GE Logiq 9 Service Manual

							Technical 
Publication
Direction 2294854-100
Revision 3
GE Medical Systems
LOGIQ™ 9 Proprietary Manual 
Copyright© 2002, 2003 by General Electric
All Rights Reserved
ADVANCED SERVICE DOCUMENTATION
PROPERTY OF GE
FOR GE SERVICE PERSONNEL ONLY
NO RIGHTS LICENSED - DO NOT USE OR COPY
DISCLOSURE TO THIRD PARTIES PROHIBITED
GE Medical Systems 
						

							GE MEDICAL SYSTEMS PROPRIETARY TO GE
D
IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL 
 i
Important Precautions
•  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.
•  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.
•  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 NICHT 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.
WARNING
AVERTISSEMENT
WARNUNG 
						

							GE MEDICAL SYSTEMSPROPRIETARY TO GE
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IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL   
ii  - 
•  ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.
•  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.
•  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.
•  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.
AV I S O
ATENÇÃO
AVVERTENZA  
						

							GE MEDICAL SYSTEMS PROPRIETARY TO GE
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IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL 
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							GE MEDICAL SYSTEMSPROPRIETARY TO GE
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IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL   
iv  - 
DAMAGE IN TRANSPORTATION - FOR USA ONLY
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 Traffic and Transportation, Milwaukee, WI (262) 827-3468 or 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 And Procedures 
Bulletins.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY
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. Other connections between pieces of 
electrical equipment, calibrations and testing shall be performed by qualified GE Medical Systems 
personnel. 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.
OMISSIONS & ERRORS
If there are any omissions, errors or suggestions for improving this documentation, please contact the 
GE Medical Systems Global Documentation Group with specific information listing the system type, 
manual title, part number, revision number, page number and suggestion details.  E-mail the information 
to :  [email protected]
GE Medical Systems employees should use the Customer Quality Assurance (CQA) System to report 
all documentation omissions, errors or suggestions.
For USA 
Only
For USA 
Only 
						

							GE MEDICAL SYSTEMS PROPRIETARY TO GE
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IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL 
 v
Revision History
List of Effected Pages
RevisionDateReason for change
0April 8, 2002Initial Release
1November 8, 2002Update for BT’02 Release, BEP and FEP changes
2April 4, 2003Update for R2.1.1 Release and hardware changes
3October 23, 2003Update for R3.0 Release and hardware changes
PagesRevisionPagesRevisionPagesRevision
Title PageN/AChapter 2 - Pre-Installation
pages 2-1 to 2-103
Chapter 7 - Diagnostics/
Troubleshooting
pages 7-1 to 7-80
3
Important Precautions
pages i to iv3Chapter 3 - Installation
pages 3-1 to 3-463
Chapter 8 - Replacement 
Procedures
pages 8-1 to 8-194
3
Rev History/LOEP
pages v to vi3Chapter 4 - Functional Checks
pages 4-1 to 4-243Chapter 9 - Replacement Parts
pages 9-1 to 9-423
Table of Contents
pages vii to xxxiv3Chapter 5 - Theory
pages 5-1 to 5-723Chapter 10 - Periodic Maintenance
pages 10-1 to 10-303
Chapter 1 - Introduction
pages 1-1 to 1-123Chapter 6 - Service Adjustments
pages 6-1 to 6-163Index
pages I to IV3
Back CoverN/A 
						

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IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL 
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CHAPTER  1
Introduction
Overview  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Chapter 1  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Service Manual   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Typical Users of the Basic Service Manual   . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2
LOGIQ™ 9 Models Covered by this Manual   . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2
Purpose of Operator Manual(s)  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2
Important Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3
Conventions Used in Book  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3
Standard Hazard Icons   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 4
Product Icons  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5
Safety Considerations  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Introduction   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Human Safety   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Mechanical Safety   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Electrical Safety  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Labels Locations   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Dangerous Procedure Warnings   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9
Lockout/Tagout Requirements (For USA Only)  . . . . . . . . . . . . . . . . . . . . . . 1 - 9
Returning/Shipping Probes and Repair Parts   . . . . . . . . . . . . . . . . . . . . . . . 1 - 9
EMC, EMI, and ESD  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10
Electromagnetic Compatibility (EMC)   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10
CE Compliance   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10
Electrostatic Discharge (ESD) Prevention  . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10
Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Contact Information   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
System Manufacturer  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12
Table of Contents 
						

							GE MEDICAL SYSTEMSPROPRIETARY TO GE
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CHAPTER  2
Pre-Installation
Overview  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
Purpose of Chapter 2  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
General Console Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Console Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Cooling   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Lighting   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Electrical Requirements  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
LOGIQ™ 9 Power Requirements   . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Inrush Current  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Site Circuit Breaker  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Site Power Outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Unit Power Plug . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Power Stability Requirements  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4
Scan Probe Environmental Requirements  . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5
Time and Manpower Requirements  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5
Facility Needs  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Purchaser Responsibilities  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Required Features  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7
Desirable Features  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7
Minimal Floor Plan Suggestion   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 8
Networking Pre-installation Requirements  . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9
Purpose of the DICOM Network Function  . . . . . . . . . . . . . . . . . . . . . 2 - 9
DICOM Option Pre-installation Requirements . . . . . . . . . . . . . . . . . . 2 - 9