GE LOGIQ 5 PRO Service Manual

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Technical Publication
Direction 2380207 Revision 7

GE Medical Systems

LOGIQ™5 PRO Service Manual
Operating Documentation
Copyright© 2006 by General Electric Co.
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GE MEDICAL SYSTEMS DIRECTION 2407381, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
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GE MEDICAL SYSTEMS
GE Medical Systems: Telex 3797371 P.O. Box 414; Milwaukee, Wisconsin 53201, U.S.A. (Asia, Pacific, Latin America, North America)
GE Ultraschall:Tel: +49 (0) 212 28 02 207 Deutschland GmbH & Co KG Beethovenstrabe 239, Postfach 11 05 60 D-42655 Solingen, Germany
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GE MEDICAL SYSTEMS D
IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL

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.
WARNING
AVERTISSEMENT
• 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, MéCA NIQUES 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 D IE SES 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.
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
• 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
AVISO
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 TRADUç ãO.
ATENÇÃO
• 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 SEGURANç A 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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IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
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.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY
All electrical Installations that are preliminary to position ing of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. Othe r conn ections between pieces o f electrical equipment, calibrations and testing sh all be perfo rm ed by qu a lifie d GE Me dic al Syst em s 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. Ma il the information to : Service Documentation, 9900 Innovation Drive (RP-2123), Wauwatosa, WI 53226, USA.
GE Medical Systems employees should use the iTrak System to report all documentation errors or omissions.
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GE MEDICAL SYSTEMS D
IRECTION 2380207, REVISION 7 LOGIQ™5 PRO SERVICE MANUAL
LEGAL NOTES
The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE Medical Systems.
GE Medical Systems may revise this publication from time to time without written notice.
TRADEMARKS
All products and their name brands are trademarks of their respective holders.
COPYRIGHTS
All Material Copyright© 2006 by General Electric Inc. All Rights Reserved
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™5 PRO SERVICE MANUAL

Revision History

Revision Date Reason for change
0 2003.5.18 Initial Release - software version R2.0.1 1 2004.3.27 R2.1.2 Software Release 2 2004.5.19 Updated Spare Parts Information on Chapter 9 3 2004.10.20 LOGIQ 5 BT’04 software release 4 2005.5.14 LOGIQ 5 BT’05 software release 5 2006.11.10 LOGIQ 5 BT’05 M4 software release 6 2007. 3. 30 Updated Spare Parts Information on Chapter 9 & Content update 7 2008. 9. 12 Insert the Function check Procedure

List of Effected Pages

Pages Revision Pages Revision Pages Revision
Title Page 7 1-1 to 1-14 7 Back Cover N/A
Warnings
i to iv
Rev Hist/LOEP
A-v to A-vi
Table of Contents
i to viii
7 2-1 to 2-10 7
7 3-1 to 3-28 7
7 4-1 to 4-26 7
5-1 to 5-44 7 6-1 to 6-14 7 7-1 to 7-44 7
8-1 to 8-118 7
9-1 to 9-20 7
10-1 to 10-32 7
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Table of Contents
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™ 5 Models Covered by this Manual . . . . . . . . . . . . . . . . . . . . . . . .1 - 2
Purpose of Operator Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 2
Important Conventions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 3
Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 3
Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 5
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 7
Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 7
Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 7
Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 8
Lockout/Tagout Requirements (For USA Only) . . . . . . . . . . . . . . . . . . . . . .1 - 12
Electromagnetic Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 13
Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 13
CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 13
Customer Assistance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 14
System Manufacture . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 14
Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 14
CHAPTER 2
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 1
Purpose of chapter 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 1
General Console Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 2
Console Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 2
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Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 3
EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 4
Scan Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 5
Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 6
Purchaser Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 6
Required Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 7
Desirable Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 7
Recommended and Alternate Ultrasound Room Layout . . . . . . . . . . . . . . .2 - 8
CHAPTER 3
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 1
Purpose of Chapter 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 1
Installation Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 1
Average Installation Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 1
Installation Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 2
Moving into Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 9
Adjusting System Clock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 9
Product Locator Installation Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 9
Preparing for Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 10
Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 10
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 10
EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 10
Completing the Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 11
Power On/Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 11
Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 14
Transducer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 14
System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 15
Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 18
On-Board Optional Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 19
External I/O Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 20
Video Specification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 23
Software/Option Configuration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 23
Loading Base System Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 25
Before You Load Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 25
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IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Managing Data, Presets and Images . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25
Save Connectivity Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25
Possible GE USB Control Panel Driver Loss . . . . . . . . . . . . . . . . . . . . . . . 3 - 28
Possible Behavior of the First Power Up After Application Load . . . . . . . . 3 - 35
GE USB Control Panel Driver Loss . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 35
Restore Patient, Report, and User-Defined Presets . . . . . . . . . . . . . . . . . . 3 - 38
Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 39
User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 39
CHAPTER 4
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
Purpose for Chapter 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
Required Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
General Procedure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
Power On/Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3
Power Off / Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 4
System Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
System B/M-Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 8
System CFM and PWD Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10
Probe/Connectors Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 11
Using Cine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 12
Image Management (QG) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
Using the CD-RW / MOD (Magneto-Optical Drive) . . . . . . . . . . . . . . . . . . . 4 - 14
Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 22
Operator I/O Movement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24
Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 26
CHAPTER 5
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1
Purpose of Chapter 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1
Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 3
Front End . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5
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Backend Processor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 16
Patient I/O (Option) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 18
External I/O (Rear Panel) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 21
Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 22
Interconnect Cabling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 23
Power Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 24
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 24
AC Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 24
DC Power (Low Voltage) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 25
Air Flow Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 28
Air Flow Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 28
Filters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 28
Fans . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 29
Service Platform. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 30
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 30
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 38
Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 39
Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 39
PM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 40
CHAPTER 6
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 1
Purpose of this chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 1
Regulatory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 1
Power Supply Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 2
LV Unit Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 2
Adjustments Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 4
Reloading the Probe Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 5
Monitor and LCD Adjustments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 8
Contrast and Brightness Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 8
LCD Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 9
1-x -
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GE MEDICAL SYSTEMS D
IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
CHAPTER 7
Diagnostics/Troubleshooting
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1
Purpose of Chapter 7 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1
Network Connectivity Troubleshooting. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Collect Vital System Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Check and Record the P4 Key Function . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Setting the P4 Key to Screen Capture . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5
Reset the P4 Key to Customer’s Functionality . . . . . . . . . . . . . . . . . . . . . . 7 - 7
Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
CHAPTER 8
Replacement Procedures
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Purpose of Chapter 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . DISAS-
SEMBLY/RE-ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
CRT Assy (FRU No. 100) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Monitor Cable Assy (FRU No. 101) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4
Monitor Cover Set (FRU No. 102) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 6
Monitor S/W Assy (FRU No. 103) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 7
Speaker Assy (FRU No. 104) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 9
Task Lamp Assy (FRU No. 105) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 11
Keyboard Block . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 13
KeyBoard Assy (FRU No. 200) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 13
KeyBoard Front Grip (FRU No. 201) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 15
Probe Holder (FRU No. 202) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 16
ECG Cable Hook (FRU No. 203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 17
OP Panel Encoder Assy (FRU No. 204) . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 18
OP Panel TGC Assy (FRU No. 205) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 20
TGC Knob Set (FRU No. 206) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 21
OP Panel A/N Keyboard Assy (FRU No. 207) . . . . . . . . . . . . . . . . . . . . . . 8 - 22
OP Panel Trackball Assy (FRU No. 208) . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 24
OP Panel HUB board Assy (FRU No. 209) . . . . . . . . . . . . . . . . . . . . . . . . 8 - 25
OP Panel LCD Assy (FRU No. 210) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 27
- 1-xi
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
OP Panel LCD Encoder Assy (FRU No. 211) . . . . . . . . . . . . . . . . . . . . . . .8 - 29
Covers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 31
Left Cover (FRU No. 300) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 31
Right Cover (FRU No. 301) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 32
Rear Cover (FRU No. 302) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 33
Rear Door Cover (FRU No. 303) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 34
Top Cover (FRU No. 304) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 35
Front Base Cover (FRU No. 305) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 37
Front Cover (FRU No. 306) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 39
OP Side L Cover (FRU No. 307) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 40
OP Side R Cover (FRU No. 308) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 42
OP Rear Cover (FRU No. 309) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 44
OP Bottom Cover (FRU No. 310) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 45
OP Curtain Cover (FRU No. 311) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 46
EMI Cover L (FRU No. 312) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 48
EMI Cover R (FRU No. 313) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 49
Side Cap (FRU No. 314) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 50
Side Fringe (FRU No. 315) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 51
Body Block. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 52
Rear Handle (FRU No. 400) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 52
Rear Panel Assy (FRU No. 401) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 54
Gas Spring Assy (FRU No. 402) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 56
Front Caster (FRU No. 403) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 58
Rear Caster (FRU No. 404) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 59
Bumper Set (FRU No. 405) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 60
Air Filter Set (FRU No. 406) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 61
PCB Boards. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 62
RLY Assy (FRU No. 500) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 62
LMT Assy (FRU No. 501) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 64
BackPlane (FRU No. 502) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 66
PCB Boards (FRU No. 503, 505~510) . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 68
DC Fan Assy(FRU No. 504) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 70
PC Block . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 71
BEP (Back End Processor) ASSY(FRU No. 600) . . . . . . . . . . . . . . . . . . . .8 - 71
SMPS Assy, Hard Disk, CD R/W (FRU No. 601, 602, 603) . . . . . . . . . . . . .8 - 72
Power Block. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 73
AC Power Assy (FRU No. 700) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 73
LV Unit (FRU No. 701) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 75
JPC Assy (FRU No. 702) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 77
Transformer (FRU No. 703) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 79
AC Power Box (FRU No. 704) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 81
Fuse Set (FRU No. 705) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 83
1-xii -
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IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Manpower . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 84
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 84
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 84
Base Load Software Load Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 84
Optional Manual Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 87
Loading Applications Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 92
Final System Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 93
Manpower . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 99
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 99
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 99
Image Management Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 99
Loading Applications Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 105
System Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 108
Installation an Optional USB Line Printer . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 109
CHAPTER 9
Renewal Parts
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1
Purpose of Chapter 9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1
List of Abbreviations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1
Renewal Parts Lists . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2
Equipment Models Covered in this Chapter . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2
CHAPTER 10
Periodic Maintenance
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Purpose of Chapter 10 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Why do Periodic Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Keeping Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Quality Assurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Periodic Maintenance Schedule. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
How often should PMs be performed? . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Special Tools, Supplies and Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4
- 1-xiii
Page 18
GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Preliminary Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 5
Input Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 7
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 7
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 8
Probe Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 9
Using a Phantom . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 10
Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 10
Safety Test Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 10
Grounding Continuity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 12
Isolated Patient Lead (Source) Leakage–Lead to Ground . . . . . . . . . . . . . .10 - 16
Isolated Patient Lead (Source) Leakage–Lead to Lead . . . . . . . . . . . . . . . .10 - 17
Isolated Patient Lead (Sink) Leakage-Isolation Test . . . . . . . . . . . . . . . . . .10 - 18
1-xiv -
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GE MEDICAL SYSTEMS D
IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Chapter 1 Introduction

Section 1-1 Overview

1-1-1 Purpose of Chapter 1

This chapter describes important issues related to safely servicing the LOGIQ™ 5 PRO scanner. The service provider must read and understand all the information presented in this manual before installing or servicing a unit.
Table 1-1 Contents in Chapter 1
Section Description Page Number
1-1 1-2 1-3 1-4 1-5
Overview Important Conventions Safety Considerations EMC, EMI, and ESD Customer Assistance

1-1-2 Purpose of Service Manual

This Service Manual provides installation and service information for the LOGIQ™ 5 PRO Ultrasound Scanning System and contains the following chapters:
1.) Chapter 1 - Introduction: Contai ns a content summary and warnings.
2.) Chapter 2 - Pre-Installation: Contains pre-installation requirements for the LOGIQ™ 5 PRO.
3.) Chapter 3 - Installation: Contains installation procedures.
4.) Chapter 4 - Functional Checks: Contains functional checks that are recommended as part of the installation, or as required during servicing and periodic maintenance.
5.) Chapter 5 - Components and Functions (Theory): Contains block diagrams and functional explanations of the electronics.
6.) Chapter 6 - Service Adjustments: Contains instructions on how to make availa ble adjustments to the LOGIQ™ 5 PRO.
7.) Chapter 7 - Diagnostics/Troubleshooting: Provides procedu res for running diagnostic or related routines for the LOGIQ™ 5 PRO.
8.) Chapter 8 - Replacement Procedures: Provides disassembly procedures and reassembly procedures for all changeable Field Replaceable Units (FRU).
9.) Chapter 9 - Renewal Parts: Contains a complete list of field replaceable parts for the LOGIQ™ 5 PRO.
10.)Chapter 10 - Care & Maintenance: Provides periodic maintenance procedures for the LOGIQ™ 5 PRO.
1-1
1-3 1-12 1-18 1-19
Chapter 1 Introduction 1-1
Page 20
GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL

1-1-3 Typical Users of the Basic Service Manual

Service Personnel (installation, maintenance, etc.).
Hospital’s Service Personnel
Contractors (Some parts of Chapter 2 - Pre-Installation)

1-1-4 LOGIQ™ 5 PRO Models Covered by this Manual

Table 1-2 LOGIQ™ 5 PRO Model Designations
Part Number Description
2381304 LOGIQ™ 5 PRO Console for Japan 2381301 LOGIQ™ 5 PRO Console for USA 2381302 LOGIQ™ 5 PRO Console for Europe 2381303 LOGIQ™ 5 PRO Console for Korea

1-1-5 Purpose of Operator Manual(s)

The Operator Manual(s) should be fully rea d and understood before operating the L OGIQ™ 5 PRO and also kept near the unit for quick reference.
1-2 Section 1-1 - Overview
Page 21
GE MEDICAL SYSTEMS D
IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL

Section 1-2 Important Conventions

1-2-1 Conventions Used in Book

Icons
Pictures, or icons, are used wherever they reinforce the printed message. The icons, labels and conventions used on the product and in the service information are described in this chapter.
Safety Precaution Messages
Various levels of safety precaution messages may be found on the equipment and in the service information. The different levels of concern are identi fied by a flag word that precedes the precautionary message. Known or potential hazards are labeled in one of following ways:
DANGER
DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL CAUSE SEVERE PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE IGNORED.
WARNINGWARNING
CAUTION
NOTICE
NOTE: Notes provide important information about an item or a procedure.
WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT CAN CAUSE SEVERE PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED.
Caution is used to indicate the presence of a hazard that will or can cause minor personal injury and property damage if instructions are ignored.
Equipment Damage Possible Notice is used when a hazard is present that can cause property damage but has absolutely no
personal injury risk.
Example: Disk drive will crash.
Information contained in a NOTE can often save you time or effort.
Chapter 1 Introduction 1-3
Page 22
GE MEDICAL SYSTEMS
N
DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL

1-2-2 Standard Hazard Icons

Important information will always be preceded by the exclamation point contained within a triangle, as seen throughout this chapter. In addition to text, several different graphical icons (symbols) may be used to make you aware of specific types of hazards that could cause harm.
Table 1-3 Standard Hazard Icons
ELECTRICAL MECHANICAL RADIATION
LASER HEAT PINCH
LASER
LIGHT
Other hazard icons make you aware of specific procedures that should be followed.
Table 1-4 Standard Icons Indicating a Special Procedure Be Used
AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION
TAG
&
LOCKOUT
Date
Signed
EYE
PROTECTIO
1-4 Section 1-2 - Important Conventions
Page 23
GE MEDICAL SYSTEMS D
IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL

1-2-3 Product Icons

The following table describes the purpose and locatio n of safety labe ls and other importan t information provided on the equipment.
Table 1-5 Product Icons
LABEL/SYMBOL PURPOSE/MEANING LOCATION
Identification and Rating Plate
Device Listing/Certification Labels
Type/Class Label
IP Code (IPX8)
Manufacturer's name and address Date of manufacture Model and serial numbers Electrical ratings
Laboratory logo or labels denoting conformance with industry safety standards such as UL or IEC.
Used to indicate the degree of safety or protection.
Indicates the degree of protection provided by the enclosure per IEC 529. IPX8 indicates drip proof.
Equipment Type BF (man in the box symbol) IEC 878-02-03 indicates B Type equipment having even more electrical isolation than standard Type B equipment because it is intended for intimate patient contact.
Equipment Type CF (heart in the box symbol) IEC 878-02-05 indicates equipment having a high degree of protection suitable for direct cardiac contact.
Rear of console near power inlet Under monitor On each probe
Rear of console Under front of monitor
Footswitch
Probe connectors PCG connector or Rear of Console
ECG connector Surgical probes
"CAUTION" The equilateral triangle is usually used in combination with other symbols to advise or warn the user.
ATTENTION - Consult accompanying documents " is intended to alert the user to refer to the operator manual or other instructions when complete information cannot be provided on the label.
"CAUTION - Dangerous voltage" (the lightning flash with arrowhead in equilateral triangle) is used to indicate electric shock hazards.
Chapter 1 Introduction 1-5
Various
Various
Various
Page 24
GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Table 1-5 Product Icons (Continued)
LABEL/SYMBOL PURPOSE/MEANING LOCATION
"Mains OFF" Indicates the power off position of the mains power switch.
"OFF/Standby" Indicates the power off/ standby position of the power switch.
CAUTION This Power Switch DOES NOT ISOLATE Mains Supply
"Mains ON" Indicates the power on position of the mains power switch.
"ON" Indicates the power on position of the power switch.
CAUTION This Power Switch DOES NOT ISOLATE
Mains Supply
"Protective Earth" Indicates the protective earth (grounding) terminal.
Rear of system adjacent to mains switch
Adjacent to On-Off/Standby Switch
Front Panel Switch
Internal
"Equipotentiality" Indicates the terminal to be used for connecting equipotential conductors when interconnecting (grounding) with other equipment.
Rear of console
1-6 Section 1-2 - Important Conventions
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GE MEDICAL SYSTEMS D
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1-2-4 WEEE Label

The following table describes the meaning of WEEE label and its translation provided on the equipment.
Table 1-6 WEEE Label
LABEL/SYMBOL LANGUAGE PURPOSE/MEANING
This symbol indicates that the waste of electrical and electronic equipme nt must
English
Czech (CZE)
not be disposed as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufactu rer for infor mation concerning the decommissioning of your equi pme n t.
Tento symbol znamená, že díly elektrických nebo elektronických zařízení nesmí být likvidovány do netříděného odpadu, ale musí být likvidovány samostatně. Obraťte se prosím na autorizovaného představitele výrobce, který poskytne informace týkající se likvidace vašeho přístroje.
Danish (DAN)
Dutch (DUT)
Catalan (CAT)
Chinese (CHN)
Dette symbol angiver, at elektrisk og elektronisk affald ikke må bortskaffes som usorteret brændbart affald, men skal indsamles særskilt. Kontakt venligst en autoriseret repræsentant for producenten for at få oplysninger om, hvordan dit udstyr skal bortskaffes.
Dit symbool geeft aan dat het afval van elektrische en elektronische apparatuur niet ongescheiden mag worden meegegeven met het huisvuil, maar apart moet worden ingeleverd. Neem contact op met een erkende vertegenwoordiger van de fabrikant voor informatie over het inleveren van uw apparatuur.
Aquest símbol indica que els residus dels equips elèctrics i electrònics s'han d'abocar per separat, no com a residus municipals no classificats. Contacteu amb un representant autoritzat del fabricant per obtenir informació sobre com desfer-vos del vostre equip.
Estonian (EST)
See märk näitab, et tarbetuks muutunud elektri- ja elektroonikaseadmeid ei tohi ära visata sortimata olmejäätmetena, vaid need tuleb eraldi kokku koguda. Seadmete käitlemise kohta küsige lisateavet tootja volitatud esindajalt.
Chapter 1 Introduction 1-7
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DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Table 1-6 WEEE Label(Continued)
LABEL/SYMBOL LANGUAGE PURPOSE/MEANING
Tämä kuvatunnus ilmaisee, että sillä merkittyä sähkö- ja
Finnish (FIN)
elektroniikkalaitetta ei saa hävittää lajittelemattomana yhdyskuntajätteenä vaan se on kerättävä talteen erikseen. Ota yhteyttä tuotteen valmistajan valtuuttamaan myyntiedustajaan ja kysy lisätietoja laitteen käytöstä poistosta.
Ce symbole indique que les déchets relatifs à l'équipement électrique et
French- France (FRA)
électronique ne doivent pas être jetés comme les ordures ménagères non-triées et doivent être collectés séparément. Contactez un repré sentant agréé du fabricant pour obtenir des informations sur la mise au rebut de votre équipement.
Dieses Symbol kennzeichnet elektrische und elektronische Geräte, die nicht mit dem gewöhnlichen, unsortierten Hausmüll entsorgt werden dü
German (GER)
rfen, sondern separat behandelt werden müssen. Bitte nehmen Sie Kontakt mit einem autorisierten Beauftragten des Herstellers auf, um Informationen hinsichtlich der Entsorgung Ihres Gerätes zu erhalten.
Greek (GRE)
Hungarian (HUN)
Icelandic (ICE)
Αυτό το σύµβολο υποδηλώνει ότι τα απόβλητα ηλεκτρικού και ηλεκτρονικού εξ οπλισµού δεν πρέπει να απορρίπτονται ως κοινά απορρίµατα, αλλά να συλλέγον ται ξεχωριστά. Παρακαλούµε επικοινωνήστε µε έναν εξουσιοδοτηµένο αντιπρό σωπο του κατασκευαστή για πληροφορίες σχετικά µε την απόρριψη του εξοπλισ
ού.
A szimbólum azt jelzi, hogy az elektromos és elektronikus készülék hulladékát tilos nem szelektív lakossági hulladékként kezelni, hanem elkülönítve kell gyű jteni. Kérjük, a berendezés leselejtezését illetőleg lépjen kapcsolatba a gyártó hivatalos ké
viseletével.
Merki þetta táknar að rafeindatækjum skal eytt á sérstakan máta, ekki m á losa rafeindatæki í hefðbundin sorphirðuílát sem óflokkað sorp. Vinsamlega hafið samband við umboðsmann framleiðanda fyrir upplý singar um hvernig tækinu skal eytt.
1-8 Section 1-2 - Important Conventions
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GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Table 1-6 WEEE Label(Continued)
LABEL/SYMBOL LANGUAGE PURPOSE/MEANING
Questo simbolo indica che i rifiuti derivanti da apparecchiature elettriche ed
Italian (ITA)
elettroniche non devono essere smaltiti come rifiuti municipali indifferenziati e devono invece essere raccolti separatamente. Per informazioni relative alle modalità di smantellamento delle apparecchiature fuori uso, contattare un ra
resentante autorizzato del fabbricante.
Japanese (JPN)
Šis apzīmējums norāda, ka no elektriskā un elektroniskā aprīkojuma
Latvian (LAT)
atkritumiem nedrīkst atbrīvoties kā no nešķirotiem mājsaimniecības atkritumiem un tie ir jāsavāc atsevišķi. Lūdzu, sazinieties ar pilnvarotu raž otāja pārstāvi, lai saņemtu informāciju par aprīkojuma ekspluatācijas pā rtraukšanu.
Lithuanian (LIT)
Norwegian (NOR)
Polish (POL)
Portuguese­Brazilian (POB)
Šis simbolis nurodo, kad elektros ir elektroninės įrangos atliekos turi būti surenkamos atskirai ir negali būti šalinamos kaip nerūšiuotos savivaldybė s tvarkomos atliekos. Informacijos apie įrangos veikimo sustabdymą kreipkitės į įgaliotąjį gamintojo atstovą.
Dette symbolet angir at elektrisk og elektronisk utstyr ikke skal kastes som restavfall, men må leveres inn separat. Ta kontakt med en autorisert representant for produsenten hvis du vil ha informasjon om hvordan utstyret skal avhendes.
Ten symbol oznacza, iż składowanie zużytych urządzeń elektrycznych i elektronicznych wraz z ogólnymi odpadami miejskimi jest zabronione. Informacji na temat miejsc składowania tego typu odpadów udziela producent sprzętu.
Este símbolo indica que os resíduos do equipamento elétrico e eletrônico não devem ser descartados no sistema de coleta de lixo municipal, e sim coletados separadamente. Favor entrar em contato com um representante autorizado do fabricante para obter informações sobre como descartar seu equipamento.
Chapter 1 Introduction 1-9
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DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Table 1-6 WEEE Label(Continued)
LABEL/SYMBOL LANGUAGE PURPOSE/MEANING
Acest simbol indică faptul că deşeurile de echipamente electrice şi
Romanian (ROM)
electronice nu au voie să fie aruncate nediferenţiat ca gunoi menajer şi c ă ele trebuie colectate separat. Vă rugăm să luaţi legătura cu un reprezentant autorizat al producătorului pentru a obţine informaţii referitoare la eliminarea ecologică a echipamentului dumneavoastră.
Символ обозначает: недопустимо выбрасывать электрическое и эле
Russian (RUS)
ктронное оборудование с неотсортированным бытовым мусором. Он о должно собираться отдельно. Для получения сведений об утилиза ции оборудования обратитесь к авторизованному представителю ко мпании-производителя.
Ovaj simbol označava da se otpad električne i elektronske opreme ne
Serbian (SCC)
sme odlagati zajedno sa običnim gradskim smećem, već se mora pokupiti posebno. Molimo vas da kontaktirate ovlašćenog predstavnika proizvođača svoje opreme, kako bi ste se informisali o njenom pravilnom rashodu.
Slovakian (SLK)
Slovenian (SLN)
Spanish-Spain (SPA)
Swedish (SWE)
Tento symbol označuje, že odpad elektrického a elektronického materiá lu sa nesmie vyhadzovať do netriedeného komunálneho odpadu, ale mus í sa likvidovať oddelene. Viac informácií o likvidácii vášho zariadenia vám poskytne poverený zástupca výrobcu.
Ta simbol obeležava da se elektronski otpad in elektronska oprema ne sme odlagati skup z navadnim mesnim otpadom, ter se mora pobrat posebej. Prosimo vas da kontaktirate pooblaščenega prodajalca opreme, kako bi se informirali o n
enem pravilnem rashodu.
Este símbolo indica que el equipo eléctrico y electrónico no debe tirarse con los desechos domésticos y debe tratarse por separado. Contacte con el representante local del fabricante para obtener más información sobre la forma de desechar el equipo.
Denna symbol anger att elektriska oc h elektroniska utrustningar inte få r avyttras som osorterat hushållsavfall och måste samlas in separat. Var god kontakta en auktoriserad tillverkarrepresentant för information angående avyttring av utrustnin
en.
1-10 Section 1-2 - Important Conventions
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GE MEDICAL SYSTEMS D
IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Table 1-6 WEEE Label(Continued)
LABEL/SYMBOL LANGUAGE PURPOSE/MEANING
Bu sembol, elektrikli ve elektronik ekipmanların sınıflandırılmamış çöp
Turkish (TUR)
olarak atılmaması ve ayrı olarak toplanması gerektiğini belirtir. Lütfen ekipmanınızın imhasıyla ilgili olarak üreticinin yetkili temsilcisine baş vurun.
The symbol is affixed to a battery to advise the user or owner thar it must be recycled or disposed of in accordance with local, state, or country laws.
English
The letter below indicates the toxic element (Pb=Lead, Cd=Cadmium, Hg=Mercury) that is contained in the battery that may require special recycling or disposal method, Please contact a GEHC representative to facilitate servicing, removal and disposal options.
Chapter 1 Introduction 1-11
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL

Section 1-3 Safety Considerations

1-3-1 Introduction

The following safety precautions must be observed duri ng all phases of operation, service and repair of this equipment. Failure to comply with these precautions or with specific warnings elsewhere in this manual, violates safety standards of design, manufacture and intended use of the equipment.

1-3-2 Human Safety

Operating personnel must not remove the system covers. Servicing should be performed by authorized personnel only. Only personnel who have participated in a LOGIQ™ 5 PRO Training are authorized to service the equipment.

1-3-3 Mechanical Safety

WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
CAUTION
CAUTION
WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.
ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT CAN EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN HANDLING AND PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A DAMAGED OR DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS CAN RESULT IN SERIOUS INJURY AND EQUIPMENT DAMAGE.
NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK, IT MAY BE DAMAGED.
Always lower and center the Opertaor I/O Panel before moving the scanner.
The LOGIQ™ 5 PRO weighs 180 kg or more, depending on installed periphera ls, (500 lbs., or more) when ready for use. Care must be used when moving it or replacing its parts. Failure to follow the precautions listed could result in injury, uncontrolled motion and costly damage.
ALWAYS: Be sure the pathway is clear. Use slow, careful motions. Use two people when moving on inclines or lifting more than 16 kg (35 lbs).
1-12 Section 1-3 - Safety Considerations
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1-3-3 Mechanical Safety (cont’d)
NOTE: Special care should be taken when transporting the unit in a vehicle:
Secure the unit in an upright position.
Lock the wheels (brake)
DO NOT use the Control Panel as an anchor point.
Place the probes in their carrying case.
Eject any Magneto Optical disk or CD from their drive.
CAUTION
Keep the heat venting holes on the monitor unobstructed to avoid overheating of the monitor.

1-3-4 Electrical Safety

To minimize shock hazard, the equipment chassis must be connected to an electrical ground. The system is equipped with a three-conductor AC power cable. This must be plugged into an approved electrical outlet with safety ground. If an extension cord is used with the system, make sure that the total current rating of the system does not exceed the extension cord rating.
The power outlet used for this equipment should not be shared with other types of equipment. Both the system power cable and the power connector meet international electrical standards.
WARNINGWARNING
DO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY CIRCUMSTANCES.
Chapter 1 Introduction 1-13
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL

1-3-5 Label Locations

NOTE: For the symbols shown in the illustration below, refer to previous pages in this chapter.
(1)
(2)
(3)
Figure 1-1 OUTSIDE MARKINGS OF LOGIQ™ 5 PRO
(Monitor)
1.) Caution for Possible injury : “Never put any device onto the Monitor”
2.) Caution for Hazardous movement : (Inside of the OP rear Cover)
3.) Defibrillator Label ““Do not use with Defibrillator”(On optional ECG Module)
1-14 Section 1-3 - Safety Considerations
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IRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
1-3-5Label Locations (cont’d).
(1)
(2)
(7)
220-240V 500VA Max
Including front printer panel
Europe/USA Console (220V)
100~120V 500VA Max
Including front printer panel
Japan/USA/Asia Console (100~120V)
(9)
(3) (4)
(5)
(6)
(8)
Circuit Breaker
On
AC Line Input
100-120V~ 50/60Hz
1250VA Max
I
or
AC Line Input
220-240V~ 50/60Hz
Off
1250VA Max
Figure 1-2 OUTSIDE MARKINGS OF LOGIQ™ 5 PRO
1.) Possible Shock Hazard
2.) Label -”Do not use the following devices near this equ ipm e nt .”
3.) Label - “The equipment weighs approximately 180kg.
4.) Prescription Devices
5.) CE Mark Label
6.) CISPR Label
7.) Voltage Range Indication Label
8.) Power Indication Label
9.) Grounding reliability Label.
Circuit Breaker
On
I
Off
(Rear)
Chapter 1 Introduction 1-15
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GE MEDICAL SYSTEMS
LOGIQ 5 PRO
DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
1-3-5Label Locations (cont’d)
GE ULTRASOUND KOREA LTD.
LOGIQ 5 PRO
1250VA
(2)
LOGIQ 5 PRO
GE ULTRASOUND KOREA
(7)
(1)
(6)
China 220V Console
LOGIQ 5 PRO
(3)
(4)
(5)
1250VA
LOGIQ 5 PRO
120V
1250VA
GE ULTRASOUND Korea
LOGIQ 5 PRO
Korea 220V Console
Figure 1-3 OUTSIDE MARKINGS OF LOGIQ™ 5 PRO
1.) UL Label
2.) Identification and Rating Plate - USA/Asia 120V Console
3.) Identification and Rating Plate - Europe/Asia/Latin America 220V Console
4.) Identification and Rating Plate - Japan 100V Console
5.) Identification and Rating Plate - Korea 220V Console
6.) Caution EIAJ Label
7.) Identification and Rating Plate - China 220V Console
1-16 Section 1-3 - Safety Considerations
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1-3-6 Dangerous Procedure Warnings

Warnings, such as the examples below, precede potentially dangerous procedures throughout this manual. Instructions contained in the warnings must be followed.
DANGER
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.
WARNINGWARNING
WARNINGWARNING
EXPLOSION WARNING DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE.
OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT CONSTITUTES A DEFINITE SAFETY HAZARD.
DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT
INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION OF THE EQUIPMENT.

1-3-7 Lockout/Tagout Requirements (For USA Only)

Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the electrical Mains plug.
Chapter 1 Introduction 1-17
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL

Section 1-4 EMC, EMI, and ESD

1-4-1 Electromagnetic Compatibility (EMC)

Electromagnetic compatibility describes a level of performance of a device within its electromagnetic environment. This environment consists of the device itself and its surroundings including other equipment, power sources and persons with which the device must interface. Inadequate compatibility results when a susceptible device fails to perform as intended due interference from its environment or when the device produces unacceptable levels of emission to its environment. This interference is often referred to as radio–frequency or electromagnetic interference (RFI/EM I) an d can be rad iated th rough space or conducted over interconnecting power of signal cables. In ad dition to electromagnetic energy, EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and disturbances in the electrical power supply.

1-4-2 CE Compliance

The LOGIQ™ 5 PRO unit conforms to all applicable conducted and radiated emission limits and to immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line transient requirements.
For applicable standards refer to the Safety Chapter in the Basic User Manual.
NOTE: For CE Compliance, it is critical that all covers, screws, sh ielding, gaskets, mesh, clamps, a re in
good condition, installed tightly without skew or stress. Proper installation following all comments noted in this service manual is required in order to achieve full EMC performance.

1-4-3 Electrostatic Discharge (ESD) Prevention

WARNINGWARNING
DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING THE NECESSARY ESD PRECAUTIONS:
1.ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP, TO THE ADVISED ESD CONNECTION POINT LOCATED ON THE REAR OF THE SCANNER (TO THE RIGHT OF THE POWER CONNECTOR).
2.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE EQUIPMENT.
1-18 Section 1-4 - EMC, EMI, and ESD
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Section 1-5 Customer Assistance

1-5-1 Contact Information

If this equipment does not work as indicated in this service manual or in the User Manual, or if you require additional assistance, please contact the loca l distributor or appropriate support resource, as listed below.
Prepare the following information before you call:
- System ID serial number.
- Software version.
Table 1-7 Phone Numbers for Customer Assistance
Location Phone Number
1-800–437–1171 USA/ Canada GE Medical Systems Ultrasound Service Engineering 4855 W. Electric Avenue Milwaukee, WI 53219
1-800-682-5327 Customer Answer Center
1-262-524-5698
Fax: +1-414-647-4125
Latin America GE Medical Systems Ultrasound Service Engineering 4855 W. Electric Avenue Milwaukee, WI 53219
Customer Answer Center
Europe GE Ultraschall Deutschland GmbH& Co. KG BeethovenstraBe 239 Postfach 11 05 60, D-42665 Solingen Germany
Asia (Singapore/ Japan) GE Ultrasound Asia Service Department - Ultrasound 298 Tiong Bahru Road #15-01/06 Central Plaza Singapore 169730
1-262-524-5300
1-262-524-5698
Fax: +1-414-647-4125
Tel: +49 212 2802 208
+49 212 2802 207
Fax: +49 212 2802 431
Tel: +65 291-8528
+81 426-482950
Fax: +65 272-3997
+81 426-482902
Chapter 1 Introduction 1-19
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL

1-5-2 System Manufacturer

Table 1-8 System Manufacturer
Manufacturer FAX Number
GE Ultrasound Korea 462-120 65-1, Sangdaewon-dong, Joong-won-Gu, Seongnam-Si, Gyeonggi-do, Korea
82-31-740-6436
1-20 Section 1-5 - Customer Assistance
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Chapter 2 Pre-Installation

Section 2-1 Overview

2-1-1 Purpose of chapter 2

This chapter provides the information required to plan and pr epare for the installatio n of a LOGIQ™ 5 . Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit. A checklist is also provided at the end of this section to help determine whether the proper planning and preparation is accomplished before the actual equipment installation is scheduled.
Table 2-1 Contents in Chapter 2
Section Description Page Number
2-1
2-2
2-3
Overview
General Console Requirements
Facility Needs
2-1
2-2
2-6
Chapter 2 Pre-Installation 2-1
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™5 PRO SERVICE MANUAL

Section 2-2 General Console Requirements

2-2-1 Console Environmental Requirements

Table 2-2 Environmental Requirements for LOGIQ™ 5 Scanners
Operational Storage Transport
Temperature
Humidity
Pressure
o
10 - 35 oC 50 - 104
30 - 85% non-condensing
700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
o
F
-10 - 60 14 - 140
30 - 90% non-condensing
C
o
F
o
-40 - 60
-40 - 140 30 - 90%
non-condensing
C
Table 2-3 Environmental Requirements for an Ultrasound Room
Item Values
Power Source
Current Rating
Radiation Shielding
Temperature
Humidity
Heat Dissipation
Floor Landing
Floor Condition
Weight
Refer to Table 2-4 on page 2-3. 15A (120V-100V); 8A (220-240V) CIRCUIT BREAKER NONE REQUIRED for ULTRASOUND ENERGY 20-26 DEG. C (68-79 DEG F) for PATIENT COMFORT 50% to 70% for PATIENT COMFORT 2000 BTU/Hr.
Approximately 680 - 800 kg/m2 without Accessories Gradient: WITHIN 5 degrees 180 kg (397lbs) without Accessories
o
F
2-2-1-1 Cooling
The cooling requirement for the LOGIQ™ 5 is 3500 BTU/hr. This figure doe s not include cooling needed for lights, people, or other equipment in the room. Each person in the room places an additiona l 300 BTU/hr. demand on the cooling system.
2-2-1-2 Lighting
Bright light is needed for system installation, updates and repairs. However, operator and patient comfort may be optimized if the room light is subdued and indirect. Therefore a combination lighting system (dim/bright) is recommended. Keep in mind that lighting controls and diameters can be a sour ce of EMI which could degrade image quality. These controls should be selected to minimize possible interface.

2-2-2 Electrical Requirements

NOTE: GE Medical Systems requires a dedicated power and ground for the proper operation of its
Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the system.
2-2 Section 2-2 - General Console Requirements
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2-2-2 Electrical Requirements (cont’d)
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the distribution panel to the Ultrasound outlet.
NOTE: Please note that image artifacts can occur, if at any time within the facility, the ground from the
main facility's incoming power source to the Ultrasound unit is only a conduit.
2-2-2-1 LOGIQ™ 5 Power Requirements
The following power line parameters should be monitored for on e week before installation. We recommend that you use an analyzer Dranetz Model 606-3 or Dranetz Model 626:
Table 2-4 Electrical Specifications for LOGIQ™ 5
PARAMETER AREA LIMITS
100V 100 VAC ±10% (90-110 VAC)
Voltage Range
Power All applications MAX. 1250 VA Line Frequency All applications 50/60Hz (±2Hz)
Power Transients All applications
Decaying Oscillation All applications
2-2-2-2 Inrush Current
Inrush Current is not a factor to consider due to the inrush current limiting properties of the power supplies.
2-2-2-3 Site Circuit Breaker
It is recommended that the branch circuit breaker for the machine be ready accessible.
CAUTION
POWER OUTAGE MAY OCCURE. The LOGIQ™ 5 requires a dedicated single branch circuit. To avoid circuit overload and
possible loss of critical care equipment, make sure you DO NOT have any other equipment operating on the same circuit.
220V 220-240 VAC ±10% (198-264 VAC) 115V 115 VAC ±10% (103-127 VAC)
Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including line frequency, synchronous, asynchronous, or aperiodic transients.
Less than 15% of peak voltage for less than 1 millisecond.
2-2-2-4 Site Power Outlets
A desiccated AC power outlet must be within reach of the unit without extension cords. Other outlets adequate for the external periphera ls, medical and test equipment neede d to support this unit must al so be present within 1 m (3.2 ft.) of the unit. Electrical insta llatio n mus t meet all current local, state, and national electrical codes.
Chapter 2 Pre-Installation 2-3
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™5 PRO SERVICE MANUAL
2-2-2-5 Unit Power Plug
If the unit arrives without the power plug, or with the wrong plug, you must contact your GE dealer or the installation engineer must supply what is locally required.
2-2-2-6 Power Stability Requirements
Voltage drop-out
Max 10 ms.
Power Transients
(All applications) Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including line frequency, synchronous, asynchronous, or aperiodic transients.

2-2-3 EMI Limitations

Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies, magnetic fields, and transient in the air wiring. The y also generate EMI. The LOGIQ™ 5 complies with limits as stated on the EMC label. However there is no guarantee that interface will not occur in a particular installation.
Possible EMI sources should be identified before the unit is installed. Electrical and electronic equipment may produce EMI unintentionally as the result of defect. These sources include:
medical lasers,
scanners,
cauterizing guns,
•computers,
•monitors,
fans,
gel warmers,
microwave ovens,
light dimmers,
portable phones. The presence of broadcast station or broadcast van may also cause interference. See for EMI
Prevention tips. See Table 2-5 for EMI Prevention tips.
Table 2-5 EMI Prevention/abatement
EMI Rule Details
Be aware of RF sources
Ground the unit
Keep the unit at least 5 meters or 15 feet away from other EMI sources. Special shielding may be required to eliminate interference problems caused by high frequency, high powered radio or video broadcast signals.
Poor grounding is the most likely reason a unit will have noisy images. Check grounding of the power cord and power outlet.
2-4 Section 2-2 - General Console Requirements
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Table 2-5 EMI Prevention/abatement
EMI Rule Details
After you finish repairing or updating the system, replace all covers and tighten all screws. Replace all screws, RF gaskets, covers, cores
Any cable with an external connection requires a magnet wrap at each end. Install the
shield over the front of card cage. Loose or missing covers or RF gaskets allow radio
frequencies to interface with the ultrasound signals.
Replace broken RF gaskets
Do not place labels where RF gaskets touch metal
Use GE specified harnesses and peripherals
Take care with cellular phones Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.
Properly dress peripheral cables
If more than 20% or a pair of fingers on the RF gaskets are broken, replace the gaskets.
Do not turn on the unit until any loose metallic part is removed.
Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit
RF leakage. Or, if a label has been found in such a position, move the label.
The interconnect cables are grounded and require ferrite beads and other shielding. Also,
cable length, material, and routing are all important; do not change from what is specified.
Do not allow cables to lie across the top of the card cage or hang out of the peripheral bays.
Loop the excess length for peripheral cables inside the peripheral bays. Attach the monitor
cables to the frame.

2-2-4 Scan Probe Environmental Requirements

Operation:10° to 35° C Storage:--10° to 60° C
NOTE: Temperature in degrees C. Conversion to Degrees F = (Degrees C * 9/5) + 32).
NOTICE
SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES OF -20 TO + 50 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.
Chapter 2 Pre-Installation 2-5
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Section 2-3 Facility Needs

2-3-1 Purchaser Responsibilities

The work and materials needed to prepare the site is the responsibility of the purchaser. Delay, confusion, and waste of manpower can be avoided by completing pre installation work before delivery. Use the PreInstallation checklist to verify that all needed steps have been taken. Purchaser reasonability includes:
Procuring the materials required.
Completing the preparations befo re de livery of the ultrasound system.
Paying the costs for any alternations and modifications not specifically provided in the sales contract.
NOTE: All electrical installation that are preliminary to the positioning of the equipment at the site
prepared for the equipment must be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, products involved (and the accompanying electrical installations) are highly sophisticated and special engineering competence is required. All electrical work on these product must comply with the requirements of applicable electrical codes. The purchaser of GE equipment must only utilize qualified personnel to perform electrical servicing on the equipment.
The desire to use a non-listed or customer provided product or to place an approved product further from the system than the interface kit allows pr esents challenges to the installation team. To avoid delays during installation, such variances should be made known to the individuals or gr oup performing the installation at the earliest possible date (preferable prior to purchase). The ultrasound suite must be clean pr o of to delivery of the machine. Carpet is not recommended because it collects dust and creates static. Potential sources of EMI (electromagnetic interference) should also be investigated before delivery. Dirt, static, and EMI can negatively impact system.

2-3-2 Required Features

NOTE: GE Medical Systems requires a dedicated power and ground for the proper operation of its
Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the distribution panel to the Ultrasound outlet.
Please note that image artifacts can occur, if at any time within the facility, the ground from the main facility's incoming power source to the Ultrasound unit is only a conduit.
Dedicated single branch power outlet of adequate amperage meeting all local and national codes which is located less than 2.5 m (8 ft.) from the unit’s proposed location
Door opening is at least 76 cm (30 in) wide
Proposed location for unit is at least 0.3 m (1 ft.) from the wall for cooling
Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with peripheral within 1 m of the unit to connect cables.
2-6 Section 2-3 - Facility Needs
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NOTE: The LOGIQ™ 5 has four outlets inside the unit. One is for the monitor and three for on board
peripherals.
Power outlets for other medical equipment and gel warmer
Power outlets for test equipment and modem within 1 m (3.2 ft.) of unit
Clean and protected space to store transducers (in their cases or on a rack)
Material to safely clean probes (done with a plastic container, never metal)
Chapter 2 Pre-Installation 2-7
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2-3-3 Desirable Features

Door is at least 92 cm (3 ft.) wide
Circuit breaker for dedicated power outlet is easily accessible
Sink with hot and cold water
Receptacle for bio–hazardous waste, like used probe sheaths
Emergency oxygen supply
Storage for linens and equipment
Nearby waiting room, lavatory, and dressing room
Dual level lighting (bright and dim)
Lockable cabinet ordered by GE for its software and proprietary manuals.
2-8 Section 2-3 - Facility Needs
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2-3-4 Recommended and Alternate Ultrasound Room Layout

Recommended standard floor plan and a minimal floor plan for ultrasound equipment:
DEDICATED ALALOG TELEPHONE LINE FOR CONNECTION TO INSITE
ROOM,
PROCESSING
FILM
DEDICATED
POWER
RECEPTACLE
18 IN.
(46 CM)
CONSOLE
LINEN SUPPLY
FILM VIEWER
FILM SUPPLIES
FILE
CABINET
SECRETARYS OR DOCTOR’S DESK
SINK
FILM VIEWER
COUNTER TOP
COUNTER
TOP
SINK
SUCTION LINE
EMERGECY OXYGEN
OVERHEAD LIGHTS DIMMER
A 14 by 17 foot Recommended Floor Plan
LINEN SUPPLY
PROBES/SUPPLIES
FOOT
SW
STOOL
EXAMINATION
TABLE
76 IN.
(193 CM)
24 IN.
(61 CM)
PATIENT
TOILET
FACILITY
DOOR
42 IN.
(107 CM)
Scale : Each square equals one square foot
EXTERNAL
PERIPHERALS
DEDICATED POWER OUTLETS
DEDICATED ANALOG TELEPHONE LINE FOR CONNECTION TO INSITE
GE CABINET FOT SOFTWARE AND MANUALS
DOOR
30 IN.
(76 CM)
24 IN. (61 CM)
FOOT
SW
STOOL
EXAMINARION
TABLE
LOGIQ 5
CONSOLE
76 IN. (193 CM)
An 8 by 10 foot Minimal Floor Plan
Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT
Chapter 2 Pre-Installation 2-9
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2-3-5 Networking Pre-installation Requirements

2-3-5-1 Purpose of DICOM Network Function
DICOM services provide the operator with clinically useful features for moving images and patient information over a hospital network. Examples of DICOM services include the transfer of images to workstations for viewing or transferring images to remote printers. As an added benefit, transferring images in this manner free up the o n-board monitor and peripherals, enabling viewing to be done while scanning continues. With DICOM, images can be archived, stored, and retrie ve d faster, ea sie r, and at a lower cost.
2-3-5-2 DICOM Option Pre-installation Requirements
To configure the LOGIQ™ 5 to work with other network connections, the site’s network administrator must provide some necessary information.
Information must include:
A host name, local port number, AE Title, IP address and Net Mask for the LOGIQ™ 5 .
The IP addresses for the default gateway and other routers at the site for ROUTING INFORMATION.
The host name, IP address, port and AE Title for each device the site wants connected to the
LOGIQ™ 5 for DICOM APPLICATION INFORMATION. A field for the make (manufacturer) and
the revision of the device, is also included. This information may be useful for solving errors.
2-10 Section 2-3 - Facility Needs
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2-3-5-2 DICOM Option Pre-installation Requirements (cont’d)
.
.
LOGIQ™ 5
Host Name
Local Port
IP Address
..
.
AE Title
ROUTING INFORMATION
ROUTER1 ROUTER2 ROUTER3
DICOM APPLICATION INFORMATION
NAME
Store 1
Store 2
Store 3
Store 4
Destination IP Addresses
... ... ...
MAKE/REVISION IP ADDRESSES PORTAE TITLE
Net Mask
Default
...
GATEWAY IP Addresses
...
... ... ...
...
...
...
...
Store 5
Store 6
Worklist
Storage Commit
MPPS
...
...
...
...
...
Figure 2-2 Worksheet for DICOM Network Information
Chapter 2 Pre-Installation 2-11
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2-12 Section 2-3 - Facility Needs
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Chapter 3 Installation

Section 3-1 Overview

3-1-1 Purpose of Chapter 3

This chapter contains information needed to install the unit. Included are references to a procedure that describes how to receive and unpack the equipment and how to file a damage or loss claim. How to prepare the facility and unit of the actual installation, and how to check and test the unit, probes, and external peripherals for electrical safety are included in this procedure. Also included in this section are guidelines for transporting the unit to a new site.
Table 3-1 Contents in Chapter 3
Section Description Page Number
3-1 Overview 3-1 3-2 Installation Reminders 3-2 3-3 Receiving and Unpacking the Equipment 3-4 3-4 Preparing for Installation 3-9 3-5 Completing the Installation 3-11 3-6 System Configuration 3-16 3-7 Available Probes 3-24 3-8 Software/Option Configuration 3-24 3-9 Connectivity Installation Worksheet 3-25
3-9 Connectivity Installation Worksheet 3-25 3-10 Insite IP Address Configuration 3-25 3-11 Loading Base System Software 3-25 3-10 Paperwork 3-26
Chapter 3 Installation 3 - 1
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Section 3-2 Installation Reminders

3-2-1 Average Installation Time

Table 3-2 Average Installation Time
Description Average Installation Time Comments
Unpacking the scanner Scanner wo/options DICOM Option InSite Option
0.5 hour
0.5 hour
0.5 hour
0.5 hour
Dependant on the configuration that is required Dependant on the amount of configuration
The LOGIQ™ 5 PRO has been designed to be installed and checked out by an experienced service technician in approximately four hours. LOGIQ™ 5 PRO consoles with optional equipment may take slightly longer.

3-2-2 Installation Warnings

1.) Since the LOGIQ™ 5 PRO weighs approximately 180 kg. (397 lb.) without options, preferably two people should unpack it. Two people are also preferable for installing any additional bulky items.
2.) There are no operator serviceable components. To prevent shock, do not remove any covers or
panels. Should problems or malfunctions occur, unplug the power cord. Only qualified service personnel should carry out servicing and troubleshooting.
NOTE: For information regarding packing labels, refer to LABELS ON PACKAGE.
3.) After being transported, the unit may be very cold or hot. If this is the case, allow the unit to
acclimate before you turn it on. It requires one hour for each 2.5°C increment if its temperature is below 10°C or above 40°C.
CAUTION
Equipment damage possibility. Turning the system on without acc limati on af ter a rriving a t sit e may cause the system to be damaged.
Table 3-3 Acclimation Time
60 55 50 45 40 35 30 25 20 15 10 5 0 -5 -10 -15 -20 -25 -30 -35 -40
°C
140 131 122 113 104 96 86 77 68 59 50 41 32 23 14 5 -4 -13 -22 -31 -40
°F
864200000002468101214161820
hrs
3 - 2 Section 3-2 - Installation Reminders
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3-2-3 Safety Reminders

DANGER
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DON’T TOUCH THE UNIT!
Two people should unpack the unit because of its weight. Two people are required whenev er a part weighing 19kg (35 lb.) or more must be lifted.
If the unit is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.
To prevent electrical shock, connect the unit t o a properly grounded power outlet. Do not use a three to two prong adapter. This defeats safety grounding.
Do NOT wear the ESD wrist strap when you work on live c ircuits and more than 30 V pea k is present.
Do not use a 20 Amp to 15 Amp adapter on the 120 Vac unit’s power cord. This unit requires a dedicated 20 A circuit and can have a 15A plug if the on boa rd peripherals do not cause the unit to draw more than 14.0 amps.
Do not operate this unit unless all board covers and frame panels are securely in place. System performance and cooling require this.
OPERATOR MANUAL(S) The User Manual(s) should be fully read and understood before operating the LOGIQ™ 5 PRO and kept near the unit for quick reference.
CAUTION
ACOUSTIC OUTPUT HAZARD Although the ultrasound energy transmitted from the LOGIQ™ 5 PRO probe is within FDA limits, avoid unnecessary exposure. Ultrasound energy can produce he at and mechanical damage.
Figure 3-6 Environmental Labels
Chapter 3 Installation 3 - 3
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GE MEDICAL SYSTEMS DIRECTION 2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL

Section 3-3 Receiving and Unpacking the Equipment

When a new system arrives, check that any components are not d amaged and a re not in short su pply. If shipping damage or shortage occurs, contact the address shown in Chapter 1.
CAUTION
CAUTION
Do not lift the unit by the Keyboard. Equipment damage may result.
The crate with the LOGIQ™ 5 PRO weighs approximately 180 kg. (397 lb.) Be prepared for a sudden shift of weight as the unit is remove d from its base (pallet)
1.) Cut the three PLASTIC BANDs.
Plastic Bands
Figure 3-7 Cutting the Plastic Bands.
3 - 4 Section 3-3 - Receiving and Unpacking the Equipment
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Section 3-3 Receiving and Unpacking the Equipment (cont’d)
2.) Lift the TOP COVER up and off.
Top Cover
Figure 3-8 Removing the top Cover
Chapter 3 Installation 3 - 5
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Section 3-3 Receiving and Unpacking the Equipment (cont’d)
3.) Remove the MONITOR CAP up and off..
Monitor Cap
Figure 3-9 Removing the monitor cap
3 - 6 Section 3-3 - Receiving and Unpacking the Equipment
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Section 3-3 Receiving and Unpacking the Equipment (cont’d)
4.) Remove the three PLASTIC JOINTs from the OUTER SLEEVE
5.) Remove the OUTER SLEEVE.
6.) Remove the INNER SLEEVE.
Inner Sleeve
Plastic Joint
Outer Sleeve
Monitor Supporter
Palette Assy
Figure 3-10 Removing Plastic Joints and Sleeves
Chapter 3 Installation 3 - 7
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Section 3-3 Receiving and Unpacking the Equipment (cont’d)
7.) Remove the PLASTIC BAG.
8.) Lift the Monitor up by pressing the UP/Down Release Button.
9.) Remove the MONITOR SUPPORTER.
10.)Pull the Bottom Plate from the bottom so that it can be used as a ramp.
11.)Unlock the front caster and carefully put the console off the PALETTE.
PLASTIC BAG
Monitor Supporter
Figure 3-11 Moving the LOGIQ™ 5 PRO from the crate
Console
Palette Base Assy
Bottom Plate
3 - 8 Section 3-3 - Receiving and Unpacking the Equipment
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3-3-1 Moving into Position

CAUTION
CAUTION
Do not lift the unit by the Keyboard. Do not tilt the unit more than 5 degrees to avoid tipping it over. To avoid injury by tipping over. Set the monitor to the lowest position before moving.
Equipment Damage Possibility. Lifting the console by holding covers may damage the covers. Do not lift the console by holding any covers.
In general, a single adult can move the LOGIQ™ 5 PRO along an even surface with no steep grades. At least two people should move the machine when large humps, grooves, or grades will be encountered. (It is better to pull from the rear rather than push from the front of the unit). Before moving, store all loose parts in the unit. Wrap transducers in soft cloth or foam to prevent damage.
Although LOGIQ™ 5 PRO is a compact and mobile machine, two people should move it over rough surfaces or up and down grades.

3-3-2 Adjusting System Clock

Set the system clock for the LOGIQ™ 5 PRO to the local time. For procedure of adjusting the system clock, refer to section 3-6-1-1 on page 16.
Fill out proper customer Information the Product Locator Installation Card. Mail this Installation Card “Product Locator” to the address corresponding to your pole.

3-3-3 Product Locator Installation Card

NOTE: The Product Locator Installation Card shown may not be same as the provided Product Locator
card.
Figure 3-12 Product Locator Installation Card

Section 3-4 Preparing for Installation

3-4-1 Verify Customer Order

Compare items received by the customer to that which is listed on the delivery order. Report any item s that are missing, back ordered or damaged.
Chapter 3 Installation 3 - 9
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3-4-2 Physical Inspection

3-4-2-1 System Voltage Settings
Verify that the scanner is set to the correct voltage. The Voltage settings for the LOGIQ™ 5 PRO Scanner is fou nd on a label to the right of the Power switch and External I/O, on the rear of the system.For the Rating Plate example, refer to Figure 1-3 "OUTSIDE
MARKINGS OF LOGIQ™ 5 PRO" on page 1-16
WARNINGWARNING
Connecting a LOGIQ™ 5 PRO scanner to the wrong voltage level will most likely destroy the scanner.
3-4-2-2 Video Formats
Check that the video format is set to the locally used video standard, NTSC or PAL.

3-4-3 EMI Protection

This Unit has been designed to minimize the effects of Electro Magnetic Interference (EMI). Many of th e covers, shields, and screws are provided primarily to protect the system from image artifacts caused by this interference. For this reason, it is imperative that all covers and hard ware are installed and secure d before the unit is put into operation.
3 - 10 Section 3-4 - Preparing for Installation
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Section 3-5 Completing the Installation

3-5-1 Power On/Boot Up

NOTE: After turning off the system, wait at least ten seconds before turning it on again. The system
may not be able to boot if power is recycled too quickly.
3-5-1-1 Scanner Power On
1.) Connect the Main Power Cable at the rear of the System.
WARNINGWARNING
Protective earth must be taken when connecting AC power cable (200V) without its plug to wall outlet.
2.) Connect the Main Power cable to an appropriate mains power outlet.
3.) Switch ON the Main Circuit Breaker at the rear of the System.
Main Circuit Breaker
Main Power Cable
Figure 3-13 Circuit Breaker
When power is applied to the Scanner, and the Rear Circuit breaker is turned ON, Power is dist ribute d to the ATX smps in the Back End Processor and Power control circuit in the AC power assy . When the Power ON/OFF key is pressed once, the power control circuit turn on the card cage and fans, and Back End Processor ,Monitor. Backend Processor starts and its software code is distributed to initiate the scanner.
4.) Press the ON/OFF
key at the keyboard paenl of the System once.
Chapter 3 Installation 3 - 11
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3-5-1-1 Scanner Power On (cont’d)
Composite
Serial
B/W
B/W Printer
Power
Figure 3-14 Power On/Off Switch Location
3-5-1-2 Power Up Sequence
1.) The Start Up Screen will be shown on the Monitor display when the system is turned ON.
2.) After initialization is complete, default mode buttons on the keyboard are lit a nd the B-Mode screen
or Patient screen (no probes are connected) is displayed on the monitor.
Figure 3-15 Start Up Screen Display
3 - 12 Section 3-5 - Completing the Installation
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3-5-1-3 Maintanance Mode for Service
1.) If the service dongle is inserted in the USB port in the rear panel during system boot up,
Maintenance access window appears.
2.) Then key in the service pass word and click OK button.
3.) When the start application widow appear, click the “Maintenence” button
Figure 3-16 maintenance Window
NOTE: Start is selected automatically when it time out.
Chapter 3 Installation 3 - 13
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3-5-2 Power Off/ Shutdown

NOTE: After turning off a system, wait at least ten seconds before turning it on again. The system may
not be able to boot if power is recycled too quickly.
3-5-2-1 Power Shutdown
NOTICE
1.) Press once the ON/OFF
2.) Click the shutdown button in the Exit dialog box as Figure 3-17 on page 3-14
3.) Switch OFF the Main Circuit Breaker at the rear of the system Refer to Figure 3-13 on page 3-11 .
4.) Disconnect the Main Power Cable is necessary. For example : Relocating the scanner.
Disconnecting the Mains Power Cable before switching OFF the Circuit Breaker will activate the uninterruptible power system (UPS) in the backend processor, forcing an ordered shutdown of the system.
key at the front of the System.
Figure 3-17 System Exit Window
NOTICE
3 - 14 Section 3-5 - Completing the Installation
The UPS serves only as a battery backup that allows for a soft shut-down of the scanner to prevent file corruption. IT DOES NOT REGULATE INCOMING VOLTAGE.
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3-5-3 Transducer Connection

1.) Connect a transducer to one of the three rightmost transducer receptacle as follows:
A.) Ensure that the transducer twist lock lever to the horizontal position. B.) Insert the transducer connector on the receptacle guide pin until it touches the receptacle
mating surface.
C.) Twist the transducer twist lock lever to vertical position to lock it in place. Twist the lever
to the horizontal position to disconnect the transducer.
NOTE: It is not necessary to turn OFF power to connect or disconnect a transducer.
Chapter 3 Installation 3 - 15
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Section 3-6 System Configuration

3-6-1 System Specifications

3-6-1-1 System Settings
Table 3-1 System Configuration
Configuration Category Description
Enables the user or service personnel to set the
Settings
1.) Press Power on/off switch.
2.) The SYSTEM EXIT window appears. Click on Logoff.
date, time, unit, language, basic information about the organization such as the institution name and department.
Figure 3-18 System EXIT window
3.) The message window appears. Click on OK.
4.) The OPERATOR LOGIN window appears.
Change the User level to Admin, then enter Password. Then click on Log on.
Figure 3-19 Operator LOGIN window
3 - 16 Section 3-6 - System Configuration
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3-6-1-1 System Settings (cont’d)
5.) Press Utility > System.
6.) Set the Hospital name, Department, Date and Time, Language, and Units.
Click on Utilities to terminate the utility function.
3-6-1-2 Physical Dimensions
The physical dimensions of the LOGIQ™ 5 PRO unit are summarized in Table 3-2 on page 3-17 . The Size of LOGIQ™ 5 PRO, with monitor and peripherals
Table 3-2 Physical Dimensions of LOGIQ™ 5 PRO
Height Width Depth Unit
135 - 145 52.0 99.0 cm
53.1 - 57.08 20.47 38.9 inches
Figure 3-20 Setting Display
Chapter 3 Installation 3 - 17
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3-6-1-2 Physical Dimensions (cont’d)
WEIGHT  : 180Kg(397lbs)    including Monitor
520
NOTE: Length is in mm  Variation +/- 10%
Composite
Serial
B/W
B/W Printer
Power
1350~1450
800~900
Figure 3-21 Overall Dimensions
3-6-1-3 Weight without Monitor and Peripherals
990
Table 3-3 Weight of LOGIQ™ 5 PRO With Monitor and Without Other Peripherals
Model Weight [kg] Weight [lbs]
LOGIQ™ 5 PRO Approximately 180 Approximately 397
3-6-1-4 Acoustic Noise Output:
Less than 70dB (A) according to DIN 45635 - 19 - 01 - KL2.

3-6-2 Electrical Specifications

Table 3-4 Electrical Specifications for LOGIQ™ 5 PRO
System Voltage Current Frequency
1 110 ~ 120 VAC 10~12A 50~60Hz 2 220 ~ 240 VAC 5~5.5A 50~60Hz
3 - 18 Section 3-6 - System Configuration
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3-6-3 On-Board Optional Peripherals

Table 3-5 List of Recording Devices
Device Manufacturer Model Video Signal
B/W Video Printer SONY
B/W Video Printer Mitsubishi
Video Cassette Recorder SONY
Video Cassette Recorder Pana sonic
A6 Color Video Printer SONY
A6 Color Video Printer Mitsubishi
A5 Color Video Printer SONY
A5 Color Printer Mitsubishi
UP-895MDW
UPD-895
P-91(AP9500)
P91W
P91E P91D
SVO-9500MD
SVO-9500-MDP
AG-MD835 AG-MD835P AG-MD835E
UP-21MD UP-21MDS UP-D21MD UP-D23MD
CP-900
CP900UM
CP-900E CP-900D
UP-50
UP51MD
CP-800
CP-800UM
CP800E
NTSC/PAL
NTSC NTSC/PAL NTSC/PAL
NTSC
PAL
NTSC
NTSC
PAL
NTSC/PAL
NTSC
NTSC NTSC/PAL
See each option installation instructions for installation and connection procedures.
NOTE: There are no external peripheral options for the LOGIQ™ 5 PRO

3-6-4 External I/O Connector Panel

Located on the rear panel are video input and output connectors, audio input and output, camera expose connectors, footswitch connector power connector and control connections for VCR, printer, and service tools.
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3-6-4 External I/O Connector Panel (cont’d)
This section indicates the pin assignment for each connector.
1
2
Serial
1 2
220-240V 500VA Max
Including front printer panel
Figure 3-22 Rear Connector Panel
NOTE: Each outer (case) ground line of peripheral/accessory connectors are protectively grounded.
Signal ground lines are not isolated, except the Service port (3). All of signal lines (include signal GND) of the Service port are isolated.
3 - 20 Section 3-6 - System Configuration
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3-6-4-1 External I/O Pin Outs
Pin No. Signal Pin No. Signal
1N/A6DSR
2RXD7RTS
3TXD8GTS
4DTR9 N/A
5GND
Table 3-6 Pin Assignments of RS232C for Remote 1 and Remote 2
Pin No. Signal Pin No. Signal
1NC6NC
2RXD7 NC
3TXD8 NC
4NC9 RI
5GND
Table 3-7 Pin Assignments of RS232C for Service
Pin No. Signal Pin No. Signal
1RED9N/A
2 GREEN 10 SGND
3BLUE11 N/A
4N/A12N/A
5 GND 13 HSYNC
6 RGND 14 VSYNC
7 GGND 15 N/A
8BGND
Table 3-8 Pin Assignments of DB15 connector for External VGA
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3-6-4-1 External I/O Pin Outs (cont’d)
Pin No. Signal Pin No. Signal
1+5 VDC3DATA +
2 DATA - 4 GND
Table 3-9 Pin Assignments of USB
Pin No. Signal Pin No. Signal
1TX+5 NC
2TX-6RX-
3RX+7 NC
4NC8NC
Table 3-10 Pin Assignments of InSite - RJ45 Male Connector
Pin No. Signal Pin No. Signal
1TX+5 NC
2TX-6RX-
3RX+7 NC
4NC8NC
Table 3-11 Pin Assignments of Ethernet
Pin No. Output Signal
1 PRINT*1
2 Signal GND
Table 3-12 Pin Assignment of Mini-Jack for Controlling B/W Printer
Pin No. Output Signal
1 SHUTTER*2
2 Signal GND
Table 3-13 Pin Assignment of Mini-Jack for Controlling Color
3 - 22 Section 3-6 - System Configuration
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3-6-5 Video Specification

Video specifications may be needed to be able to connect laser cameras or other devices to the LOGIQ™ 5 PRO.
Table 3-14 Video Specifications
1024x768
Timing Parameter
Horizontal Rate [kHz] 60.02 31.25 31.47 37.88 46.88 48.36
Horizontal Period [µs] 16.66 32.00 31.78 26.40 21.33 20.68
Pixel Clock [MHz] 78.75 29.50 24.55 40.00 49.50 65.00
H Blank Width s] 3.66 5.97 5.70 6.40 5.17 4.92
H Sync Width s] 1.22 2.34 2.36 3.20 1.62 2.09
H Front Porch s] 0.20 0.75 0.73 1.00 0.32 0.37
Active Horizontal Period s] 13.00 26.03 26.07 20.00 16.16 15.75
Vertical Rate [Hz] 75.03 50.00 59.94 60.32 75.00 60.00
Vertical Period [ms] 13.33 20.00 16.68 16.58 13.33 16.67 V Sync Width [lines=ms] 32=0.53 49=1.57 45=1.43 28=0.74 25=0.53 38=0.79 V Front Porch [lines=µs] 3=50.00 5=160.00 6=190.70 4=105.60 3=64.00 6=124.10
Equalization Gate [lines=µs] 1=16.66 5=160.0 6=190.7 1=26.4 1=21.3 3=62.00
Lines: Field/Frame 800 625/625 525/525 628 625 806
Active Lines/Frame 768 576 480 600 600 768
75Hz
768x576
50Hz
640x480
60Hz
800x600
60Hz
800x600
75Hz
1024x768
60Hz
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Section 3-7 Available Probes

See Specifications in the LOGIQ™ 5 PRO User Reference Manual for probes and intended use. See Chapter 9, for part numbers to be used when ordering new or replacement probes.

Section 3-8 Software/Option Configuration

Refer to the LOGIQ™ 5 PRO Basic User Manual, Chapter 16, Customizing Your System for information on configuring items like Hospital, Department, Language, Units (of measure), Date, Time and Date Format.
For information on configuring Software Options, Refer to the LOGIQ™ 5 PRO Basic User Manual, Chapter 16, Customizing Your System.
For information on configuring DICOM Connectivity, Refer to the LOGIQ™ 5 PRO Basic User Manual, Chapter 16, Customizing Your System.
3 - 24 Section 3-7 - Available Probes
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Section 3-9 Connectivity Installation Worksheet

Site System Information
Site:
Dept.:
LOGIQ SN:
CONTACT INFORMATION
Name
TCP/IP Settings
Name - AE Title:
Type:
Title
Floor:
Room:
REV:
Phone
Comments:
E-Mail Address
IP Settings
IP Address:
Subnet Mask:
Default Gateway:
Services (Destination Devices)
Device Type
1 2 3 4 5 6 7 8 9 10 11 12
Manufacturer
Name
Remote Archive Setup
Remote Archive IP:
Remote Archive Name:
IP Address
Port
AE Title
Chapter 3 Installation 3 - 25
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Section 3-10 Paperwork

NOTE: During and after installation, the documentation (i.e. User Manuals, Installation Manuals...) for the
peripheral units must be kept as part of the original system documentation. This will ensure that all relevant safety and user information is availa b le du rin g th e op er a tion and ser vice of th e com p let e system.

3-10-1 Product Locator Installation

NOTE: The Product Locator Installation Card shown may not be same as the provided Product Locator
card.
Figure 3-23 Product Locator Installation Card

3-10-2 User Manual(s)

Check that the correct User Manual(s) for the system and software revision, is included with the installation. Specific language versions of the User Manual may also be available. Check with your GE Sales Representative for availability.
3-10-2-1 Reference off-board peripherals and options
None.
3 - 26 Section 3-10 - Paperwork
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Chapter 4 Functional Checks

Section 4-1 Overview

4-1-1 Purpose of Chapter 4

This chapter provides procedures for quickly checking major functions of the LOGIQ™ 5 PRO scanner diagnostics by using the built-in service software, and power supply adjustments.
Table 4-15 Contents in Chapter 4
Section Description Page Number
4-1 Overview 4-1
4-2 Required Equipment 4-1
4-3 General Procedure 4-2
4-4 Software Configuration Checks 4-20
4-5 Peripheral Checks 4-21
4-6 Peripheral Checks 4-21
4-7 Site Log 4-24
\
NOTICE
Most of the information pertaining to this Functional Checks chapter is found in the LOGIQ™ 5 PRO Quick Guide (Direction Number 2380205-100).

Section 4-2 Required Equipment

An empty (blank) MO Disk.
At least one transducer. See “Probe/Connectors Usage (QG)” on page 28. for an overview. (normally you should check all the transducers used on the system.)
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Section 4-3 General Procedure

CAUTION
SYSTEM REQUIRES ALL COVERS Operate this unit only when all board covers and frame panels are securely in place. The covers are required for safe operation, good system performance and cooling purposes.
NOTICE
Lockout/Tagout Requirements (For USA only) Follow OSHA Lockout/Tagout requirements by ensuring you are in total co ntro l of the Po wer Ca ble
on the system.
TAG
&
LOCKOUT
Date
Signed

4-3-1 Power On/Boot Up

NOTE: After turning off the system, wait at least ten seconds before turning it on again. The system
may not be able to boot if power is recycled too quickly.
4-3-1-1 Scanner Power On
1.) Connect the Main Power Cable to the back of the System.
2.) Ensure the Cable Clip slips securely over the shoulders on the molded plug.
3.) Connect the Main Power cable to an appropriate mains power outlet.
4.) Switch ON the Main Circuit Breaker at the rear of the System.
4 - 2 Section 4-3 - General Procedure
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4-3-1-1 Scanner Power On (cont’d)
Main Circuit Breaker
Main Power Cable
Figure 4-24 Circuit Breaker
NOTE: When power is applied to the Scanner, and the Rear Circuit breaker is turned ON, Power is
distributed to the ATX smps in the Back End Processor and Power control circuit in the AC power assy . When the Power ON/OFF key is pressed once, the power control circuit turn on the card cage and fans, and Back End Processor ,Monitor. Backend Processor starts and its software code is distributed to initiate the scanner.
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4-3-1-1 Scanner Power On (cont’d)
5.) Press the ON/OFF
key at the front of the System once.
Composite
Serial
B/W
B/W Printer
Power
Figure 4-25 Power On/Off Standby Switch Location

4-3-2 Power Off / Shutdown

NOTE: After turning off a system, wait at least ten seconds before turning it on again. The system may not be
able to boot if power is recycled too quickly.
4-3-2-1 Scanner shutdown
1.) Press the On/Off key at the front of the system once to display the SYSTEM - EXIT menu.
2.) Select Shutdown from the SYSTEM - EXIT menu.
Figure 4-26 System Exit Menu for System Shutdown
4 - 4 Section 4-3 - General Procedure
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4-3-2-2 Switch off the scanner
1.) Switch OFF the Circuit Breaker at the back of the scanner.
2.) Disconnect the Mains Power Cable is necessary. For example: Servicing or relocating the scanner.
NOTICE
Disconnecting the Mains Power Cable before switching OFF the Circuit Breaker will activate the uninterruptible power system (UPS) in the Back End Processor, forcing an ordered shutdown of the system.

4-3-3 System Features

4-3-3-1 Control Panel
Figure 4-27 Control Panel Tour
1.) Video
2.) Audio On/Off and Volume
3.) TGC
4.) Reverse
5.) Additional Feature Keys
6.) Keyboard
7.) Mode/Gain Keys
8.) Imaging/Measurement Keys
9.) Depth
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4-3-3-1 Control Panel (cont’d)
10.)Imaging Feature Keys
11.)Freeze
12.)Probe and Cord Holder
13.)Gel Holder
14.)New Patient
15.)Application
16.)Report
17.)End Exam
18.)Mode Parameter
19.)Utility
20.)Top Menu control keys
21.)Submenu control keys
22.)Print keys
4-3-3-2 Sub Menu Control KeysMenu Key Panel
Figure 4-28 Menu Key Tour
1.) Patient: Enter Patient screen
2.) Reports: Activates default report and Measurement Selection Menu of report choices.
3.) End Exam: Activates Image Management and Measurement Selection Menu with end of exam options.
4.) Utility: Activates the configuration system.
5.) Applications: Select the application to use and Probe select.
6.) Mode Paramenters: To toggle between the Primary menus of different modes
7.) Top menu Controls : Activates the changes of functions in the Top menu.
8.) Sub menu controls: Activates Sub Menu for Modes and toggles/changes functions.
At the bottom of the Keypad, there are five combinat ion rotary dials/push buttons. The functionality of these rotaries is changed, depending upon the currently displayed menu. Press the button to switch between controls (as with Focus Position/Number), or rotate the dial to adjust the value.
4 - 6 Section 4-3 - General Procedure
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4-3-3-3 Monitor Display
1234
1234
12
12
5
5
13
6
6 7
7
13
14
14
8
8 9
9
10
10
11
11
19 20 21
19 20 21
Figure 4-29 Monitor Display Tour
Table 4-16 Monitor Display Features
1. Institution/Hospital Name, Date, Time, Operator Identification
3. Patient Name, Patient Identification 4. GE Symbol : Probe Orientation Marker. Coincides with a
5. Image Preview 6. Gray/Color Bar
7. Cine Gauge 8. Measurement selection Menu
9. Image 10. Measurement
11. Result window 12. Imaging Paramenters by mode
13. Power Output Readout, system status 14. Focal Zone
15. Depth Scale 16. Body Pattern
17. TGC 18. Image Management Menu : Menu, Delete, and Image
19. Image Palette 20. System Messages Display
21. Trackball Fucntionality Status 22.
2. Probe Identifier, Exam Study
probe orientation marking on the probe.
Manager
15
15 17
17
16
16
18
18
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4-3-4 System B/M-Mode Checks

For a basic functional check of the system’s different modes, the Quick Guide will familiarize you with image optimization for B-Mode, M-Mode, Color Flow, and Doppler.
Table 4-17 B/M-Mode Functions
Optimizes image quality and allows user to reduce beam
Power Output (Acoustic Power)
Dynamic Range
Focus Number and Position
intensity. 10% increments between 0-100%. Values greater than 0.1 are displayed
Dynamic Range controls how echo intensities are converted to shades of gray, thereby increasing the adjustable range of contrast.
Increases the number of transmit focal zones or moves the focal zone(s) so that you can tighten up the beam for a specific area. A graphic caret corresponding to the focal zone position(s) appears on the right edge of the image.
Rejection
Edge Enhance
Frame Average
Colorize
Gray Map
Rotation (Up/Down) Rotates the image by selecting the value from the pop up menu.
Frequency
Frame Rate/Resolution
B Flow
Selects a level below which echoes will not be amplified (an echo must have a certain minimum amplitude before it will be processed).
Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures. Adjustments to M Mode's edge enhancement affects the M Mode only.
Temporal filter that averages frames together. This has the effect of presenting a smoother, softer image.
Enables gray scale image colorization. To deactivate, reselect a Gray Map.
Determines how the echo intensity levels received are presented as shades of gray.
Multi Frequency mode lets you downshift to the probe's next lower frequency or shift up to a higher frequency.
Optimizes B Mode frame rate or spatial resolution for the best possible image.
Provides intuitive representation of non-quantitative hemodynamics in vascular structures.
Sensitivity/PRI Adjusts the sample rate for the flow signal.
Background On/Off
Sweep Speed Changes the speed at which the timeline is swept.
Background On lets you view the anatomy roadmap; Background Off lets you view just flow information.
4 - 8 Section 4-3 - General Procedure
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4-3-5 System CFM and PWD Checks

Table 4-18 CFM and PWD Functions
Baseline
PRF/Wall Filter
Angle Correct
Threshold
Map
Invert
Packet Size
Quick Angle Correct Quickly adjusts the angle by 60 degrees
Doppler Display Formats
Adjusts the baseline to accommodate faster or slower blood flows to eliminate aliasing.
Velocity scale determines pulse repetition frequency. If the sample volume gate range exceeds single gate PRF capability, the system automatically switches to high PRF mode. Multiple gates appear, and HPRF is indicated on the display.
Estimates the flow velocity in a direction at an angle to the Doppler vector by computing the angle between the Doppler vector and the flow to be measured
Threshold assigns the gray scale level at which color information stops.
Allows a specific color map to be selected. After a selection has been made, the color bar displays the resultant map.
Allows blood flow to be viewed from a different perspective, i.e. red away (negative velocities) and blue toward (positive velocities). The real-time or frozen image can be inverted.
Controls the number of samples gathered for a single color flow vector.
Display layout can be preset to have B-Mode and Time-motion side-by-side or over-under.
In the side-by-side layout, there are three display alternatives defined: equal priority, time-motion priority or time-motion with B-Mode reference.
In the over-under layout, there are three display alternatives defined: time-motion priority, B Mode priority or equal priority.
Sample Volume Gate Length Sizes the sample volume gate
Scan Area
Slants the B-Mode or Color Flow linear image left or right to get more information without moving the probe
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4-3-6 Basic Measurements

NOTE: The following instructions assume that you first scan the patient and then press Freeze.
4-3-6-1 Distance and Tissue Depth Measurements
1.) Press MEASURE
2.) To position the active caliper at the start point (distance) or the most anterior point (tissue depth), move the TRACKBALL
3.) To fix the start point, press Set. The system fixes the first caliper and displays a seco nd active caliper.
4.) To position the second active caliper at the end point (distance) or the most posterior point (tissue depth), move the TRACKBALL
5.) To complete the measurement, press SET value in the measurement results window.
Before you complete a measurement:
To toggle between active calipers, press MEAS URE To erase the second caliper and the current data measured and start the measurement again, press
CLEAR
NOTE: To rotate through and activate previously fixed calipers, turn CURSOR SELECT NOTE: After you complete the measurement, to erase all data that has been measured to this point,
but not data entered onto worksheets, press CLEAR
4-3-6-2 Circumference/Area (Ellipse) Measurement
1.) Press MEASURE
2.) To position the active caliper, move the TRACKBALL
3.) To fix the start point, press SET
4.) To position the second caliper, move the TRACKBALL
5.) Turn the ELLIPSE
once.
caliper.
once; an active caliper displays.
.
.
. The system displays the distance or tissue depth
.
.
.
once; an active caliper displays.
.
. The system fixes the first caliper and displays a second active
.
control; an ellipse with an initial circle shape appears.
NOTE: Be careful not to press the Ellipse control as this activates the Body Pattern.
6.) To position the ellipse and to size the measured axes (move the calipers), move the
TRACKBALL
7.) To increase the size, turn the ELLIPSE turn the ELLIPSE
8.) To toggle between active calipers, pr es s MEASURE
9.) To complete the measurement, press SET in the measurement results window.
Before you complete a measurement:
- To erase the ellipse and the current data measured, press CLEAR
is displayed to restart the measurement.
- To exit the measurement function without completing the measurement, press CLEAR
second time.
4 - 10 Section 4-3 - General Procedure
.
control in a clockwise direction. To decrease the size,
control in a counterclockwise direction.
.
. The system displays the circumference and area
once. The original caliper
a
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4-3-6-3 Worksheets
Measurement/Calculation worksheets are available to display and edit measurements and calculations. There are generic worksheets as well as Application specific worksheets. The worksheets are selected from the Measurement icon on the monitor screen after pressing measurement key.
4-3-6-4 Report Pages
Measurements/Calculations that are included on the worksheet can also be di splayed on Report Pages. Report Pages can be customized to meet the appr o pr iate needs of the user.
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4-3-7 Probe/Connectors Usage

4-3-7-1 Connecting a probe
1.) Place the probe's carrying case on a stable surface and open the case.
2.) Carefully remove the probe and unwrap the probe cable.
3.) DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable damage.
4.) Turn the connector locking handle counterclockwise.
5.) Align the connector with the probe port and carefully push into place.
6.) Turn the connector locking handle cloc kwise to secure the probe connector.
7.) Carefully position the probe cable in the probe cord holder spot so it is free to move, but not resting on the floor.
4-3-7-2 Activating the probe
Press the Appilcation button on the menu key panel in keyboard Select the appropriate probe from the probe indicators on the monitor screen. The probe activates in the currently-selected operati ng mode. The probe's default settings for the mode
and selected exam are used automatically.
4-3-7-3 Deactivating the probe
When deactivating the probe, the probe is automatically placed in standby mode.
1.) Press the Freeze key.
2.) Gently wipe the excess gel from the face of the probe. (Refer to the Basic User Manual for complete probe cleaning instructions.)
3.) Carefully slide the probe around the right side of the keyboard, toward the probe holder. Ensure that the probe is placed gently in the probe holder.
4-3-7-4 Disconnecting the probe
Probes can be disconnected at any time. However, the probe should not be selected as the active probe.
1.) Move the probe locking handle counterclockwise. Pull the probe and connector straight out of the probe port.
2.) Carefully slide the probe and connector away from the p robe port a nd arou nd the ri ght side of the keyboard. Ensure the cable is free.
3.) Be sure that the probe head is clean before placing the probe in its storage box.
4 - 12 Section 4-3 - General Procedure
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4-3-8 Using Cine

4-3-8-1 Activating CINE
Press FREEZE left most button on the menu key panel of keyboard. To stop CINE Loop playback. press Run/Stop.
4-3-8-2 Quickly Move to Start/End Frame
Press FIRST
4-3-8-3 Start Frame/End Frame
Turn the START FRAME right to move forward through the CINE Loop.
, then roll the TRACKBALL to activate CINE. To start CINE Loop playback, press the
to move to the first CINE frame; press LAST to move to the last CINE frame.
dial to the left to move to the beginning of the CINE Loop. Turn the dial to the
Turn the END FRAME move backward through the CINE Loop.
4-3-8-4 Adjusting the CINE Loop Playback Speed
Turn the LOOP SPEED
4-3-8-5 Disconnecting B-Mode CINE from Timeline CINE
To review the B-Mode CINE Loop only, press CINE MODE SELECTION To review the Timeline CINE Loop only, press CINE MODE SELECTION To return to linked B-Mode and Timeline CINE Loop review, press CINE MODE SELECTION
B/TL
.
4-3-8-6 Moving through a CINE Loop Frame By Frame
Turn FRAME BY FRAME
dial to the right to move to the end of the CINE Loop. Turn the dial to the left to
dial right/left to increase/decrease the CINE Loop playback speed.
to move through CINE memory one frame at a time.

4-3-9 Image Management (QG)

For Image Management functionality refer to the LOGIQ™ 5 PRO Quick Guide. It talks about several topics:
Clipboard
Printing Images
Browsing and Managing an Exam’s Stored Image
Connectivity, and Dataflow Concept and Creation
Starting an Exam
Configuring Connectivity
•TCP/IP
Services (Destinations)
Buttons
Views Verifying and Pinging a Device
and select B ONLY.
and select TL ONLY.
and select
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4-3-10 Using the CD-RW / MOD (Magneto-Optical Drive)

4-3-10-1 Using the CD-RW
NOTICE
NOTICE
Never move the unit with a disk in the CD-RW because the drive actuator will not be locked and the CD-RW could break.
1.) Push the EJECT
button, the disk tray will appear.
2.) Put the disk onto the disk tray.
3.) Press the EJECT
button to insert the disk into the CD-RW device.
4.) There are a number of methods to eject a disk from the CD-RW. Ejection is automatic in some cases. Manual ejection methods, listed in preferred order of use, are:
a.) Press EJECT b.) Press and hold EJECT
button on the CD-RW while system is ON.
button while the system is booting.
c.) Mechanical ejection. Insert the end of a paper clip into the hole next to the EJECT button while
system power is OFF.
Avoid mechanical ejection whenever possible. Mechanica l ejection leaves the actuator unlocked and the MOD susceptible to d amage if moved. If forced to use t his method, r eboot the system, then insert and eject a known good disk using one of the othe r methods.
CD-RW Drive
Eject Button
Figure 4-30 CD-RW drives
4 - 14 Section 4-3 - General Procedure
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4-3-10-2 Using the MOD (Magneto-Optical Drive)
The 3.5 inch Magneto-Optical disk drive supports the following densities:
Standard: 1.3GB; 640MB; 540MB; 230MB; and 128MB Overwrite: 1.3GB; 640MB; and 540MB
1.) Before installing an MO disk in the MOD, check the MO disk for loose hardware or damaged labels which could jam inside the MOD. Also, ensure that the slide switch in one corner of the disk is set so that the disk is write enabled (disk hole closed).
2.) Insert the disk into the MOD with the label facing up.
NOTICE
Never move the unit with a disk in the MOD because the drive actuator will not be lo cked and the MOD could break.
3.) There are different methods to eject a disk from the MOD. In some cases disk ejection is automatic. Manual ejection methods are listed below in preferred order from best (1 ) to worst (4).
a.) When in Archive Menu, use the softkey choice –or– click Image Presets up, then click the left
softkey switch up for ARCHIVE
b.) Press the EJECT
switch on the MOD while system is ON. c.) Press and hold the EJECT d.) Mechanical ejection. Insert the end of a paper clip into the h ole next to the EJECT
, then toggle the switch under EJECT MOD.
switch while the system is booting.
switch while
system power is OFF.
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4-3-11 Backup and Restore Database, Preset Configurations and Images

NOTICE
4-3-11-1 Formatting Media
Avoid mechanical ejection whenever possible. Mechanical ejection leaves the actuator unlocked and the MOD susceptible to damage if mov ed. If forced to use this method, re boot the system, then insert and eject a known good disk using one of the other manual ejection methods.
1.) To format the backup media, CD-ROM or MOD, select the UTILITY
2.) Select CONNECTIVITY monitor screen. Properly label and Insert the backup media.
3.) Select the media type from the drop down menu.
4.) Enter the label for the media as shown in Figure 4-31. It is best to use all capital letters with no spaces or punctuation marks.
button on the Menu panel.
, then TOOL( in case of BT05 SW, REMOVABLE MEDIA )on the
Figure 4-31 Format and Verify Media
5.) The Ultrasound system displays a pop-up menu, as shown in Figure 4-32. When the formatting has been completed, press OK
6.) If desired, verify that the format was successful by returning to Utility>Connectivity>Tools (in case of BT05 SW, Removable Media) and selecting VERIFY
Figure 4-32 Format Successful Pop-up Menu
4 - 16 Section 4-3 - General Procedure
to continue.
as shown in Figure 4-31.
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4-3-11-2 Backup System Presets and Configurations
NOTE: Always backup any preset configurations before a software reload. This ensures that if the presets need
to be reloaded, after the software update, they will be the same ones the customer was using prior to service.
1.) Insert a formatted MOD (Magneto-Optical Disk) or CD-R into the drive.
2.) On the Touch Panel, press UTILITY
3.) On the Utility Touch Panel, press SYSTEM
4.) On the monitor display, select BACKUP/RESTORE
.
.
.
NOTE: If you are not logged in as GE Service or with administrator privileges, the Operator Login
window is displayed. Log on with administrator pr ivile ge s.
5.) In the Backup list, select Patient Archive, Report Archive, System Configuration and User Defined Configuration.
6.) In the Media field, select MO or CD-RW.
7.) Select BACKUP
.
The system performs the backup. As it proceeds, status information is displayed on the Backup/Restore screen.
Check here to backup presets and configurations
Figure 4-33 Backup/Restore Menu
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4-3-11-3 Restore System Presets and Configurations
CAUTION
The restore procedure overwrites the existin g database on the local hard drive. Make sure to insert the correct MOD or CD-R.
1.) Insert the Backup/Restore MOD (Magneto-Optical Disk) or CD-R into the drive.
2.) On the Touch Panel, press UTILITY
3.) On the Utility Touch Panel, press SYSTEM
4.) On the monitor display, select BACKUP/RESTORE
.
.
.
NOTE: If you are not logged in with administrator privileges, the Operator Login window is displayed.
Log on with administrator privileges.
5.) In the Restore list, select Patient Archive, Report Archive, System Con figuration and User Defined Configuration.
6.) In the Media field, select the Backup/Restore MOD or CD-RW.
7.) Select RESTORE
.
The system performs the restore. As it proceeds, status information is displayed on the Backup/Restore screen.
Figure 4-34 Backup/Restore Menu
Check here to restore presets and configurations
4 - 18 Section 4-3 - General Procedure
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4-3-11-4 Archiving Images
To export an exam(s) to a compatible Ultrasound system:
1.) Format the removable media (MOD or CD-ROM) . Label the removable media. Answer Yes/OK to the messages.Press Patient. Deselect any selected patient(s) in the search portion of the Patient screen. Press Exam Data Transfer (located at the upper, left-hand corner of the Patient menu).
Figure 4-35 Exam Data Transfer
2.) Select Export task Button.
Figure 4-36 Task button
3.) The [From] combo box is not active. It displays Local Archive. The [To] combo box is active. Select the type of removable media MOD or CD Rom. Then please wait until the patient list is visible.
Figure 4-37 To Combo Box
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4-3-11-4 Archiving Images (cont’d)
4.) In the patient list at the top of the Patient menu, select the patient(s) you want to export. You can use Windows commands to select more than one patient. To select a consecutive list of patients, click the cursor on the first name, move the cursor to the last name, then press and hold down the Shift+right Set key to select all the names. To select a non-consecutive list of patients, click the cursor at the first name, move the cursor to the next name, then press and hold down the Ctrl+right Set key, move the cursor to the next name, then press and hold down the Ctrl+right Set key again, etc. You can also search for patients via the Search key and string. Or, Select All Button from the Patient Menu:
Figure 4-38 Source Section
NOTE: You need to use your best judgment when moving patients' images. If there are lots of images
or loops, then only move a few patients at a time.
5.) Once you have selected all of the patients to export, press Transfer Button as shown in Figure 4-38.
6.) The progress bar appears as the copy is taking place. Once transfer completed, the exported patient list will be shown as Figure 4-39..
Figure 4-39 Destination Section of Patient Screen
7.) Press F3 to eject the media. Specify that you want to finalize the CD-ROM.
4 - 20 Section 4-3 - General Procedure
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4-3-12 ECG Check Out (this option is currently not available on the LOGIQ™ 5 PRO

Connect the ECG Harness and check:
Table 4-19 ECG Harness Check
Step Task to do Expected Result(s)
Connect the ECG at the Connector on the Front of the
1. scanner.
It will display a curve along the bottom edge of the image sector
Chapter 4 Functional Checks 4 - 21
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Section 4-4 Application Turnover Checklist

Complete these checks before returning the scanner to customer for use:
1.) TBD

Section 4-5 Software Configuration Checks

Table 4-20 Software Configuration Checks
Step Task to do Expected Result(s)
1.
Check Date and Time setting Date and Time are correct
2.
Check that Location (Hospital Name) is correct Location Name is correct
3.
Check Language settings Desired Language is displayed
4.
Check assignment of Printer Keys Print1-4 Keys are assigned as desired by the customer
5.
Check that all of the customer’s options are set up correct All authorized functions are enabled
4 - 22 Section 4-4 - Application Turnover Checklist
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Section 4-6 Peripheral Checks

Check that peripherals work as described below:
Table 4-21 Peripheral Checks
Step Task to do Expected Result(s)
1.
Press (FREEZE
) Stop image acquisition.
Press (PRINT 1
2. keyboardl
3.
Press VIDEO
4.
Press UPDATE MENU Use the alphanumeric keyboard to enter
5. the counter number in the counter field.
6.
Press SET COUNTER
7.
Press VIDEO
8.
Press REC/PAUSE
9.
Press REC/PAUSE
Press VIDEO
10. assignable play
Use the Assignable keys on the Control
11.
Panel
While in playback mode, use the
12.
TRACKBALL
speed and scroll through the record.
) or (PRINT 2) on the
on the keyboard. To start the video counter at a different point:
in the Trackball area. The Video Set Counter / Search Dialog window is displayed
to save the change. Number is saved
on the Control Panel to return to the scanning mode
on the Control panel.
on the Control panel.
on the Control Panel and the
to adjust the video playback
The image displayed on the screen is printed on B&W or Color printer, depending on the key assignment configuration
Number appears
to Start Recording A red dot is displayed in the VCR status area on the Title bar to indicate
that recording has begun To Stop recording
The video status icon is changed to (Pause)
To start, Play back an examination
to perform actions on the recorded session, such as stop, pause, rewind or fast forward.
The video status icon in updated accordingly.
To search on the tape
13.
Press the assignable PAUSE
14.
When playing back an examination
Press (FREEZE
15. recorded session.
) while playing back a
to stop the tape at the desired frame. part of it can be stored on the computer’s memory as a cineloop.The
cineloop enables the user to perform further operations on the stored section (see for further information on cineloop operation).
To store a recorded sequence as a cineloop. The last few seconds are stored as a cineloop.
Chapter 4 Functional Checks 4 - 23
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Section 4-7 Site Log

Table 4-22 Site Log
Date Service person Problem Comments
4 - 24 Section 4-7 - Site Log
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