELTENDEN SICHERHEITSVORKEHRUNGEN NICHT GENAU BEACHTET WERDEN Dieser Apparat entspricht in seiner Bauweise strengsten elektrischen und mechanischen Sichereitsnormen, doch in den Händen unbefugter oder unqualifizierter Personen wird er zu einer Gefahrenquelle. Übermäßige Röntgenbestrahlung ist für den menschlichen Organismus schädlich. Deswegen sind hinreichende Vorsichtsmaßnahmen erforderlich, um zu verhindern, daßunbefugte oder unqualifizierte Personen solche Geräte bedienen oder sich selbst und andere Personen deren Bestrahlung aussetzen können. Vor Inbetriebnahme dieses Apparats sollte sich das qualifizierte und befugte Bedienungspersonal mit den geltenden Kriterien für den gefahrlosen Strahleneinsatz durch sorgfältiges Studium des Hefts Nr. 26 der Internationalen Kommission für Strahlenschutz (ICRP) vertraut machen: Empfehlungen der Internationalen Kommission für Strahlenschutz und anderer nationaler Normenbehörden.

 

TOC Preinstallation Installation Functional Check

Service Procedures Renewal Parts Schematics   TOC

Theory

Schematic Symbols/Abbreviations

GE Medical Systems 

REV 2

STENOSCOP 2 6000/9000 C.C.D. – M.D.A. sm 826 921 P615

SUMMARY 2 – PREINSTALLATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2. 1

2–1

BASIC CONFIGURATION – OPTIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2. 1

2–2

DOSE AREA PRODUCT METER SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . .

2. 4

2–3

IMAGER 16/22 CCD SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2. 5

2–4

MONITOR SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2. 11

3 – INSTALLATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3. 1

3–1

RECEPTION OF THE MOBILE SURGICAL UNIT . . . . . . . . . . . . . . . . . . . . . . . . . .

3. 1

3–2

MAIN SUPPLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3. 5

3–3

INTERCONNECTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3. 7

3–4

EQUIPMENT INSTALLATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3. 7

3–5

CDRH CERTIFICATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3. 8

3–6

DR4 / MD10 COMPONENTS INTERCONNECTIONS. . . . . . . . . . . . . . . . . . . . . . . . .

3 . 10

3–7

MDA COMPONENTS INTERCONNECTIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3 . 11

3–8

COMPONENTS POWER SUPPLY WIRING. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3 . 12

3–9

CCM 620 – Photography parameters setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3 . 13

4 – FUNCTIONAL CHECK . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 1

4–1

MECHANICAL TESTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 3

4–2

CDRH COMPLIANCE TEST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 5

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STENOSCOP 2 6000/9000 C.C.D. – M.D.A.

GE Medical Systems 

RE V 2

sm 826 921 P615

SUMMARY (CONT (CON T.)

6 – SERVICE PROCEDURES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

6. 1

6–1

PREVENTIVE MAINTENANCE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

6. 1

6–2

CORRECTIVE MAINTENANCE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

6. 3

6–3

JOB CARDS SYNOPTIC TABLE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

6. 6

6–4

DISASSEMBLY/REASSEMBLY SHEETS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

6. 6

6–5

ADJUSTMENT SHEETS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

6. 110

MECHANICAL ADJUSTMENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6. 111 ELECTRONIC ADJUSTMENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6. 127   6–6

LIST OF USED MEASURING EQUIPMENT. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

6. 217

7 – SCHEMATICS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

7. 1

7–1

IDENTIFICATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ID

7. 3

7–2

S CHOTTKY DIODES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . SC

7. 3

7–3

LIST OF SYMBOLS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . LI

7. 3

7–4

LIST OF THE ABBREVIATIONS USED IN THE SCHEMATICS . . . . . . . . . . . . . . .

7. 4

7–5

USE OF THE SCHEMATICS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

7. 8

9 – SPARE PARTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9–1

STENOSCOP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

9. 1 9.1

9–2

LASER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

9 . 70

9–3

DOSE AREA PRODUCT METER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

9 . 72

9–4

IMAGER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

9 . 74

9–6

MONITOR . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

9 . 90

9–7

KITS (MONITOR CART) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

9 . 92

SCHEMATICS A3 (see TOC page A – i) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

A–i

  ii

 

TOC Preinstallation Installation Functional Check

Service Procedures Renewal Parts Schematics   TOC

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Schematic Symbols/Abbreviations

STENOSCOP 2 6000/9000 C.C.D. – M.D.A.

GE Medical Systems 

REV 2

sm 826 921 P615

REVISION HISTORY RE V A 0

DATE

TYPE OF MODIFICATION

August, 1996 November, 1996

Preliminary release from engineering validation. Product document release.

1 2

January, February,

1997 1998

Update and corrections. M5 version; update and corrections. + RG 251 : II input dose clarification. + RG 256 : gain adjustment procedure revised because of the release of a new Sony CCD module.

LIST OF EFFECTIVE PAGES PAGE

REVISION

PAGE

REVISION

PAGE

REVISION

NUMBER

NUMBER

NUMBER

NUMBER

NUMBER

NUMBER

Title page Safe Sa fety ty In Inst stru ruct ctio ions ns

2 2

Summary i to ii Rev. history iii to iv

Chapter 2 Table Tab le of contents 2–i to 2–ii 2–1 to 2–12

Chapter 3 Table Tab le of contents 3–i to 3–ii Prod. 3–iii to 3–iv

2 2

2 2

2 2

Chapter 6 Table of contents 6–i to 6–viii 6–1 to 6–218

2 2

Chapter 7 Table of contents 7–i to 7–ii 7–1 to 7–10

2 2

Chapter 9 Table of contents 9–i to 9–ii 9–1 to 9–98

2 2

3–1 to 3–14

Chapter 4 Table Tab le of contents 4–i to 4–ii 4–1 to 4–14

2

Schematics –Din A3 Table of contents A–i to A–ii A–1 to A–78

2 2

2 2

  iii

 

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Theory

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GE Medical Systems 

RE V 2 Blank page

STENOSCOP 2 6000/9000 C.C.D. – M.D.A. sm 826 921 P615

  iv

 

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Theory

Schematic Symbols/Abbreviations

GE Medical Systems 

STENOSCOP 2 6000/9000 C.C.D. – M.D.A.

REV 2

sm 826 921 P615 CHAPTER 2 – PREINSTALLATION

TABLE OF CONTENTS 2–1

STENOSCOP : BASIC CONFIGURATION – OPTIONS. . . . . . . . . . . . . . . . . . . . . . .

2.1

2–2

DOSE AREA PRODUCT METER SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . .

2.4

2–2–1

Model 841–SO Chamber : . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.4

2–2–2

Electronic Enclosure : . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.4

2–2–3

Display Unit : not used with MDA Memory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.4

2–2–4

Power Supply : . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.4

2–2–5

Cable : . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.4

2–3

IMAGER 16/22 CCD SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.5

2–3–1

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.5

2–3–2

Composition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.5

2–3–3

Safety Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.5

2–3–4

Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.6

2–3–5

Special Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2.9

2–3–6

MAINTENANCE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2 . 10

MONITOR SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2 . 11

2–4

2–4–1

Physical Characteristics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2 . 11

2–4–2

Power Input . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2 . 11

2–4–3

Video Input . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2 . 11

2–4–4

Rotating Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2 . 11

2–4–5

Environmental Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2 . 11

2–4–6

Regulations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

2 . 12

2.i

 

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GE Medical Systems 

RE V 2 Blank page

STENOSCOP 2 6000/9000 C.C.D. – M.D.A. sm 826 921 P615

2 . ii

 

TOC Preinstallation Installation Functional Check

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Schematic Symbols/Abbreviations

STENOSCOP 2 6000/9000 C.C.D. – M.D.A.

GE Medical Systems 

REV 2

sm 826 921 P615

2 PREINSTALLA PR EINSTALLATION TION 2.

2–1 2– 1

STEN ST ENOS OSCO COP P : BAS BASIC IC CO CONF NFIG IGUR URA ATI TION ON – OPT OPTIO IONS NS.. According to the order specifications, the STENOSCOP Series 6000 / 9000 C.C.D. is available in 4 models. MODEL TCB92 601 P 478 TCB92 601 P 479 TCB92 601 P 480 TCB92 601 P 481

STENO 2 STENO 2 STENO 2 STENO 2

6000 6000 9000 9000

CCD CCD CCD CCD

50 Hz 60 Hz 50 Hz 60 Hz

The components of these models are listed in 2 charts and indexed according to the following criteria :  OO , OF , SOF , ACC , C , USA

OO : OBLIG OBLIGA ATOR TORY Y option necess necessary ary for the operatio operation n of the unit To be ordered separately.

ACUL LTATIV TIVE E Opti Option on OF : FACU To be ordered separately.

SOF : OBLIGATOR OBLIGATORY Y option necessary for the operation of the unit but DEPENDING of THE FACULTATIVE Option Components supplied according to the FACULTATIVE Option ACC : Spécific ccomponents omponents To be ordered separately. C :

Consommable To be ordered separately.

USA : Supplied direct by GE – USA following the GE – CGR CGR spécifications.

2.1

   

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STENOSCOP 2 6000/9000 C.C.D. – M.D.A.

GE Medical Systems 

RE V 2

sm 826 921 P615

STENOSCOP 2 CONFIGURATION CONFIGURATION – Only for information MODEL TCB92 601 P 481 TCB92 601 P 480 TCB92 601 P 479 TCB92 601 P 478

STENO 2 STENO 2 STENO 2 STENO 2

9000 9000 6000 6000

COMPONENTS DESCRIPTION

CCD CCD CCD CCD

60 Hz 50 Hz 60 Hz 50 Hz

CATALOG NUMBER

478

479

480

481

STENO 2 –MOBILE FRAME ASM (with XR head, without monitor cart)

OO

OO

OO

OO

BASE 6000 / 9000

OO

OO

OO

OO

KIT STENO 6000 / 9000 CCD PEG

OO

OO

OO

OO

IMAGER 16 (6”) CCD 50 Hz

OO OO

IMAGER 16 (6”) CCD 60 Hz

OO

IMAGER 22 (9”) CCD 50 Hz

OO

IMAGER 22 (9”) CCD 60 Hz

16 CCD IMAGER KIT (collimator + screened mylar) 22 CCD IMAGER KIT (collimator + screened mylar)

CASSETTE HOLDER (16) 24 x 30 cm

(1)

B92 601 P325

OO

OO

OF

OF

OO

OO

CASSETTE HOLDER (16) 9,5” x 9,5”

B92 601 P326

CASSETTE HOLDER (16) 10” x 12”

B92 601 P358 (1)

CASSETTE HOLDER (22) 24 x 30 cm CASSETTE HOLDER (22) 9,5” x 9,5” CASSETTE HOLDER (22) 10” x 12”

RAD REMOVAL GRID  24 x 30 cm (8:1, 28 L / cm)

(1)

OF OF

OF

B92 601 P327

OF

OF

B92 601 P328 B92 601 P359

OF

OF OF

ACC ( 1 )

ACC

ACC

ACC

ACC

ACC

OO

OO

OO

B95 601 P172

RAD REMOVAL GRID 9,5” x 9,5” (10:1, 44L / cm )

B93 601 P157

RAD COLLIMATOR COLLIMATOR KIT 24 x 30 cm

B92 601 P453

RAD COLLIMATOR COLLIMATOR KIT 9.5” x 9.5”

B92 601 P454

ACC

OO

OO

OO

TV MONITOR FFD NOT N OT ROT.( with MDA )

2153979

OO

OO

OO

OO

TV MONITOR FFD/ROT FFD/ROT.. (+ / – 170o) (with DR memory)

2153980

OO

OO

OO

OO

2nd TV MONITOR FFD/ROT FFD/ROT.. (+ / – 170o) (with DR memory)

2153980

OF

OF

OF

OF

1 MONITOR KIT (with shelf)

OO

OO

OO

OO

2 MONITOR KIT (with shelf)

OF

OF

OF

OF

2.2

   

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STENOSCOP 2 6000/9000 C.C.D. – M.D.A.

GE Medical Systems 

REV 2

sm 826 921 P615

CATALOG Nber

448

449

450

451

MDA MEMORY

B92 601 P494

OF ( 2 )

OO

OO

OO

Seq. Low Speed

B92 601 P495

OF

OF

OF

OF

Seq. Mid Speed

B92 601 P496

OF

OF

OF

OF

Seq. High Speed

B92 601 P497

OF

OF

OF

OF

Soft Measure

B92 601 P500

OF

OF

OF

OF

Soft Vascular 1 Soft Vascular 2

B92 601 P501 B92 601 P502

OF OF

OF OF

OF OF

OF OF

DR4 MEMORY + KIT

B92 601 P441

OF ( 2 )

OO

OO

OO

MD10 MEMORY + KIT

B92 601 P442

OF ( 2 )

OO

OO

OO

OF ( 3 )

OF

OF

OF

COMPONENTS DESCRIPTION

MD10 KEY BOARD CCM 620–1 VISIPLEX CAMERA 625L

B92 601 P385

SOF

SOF

SOF

SOF

CCM 620–1 VISIPLEX CAMERA 525L

B92 601 P395

SOF

SOF

SOF

SOF

CCM 620–2 VISIPLEX CAMERA 625L

B92 601 P443

SOF

SOF

SOF

SOF

CCM 620–2 VISIPLEX CAMERA 525L

B92 601 P444

SOF

SOF

SOF

SOF

CCM 620–1 + 4 VISIPLEX CAMERA 625L

B92 601 P445

SOF

SOF

SOF

SOF

CCM 620–1 + 4 VISIPLEX CAMERA 525L

B92 601 P446

SOF

SOF

SOF

SOF

SOF

SOF

SOF

SOF

SOF

SOF

SOF

SOF

FILM IMAGER KIT /STENO 6000/9000 PAPER IMAGER UP890 CEI/ 220V

861 190 P035

PAPER IMAGER UP880 UL/ 110V

861 190 P045

PAPER IMAGER SONY UP910 CEI/ 220V

861 190 P015

PAPER IMAGER SONY UP910/ 110V

861 190 P025

PAPER IMAGER KIT / STENO 6000/9000

SOF SOF

SOF

SOF SOF

SOF

VCR S–VHS SONY 220V/ 625 L/ CEI / RS232

B92 601 P503

SOF

SOF

VCR S–VHS SONY 110V/ 525 L/ UL / RS232 KIT VCR .SONY STENO 6000/9000

B92 601 P504 B92 601 P505

SOF

SOF SOF

SOF

SOF SOF

STERILE DRAPES SET (cloth)

B92 601 P350

C

C

C

C

DISPOSABLE STERILE DRAPES SET

B92 601 P357

C

C

C

C

PM STAND ALONE KIT

B92 601 P506

OO

OO

OO

OO

XR HANDSWITCH KIT

B92 601 P338

OF

OF

OO

OO

KIT LASER IMAGER 16 (6”)

B92 601 P457

OF

OF

KIT LASER IMAGER 22 (9”)

B92 601 P458

OF

OF

KIT LASER CUVE

832 139 G015

OF

OF

OF

OF

KIT DAP

B92 601 P459

OF

OF

OF

OF

( 1 )  Not for USA ( 2 )  One of those is obligatory ( 3 )  With MD10 memory only

2.3

 

TOC Preinstallation Installation Functional Check

Service Procedures Renewal Parts Schematics   TOC

Theory

Schematic Symbols/Abbreviations

GE Medical Systems 

RE V 2

STENOSCOP 2 6000/9000 C.C.D. – M.D.A. sm 826 921 P615

2–2 2– 2

DOSE DO SE AR AREA EA PR PROD ODUC UCT T MET METER ER SP SPEC ECIF IFIC ICA ATI TION ONS. S.

2–2–1

Model 841–SO Chamber : 

Type:: full field ion chamber. Type



Chamber active area: 72.38 cm2.



Dose area product rates: 1 mGycm 2s–1 to 400000 mGycm2s–1.



2–2–2



Energy range: 50 KVp to 150 KVp. Chamber sensitivity: 130 pC/mGycm2.



Absorption: less than 0.5 mm Al.



Connection: 2 sets of co–axial cable.



Warm up time: 8–10 minutes.



Transparency: greater than 75 %.

Electronic Enclosure : 

Calibration and offset adjustment: user accessible controls.



Weight: 0.200 Kg.



Signal processing: assembly contains integrated electronics.



Testt and reset push buttons. Tes



Power on indication.

Physical size: 165mm x 44mm x 28mm. Display Unit : not used with MDA Memory 

2–2–3



Display: 8 digit LCD with reset r eset and test function.



Display units: mGycm2.



Dose area product range: 1 mGycm 2 to 99,999,999 mGycm2.



Free running rate: 10 KHz.



Response time: dose rate dependent 1 ms – 5 seconds.

2–2–4

2–2–5



Power input: < 120 mA at 24 VDC.



Power input range: 15 – 28 VDC.



Testt & reset buttons. Tes



Overall size (including overlay): 120mm x 30mm x 19.5mm.



Weight: approximately 200g.



Local supply at Image Intensifier: 24 VDC, 120 mA (tolerance 15 – 28 VDC).



Co–axial cable: RG174.



Type:: 9 mm oval cross section, pvc insulated 6 core. Type



Length: X–ray machine specific.

Power Supply :

Cable :

2.4

 

TOC Preinstallation Installation Functional Check

Service Procedures Renewal Parts Schematics   TOC

Theory

Schematic Symbols/Abbreviations

GE Medical Systems 

REV 2 2–3 2– 3

STENOSCOP 2 6000/9000 C.C.D. – M.D.A. sm 826 921 P615

IMA MAGE GER R 16/ 16/2 22 CCD CCD SP SPE ECI CIFI FICA CATI TION ONS. S.

2–3–1

Overview The Imageur 22 Stenoscop CCD* and 16 Stenoscop CCD are compact image intensifier (II) systems used to: 

Convert radiology images to a video image (625– or 525–line).



Display this image on a TV monitor. The Imageurs Stenoscop are intended to equip mobile surgical units Stenoscop 2 – 6000/9000. The different versions of the Imageur I mageur Stenoscop are:



Imageur 22 Stenoscop CCD 625 L



Imageur 22 Stenoscop CCD 525 L

 

2–3–2

Imageur 16 Stenoscop CCD 625 L Imageur 16 Stenoscop CCD 525 L

Composition The Imageur Stenoscop CCD includes the following subassemblies: 

Mechanical mount,



II tube (image intensifier),



High voltage power supply,



Optical unit, equipped with a CCD sensor. The front cover is fitted with an anti–scatter grid which is protected by a sheet of Impax.

* Charged–Coupled Device.

2–3–3

Safety Instructions

CAUTION

The Imageur contains Extra High Voltage circuits indicated by a  DANGER – HIGH VOLTAGE label.



Pay close attention to high–voltage safety warnings (label:

).



All disassembly should be performed by the Field Engineer only.



Before any disassembly of the Imageur, ensure that the unit is not under power.



Before using the Imageur, ensure that it is correctly connected to ground by the yellow/green ground wire connecting the power supply chassis to the II assembly.

2.5

 

TOC Preinstallation Installation Functional Check

Service Procedures Renewal Parts Schematics   TOC

Theory

Schematic Symbols/Abbreviations

GE Medical Systems 

STENOSCOP 2 6000/9000 C.C.D. – M.D.A.

RE V 2 2–3–4

sm 826 921 P615 Specifications

2–3–4–1 Regulations The Imageur complies with the following regulations:

UL 187. 

CSA 22–2 114.



IEC 601–1.



JIS Z 4701 (Reference to IEC 601 – General Rule for Medical X–Ray Equipment).



JIS Z 4721 (Medical X–Ray Intensifier).



CDRH – Code of Federal Regulation 21 CFR.



REDACT.



GE 806–1 thru 806–14.



EMC – According to IEC 601–1–2.

2–3–4–2 Operating conditions



Temperature

– Operating – St Stor orag age/ e/tr tran ansp spor ortt

  0°C thru 45°C   – 40°C thru 70°C (IEC Standard 601–1)



Relative humidity

– Operating

 B00 C00 D00

2 4

RESET

>B020 C00 D00

Hit once the key to select the CONTRAST with the keys

1 3

Then adjust the contrast with the keys

>B020 C250 D00 1 3

Press the button

2 4 and set the appropriate DENSITY ( 50 or 60 Hz )

RESET

>B020 C250 D050

Store these new values with the ” PROGRAM ” button.

Refer to the CCM 620 manual for more details over these adjustments.

3 . 14

 

TOC Preinstallation Installation Functional Check

Service Procedures Renewal Parts Schematics   TOC

Theory

Schematic Symbols/Abbreviations

GE Medical Systems 

STENOSCOP 2 6000/9000 C.C.D. – M.D.A.

REV 2

sm 826 921 P615 CHAPTER 4 – FUNCTIONAL CHECK

TABLE OF CONTENTS 4–1

MECHANICAL TESTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 3

4–1–1

DISPLACEMENT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 3

4–1–2

WIG–WAG of ”C” ARM ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 3

4–1–3

IN–OUT MOTION OF ”C” ARM ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 3

4–1–4

C – ARM ROTATION AROUND THE HORIZONTAL AXIS . . . . . . . . . . . . . . . .

4. 3

4–1–5

ORBITAL ROTATION OF C–ARM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 4

4–1–6

STABILITY OF ”C” ARM ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 4

4–1–7

C–ARM UP–DOWN MOTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 4

CDRH COMPLIANCE TEST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 5

4–2

4–2–1

GENERATOR OPERATOR INDICATORS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 5

4–2– 4– 2–2 2

LEAKA LEA KAGE GE RA RADI DIA ATIO TION N TES TESTI TING NG OF TH THE E DI DIAG AGNO NOSTI STIC C

4–2–3

SOURCE ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . PRIMARY BARRIER PROTECTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 5 4. 6

4–2–4

RADIATION LEAKAGE OF THE IMAGE INTENSIFIER ASSEMBLY . . . . . . .

4. 6

4–2–5

KV PEAK MEASUREMENT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 6

4–2–6

FLUORO mA MEASUREMENT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 7

4–2–7

TUBE CURRENT EXPOSURE TIME PRODUCT . . . . . . . . . . . . . . . . . . . . . . . . .

4. 8

4–2–8

FLUOROSCOPY TIMER. (Not required for tube replacement or re–load). . . . . .

4. 8

4–2–9

REPRODUCIBILITY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 9

4–2–10

QUALITY CONTROL OF THE X RADIATION . . . . . . . . . . . . . . . . . . . . . . . . . .

4. 10

4–2–11

MAX FLUOROSCOPIC ENTRANCE EXPOSURE RATE . . . . . . . . . . . . . . . . . .

4. 11

4–2–12

ALIGNMENT OF THE X–RAY FIELD AND SPOT FILM CASSETTE . . . . . . .

4. 12

4–2– 4– 2–13 13

ALIGNM ALIG NMEN ENT T OF THE THE EDG EDGES ES OF OF THE THE X–RA X–RAY Y FIELD FIELD WITH WITH THE EDGES OF THE FLUOROSCOPIC IMAGE RECEIVER . . . . . . . . . . . . . . .

4. 13

4.i

 

TOC Preinstallation Installation Functional Check

Service Procedures Renewal Parts Schematics   TOC

Theory

Schematic Symbols/Abbreviations

GE Medical Systems 

RE V 2 Blank page

STENOSCOP 2 6000/9000 C.C.D. – M.D.A. sm 826 921 P615

4 . ii

 

TOC Preinstallation Installation Functional Check

Service Procedures Renewal Parts Schematics   TOC

Theory

Schematic Symbols/Abbreviations

GE Medical Systems 

STENOSCOP 2 6000/9000 C.C.D. – M.D.A.

REV 2

sm 826 921 P615

4 FUNCTIONAL CHECK 4.

4.1

 

TOC Preinstallation Installation Functional Check

Service Procedures Renewal Parts Schematics   TOC

Theory

Schematic Symbols/Abbreviations

GE Medical Systems 

RE V 2

STENOSCOP 2 6000/9000 C.C.D. – M.D.A. sm 826 921 P615

4 3 2

1 5