Professional Documents
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Technical Publications: Revision 8
Technical Publications: Revision 8
Publications
2242062
Revision 8
CT Sytec/Sytec i Series
Renewal Parts
Operating Documentation
GE MEDICAL SYSTEMS CT SYTEC/SYTEC i SERIES RENEWAL PARTS
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WARNING WARNUNG
D DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE D VERSUCHEN SIE NICHT, DAS GERÄT ZU REPARIEREN, BEVOR DIESES
MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD. KUNDENDIENST–HANDBUCH NICHT ZU RATE GEZOGEN UND
VERSTANDEN WURDE.
D FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE D WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU
SERVICE PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, VERLETZUNGEN DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS
MECHANICAL OR OTHER HAZARDS. ODER DES PATIENTEN DURCH ELEKTRISCHE SCHLÄGE,
MECHANISCHE ODER SONSTIGE GEFAHREN KOMMEN.
AVERTISSEMENT
AVISO
D CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS. D ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.
D SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE D SI ALGÚN PROVEEDOR DE SERVICIOS AJENO A GEMS SOLICITA UN
AUTRE LANGUE QUE L’ANGLAIS, C’EST AU CLIENT QU’IL INCOMBE DE IDIOMA QUE NO SEA EL INGLÉS, ES RESPONSABILIDAD DEL CLIENTE
LE FAIRE TRADUIRE. OFRECER UN SERVICIO DE TRADUCCIÓN.
D NO SE DEBERÁ DAR SERVICIO TÉCNICO AL EQUIPO, SIN HABER
D NE PAS TENTER D’INTERVENTION SUR LES ÉQUIPEMENTS TANT QUE LE CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.
MANUEL SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS.
D LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE
D LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAÎNER CHEZ LE EL PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN
TECHNICIEN, L’OPÉRATEUR OU LE PATIENT DES BLESSURES DUES À LESIONES PROVOCADAS POR CAUSAS ELÉCTRICAS, MECÁNICAS O DE
DES DANGERS ÉLECTRIQUES, MÉCANIQUES OU AUTRES. OTRA NATURALEZA.
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GE MEDICAL SYSTEMS CT SYTEC/SYTEC i SERIES RENEWAL PARTS
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ATENÇÃO
AVVERTENZA
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CAUTION
DAMAGE IN TRANSPORTATION
Do not use the following devices near this equipment. Use of these devices
All packages should be closely examined at time of delivery. If damage is near this equipment could cause this equipment to malfunction.
apparent, have notation “damage in shipment” written on all copies of the
freight or express bill before delivery is accepted or “signed for” by a General Devices not to be used near this equipment:
Electric representative or a hospital receiving agent. Whether noted or
concealed, damage MUST be reported to the carrier immediately upon Devices which intrinsically transmit radio waves such as; cellular phone,
discovery, or in any event, within 14 days after receipt, and the contents and radio transceiver, mobile radio transmitter, radio–controlled toy, etc.
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 Keep power to these devices turned off when near this equipment.
period.
Medical staff in charge of this equipment is required to instruct technicians,
Call Traffic and Transportation, Milwaukee, WI (414) 827–3449 / 8*285–3449 patients an
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.
GE personnel, please use the GEMS CQA Process to report all omissions,
errors, and defects in this documentation. Customers, please contact your
GE Sales or Service representatives.
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GE MEDICAL SYSTEMS CT SYTEC/SYTEC i SERIES RENEWAL PARTS
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REVISION HISTORY
PAGE REV PAGE REV PAGE REV PAGE REV PAGE REV
Title page . . . . . . . . . . 8 Tab 1 (System) Tab 2 (Operator Console) 2–1 to 2–9 . . . . . . . . . . 6 1–8 . . . . . . . . . . . . blank
Title page rear . . blank 1–1 . . . . . . . . . . . . . . . . 0 1–1 to 1–6 . . . . . . . . . . 2 2–1 to 2–6 . . . . . . . . . . 5
Tab 5 (Table)
a to d . . . . . . . . . . . . . . 0 1–2 . . . . . . . . . . . . blank 2–1 to 2–7 . . . . . . . . . . 8
1–1 to 1–9 . . . . . . . . . . 0 Tab APPENDIX
A .................. 8 2–1 to 2–5 . . . . . . . . . . 0 2–8 . . . . . . . . . . . . blank
1–10 . . . . . . . . . . . blank A–1 to A–4 . . . . . . . . . 0
B . . . . . . . . . . . . . . blank 2–6 . . . . . . . . . . . . . . . . 1
Tab 3 (Gantry) 2–1 to 2–6 . . . . . . . . . . 0
i to ii . . . . . . . . . . . . . . . 0 2–7 . . . . . . . . . . . . . . . . 0
1–1 to 1–9 . . . . . . . . . . 0
ii . . . . . . . . . . . . . . blank 2–8 . . . . . . . . . . . . blank Tab 7 XG Blank/Rear cover . . . . –
1–8 . . . . . . . . . . . . blank
1–1 to 1–7 . . . . . . . . . . 0
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GE MEDICAL SYSTEMS CT SYTEC/SYTEC i SERIES RENEWAL PARTS
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CONTENTS
i
GE MEDICAL SYSTEMS CT SYTEC/SYTEC i SERIES RENEWAL PARTS
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GE MEDICAL SYSTEMS CT SYTEC/SYTEC i SERIES RENEWAL PARTS
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1-1 SUBSYSTEM
4
2
2-1 SUBSYSTEM
2-3 ACCESSORIES
2-6 SOFTWARE
SECTION 1 – OC ILLUSTRATION
OC PRIMARY COMPONENT 4 2
1-1 OC ASSY
Desktop
1–7
1–5
1–140
1–23
1–102 1–25
DC Power Supply
1–44
1–45
1–43
1–21
ÂÂÂÂÂÂÂ
1–100
ÂÂÂÂÂÂÂ
1–20
ÂÂÂÂÂÂÂ
ÂÂÂÂÂÂÂ
Â
 ÂÂÂÂÂÂ
ÂÂÂÂÂÂ
 ÂÂÂÂÂÂ
ÂÂÂÂÂÂ
1–41
ÂÂÂÂÂÂ
ÂÂÂÂÂÂ
1–42
1–40
1–144
AC Power Supply
1–1–7
1–1–6
1–1–5
1–1–3
1–1–1
1–1–2
1–1–4
1–22
1–1
1–66
1–2–6 ÅÅÅÅÅÅÅÅ
ÅÅÅÅÅÅÅÅ
ÅÅÅÅÅÅÅÅ
1–2–6–1
ÅÅÅÅÅÅÅÅ
ÅÅÅÅÅÅÅÅ
ÅÅÅÅÅÅÅÅ
1–141
1–304
1–2
2–7
2–2
ÔÔ
2–5
ÔÔ
2–6
2–3
2–4
2–8
2–1
OC PRIMARY COMPONENT
OPTION
1–307
1–308
1–424
1–405
1–339
1–164
1-1 GANTRY ASSY (continued) 1–163
1–830
Gantry Stationary
1–404
1–204
1–403
1–176
1–206
1–202
1–181
1–425
1–101
1–402
1–412
1–156
1–401 1–413
1–416
1–414
1–160
1–419
1–415
1–418
1–406 1–157
1–312
1–1
1–407
1–4 1–44
1–5
1–45
1–115
1–54
1–120 1–57
1–740
1–104
1–53
1–3–31
1–3
1–6 1–105
1–7
1–81
1–82
ÂÂÂÂÂÂÂÂÂ
ÂÂÂÂÂÂÂÂÂ
1-1 GANTRY ASSY (continued)
ÂÂÂÂÂÂÂÂÂ
ÂÂÂÂÂÂ
ÂÂÂÂÂÂÂÂÂ
ÂÂÂÂÂÂ
ÂÂÂÂÂÂÂÂÂÂ
Gantry Rotational (2/3)
ÂÂÂÂÂÂÂÂÂ
ÂÂÂÂÂÂ
ÂÂÂÂÂÂÂÂÂÂ
ÂÂÂÂÂÂÂÂÂ
ÂÂÂÂÂÂÂÂÂÂ
ÂÂÂÂÂÂ
ÂÂÂÂÂ
ÂÂÂÂÂÂÂÂÂÂ
ÂÂÂÂÂÂ
1–7–1
ÂÂÂÂÂ
ÂÂÂÂÂÂ
1–7–2
1–7–22
1–7–25
1–7–24
1–7–26 1–7–23
1–7–27
1–7–28
1–5–2
1–5–57
1–247
1–245 1–246
1–252
1–251
1–241
1–242
1–243
1–244
1–227
1–228
1–249
1–233
1–248
IMPORTANT NOTE:
When replacing the Collimator as assemble, take attention to the rating plate attached on the collimator cover:
When the new collimator Assy does not contain the rating plate, reuse the current collimator cover, on which the rating plate is
attached.
When the new collimator Assy contains the rating plate, attach the rating plate onto the new collimator cover. It is not necessary
to reuse the current collimator cover.
1–254
1–255
1–291
1–293
1–283
1–235
1–295
1–171
1–145
1–189
1–113
1–149
1–183 1–182
1–160
1–204
Hydraulic Systems
1–60
1–93 1–60 1–57
1–64
1–81
1–96
1–59 1–59
1–65
1–57
1–98
1–97 1–97
Lower Side
For Table 2129565/2129566 For Table 2109041/2109042
1–249
1–250 1–250
1–101
1–102
1–189
1–249
1–130
1–233
1–110
1–67
1–68
1–91
1–95
1–142
1–164
Hydraulic System
Type A Type B
1–185 1–185
1–187 1–187
1–199 1–199
Lower Side
1–162
1–165
1–166
SECTION 1 – XG ILLUSTRATION
1
XG PRIMARY COMPONENT
1–QM2 1–K6∼8
Upper Portion 1–QM1
1–F3
1–121
1–(F3)
1–C1
1–280
1–R6∼8
1–R9
1–PS1
1–T3
1–D1∼2
1–270
1–L1
1–T4
1–RL18
1–DM1∼3
1–R4 1–235
1–279
1–RL16 1–PS3
1–PS2
1–RL15
1–RL17
1–1
1–CT2
1–F5
1–F2
1–CT1
1–R1
1–R2
1–R3
1–K4
1–CB6
1–1–85
1–1–61
1–1–62
1–1–C1
1–1–C2
1–1–C3
1–1–C4
1–453
1–452
1–F1 1–239
1–F4
1–RL13
1–RL14
1–2
1–K3 1–T2
1–T1
1–K2
1–2–1–3
1–2–40
1–2–105
1–2–1
1–2–102
1–2–2
1–2–3
1–2–39
1–2–40
1–2–104 1–2–3
1–2–101
1–2–2
1–2–39
PRIMARY COMPONENT
2-1-2 HV Tank
Direct Current
Type B
A–1
GE MEDICAL SYSTEMS CT SYTEC/SYTEC i SERIES RENEWAL PARTS
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Contrast
Start
Brightness
Table Set
Intercom
–10_C
A–2
GE MEDICAL SYSTEMS CT SYTEC/SYTEC i SERIES RENEWAL PARTS
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Symbol Description
System storage prior to installation:
Maintain non–condensing storage
humidity below 95%
DO NOT store system longer than 90
days
Humidity 5–95%
Excluding Condensation
A–3
GE MEDICAL SYSTEMS CT SYTEC/SYTEC i SERIES RENEWAL PARTS
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CLASS 1 EQUIPMENT EQUIPMENT not suitable for use in the presence of a FLAMMABLE ANES-
Any permanently installed equipment containing operator or patient accessi- THETIC MIXTURE WITH AIR or WITH OXYGEN or NITROUS OXIDE
ble surfaces must provide backup protection against electric shock,in case
the BASIC INSULATION fails. In addition to BASIC INSULATION,Class1
equipment contains a direct connection to a PROTECTIVE(EARTH) CON-
DUCTOR which prevents shocks when a person touches a broken piece of
equipment or touches two different equipment surfaces simultaneously.
CLEANING
TYPE B EQUIPMENT
CLASS I, II, or III EQUIPMENT or EQUIPMENT with INTERNAL ELEC-
The ProSpeed S series system is NOT WATERPROOF. It is NOT designed
TRICAL POWER SOURCES provide an adequate degree of protection
to protect internal components against the ingress of liquids.Clean external
against electric shock arising from (allowable) LEAKAGE CURRENTS or a
breakdown in the reliability of the protective earth connection. system surfaces(Gantry,table,consoles and accessories)with a soft cloth
dipped in hot water and wrung DAMP/DRY. (NOT dripping!) IF NECESSARY,
ORDINARY EQUIPMENT use only mild (dish washing liquid) soap to remove dirt.
Enclosed EQUIPMENT without protection against the ingress of water.
OPERATION 0f EQUIPMENT
CONTINUOUS OPERATION WITH INTERMITTENT LOADING. NOTICE
Operation in which EQUIPMENT is connected continuously to the SUPPLY
Avoid damage to equipment! Some ”spray and
MAINS. The stated permissible loading time is so short that the long term
on–load operating temperature is not attained. The ensuing interval in load- wipe”cleaners etch and permanently cloud
ing is, however, not sufficiently long for cooling down to the long term no–load clear plastic surfaces!! Use only warm water and mild
operating temperature. liquid soap to clean surfaces.
A–4
GE Medical Systems: Telex 3797371
P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.
(Asia, Pacific, Latin America, North America)