Renewal Parts
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GE Medical Systems gemedical.com
Technical Publications Direction 2173228−100 Revision 15
AMX−4+ Renewal Parts (Model 2169360 Series)
Copyrighte 1996, 1997, 1999, 2000, 2003 and 2004 By General Electric Co. All Rights Reserved
AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100 THIS PAGE INTENTIONALLY LEFT BLANK.
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
− THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.
WARNING
− 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.
− CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.
AVERTISSEMENT
− 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.
WARNUNG
− DIESES KUNDENDIENST−HANDBUCH 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, DAS GERÄT ZU REPARIEREN, BEVOR DIESES KUNDENDIENST−HANDBUCH ZU RATE GEZOGEN UND VERSTANDEN WURDE. − WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN DURCH ELEKTRISCHE SCHLÄGE, MECHANISCHE ODER SONSTIGE GEFAHREN KOMMEN.
− ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.
AVISO
− SI ALGÚN PROVEEDOR DE SERVICIOS AJENO A GEMS SOLICITA UN IDIOMA QUE NO SEA EL INGLÉS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN SERVICIO DE TRADUCCIÓN. − NO SE DEBERÁ DAR SERVICIO TÉCNICO 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.
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
ATENÇÃO
− 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. − NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA. − O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELÉTRICOS, MECÂNICOS OU OUTROS.
AVVERTENZA
− 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. − NON TENERE CONTO 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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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
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, Medical Systems 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 everyone 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 take adequate steps to protect against injury. The equipment is sold with the understanding that the General Electric Company, Medical Systems Group, its agents, and representatives have no responsibility for injury or damage which may result from improper use of the equipment. Various protective material and devices are available. It is urged that such materials or devices be used. CAUTION: United States Federal law restricts this device to use by or on the order of a physician.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT 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 Medical 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.
DAMAGE IN TRANSPORTATION All packages should be closely examined at time of delivery. If damage is 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 Electric representative or a 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 Traffic and Transportation, Milwaukee, WI (414) 827−3468 / 8*285−3468 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 & Procedure Bulletins. 6/17/94
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100 THIS PAGE INTENTIONALLY LEFT BLANK.
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
TABLE OF CONTENTS AMX−4+ RENEWAL PARTS... MAJOR COMPONENTS, 2169360, −2, −3, −4, −5, −6, −7, −8, −9, −10... AMX4+ TOP LEVEL BASE ASSEMBLY (INCLUDES 46−302158G2)... HORIZONTAL ARM ASSEMBLY, 46−302156G1, AMX3A2... 76” COLUMN ASSEMBLY, 2174198 & 70” COLUMN ASSEMBLY, 2174198−2... CARRIAGE ASSEMBLY, 46−270306G3... AMX−4+ GENERATOR ASSEMBLY, 46−315159G7/8... DRIVE ELECTRONICS MODULE ASSEMBLY, 46−315340G1, AMX1A5... X−RAY CONTROL MODULE ASSEMBLY, 46−303897G2, AMX1A4... DRIVE HANDLE ASSEMBLY, 46−302276G2... BATTERY CHARGER & ROTOR CONTROL ASSEMBLY... CASSETTE DRAWER ASSEMBLY, 46−270231G2... COVER ASSEMBLY (EMC, GRAY #4), 46−303626G4... HV TRANSFORMER ASSEMBLY (46−270954G1), T3432AP AMX1A6... COLLIMATOR ASSEMBLY (46−270615P2), (2141235), T3497T...
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11 13 33 37 41 45 47 51 53 55 57 59 60 61 65
AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100 THIS PAGE INTENTIONALLY LEFT BLANK.
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
REVISION HISTORY
REV
DATE
0 1 2 3 4 5 6 7 8 9 10 11 12
Dec. 13, 1996 Mar. 7, 1997 Mar. 28, 1997 June 24, 1997 Aug. 14, 1997 Dec. 1, 1997 Dec. 10, 1997 Sept. 23, 1998 Dec. 7, 1998 Mar. 7, 2000 Aug. 8, 2000 Dec. 10, 2001 Aug. 23, 2004
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Feb. 14, 2008
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26OCT2009
15
24SEP2010
REASON FOR CHANGE
Initial release. Changes to battery installation, drive relay for M4 release. Added cord plugs to Page 10. Added collimator; updated vertical column, horizontal column lock latch. High Impact Inspection. Removed screws and added pins to 2169360, item 280. Added reference to furnished items in Introduction. Updated Collimator Assembly (46−270615P2). Updated 2169360, item 19 to 46−267217P22, FUSE. Updated Drive Handle Assembly, 46−302276G1. Updated 46−315159G9/10, item 13, Power Supply to 46−302350P4. Added Part numbers for Panasonic batteries and LVLE power supply. Document revision was changed to ’12’ by error during ePDM revisions of the AMX documentation set. There is no difference between revision 11 and revision 12 of this document. Removed items 239, 246, 247, 248 from 2169360BOM. Updated item 245 from 46−315954P2 to 5291366 “AMX Film Bin Finger Pinch IEC Symbol Label”. In BOM 46−315159, replaced part number 46−270985P2 (solenoid) with 5316584 (ECO 2065241), added part numbers 5316575 (Latch Base Assembly) and 5316585 (Latch Assembly with Hall Effect Sensor). ECO 2065241. Updated Battery Charger & Rotor Control Assembly figure and BOM to add notes regarding new rotor board 5350020 and kit 5391091. ECO 2106236.
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100 THIS PAGE INTENTIONALLY LEFT BLANK.
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
AMX−4+ RENEWAL PARTS Indentification See Illustration 1. The AMX−4+ is identified by Model Number on the rating plate located on the top cover. Model part and catalog numbers are identified in Table 1. This direction contains renewal parts for these units. TABLE 1 AMX−4+ MODELS
Description
Part number
catalog number
domestic
2169360−7
a0659f
domestic, aec
2169360−8
a0659fa
domestic, tech switch
2169360−9
a0659fc
domestic, aec, tech switch
2169360−10
a0659fb
iec, emc
2169360
a0659a
iec, emc, aec
2169360−2
a0659aa
iec, emc, tech switch
2169360−3
a0659ab
iec, emc, aec, tech switch
2169360−4
a0659ac
japan
2169360−5
a0659c
japan short column
2169360−6
a0659d
ILLUSTRATION 1 AMX−4+ IDENTIFICATION
RATING PLATE
Furnished items such as manuals, labels and touchup paint are listed in Direction 2173222−100 AMX−4+ Installattion (Model 2169360 Series).
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100 THIS PAGE INTENTIONALLY LEFT BLANK.
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
MAJOR COMPONENTS, 2169360, −2, −3, −4, −5, −6, −7, −8, −9, −10
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
MAJOR COMPONENTS, 2169360, −2, −3, −4, −5, −6, −7, −8, −9, −10 (FRONT, SIDE AND TOP COVERS)
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
MAJOR COMPONENTS, 2169360, −2, −3, −4, −5, −6, −7, −8, −9, −10 (TOP COVER ASSEMBLY)
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
MAJOR COMPONENTS, 2169360, −2, −3, −4, −5, −6, −7, −8, −9, −10 (HORIZONTAL ARM, COLLIMATOR AND TUBE UNIT ASSEMBLY)
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
MAJOR COMPONENTS, 2169360, −2, −3, −4, −5, −6, −7, −8, −9, −10 (CABLE INSTALLATION)
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
MAJOR COMPONENTS, 2169360, −2, −3, −4, −5, −6, −7, −8, −9, −10 (BATTERY INSTALLATION − GENESIS BATTERIES)
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
MAJOR COMPONENTS, 2169360, −2, −3, −4, −5, −6, −7, −8, −9, −10 (BATTERY INSTALLATION − PANASONIC BATTERIES)
CABLE 7 SENSE LEAD
CABLE 6
CABLE 7 (2) SEE NOTE 2 BATTERY SEPARATOR PAD TYPICAL (4 PLACES) SEE NOTE 3
CABLE 4 SENSE LEAD CABLE 8
CABLE 4 TO CIRCUIT BREAKER
CABLE 1 SENSE LEAD
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CABLE 7 SENSE LEAD
CABLE 3 CABLE 3 SENSE LEAD
CABLE 1 SEE NOTE 2
SEE NOTE 2
CABLE 6 SENSE LEAD battery test terminal strip CABLE 5 CABLE 5 SENSE LEAD
CABLE 1 CABLE 1 SENSE LEAD
SEE NOTE 2 CABLE 2 SENSE LEAD CABLE 2 TO GROUND STUD
NOTE 1: THERE ARE NO INSULATORS #3 & #7. NOTE 2: DON’T CONFUSE INSULATOR #4 WITH INSULATOR #1. INSULATOR #4 HAS TWO NON−FUNCTIONAL HOLES. INSULATOR #1 HAVE TWO CUP−SHAPED BUMPS WITH NO HOLES. INSULATOR #1 MUST BE ORIENTED WITH BUMPS POINTING AWAY FROM YOU. NOTE 3: ADD BATTERY SEPARATOR PADS BETWEEN BATTERIES 1 & 3, 2 & 4, 5 & 6, AND 7 & 8. DON’T REMOVE PAPER BACKING FROM BATTERY SEPARATOR PADS. ORIENT PADS WITH PAPER BACKING FACING UP.
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AMX−4+ RENEWAL PARTS (MODEL 2169360 SERIES)
GE MEDICAL SYSTEMS REV 15
DIRECTION 2173228−100
MAJOR COMPONENTS, 2169360, −2, −3, −4, −5, −6, −7, −8, −9, −10 (DETAIL VIEWS)
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