GE LOGIQ BOOK BASIC SERVICE MANUAL_SM_2300141_13 Two & Six-Place (Macro) Kjeldahl Distillation Systems Models 2128501 2127601 2127602 2127603
Page 1
Technical
Publication
Direction 2300141
Revision 13
GE Medical Systems
LOGIQ™ Book Service Manual
GE Medical Systems
Operating Documentation
Copyright© 2002, 2003, 2004, 2005 by General Electric Co.
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK 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, MéCANIQUES OU AUTRES.
WARNUNG
• DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER
SPRACHE.
• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENö TIGT, IST
ES AUFGABE DES KUNDEN FüR EINE ENTSPRECHENDE ÜBERSETZUNG ZU
SORGEN.
• VERSUCHEN SIE NICHT, DAS GERä T ZU REPARIEREN, BEVOR DIESES
KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN
WURDE.
• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN
DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN
DURCH ELEKTRISCHE SCHLä GE, MECHANISCHE ODER SONSTIGE
GEFAHREN KOMMEN.
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE M ANUAL
• ESTE MANUAL DE SERVICIO Só LO EXISTE EN INGLé S.
• SI ALGúN PROVEEDOR DE SERVICIOS AJENO A GEMS SOLICITA UN IDIOMA
QUE NO SEA EL INGLéS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN
SERVICIO DE TRADUCCIó N.
• NO SE DEBERá DAR SERVICIO Té CNICO 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, MECá NICAS O DE OTRA
NATURALEZA.
• ESTE MANUAL DE ASSISTêNCIA TéCNICA Só SE ENCONTRA DISPONíVEL EM
INGLêS.
• SE QUALQUER OUTRO SERVIç O DE ASSISTê NCIA Té CNICA, QUE Nã O A
GEMS, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, é DA
RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIç OS DE TRADUç ã O.
ATENÇÃO
• Nã O TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTêNCIA TéCNICA.
• O Nã O CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANç A
DO TéCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELéTRICOS,
MECâ NICOS 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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DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE M ANUAL
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 positioning of the equipment at the site prepared for the
equipment shall be performed by licensed electrical contractors. Other connections between pieces of
electrical equipment, calibrations and testing shall be performed by qualified GE Medical Systems
personnel. In performing all electrical work on these products, GE will use its own specially trained field
engineers. All of GE’s electrical work on these products will comply with the requirements of the
applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to perform
electrical servicing on the equipment.
OMISSIONS & ERRORS
If there are any omissions, errors or suggestions for improving this documentation, please contact the
GE Medical Systems Global Documentation Group with specific information listing the system type,
manual title, part number, revision number, page number and suggestion details. E-mail the information
to : UltrasoundDocError@med.ge.com
GE Medical Systems employees should use the iTrak System to report all documentation errors or
omissions.
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DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Revision History
Revision Date Reason for change
0 Oct 29, 2002 Initial
1 Jan 27, 2003 Update
2 Apr 23, 2003 Update
3 Nov 12,2003 Update
4 Nov 28,2003 Spare parts update
5 Jan 16, 2004 ACDC update
6 Apr 27, 2004 FRU and peripheral update
7 May 11, 2004 Delete the user logon procedure
8 May 26, 2004 Change rating platelabel
9 Jun 08, 2004 Software version & Spare parts update
10 Jun 18, 2004 Add AUS console & USB HUB
11 July 19, 2004 FRU list update
12 Aug 20, 2004 Software version update
13 Jan 24, 2005 Add one Note for Linksys Wireless Lan Adapter
List of Effected Pages
Pages Revision Pages Revision Pages Revision
Title Page 13
Important Precautions
pages i to iv
Rev History/LOEP
pages v to vi
Table of Contents
pages vii to xx
Chapter 1 - Introduction
pages 1-1 to 1-14
13
13
13
13
Chapter 2 - Pre-Installation
pages 2-1 to 2-10
Chapter 3 - Installation
pages 3-1 to 3-26
Chapter 4 - Functional Checks
pages 4-1 to 4-32
Chapter 5 - Theory
pages 5-1 to 5-32
Chapter 6 - Service Adjustments
pages 6-1 to 6-4
Chapter 7 - Diagnostics/
13
13
13
13
13
Troubleshooting
pages 7-1 to 7-18
Chapter 8 - Replacement
Procedures
pages 8-1 to 8-2
Chapter 9 - Replacement Parts
pages 9-1 to 9-16
Chapter 10 - Periodic Maintenance
pages 10-1 to 10-20
Index
pages I to II
Back Cover 13
13
13
13
13
13
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DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE M ANUAL
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Table of Contents
CHAPTER 1
Introduction
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Chapter 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Chapter Contents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Typical Users of the Basic Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2
LOGIQ™ Book Models Covered by this Manual . . . . . . . . . . . . . . . . . . . . . 1 - 2
Purpose of Operator Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2
Important Conventions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3
Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3
Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 4
Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5
Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Labels Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10
Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Lockout/Tagout Requirements (For USA Only) . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
EMC, EMI, and ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12
Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12
CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12
Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12
Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13
Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13
System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14
1 Table of Contents
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CHAPTER 2
Pre Installation
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
Purpose of this chapter 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
Chapter Contents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
General Console Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Console Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Lighting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
LOGIQ™ Book Power Requirements . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Inrush Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Site Circuit Breaker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Site Power Outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Unit Power Plug . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Power Stability Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4
Scan Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5
Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Recommended Ultrasound Room Layout . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Purchaser Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Required Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7
Desirable Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7
Recommended and Alternate Ultrasound Room Layout . . . . . . . . . . 2 - 8
Networking Pre-installation Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9
Stand Alone Scanner (without Network Connection) . . . . . . . . . . . . 2 - 9
Scanner Connected to Hospital’s Network . . . . . . . . . . . . . . . . . . . . 2 - 9
Purpose of DICOM Network Function . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9
DICOM Option Pre-installation Requirements . . . . . . . . . . . . . . . . . . 2 - 9
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CHAPTER 3
Installation
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1
Purpose of Chapter 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1
Average Installation Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1
Installation Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Receiving and Unpacking the Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3
Moving into Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 6
Packing the Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 6
Preparing for Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
System Voltage Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
Completing the Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Power On / Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Scanner Power On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Turn on the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
Back-end Processor Power Down . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
Scanner Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10
Transducer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10
System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11
System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11
Physical Dimensions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11
Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12
Approved on-board peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12
Reference other peripherals and options . . . . . . . . . . . . . . . . . . . . . 3 - 12
Connecting Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 13
Peripherals/Accessories Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 13
Rear Panel Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 13
Connect peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 17
Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 23
Software/Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 23
Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 24
Table of Contents 3
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Loading Base Image Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25
Upgrading Application Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 27
Functional Check-out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 30
Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31
Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31
User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31
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DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
CHAPTER 4
Functional Checks
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
Purpose for Chapter 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
Required Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
General Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
Power On/Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
Scanner Power On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
Turn on the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3
Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3
Back-end Processor Power Down . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3
Scanner Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 4
Suspend . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 4
Archiving and Loading Presets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
Archiving Presets to an CD-R disk . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
Loading Presets from an CD-R disk . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
Adjusting the Display Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6
Brightness . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6
Lockout/Tagout Requirements (For USA Only) . . . . . . . . . . . . . . . . . . . . . 4 - 6
System Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7
Control Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7
LOGIQ™ Book SoftMenu Key Tour . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 8
Monitor Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
B Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10
B Mode OP Panel Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 11
B Mode Softmenu Key . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 12
M Mode Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
M Mode OP Panel Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 14
M Mode Softmenu Key . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 15
Color Flow Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 16
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 16
Color Flow Mode OP Panel Controls . . . . . . . . . . . . . . . . . . . . . . . . 4 - 17
Color Flow Mode Softemenu Key . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 18
Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20
Doppler Mode OP Panel Controls . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 21
Doppler Mode OP Panel Controls . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 22
Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24
Distance and Tissue Depth Measurements . . . . . . . . . . . . . . . . . . . 4 - 24
Circumference/Area (Ellipse) Measurement . . . . . . . . . . . . . . . . . . 4 - 24
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Worksheets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Report Pages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Probe/Connectors Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Connecting a probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Activating the probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Deactivating the probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Disconnecting the probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Using Cine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 26
Activating CINE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 26
Quickly Move to Start/End Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 26
Start Frame/End Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 26
Adjusting the CINE Loop Playback Speed . . . . . . . . . . . . . . . . . . . . 4 - 26
Moving through a CINE Loop Frame By Frame . . . . . . . . . . . . . . . . 4 - 26
Image Management (QG) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 26
Backup and Restore Database, Preset Configurations and Images . . . . . . 4 - 27
Formatting Media . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 27
Backup System Presets and Configurations . . . . . . . . . . . . . . . . . . . 4 - 28
Restore System Presets and Configurations . . . . . . . . . . . . . . . . . . 4 - 29
Archiving Images . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 30
Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 32
Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 32
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CHAPTER 5
Components and Functions (Theory)
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1
Block Diagrams and Theory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2
Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5
Front End . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6
The Back End . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7
Top Console . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7
External I/O . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 8
Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 8
Wiring . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 9
PWA Assy Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10
MST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10
Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10
DFP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 11
Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 12
DTX . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 13
Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 13
DCNN . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 14
Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 14
Keyboard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 15
Scan Control Board LEDs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 16
Power Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 17
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 17
AC Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 17
DC Power (Low Voltage) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 18
Battery charging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 19
Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 19
Air Flow Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 20
Fans . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 21
Common Service Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 22
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 22
Global Service User Interface (GSUI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 22
Internationalization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 22
Service Login . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 22
Access / Security . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 22
The usage for security cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 23
Service Home Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 24
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Error Logs Tab ( Not available on LOGIQ Book now) . . . . . . . . . . . . . . . . . 5 - 25
Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 26
Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 27
Search . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 27
Exit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 28
Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 29
Diagnostics Execution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 29
Diagnostic Reports . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 29
Image Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 30
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 30
Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
PM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
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CHAPTER 6
Service Adjustments
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1
Purpose of this chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1
Monitor Adjustments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
Adjustments Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
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CHAPTER 7
Diagnostics/Troubleshooting
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1
Purpose of Chapter 7 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1
Gathering Trouble Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Collect Vital System Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Collect a Trouble Image with Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3
Screen Captures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Check and Record the P3 Key Function . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Setting the P3 Key to Screen Capture . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5
Capturing a Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
Reset the P3 Key to Customer’s Functionality . . . . . . . . . . . . . . . . . . . . . . . 7 - 7
Global Service User Interface (GSUI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 8
Enter global service user interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 8
Active Diagnostic Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
Update FPGA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
Control Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
Button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
Loop Count . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
Progress Indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
Short Text Message . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
Background Color . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 11
Common Diagnostics. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12
Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12
Disruptive Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12
System Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12
PC Diagnostics (Non-Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
CPU Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
Hard Drive Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
Memory Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
CD/DVD Drive Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
Video Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
USB Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
PC Diagnostics (Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
Keyboard Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
LCD Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
LOGIQ™ Book Diagnostic Descriptions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 14
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 14
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FRU Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 15
MST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 15
DFP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 16
DTX . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 17
DCNN . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18
PC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 19
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CHAPTER 8
Replacement Procedures
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Purpose of Chapter 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Disassembly/Re-assembly. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Warning and Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Handle Assy (FRU No. 312) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Needed Manpower . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Mounting procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Trackball Roller Cleaning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4
Needed Manpower . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4
Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4
12 Table of Contents
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DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
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
OPERATOR CONSOLE ASSY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 3
Keyboard Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4
Bottom Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4
Accessories and Kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 5
Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 7
Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 8
Table of Contents 13
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CHAPTER 10
Care & Maintenance
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Periodic Maintenance Inspections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Purpose of Chapter 10 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Why do Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Keeping Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Quality Assurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Maintenance Task Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
How often should care & maintenance tasks be performed? . . . . . . . . . . . . 10 - 2
Tools Required. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4
Special Tools, Supplies and Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4
Specific Requirements for Care & Maintenance . . . . . . . . . . . . . . . . 10 - 4
System Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 5
Preliminary Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 5
Functional Checks (See Also Chapter 4) . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6
System Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6
Peripheral/Option Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Input Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
AC/DC Adapter Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
General Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 8
Optional
Probe Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
Diagnostic Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
View the Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
Probe Related Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
Basic Probe Care . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
Basic Probe Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
Using a Phantom . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 10
Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 10
Safety Test Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 10
GEMS Leakage Current Limits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 11
Outlet Test - Wiring Arrangement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 12
Chassis Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13
Definition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13
Generic Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13
14 Table of Contents
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Data Sheet for enclosure Source Leakage Current . . . . . . . . . . . . . 10 - 14
Probe Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 15
Definition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 15
Generic Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 15
No Meter Probe Adapter Procedure . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16
Data Sheet for Transducer Source Leakage Current . . . . . . . . . . . 10 - 17
When There's Too Much Leakage Current... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 18
Table of Contents 15
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DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
16 Table of Contents
Page 25
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK 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 this ultrasound machine. The service
provider must read and understand all the information presented here before installing or servicing a
unit.
1-1-2 Chapter Contents
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
1-1-3 Purpose of Service Manual
This Service Manual provides service information for the LOGIQ™ Book Ultrasound Scanning System.
It contains the following chapters:
1.) Chapter 1 - Introduction: Contains a content summary and warnings.
2.) Chapter 2 - Pre Installation: Contains pre-installation requirements for the LOGIQ™ Book.
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 available adjustments to
the LOGIQ™ Book.
7.) Chapter 7 - Diagnostics/Troubleshooting: Provides procedures for running diagnostic or related
routines for the LOGIQ™ Book.
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™
Book.
10.)Chapter 10 - Care & Maintenance: Provides periodic maintenance procedures for the LOGIQ™
Book.
1-1
1-3
1-7
1-12
1-13
Chapter 1 Introduction 1-1
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
1-1-4 Typical Users of the Basic Service Manual
• Service Personnel (installation, maintenance, etc.).
• Hospital’s Service Personnel
• Contractors (Some parts of Chapter 2 - Pre-Installation)
1-1-5 LOGIQ™ Book Models Covered by this Manual
Table 1-2 LOGIQ™ Book Model Designations
Part Number Description
H41402LA LOGIQ™ Book B/W Console for USA
H41402LC LOGIQ™ Book B/W Console for Europe
H41402LB LOGIQ™ Book B/W Console for China
H41422LA LOGIQ™ Book CFM/DOP. Console for USA
H41422LC LOGIQ™ Book CFM/DOP. Console for Europe
H41422LB LOGIQ™ Book CFM/DOP. Console for China
H41442LB LOGIQ™ Book CFM/DOP. Console for AUS
1-1-6 Purpose of Operator Manual(s)
The Operator Manual(s) should be fully read and understood before operating the LOGIQ™ Book and
also kept near the unit for quick reference.
1-2 Section 1-1 - Overview
Page 27
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK 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 identified 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
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK 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
Signed
Date
EYE
PROTECTION
1-4 Section 1-2 - Important Conventions
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
1-2-3 Product Icons
The following table describes the purpose and location of safety labels and other important information
provided on the equipment.
Table 1-5 Warnings
LABEL/SYMBOL PURPOSE/MEANING LOCATION
Identification and Rating Plate • Manufacture’s name and address
• Date of manufacture
• Model and serial numbers
• Electrical ratings (Volts, Amps, phase,
and frequency)
Type/Class Label Used to indicate the degree of safety or
protection.
IP Code (IPX1) Indicates the degree of protection
provided by the enclosure per IEC60
529. Can not be used in operating room
environment.
Equipment Type BF (man in the box
symbol) IEC 878-02-03 indicates B
Type equipment having a floating
applied part.
Bottom panel of the console
Bottom panel of the adapter
Foot Switch
Probe connectors
“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.
“ON” indicates the power on position of
the power switch.
“Standby” indicates the power stand by
position of the power switch.
CAUTION
This Power Switch DOES NOT
ISOLATE Mains Supply
Various
Various
Various
Adjacent to On/Standby Switch
Chapter 1 Introduction 1-5
Page 30
GE MEDICAL SYSTEMS
REF
SN
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Table 1-5 Warnings
LABEL/SYMBOL PURPOSE/MEANING LOCATION
“TUV” Listing and Certification Mark is
used to designate conformance to
nationally recognized product safety
standards. The Mark bears the name
and /or logo of the testing laboratory,
product category, safety standard is
assessed and a control number.
Date of manufacture.
The date could be a year, year and
month, or year, month and day, as
appropriate. See ISO 8601 for date
formates.
Bottom panel of the console
Rating Plate
REF
SN
Catalog or model number. Rating Plate
Serial number Rating Plate
Equipment Class II.
For products not relying protective earth
such as products having double or
reinforced insulation.
Direct Current.
For products to be powered from a DC
supply.
Rating Plate
Rating Plate
1-6 Section 1-2 - Important Conventions
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Section 1-3 Safety Considerations
1-3-1 Introduction
The following safety precautions must be observed during 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™ Book Training are authorized to service the
equipment.
1-3-3 Mechanical Safety
WARNINGWARNING
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.
WARNINGWARNING
CAUTION
NOTE: Special care should be taken when transporting the unit in a vehicle:
Never use a probe that has fallen to the floor. Even if it looks ok, it may be damaged.
The LOGIQ™ Book weights 4.2kg or more, depending on installed peripherals, when ready for
use. To avoid possible injury and equipment damage:
ALWAYS:
• Use the handle to move the system.
• Do not let the system strike walls or door frame.
• Limit movement to a slow careful walk.
• Before transporting, place the system in its special storage case.
• Ensure that the system is firmly secured while inside the vehicle.
• Secure system with straps or as directed otherwise to prevent motion during transport.
• Prevent vibration damage by driving cautiously. Avoid unpaved roads, excessive speeds, and
erratic stops or starts.
Chapter 1 Introduction 1-7
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
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 protective ground.
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.
1-3-5 Labels Locations
Figure 1-1 Label Location (oversea)
1-8 Section 1-3 - Safety Considerations
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Labels Locations (cont’d)
Figure 1-2 Label Location (China)
Chapter 1 Introduction 1-9
Page 34
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
1-3-6 Battery Safety
To avoid the risk of injury, follow the warning and cautions to make sure that the battery does not burst,
ignite, or generate heat of fumes.
WARNINGWARNING
CAUTION
• The battery has a safety device. Do not disassemble or alter the battery.
• Charge the batteries only when the ambient temperature is between 0° and 40° C (32° and
104° F).
• Do not short-circuit the battery by directly connecting the negative terminals with metal
objects.
• Do not heat the battery or discard it in a fire.
• Do not expose the battery to temperature over 60° C (140° F). Keep it away from fire and other
heat sources.
• Do not charge the battery near a heat source, such as a fire or heater.
• Do not leave the battery in direct sunlight.
• Do not drop packs from height to prevent them from possible malfunction damage.
• Do not pierce the battery with a sharp object, hit it, or step on it.
• Do not use a damaged battery.
• Do not solder a battery.
• Do not connect the battery to an electrical power outlet.
• Do not contact PCM directly to prevent packs from ESD damage.
• In the case of longer non-use of the LOGIQ Book, remove the battery is necessary.
To avoid the battery bursting, igniting, or fumes from the battery causing equipment damage,
observe the following precautions:
• Do not immerse the battery in water or allow it to get wet.
• Do not put the battery into a microwave oven or pressurized container.
• If the battery leaks or emits an odor, remove it from all possible flammable sources.
• If the battery emits an odor or heat, is deformed or discolored, or in a way appears abnormal
during use, recharging or storage, immediately remove it and stop using it.
If you have any questions about the battery, consult GE or your local
representative.
• Store the battery between -20° C (-4° F) and 60° C (140°F).
• Use only GE recognized batteries.
• In case of the long term (3 months or more) storage:
• Store the battery in a temperature range of 10° C (50° F) and 30° C (86°F).
• When charging for the first time after long-term storage. Recover such packs
to original performance through repeating several cycles of full charging and
discharging.
• When store packs for more than 6 months, charge at lease once charging
require per 6 months to prevent leakage and deterioration in performance
due to self-discharging.
NOTICE
The battery shall be shipped in about 30% charged state. Those packs have to be fully charged and
discharged up to 3 times to utilize Li-lon smart packs before use.
1-10 Section 1-3 - Safety Considerations
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DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
1-3-7 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.
1-3-8 Lockout/Tagout Requirements (For USA Only)
Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the electrical Mains
plug.
1-3-9 Returning/Shipping Probes and Repair Parts
Equipment being returned must be clean and free of blood and other infectious substances.
GEMS policy states that body fluids must be properly removed from any part or equipment prior to
shipment. GEMS employees, as well as customers, are responsible for ensuring that parts/equipment
have been properly decontaminated prior to shipment. Under no circumstance should a part or
equipment with visible body fluids be taken or shipped from a clinic or site (for example, body coils or
an ultrasound probe).
The purpose of the regulation is to protect employees in the transportation industry, as well as the
people who will receive or open this package.
NOTE: The US Department of Transportation (DOT) has ruled that “ items that were saturated and /or
dripping with human blood that are now caked with dried blood; or which were used or intended
for use in patient care” are “ regulated medical waste” for trabsportatin purposes and must be
transported as a hazardous material.
NOTE: THE USER/SERVICE STAFF SHOULD DISPOSE ALL THE WASTE PROPERLY AS PER
FEDERAL, STATE, AND LOCAL WASTE DISPOSAL REGULATION.
Chapter 1 Introduction 1-11
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK 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/EMI) and can be radiated through
space or conducted over interconnecting power of signal cables. In addition 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™ Book 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, shielding, gaskets, mesh, clamps, are 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:
FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE
EQUIPMENT.
1-12 Section 1-4 - EMC, EMI, and ESD
Page 37
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
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 local distributor or appropriate support resource, as
listed below.
Prepare the following information before you call:
- System ID serial number.
- Software version.
Table 1-6 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
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
1-262-524-5698
Fax: +1-414-647-4125
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 1-13
Page 38
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
1-5-2 System Manufacturer
Table 1-7 System Manufacturer
Manufacturer Phone Number
GE Medical Systems (China) Co., Ltd.
No.19, Changjiang Road, Wuxi, Jiangsu, P.R. China 214028
TEL: +86 510-5225888
FAX: +86 510-5226688
1-14 Section 1-5 - Customer Assistance
Page 39
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Chapter 2
Pre Installation
Section 2-1 Overview
2-1-1 Purpose of this chapter 2
This chapter provides the information required to plan and prepare for the installation of a LOGIQ™
Book. Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit.
2-1-2 Chapter Contents
Table 2-8 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
Page 40
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Section 2-2 General Console Requirements
2-2-1 Console Environmental Requirements
Table 2-9 Environmental Requirements for LOGIQ™ Book Scanners
Operational Storage Transport
Temperature
Humidity
Pressure
Temperatures in degree C, conversion to degree F = (degree C*(9/5) + 32)
2-2-1-1 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 source
of EMI which could degrade image quality. These controls should be selected to minimize possible
interface.
2-2-2 Electrical Requirements
10 - 40 degree C -5 - 50 degree C -5 - 50 degree C
30 - 75%
non-condensing
700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
10 - 90%
non-condensing
10 - 90%
non-condensing
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.
2-2-2-1 LOGIQ™ Book Power Requirements
Table 2-10 Electrical Specifications for LOGIQ™ Book
Adapter Name Voltage Power Tolerances Current Frequency
LBAC - 66 100-240 VAC 120VA ±10% 1.2-0.5 A 50-60 Hz
GE - 90W 100-240 VAC 108VA ±10% 1.08-0.45A 50-60HZ
2-2 Section 2-2 - General Console Requirements
Page 41
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
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.
Table 2-11 Inrush Current
Inrush Current
Voltage
100V 0.38A 0.41A
240V 0.20A 0.21A
2-2-2-3 Site Circuit Breaker
It is recommended that the branch circuit breaker for the machine be readily accessible.
2-2-2-4 Site Power Outlets
A dedicated AC power outlet must be within reach of the unit without extension cords. Other adequate
outlets for the external peripherals, medical and test equipment needed to support this unit must also
be present within 1 m (3.2 ft.) of the unit. Electrical installation must meet all current local, state, and
national electrical codes.
2-2-2-5 Unit Power Plug
If the unit arrives without a 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.
Console Only Console with all peripherals
Chapter 2 Pre Installation 2-3
Page 42
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
2-2-3 EMI Limitations
Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies,
magnetic fields, and transient in the air wiring. They also generate EMI. The LOGIQ™ Book 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 a broadcast station or broadcast van may also cause interference.
See Ta ble 2 - 12 for EMI Prevention tips.
Table 2-12 EMI Prevention/abatement
EMI Rule Details
Be aware of RF sources
Ground the unit
Replace all screws, RF
gaskets, covers, cores
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
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.
After you finish repairing or updating the system, replace all covers and tighten all screws.
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 interfere with the ultrasound signals.
If more than 20% or a pair of the fingers on an RF gasket are broken, replace the gasket.
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.
2-4 Section 2-2 - General Console Requirements
Page 43
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
2-2-4 Scan Probe Environmental Requirements
Operation:10° to 40° 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
-10 TO + 60 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
Page 44
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Section 2-3 Facility Needs
2-3-1 Recommended Ultrasound Room Layout
2-3-1-1 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.
User the Pre Installation checklist to verify that all needed steps have been taken,
Purchaser reasonability includes:
• Procuring the materials required.
• Completing the preparations before delivery 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 presents challenges to the installation team. To avoid
delays during installation, such variances should be made known to the individuals or group performing
the installation at the earliest possible date (preferable prior to purchase).
The ultrasound suite must be clean prior 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.
2-6 Section 2-3 - Facility Needs
Page 45
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
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 0.2m (0.67 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.
• 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)
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.
Chapter 2 Pre Installation 2-7
Page 46
GE MEDICAL SYSTEMS
f
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
2-3-3-1 Recommended and Alternate Ultrasound Room Layout
Recommended standard floor plan and a minimal floor plan for ultrasound equipment:
FILM VIEWER
FILM SUPPLIES
FILE
CABINET
SECRETARYS OR
DOCTOR’S DESK
SINK
ROOM,
PROCESSING
FILM
FILM VIEWER
COUNTER TOP
LINEN SUPPLY
PROBES/SUPPLIES
18 IN.
(46 CM)
DEDICATED
POWER
RECEPTACLE
COUNTER
TOP
SINK
OVERHEAD
LIGHTS DIMMER
SUCTION LINE
EMERGECY
OXYGEN
DOOR
42 IN.
(107 CM)
CONSOLE
FOOT
SW
(193 CM)
STOOL
76 IN.
A 14 by 17 foot Recommended Floor Plan
Scale : Each square equals one square
LINEN SUPPLY
EXAMINATION
TABLE
24 IN.
(61 CM)
PATIENT
TOILET
FACILITY
EXTERNAL
DOOR
30 IN.
(76 CM)
24 IN.
(61 CM)
FOOT
SW
STOOL
EXAMINARION
TABLE
PERIPHERALS
LOGIQ Book
CONSOLE
76 IN.
(193 CM)
DEDICATED POWER
OUTLETS
GE CABINET
FOT SOFTWARE
AND MANUALS
An 8 by 10 foot Minimal Floor Plan
Figure 2-3 RECOMMENDED ULTRASOUND ROOM LAYOUT
2-8 Section 2-3 - Facility Needs
Page 47
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
2-3-4 Networking Pre-installation Requirements
2-3-4-1 Stand Alone Scanner (without Network Connection)
None.
2-3-4-2 Scanner Connected to Hospital’s Network
Supported networks:
Wireless LAN
2-3-4-3 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 frees up the on-board monitor and peripherals, enabling viewing to be done while
scanning continues. With DICOM, images can be archived, stored, and retrieved faster, easier, and at
a lower cost.
2-3-4-4 DICOM Option Pre-installation Requirements
To configure the LOGIQ™ Book 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™ Book.
• 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™ Book 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.
Chapter 2 Pre Installation 2-9
Page 48
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
2-3-4-4 DICOM Option Pre-installation Requirements (cont’d)
.
.
LOGIQ™
Host Name
AE Title
Local Port
IP Address
Net Mask
..
.
...
ROUTING INFORMATION
ROUTER1
ROUTER2
ROUTER3
DICOM APPLICATION INFORMATION
NAME
Store 1
Store 2
Store 3
Store 4
Store 5
Store 6
Destination
IP Addresses
...
...
...
MAKE/REVISION IP ADDRESSES PORTAE TITLE
Default
GATEWAY IP Addresses
...
...
...
...
...
...
...
...
...
...
Worklist
Storage
Commit
MPPS
Figure 2-4 Worksheet for DICOM Network Information
2-10 Section 2-3 - Facility Needs
...
...
...
Page 49
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
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 3-13 Contents in Chapter 3
Section Description Page Number
3-1
3-2
3-3
3-4
3-5
3-6
3-7
3-8
3-9
3-10
3-11
Overview
Receiving and Unpacking the Equipment
Packing the Equipment
Preparing for Installation
Completing the Installation
System Configuration
Software/Option Configuration
Connectivity Installation Worksheet
Loading Base Image Software
Upgrading Application Software
Paperwork
3-1-2 Average Installation Time
Table 3-14 Average Installation Time
Description Average Installation Time Comments
Unpacking the scanner
Scanner wo/options
DICOM Option
20 minutes
30 minutes
30 minutes
3-1
3-3
3-6
3-7
3-8
3-11
3-23
3-24
3-25
3-27
3-31
Dependent on the configuration that is required
Dependent on the amount of configuration
The LOGIQ™ Book installation and functional checkout will take approximately one hour. LOGIQ™
Book consoles with optional equipment may take slightly longer.
Chapter 3 Installation 3-1
Page 50
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
3-1-3 Installation Warnings
11.)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.
NOTE: For information regarding packing labels, refer to LABELS ON PACKAGE.
12.)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 it's temperature is
below 10°C or above 40°C.
DANGER
Equipment damage possibility. Turning the system on without acclimation after arriving at site
may cause the system to be damaged.
Table 3-15 Time for Settlement
60 55 50 45 40 35 30 25 20 15 10 5 0 -5 -10 -15 -20 -25 -30 -35 -40
°C
14013112211310495867768595041322314 5 -4-13-22-31-40
°F
864200000002468101214161820
hrs
3-1-4 Safety Reminders
DANGER
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!
CAUTION
DANGER
DANGER
DANGER
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 to a properly grounded power outlet. Do not use a
three to two prong adapter. This defeats safety grounding.
Do not operate this unit unless all board covers are securely in place.
OPERATOR MANUAL(S)
The User Manual(s) should be fully read and understood before operating the LOGIQ™ Book
and kept near the unit for quick reference.
DANGER
ACOUSTIC OUTPUT HAZARD
Although the ultrasound energy transmitted from the LOGIQ™ Book probe is within FDA limits,
avoid unnecessary exposure. Ultrasound energy can produce heat and mechanical damage
3-2 Section 3-1 - Overview
Page 51
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Section 3-2 Receiving and Unpacking the Equipment
When a new system arrives, check that any components are not damaged and are not in short supply.
If shipping damage or shortage occurs, contact the address shown in Chapter 1.
1.) Cut the four PLASTIC BANDs.
2.) Cut the adhesive tape and open top covers of paper carton.
Adhesive tape
Plastic Bands
1
2
Figure 3-5 Open top covers of paper carton.
Chapter 3 Installation 3-3
Page 52
GE MEDICAL SYSTEMS
Console and
s
Accessories Package
er
rubber band
d
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Section 3-2 Receiving and Unpacking the Equipment (cont’d)
3.) Take out the Paper pad.
4.) Take out console together with 2 interleavers.
5.) Take out the interleavers beside Accessories Package.
6.) Take out Accessories Package..
Paper pa
interleaver
interleav
Figure 3-6 Unpacking the equipment
CAUTION
Do not lift the unit by the rubber band. Equipment damage may result.
3-4 Section 3-2 - Receiving and Unpacking the Equipment
Page 53
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Section 3-2 Receiving and Unpacking the Equipment (cont’d)
7.) Remove 2 interleavers.
8.) Remove plastic bag.
Interleaver
Plastic bag
Interleaver
Console
Figure 3-7 Removing interleavers and plastic bag
Chapter 3 Installation 3-5
Page 54
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Section 3-2 Receiving and Unpacking the Equipment (cont’d)
NOTE: Check the shipping container for special instructions. Verify that the container is intact. In some
cases a secondary container may be used. If so, ask the carrier for unpacking instructions.
50ºC
4
Humidity 10-90%
Excluding Condensation.
Figure 3-8 Labels on Package
-5ºC
Air Pressure
700-1060hpa
CAUTION
Please carefully unpack the system, and do not dispose the package of LOGIQ™ Book, so that
it can be reused for service.
3-2-1 Moving into Position
CAUTION
CAUTION
Do not lift the unit by the rubber band. Use handle to move system.
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™ Book. Before moving, store all loose parts in original
accessory box or in back pack. Return probes to original box.
Section 3-3 Packing the Equipment
Please pack LOGIQ™ Book in the reverse order of unpacking.
3-6 Section 3-3 - Packing the Equipment
Page 55
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
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 items
that are missing, back ordered or damaged.
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™ Book
Scanner is found on a label located on the AC adapter.
• 220-240VAC(China); 100-120VAC(USA/Asia); 220-240VAC(Europe, Latin America)
WARNINGWARNING
Connecting a LOGIQ™ Book scanner to the wrong voltage level will most likely destroy
the scanner.
3-4-3 EMI Protection
This Unit has been designed to minimize the effects of Electro Magnetic Interference (EMI). Many of the
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 hardware are installed and secured
before the unit is put into operation.
Chapter 3 Installation 3-7
Page 56
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Section 3-5 Completing the Installation
3-5-1 Power On / Boot Up
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.
3-5-1-1 Scanner Power On
Lower the handle. Plug the AC adapter output connector into the system DC input port (located on the
system’s rear panel) with the arrow side upward. Plug the AC adapter power cord into a grounded,
protective earth outlet.
Figure 3-9 connect AC adapter
When power is applied to the scanner, power is distributed to the Cooling Unit, Control Panel, LCD,
Peripherals and the Back-end Processor.
CAUTION
3-8 Section 3-5 - Completing the Installation
The system should rest on the handle to allow an air gap to prevent overheating.
Page 57
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
3-5-1-2 Turn on the system
Press the Power On/Off switch at the front of the system once.
Power On/Off switch
Figure 3-10 Power On/Off Switch
When the Power On/Off switch on the Control Panel is pressed once, the Back-end Processor starts
and the software code is distributed to initiate the scanner.
No status messages are displayed during this process.
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 Back-end Processor Power Down
To power down the system:
1.) Press the Power On/Off switch at the front of the system once.
2.) The System-Exit window is displayed.
Figure 3-11 System Exit Window
3.) Using the Trackball or Select key, select Shutdown.
4.) The shutdown process takes a few seconds and is complete when the power status LED is turned
off.
5.) Disconnect the probes.Clean or disinfect all probes as necessary. Store them in their shipping
cases to avoid damage.
6.) Close LCD cover.
Chapter 3 Installation 3-9
Page 58
GE MEDICAL SYSTEMS
probe latch
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
3-5-2-2 Scanner Shutdown
Disconnect the Mains Power Cable if necessary. For example: Relocating the scanner.
3-5-3 Transducer Connection
1.) Carefully open the system LCD display, plug the probe connector into the probe port, then lock the
probe latch upward.
NOTE: Please ensure that the probe latch is in an unlocked position before you connect the probe to the
systsem.
probe latch
Figure 3-12 Connect the probe
NOTE: It is not necessary to turn OFF power to connect or disconnect a probe.
3-10 Section 3-5 - Completing the Installation
Page 59
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Section 3-6 System Configuration
3-6-1 System Specifications
3-6-1-1 Physical Dimensions
The physical dimensions of the LOGIQ™ Book console are summarized in Figure 3-13 on page 3-11 .
Table 3-16 Physical Dimensions of LOGIQ™ Book
Height Width Depth Unit
78-99.5 350 280-320 mm
3.07-3.92 13.78 11-12.6 inches
WEIGHT: 4.2KG (9.2 lb.)
NOTE: Length is in mm
99.5
350
Figure 3-13 Overall Dimensions
78
280
320
Chapter 3 Installation 3-11
Page 60
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
3-6-2 Electrical Specifications
Table 3-17 Electrical Specifications for LOGIQ™ Book
Adapter Voltage Tolerances Current Frequency
LBAC-66 100-240 VAC +/-10% 1.2-0.5 A 50/60Hz
GE-90W 100-240 VAC +/-10% 1.08-0.45 A 50/60Hz
3-6-3 Approved on-board peripherals
Table 3-18 Approved on-board peripherals
Device Manufacturer Model Interface
B/W Printer SONY UP-D895 USB
Digital Color Printer SONY UP-D23MD USB
USB CD-RW IOMEGA CDRW 38402EXT2-B USB
Wireless LAN Adapter Linksys WPC55AG PCMCIA
Network Adapter Netgear P/N:FA411 PCMCIA
USB Lamp KENSINGTON FlyLight USB
VCR Sony SVO-9500MD/MDP
Video Adapter Focus Tview Micro-NTSC/PAL USB & SVGA
USB Memory LEXAR/IOMEGA
Bluetooth Adapter 3com 3CREB96B USB
Bluetooth Printer HP HP450/HP995CK USB
Footswitch Whanam FSU2001 USB
USB HUB PENGHONG PH-USB500 USB
JUMPDRIVE 256M/512M,
Mini 128/256MB
USB
NOTE: See each option installation instructions for installation and connection procedures.
WARNINGWARNING
Network Adapter (FA411) must be worked with patient isolation box (P/N :EP200132) ,
for details ,please refer to option manual.
3-6-3-1 Reference other peripherals and options
•Foot Switch
3-12 Section 3-6 - System Configuration
Page 61
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
3-6-4 Connecting Cables
WARNINGWARNING
Equipment damage possibility. Be sure to use the following recommended connecting cables to connect
recording devices and a network with LOGIQ™ Book console.
Table 3-19 List of Connecting Cables
Name Part No. Figure NOTE
USB Cable 2362186
USB Cable TBD
3-6-5 Peripherals/Accessories Connector Panel
LOGIQ™ Book peripherals and accessories can be properly connected using the rear connector panel.
3-6-5-1 Rear Panel Connector
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 printer, and
service tools.
For USB Printer
For USB CD-RW
Chapter 3 Installation 3-13
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Rear Panel Connector (cont’d)
This section indicates the pin assignment for each connector.
1
3
4
2
Figure 3-14 Rear Connector Panel
1.) PCMCIA Port for PC Card
2.) SVGA Output (CRT monitor option is not supported)
3.) Two interchangeable USB Port (Digital Printer, CD-RW and/or Foot Switch, exe)
4.) Port for DC input (AC Adapter)
NOTICE
The USB devices should be connected to LOGIQ™ Book first , power on USB devices before turning
LOGIQ™ Book to work.
NOTE: After User insert the PC Card into the PCMCIA Port, a “Beep” of buzzer will be heard, which means the
Card works properly, otherwise, please pull out the Card and insert again.
NOTE: Each outer (case) ground line of peripheral/accessory connectors are protectively grounded.
Signal ground lines are not isolated.
3-14 Section 3-6 - System Configuration
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3-6-5-1 Rear Panel Connector (cont’d)
1. Pin Assignment of DC/DC input
Connector: 3 Pin, Female
Table 3-20 Pin Assignments of DC/DC input
Pin No. Signal Pin No. Signal
1+3 -
2NC
2. Pin Assignment of USB
Table 3-21 Pin assignment of USB1
Pin No. Signal Pin No. Signal
1+5VDC3DATA+
2 DATA- 4 GND
Table 3-22 Pin assignment of USB2
Pin No. Signal Pin No. Signal
1+5VDC3DATA+
2 DATA- 4 GND
3. Pin assignment of RS232C for external VGA
Connector: D-SUB, 15Pin, Female
Table 3-23 Pin Assignments of RS232C for External VGA
Pin No. Signal Pin No. Signal
1RED9 N/A
2 GREEN 10 SGND
3BLUE11 N/A
4N/A12N/A
5 GND 13 HSYNC
6 RGND 14 VSYNC
7 GGND 15 N/A
8BGND16
Chapter 3 Installation 3-15
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Rear panel Connector (cont’d)
4. Pin Assignment of PCMCIA
Connector:
Table 3-24 Pin Assignments of PCMCIA
Pin No. Signal Pin No. Signal
1 DGND 35 DGND
2 BCDATA3 36 BCD1#
3 BCDATA4 37 BCDATA11
4 BCDATA5 38 BCDATA12
5 BCDATA6 39 BCDATA13
6 BCDATA7 40 BCDATA14
7 BCE1# 41 BCDATA15
8 BCADR10 42 BCE2#
9 BOE# 43 BVS1#
10 BCADR11 44 BIORD#
11 BCADR9 45 BIOWR#
12 BCADR8 46 BCADR17
13 BCADR13 47 BCADR18
14 BCADR14 48 BCADR19
15 BWE_C# 49 BCADR20
16 BRDY_IREO# 50 BCADR21
17 PPCMVCCB 51 PPCMVCCB
18 PPCMVPPB 52 PPCMVPPB
19 BCADR15 53 BCADR22
20 BCADR16 54 BCADR23
21 BCADR12 55 BCADR24
22 BCADR7 56 BCADR25
23 BCADR6 57 BVC2#
24 BCADR5 58 BRESET
25 BCADR4 59 BWAIT#
26 BCADR3 60 BINPACK#
27 BCADR2 61 BREG#
28 BCADR1 62 BBCD2
3-16 Section 3-6 - System Configuration
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Pin No. Signal Pin No. Signal
29 BCADR0 63 BBCD1
30 BCDATA0 64 BCDATA8
31 BCDATA1 65 BCDATA9
32 BCDATA2 66 BCDATA10
33 BIOCS16# 67 BCD2#
34 DGND 68 DGND
3-6-5-2 Connect peripherals
A.) Connect B/W printer to the system.
B/W Printer can be properly connected using USB Port1 or USB Port 2.(Figure 3-15).
Figure 3-15 Connect B/W printer to the system
B.) Connect UP-D23MD color printer to the system.
UP-D23MD Color Printer can be properly connected using USB Port1 or USB Port 2(Figure 3-16).
Figure 3-16 Connect digital color printer to the system
Chapter 3 Installation 3-17
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3-6-5-2 Connect peripherals (cont’d)
C.) Connect CD-RW to the system.
CD-RW can be properly connected using USB Port1 or USB Port2.
Figure 3-17 Connect CD-RW to the system
Iomega CD-RW drive recommended media list
Media issues are common throughout the CD-RW drive industry. Because CD media vendors often
change disc suppliers, quality levels may change due to manufacturing differences. This means that
you may encounter CD creation problems with media that may have worked successfully before.
Overall system configuration and other factors may also affect the success of creating a CD.
The following media types have been tested. Iomega highly recommends that you use the media types
on this list when creating your CDs.
Not all brands of media have been tested and, therefore, you may encounter success with other brands
not listed. This list will be updated as other media is tested and approved.
Table 3-25 Iomega CD-RW drive recommended media list
Brand Name Type Product Code Speed
Acer CDR80 Acer Media 40x-1x
Digital Research CDR80 DRCDR3250 32x-1x
Fuji Photo Film CDR74 CD-R74C 24x-1x
Fuji Photo Film CDR74 CD-R650D 24x-1x
Fuji Photo Film CDR80 CD-R700D 24x-1x
Hi-Val CDR80 CDR80 16x 24x-1x
Imation CDR80 CDR80 16x 24x-1x
Iomega Verbatim CDR CD-R74 32x-1x
Kodak CDR CDR Ultima 16x-1x
3-18 Section 3-6 - System Configuration
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Table 3-25 Iomega CD-RW drive recommended media list
Brand Name Type Product Code Speed
Kodak CDR CDR Gold Ultima 16x-1x
Mitsui CDR CDR74 32x-1x
Mitsui CDR CDR80 32x-1x
Mitsubishi Chemical Ultra CDRW - 24x
Mitsubishi Chemical HS CDRW RW74EU1 12x/10x/8x/4x
Mitsubishi Chemical CDRW RW74Q1 4x/2x
Mitsubishi Chemical CDRW RW74U1P 4x/2x
Ricoh CDR74 Type 74R-SG 24x-1x
Ricoh CDR74 Type 74-SFSGH2 24x-1x
Ricoh CDR80 CD-R Type 80 24x-1x
Ricoh HS CDRW CDRW 74 10x 12x/10x/8x/4x
Ricoh CDRW 74R-AZ2 4x/2x
Ricoh CDRW 74R-AZ2M3 4x/2x
Ricoh CDRW 74R-AZ2M4 4x/2x
Ricoh CDRW 74R-AZ 2x
Ricoh CDRW 74R-AZAM 2x
Samsung CDR74 Premium CDR-74 32x-1x
Sentinel CDR74 CDR74 Hyperspeed 16x-1x
TDK 48x - 48x-1x
TDK CDR74 CD-R74S 24x-1x
TDK CDR74 CD-R74A 24x-1x
TDK CDR80 CD-R80A 24x-1x
TDK CDRW CD-RW74 4x/2x
Verbatim CDR DataLifePlus CD-R 700 48x-1x
Verbatim CDR DataLifePlus CD-R 650 24x-1x
Verbatim DataLifePlus CD-RW 650 4x/2x
Yamaha CDRW CD-RW74M4 4x/2x
Chapter 3 Installation 3-19
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3-6-5-2 Connect peripherals (cont’d)
D.) Connect Foot Switch to the system.
Foot Switch can be properly connected using USB Port1 or USB Port2.
Figure 3-18 Connect Foot Switch to the system
E.) Connect Wireless LAN Adapter to the system.
Wireless LAN Adapter can be properly connected using Signal Port for Card.
Wireless
LAN Adapter
Figure 3-19 Connect Wireless LAN Adapter to the system
NOTE: When install Linksys Wireless Lan Adapter, please contact GE Service Engineer to complete
the installation.
F.) Connect the CRT to the system.
CRT can be properly connected using the SVGA output.
3-20 Section 3-6 - System Configuration
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3-6-5-2 Connect peripherals (cont’d)
G.) Connect the USB Lamp to the system. The USB Lamp can be properly connected using USB port
1 or 2.
Figure 3-20 USB Lamp connection
H.) Connect the Video Adapter and VCR to the system. The Video Adapter can be properly connected
using SVGA output and USB port 1 or 2.
Figure 3-21 Video Adapter and VCR Connection
I.) Connect the USB Memory to the system. The USB Memory can be properly connected using USB
port 1 or 2 (LEXAR USB Memory can only be properly connected using USB Port 1, the right one
in the Figure 3-22 on page 3-21 ).
Figure 3-22 USB Memory Connection
Chapter 3 Installation 3-21
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3-6-5-2 Connect peripherals (cont’d)
J.) Connect the Bluetooth printer to the system. The Bluetooth printer can be properly connected using
USB port 1.
Figure 3-23 Bluetooth Printer
NOTE: Please refer to the operation manual of each peripheral for information needed by the user to
operate the system safely.
For detailed installation information, please refer to the LOGIQ Book Peripheral Installation Instruction
manual.
3-22 Section 3-6 - System Configuration
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3-6-6 Available Probes
See in specification in the LOGIQ™ Book User Reference Manual for Probes and intended use.
Table 3-26 List of Probes
Probe Name Material of Headshell Area of Using TYPE Catalog Number Part Number
3C-RS NORYL GENERAL PURPOSE CONVEX H40402LL 2290776
10Lb-RS LEXAN
E8C-RS VALOX
8C-RS VALOX
i12L-RS ABS(GE)
8L-RS VALOX
SMALL PARTS
PERIPHERAL VASCULAR
TRANSVAGINAL
TRANSRECTAL
VETERINARY
PEDIATRIC
NEONATAL
INTRAOPERATIVE
SMALL PARTS
VASCULAR PEDIATRICS
SMALL PARTS
PERIPHERAL VASCULAR
LINEAR H40402LM 2290778
MICRO-CONVEX H40402LN 2290777
MICRO-CONVEX H40402LS 2354971
LINEAR H40402LW 2377942
LINEAR H40402LT 2376127
Section 3-7 Software/Option Configuration
Refer to the LOGIQ™ Book 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™ Book Basic User Manual,
Chapter 16, Customizing Your System.
For information on configuring DICOM Connectivity, Refer to the LOGIQ™ Book Basic User Manual,
Chapter 16, Customizing Your System.
Chapter 3 Installation 3-23
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Section 3-8 Connectivity Installation Worksheet
Site System Information
Site:
Dept:
LOGIQ SN:
CONTACT INFORMATION
Name
TCP/IP Settings
Name - AE Title:
IP Settings
IP Address:
Subnet Mask:
Default Gateway:
Type:
Title
Floor:
Room:
REV:
Phone
Remote Archive Setup
Remote Archive IP:
Remote Archive Name:
Comments:
E-Mail Address
Services (Destination Devices)
Device Type
1
2
3
4
5
6
7
8
9
10
11
12
3-24 Section 3-8 - Connectivity Installation Worksheet
Manufacturer
Name
IP Address
Port
AE Title
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Section 3-9 Loading Base Image Software
NOTE: While it is believed to be unnecessary, It would not hurt to disconnect the system from the
network and remove all transducers.
1.) Insert the disk labeled “Base System Software Load Image” into the CDROM drive.
2.) Properly turn off the scanner by momentarily pressing the Power On/Off Switch. Select
Shutdown from the System Exit menu. Wait for the Power On/Off Switch to turn amber.
3.) If the system will not shutdown normally, hold down the Standby Switch until the light turns
from green to amber.
Figure 3-24 Shutdown Dialog Box
4.) Turn on the scanner. You will see a message displayed on the LCD as shown in Figure 3-25
on page 3-25 .
Figure 3-25 System Update
5.) Press down Key on the Keyboard to choose “System Update”
NOTE: LOGIQ™ Book application software will be started automatically if you do not press down key in 3
seconds after the message displayed.
6.) You will see System Update Wizard displayed on the screen as shown in Figure 3-26 on page
3-26 .
Chapter 3 Installation 3-25
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Loading Base Image Software (cont’d)
Figure 3-26 Update Wizard
7.) Click “Update” button. It will take about 15 minutes for system updating, then shut down system
automatically while updating finished.
8.) Remove “Base System Software Image” CDROM from CD-RW.
3-26 Section 3-9 - Loading Base Image Software
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Section 3-10 Upgrading Application Software
WARNINGWARNING
While the software install procedure is designed to preserve data, you should save any
patient data, images, system setups to a CD-RW or hardcopy.
1.) Disconnect the system from the network.
2.) Place the “Application Software” CD-ROM into the CD-ROM drive.
3.) Power Down the scanner.
4.) Power up the scanner. Wait for a dialog box like the one in Figure 3-27 on page 3-27 .
Figure 3-27 Start Application Window
5.) Select INSTALL SW ...
6.) There will be two dialog boxes popping up warning you that you are about to install new
software as shown in Figure 3-28 on page 3-27 . In both cases click OK.
.
Figure 3-28 Start Loader Dialog Boxes
7.) Now you just have to wait till the Software loads (Approximately for 10 minutes).
8.) When the process has completed, the window will turn dark and you will see the following
message in Figure 3-29 on page 3-28 .
Chapter 3 Installation 3-27
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Upgrading Application Software (cont’d)
Figure 3-29 Software Load Complete
9.) When it completes loading the system will reboot.
10.)Remove the CD from the drive.
If possible, while the system is rebooting remove the CD from the drive. If you didn’t do that don’t worry
you will get a dialog box like the one shown in Figure 3-30 on page 3-28 .
Figure 3-30 Start Software
11.)REMOVE the Applications CD
12.)From the Start Applications dialog box, select START
13.)Select UPGRADE button to upgrade the FPGA while the following message box appears by
pressing the unmarked key of the trackball.
Figure 3-31 Upgrade FPGA
3-28 Section 3-10 - Upgrading Application Software
.
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Upgrading Application Software (cont’d)
14.)Click on the SHUT DOWN button to shut down the system after FPGA upgrade completing.
Figure 3-32 FPGA Upgrade
Chapter 3 Installation 3-29
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3-10-1 Functional Check-out
1.) Power on LOGIQ Book scanner and wait until system booting to main screen.
2.) Press UTILITY key on control panel.
3.) Choose the ABOUT button on the right.
Figure 3-33
4.) Check whether "Software version" is the right version for use.
Figure 3-34
3-30 Section 3-10 - Upgrading Application Software
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Section 3-11 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 available during the operation and service of the complete
system.
3-11-1 Product Locator Installation
NOTE: The Product Locator Installation Card shown may not be same as the provided Product Locator
card.
3-11-2 User Manual(s)
User 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.
Figure 3-35 Product Locator Installation Card
Chapter 3 Installation 3-31
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3-32 Section 3-11 - Paperwork
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Chapter 4
Functional Checks
Section 4-1 Overview
4-1-1 Purpose for Chapter 4
This chapter provides procedures for quickly checking major functions of the LOGIQ™ Book console,
diagnostics by using the built-in service software, and power supply adjustments.
Table 4-27 Contents in chapter 4
Section Description Page Number
4-1
4-2
4-3
4-4
4-5
Section 4-2 Required Equipment
To perform these tests, you'll need any of the sector, linear, or convex transducers.
(normally you should check all the transducers used on the system)
Overview
Required Equipment
General Procedure
Software Configuration Checks
Peripheral Checks
4-1
4-1
4-2
4-32
4-32
Chapter 4 Functional Checks 4-1
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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 control of the Power Cable
on the system.
TAG
&
LOCKOUT
Date
Signed
4-3-1 Power On/Boot Up
After AC/DC is connected correctly to the scanner, the power is applied to the scanner. When the
Control panel Power On/Off key is pressed once, the System starts.
4-3-1-1 Scanner Power On
Lower the handle. Plug the AC adapter output connector into the system DC input port (located on the
system’s rear panel) with the arrow side upward. Plug the AC adapter power cord into a grounded,
protective earth outlet.
Figure 4-36 connect AC adapter
4-2 Section 4-3 - General Procedure
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Scanner Power On (cont’d)
When power is applied to the scanner, power is distributed to the Cooling Unit, Control Panel, LCD,
Peripherals and the Back-end Processor.
4-3-1-2 Turn on the system
Press the Power On/Off switch at the front of the system once.
Power On/Off switch
Figure 4-37 Power On/Off Switch
When the Power On/Off switch on the Control Panel is pressed once, the Back-end Processor starts
and the software code is distributed to initiate the scanner.
No status messages are displayed during this process.
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 Back-end Processor Power Down
To power down the system:
1.) Press the Power On/Off switch at the front of the system once.
2.) The System-Exit window is displayed.
Figure 4-38 System Exit Window
3.) Using the Trackball or Select key, select Shutdown.
Chapter 4 Functional Checks 4-3
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Back-end Processor Power Down (cont’d)
4.) The shutdown process takes a few seconds and the power off sequence is complete when the
power status LED is turned off.
5.) Disconnect the probes.Clean or disinfect all probes as necessary. Store them in their shipping
cases to avoid damage.
6.) Close LCD cover.
4-3-2-2 Scanner Shutdown
Disconnect the Mains Power Cable is necessary. For example: Relocating the scanner.
CAUTION
DO NOT unplug and/or transport the unit until after the power off sequence has been completed.
Failure to do so may result in corrupted patient files.
4-3-2-3 Suspend
Suspend mode is triggered by suspend event. In LOGIQ™ Book system, there are two kinds of suspend
events.
1.) Close the LCD cover.
2.) Idle time longer than time set system BIOS.
After LOGIQ™ Book system enters suspend, power supply is maintained but all functions other than
those associated with power management are suspended. Currently running applications are also
temporarily paused. When suspend is entered, SUSSTAT# (suspend status flag) is asserted low, and
this signal may be then used to set peripheral devices to their Low Power mode. System should stop
scanning and cut off Analog 5V, +/-SHV, +/-THV. There is a LED on panel indicates suspend status,
see Figure 4-39 on page 4-4 . LED Green means suspend ON, turning off means suspend OFF. At this
time, all fans in the system running in half speed.
Figure 4-39 LED indicates suspend status
There is no transfer of saved data to and from the hard disk, nor any turning on or off of power supplies,
allowing this mode to be entered and resumed from rapidly.
4-4 Section 4-3 - General Procedure
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4-3-3 Archiving and Loading Presets
NOTE: Always save presets before any software reload. This ensures the presets loaded after the software
reload are as up–to–date as possible.
All user presets except changes to Summary, Anatomy, and Biometry pages, can be saved on an CDR disk for reloading on the system.
NOTICE
Presets should NOT be saved on the same CD-R disk as images. The Archive Menu lists the images
but does NOT list the presets stored on a CD-R disk.
4-3-3-1 Archiving Presets to an CD-R disk
1.) Insert an empty (blank) CD-R disk into the CD-RW.
2.) Access to the Utility Menu, and select Admin. The Backup sheet will be shown on the monitor.
Figure 4-40 Backup Sheet
3.) Select the item to back up either from Resource Files.
4.) Enter backup destination or browse through the disk to locate the destination.
5.) Select Backup now. The backup status for each item is displayed on the Result column.
4-3-3-2 Loading Presets from an CD-R disk
1.) Insert the CD-R disk with the archived Presets into the CD-RW.
2.) Access to the Utility Menu, and select Admin. The Restore sheet will be shown on the LCD display.
(see Figure 4-40 on page 4-5 )
3.) Select the item to restore either from Resource Files.
4.) Enter restore destination or browse through the disk to locate the destination.
5.) Select Restore. The restore status for each item is displayed on the Result column.
Chapter 4 Functional Checks 4-5
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4-3-4 Adjusting the Display Monitor
4-3-4-1 Brightness
To adjust the brightness:
Adjust the Brightness Slide pots, located on the right of side of the LCD, see Figure 4-41 on page 4-6 .
Figure 4-41 Brightness Slide pots
Record the final brightness setting and leave this information with the system.
4-3-5 Lockout/Tagout Requirements (For USA Only)
Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the AC plug.
4-6 Section 4-3 - General Procedure
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4-3-6 System Features
4-3-6-1 Control Panel
1
12
2
3
4
1.) TGC
2.) New Patient
3.) End Exam
4.) Mode/Gain/Auto Keys
5.) Preset Key
6.) Imaging/Measurement Keys
7.) Depth
8.) Reverse
9.) Image Keys
10.)Print Keys
11.)Freeze
12.)Keyboard
5
Figure 4-42 Control Panel Tour
6
6
7
8
9
10
11
Chapter 4 Functional Checks 4-7
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4-3-6-2 LOGIQ™ Book SoftMenu Key Tour
In general, there are three types of softMenu keys: Paddle Switch, Push Button and two-button key.
1
1.) The Paddle Switch is used to access the Sub SoftMenu.
2.) The Push Button Softkey is used to toggle between line one and line two.
3.) The up/down Two-button Softkeys are used to increase/decrease quantities.
2
Figure 4-43 SoftMenu Key Tour
3
4-8 Section 4-3 - General Procedure
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4-3-6-3 Monitor Display
10
11
1
2
3
12
4
5
6
13
7
14
8
15
17
9
16
18
19
20
21
22
23
Figure 4-44 Monitor Display Tour
Table 4-28 Monitor Display Features
1. Institution/Hospital Name, Date, Time, Operator
Identification, system status (real-time of frozen).
2. Patient Name, Patient Identification. 14. Focal Zone.
3. Acoustic Output Readout, 15. TGC (not shown on the image).
4. GE Symbol: Probe Orientation Marker. Coincides with a
probe orientation marking on the probe.
5. Image Preview. 17. Depth Scale.
6. Gray/Color Bar. 18. SoftMenu
7. Cine Gauge. 19. Caps Lock: On/Off.
8. Measurement Summary Window. 20. Start Menu icon.
9. Image. 21. Battery icon.
10. Measurement. 22. Card icon.
11. Results Window. 23. Trackball Functionality Status: Scroll, M&A (Measurement
12. Probe Identifier. Exam Study.
13. Imaging Parameters by Mode (current mode highlighted).
16. Body Pattern.
and Analysis), Position, Size, Scan Area Width and Tilt.
Chapter 4 Functional Checks 4-9
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4-3-7 B Mode Checks
4-3-7-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-23, in Chapter 3 Installation
to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already))
SoftMenu Key
Primary Menu
Secondary Menu
Frame Average
Biopsy
Line Density
Focus Width
B Softner
Suppression
Power Output
TGC
Zoom
Frequency
Gray Map
Dynamic Range
Rejection
Focus Position
Colorize
Edge Enhance
Updown Invert
Focus Number
Depth
Reverse
B Mode
Scan Area
Freeze
Figure 4-45 Controls available in B Mode
Figure 4-46 B Mode Screen Picture Example
4-10 Section 4-3 - General Procedure
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4-3-7-2 B Mode OP Panel Controls
Table 4-29 B Mode Control Panel Controls
Step Task Expected Result(s)
1
Press B Mode key B Mode Starts
Adjust the field of view. Increasing the depth
may view larger/deeper structures rates, and
2
Adjust Depth
3
Adjust Gain
4
Adjust Focus
5
Activate Auto Optimize
7
Adjust Time Gain Compensation (TGC)
8
Adjust Scan Area
9
Adjust Zoom
10
Zoom Clear Clear Zoom to normal condition.
11
Reverse
decreasing the depth may view near the skin
line.Press Up/Down Button to increase/
decrease. Depth displays on the monitor in
cm.
Controls the amount of echo information
displayed in an image. Turn B Mode dial to
the left/right to increase/decrease Gain. Gain
displays on the monitor in G (dB).
Increases the number of focal zones or
moves the focal zone(s) to tighten up the
beam for specific area. Press the control to
toggle between Focus Position and Focus
Number. Press Up/Down Button to move or
adjust the focal numbers.
Optimize the image based upon a specified
region of interest or anatomy. Press the
Center Button in the Gain Dial to toggle the
ATO/ACE On and Off.
Amplifies the returning signals to correct for
the attenuation caused by tissues at
increasing depth. TGC slide pots spaced
proportional to the depth. Move the slide pots
to the left/right to decrease/increase TGC. A
TGC curve appears on the display.
Widen or narrow the size of the sector angle
to maximize the image’s region of interest
(ROI). Press Scan Area and move the
Trackball to narrow/widen the angle.
Changes the location of the focal point(s). A
triangular focus marker indicates the depth of
the focal point.
Toggles the left/right orientation of the scan
image.
Chapter 4 Functional Checks 4-11
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DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
4-3-7-3 B Mode Softmenu Key
Table 4-30 B Mode Softmenu Key
Step Task Expected Result(s)
Selects a level below which echoes will not be
1
Adjust Rejection
2
Activate Colorize
3
Adjust Edge Enhance
4
Activate Gray Map
5
Adjust Frequency
6
Adjust Frame Average
7
Adjust Rotation
9
Adjust Line Density
10
Power output
11
Dynamic Range
12
Focus Number and Position
amplified (an echo must have a certain
minimum amplitude before it will be
processed).
Enables gray scale image colorization. To
deactivate, reselect a Gray Map.
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.
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.
Temporal filter that averages frames together.
This has the effect of presenting a smoother,
softer image.
Rotates the image by selecting the value from
the pop-up menu.
Optimizes B Mode frame rate or spatial
resolution for the best possible image.
Optimizes image quality and allows user to
reduce beam 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.
4-12 Section 4-3 - General Procedure
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DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
4-3-8 M Mode Controls
4-3-8-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-23, in Chapter 3 Installation
to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
secondary Menu
Rejection
Power Output
Gain
M Mode
Primary Menu
Gray Map
Dynamic Range
Sweep Speed
Display Format
Full Timeline
Colorize
Edge Enhance
M Cursor
Figure 4-47 Controls available in M Mode
Figure 4-48 M Mode Screen Picture Example
Chapter 4 Functional Checks 4-13
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
4-3-8-2 M Mode OP Panel Controls
Table 4-31 M Mode OP Panel Controls
Step Task Expected Result(s)
1
Press M Mode key M Mode Starts
Controls the amount of echo information
2
Adjust Gain
3
Display M-Mode Cursor
displayed in an image. Turn B Mode dial to
the left/right to increase/decrease Gain. Gain
displays on the monitor in G (dB).
Displays the M-Mode cursor on the B-Mode
image. Press Cursor and Trackball to position
M-Mode Cursor.
4-14 Section 4-3 - General Procedure
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
4-3-8-3 M Mode Softmenu Key
Table 4-32 M Mode Softmenu Key
Step Task Expected Result(s)
Selects a level below which echoes will not be
1
Adjust Rejection
2
Adjust Sweep Speed
3
Adjust Edge Enhance
4
Activate Gray Map
6
Activate Colorize
7
Activate Full Timeline
8
Select Display Format
9
Adjust Dynamic Range
10
Power output
amplified (an echo must have a certain
minimum amplitude before it will be
processed).
Changes the speed at which the time line is
swept. The following speed values are
available, 1, 2, 3, 4, 6, 8, 12, 16.
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.
Determines how the echo intensity levels
received are presented as shades of gray.
Enables gray scale image colorization. To
deactivate, reselect a Gray Map.
Displays only timeline screen. Press the Full
Timescreen to activate.
Select the format to display B image and M
image on the LCD. Press Display Format,
and select from the pop up menu.
Dynamic Range controls how echo
intensities are converted to shades of gray,
thereby increasing the adjustable range of
contrast.
Optimizes image quality and allows user to
reduce beam intensity. 10% increments
between 0-100%. Values greater than 0.1 are
displayed.
Chapter 4 Functional Checks 4-15
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DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
4-3-9 Color Flow Mode Checks
4-3-9-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-23, in Chapter 3 Installation
to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
Primary Menu
Secondary Menu
Baseline
Dynamic Range
Power Output
Line Density
Transparency Map
Focus Position
Duplex/Triplex
ACE
Capture
Spatial Filter
Frequency
Frame Average
Angle Steer
Packet Size
PRF
Color Map
Threshold
Color Invert
Wall Filter
CF Mode
Gain
Figure 4-49 Controls available in Color Flow Mode
Figure 4-50 CFM Mode Screen Picture Example
4-16 Section 4-3 - General Procedure
Page 97
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
4-3-9-2 Color Flow Mode OP Panel Controls
Table 4-33 Color Flow Mode OP Panel Controls
Step Task Expected Result(s)
1
Press CFM-Mode key CFM Mode Starts
Amplifies the overall strength of the echoes
2
Adjust Gain
processed in the Color Flow window. Turn the
Gain dial (CFM Mode key) to the left/right to
increase/decrease Gain.
Chapter 4 Functional Checks 4-17
Page 98
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
4-3-9-3 Color Flow Mode Softemenu Key
Table 4-34 Color Flow Mode Softmenu Key
Step Task Expected Result(s)
1
Threshold
2
Packet Size
3
Select Color maps
4
Adjust Frequency
5
Set Frame Average
6
Color Invert
7
Adjust LIne Density
8
Activate Spatial Filter
9
Adjust Dynamic Range
10
Activate ACE
11
Adjust Angle Steer
12
Move Baseline
Change PRF
13
(Pulse Repetition Frequency)
14
Transparency Map
15
Focus Position
16
Capture
Threshold assigns the gray scale level at
which color information stops.
Controls the number of samples gathered for
a single color flow vector.
Allows a specific color map to be selected.
After a selection has been made, the color
bar displays the resultant map.
Enables the adjustment of the probe’s
operating frequency. Press Frequency and
select desired value. The selected frequency
is displayed in the status window.
Averages color frames. Press Frame
Average up/down to smooth temporal
averaging.
Views blood flow from a different perspective.
Press Invert to reverse the color map.
Trades frame rate for sensitivity and spatial
resolution. If the frame rate is too slow,
reduce the size of the region of interest,
select a different line density setting, or
reduce the packet size.
Dynamic Range controls how echo
intensities are converted to shades of gray,
thereby increasing the adjustable range of
contrast.
Eliminates the motion artifacts. Press Ace to
activate.
Slants the Color Flow region of interest or the
Doppler line to obtain a better Doppler angle.
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.
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.
4-18 Section 4-3 - General Procedure
Page 99
GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
Table 4-34 Color Flow Mode Softmenu Key
Step Task Expected Result(s)
Optimizes image quality and allows user to
17
18
Power output
Wall Filter
reduce beam intensity. 10% increments
between 0-100%. Values greater than 0.1 are
displayed.
Wall Filter insulates the Doppler signal from
excessive noise caused from vessel
movement.
Chapter 4 Functional Checks 4-19
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GE MEDICAL SYSTEMS
DIRECTION 2300141, REVISION 13 LOGIQ™ BOOK SERVICE MANUAL
4-3-10 Doppler Mode Checks
4-3-10-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-23, in Chapter 3 Installation
to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
Secondary Menu
Rejection
Dynamic Range
Display Format
Full Timeline
Trace Direction
Auto Calculations
Modify Calcs
Trace Method
Trace Sensitivity
Trace Method
Spectral Average
Power Output
PW Mode
Gain
Primary Menu
Frequency
Baseline
Quick Angle
Sweep Speed
PRF
SV Length
Colorize
Angle Correct
Spectral Invert
Wall Filter
M/D Cursor
B Pause
Figure 4-51 Controls available in Doppler Mode
Figure 4-52 Doppler Mode Screen Picture Example
4-20 Section 4-3 - General Procedure
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