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LOGIQ F Series Basic Service manual_SM_5446617-100_10
LOGIQ F Series Basic Service Manual
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GE LOGIQ F Series Basic Service manual_SM_5446617-100_10 LOGIQ F Series Basic Service Manual

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Page 1
GE
LOGIQ F Series
Basic Service Manual
Part Number: 5446617-100
Revision: 10
Page 2
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GE LOGIQ F SERIES D

Important Precautions

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GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
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GE LOGIQ F SERIES D
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GE LOGIQ F SERIES
G
D
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 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 Global Documentation Group with specific information listing the system type, manual title, part number, revision number, page number and suggestion details.
Mail the information to:
Service Documentation, GE Medical Systems (China) Co., Ltd. No.19 Changjiang Road WuXi National Hi-Tech Development Zone Jiangsu, P.R China 214028 TEL: +86 510 85225888; FAX: +86 510 85226688
GE Healthcare employees should use TrackWise to report service documentation issues. These issues will then be in the internal problem reporting tool and communicated to the writer.
SERVICE SAFETY CONSIDERATIONS
DANGER
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.
WARNIN
Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and kneeling pad, to reduce the risk of injury.
For a complete review of all safety requirements, see the Chapter 1, Safety Considerations section in the Service Manual.
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GE LOGIQ F SERIES D
LEGAL NOTES
The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE.
GE may revise this publication from time to time without written notice.
PROPRIETARY TO GE
Permission to use this Advanced Service Software and related documentation (herein called the material) by persons other than GE employees is provided only under an Advanced Service Package License relating specifically to this Proprietary Material. This is a different agreement from the one under which operating and basic service software is licensed. A license to use operating or basic service software does not extend to or cover this software or related documentation.
If you are a GE employee or a customer who has entered into such a license agreement with GE to use this proprietary software, you are authorized to use this Material according to the conditions stated in your license agreement.
However, you do not have the permission of GE to alter, decompose or reverse-assemble the software, and unless you are a GE employee, you MAY NOT COPY the Material. The Material is protected by Copyright and Trade Secret laws; the violation of which can result in civil damages and criminal prosecution.
If you are not party to such a license agreement or a GE Employee, you must exit this Material now.
TRADEMARKS
All products and their name brands are trademarks of their respective holders.
COPYRIGHTS
All Material Copyright© 2013-2017 by General Electric Company Inc. All Rights Reserved.
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GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL

Revision History

Revision Date Reason for change
1 2013/01/10 Initial Release.
2 2013/06/15 Update for CRU part list update.
3 2013/10/09 Update for CRU part list update.
4 2014/05/20 Update for AC power cord update.
5 2014/10/29 Update for printer list update
6 2015/09/16 Update for CRU part list update.
7 2016/05/25 Update peripheral list
8 2016/08/22 Update peripheral list
9 2017/01/05 Add keyboard film attaching process and spare part
10 2017/09/25 Update the unpacking procedure of the equipment for sea transportation

List of Effected Pages(LOEP)

Pages Revision Pages Revision
Title Page N/A
Important Precautions
i to ix
Table of Contents
pages i to xii
Chapter 1 - Introduction
pages 1-1 to 1-14
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 4-33
10
10
10
10
10
10
Chapter 7 - Diagnostics/Troubleshooting
Chapter 8 - Replacement Procedures
Chapter 5 - Theory
pages 5-1 to 5-4
Chapter 6 - Service Adjustments
pages 6-1 to 6-2
pages 7-1 to 7-10
pages 8-1 to 8-14
Chapter 9 - Replacement Parts
pages 9-1 to 9-6
Chapter 10 - Periodic Maintenance
pages 10-1 to 10-18
pages I to II
Index
10
10
10
10
10
10
10
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GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
CHAPTER 1
Introduction
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Chapter 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Typical Users of the Basic Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2
Purpose of Operator Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2
LOGIQ F Series Models Covered by this Manual . . . . . . . . . . . . . . . . . . . . 1 - 2
Peripheral List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3
Important Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6
Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6
Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9
Label Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9
Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10
Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . 1 - 10
EMC, EMI, and ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Lockout/Tagout (LOTO) requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12
Customer Assistance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13
Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13
System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14
Factory Site . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14
Table of Contents 1
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GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
CHAPTER 2
Site Preparations
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
Purpose of chapter 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
General Console Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Console Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4
Scan Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5
Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Purchaser Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Required Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7
Recommended and Alternate Ultrasound Room Layout . . . . . . . . . . . . . . . 2 - 8
Networking Pre-installation Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9
Table of Contents 2
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GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
CHAPTER 3
System Setup
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1
Purpose of Chapter 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1
Setup Reminders. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Average Installation Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Installation Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3
Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4
Receiving and Unpacking the Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 5
Moving into Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
Product Locator Installation Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
Preparing for Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Completing the Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
Power On / Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
Transducer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10
System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11
System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11
Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12
On-Board Optional Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12
Connecting Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12
Peripherals/Accessories Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 13
Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21
Software/Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21
Connectivity Installation Worksheet. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 22
Loading Base Image Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 23
Software Version check out. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 24
Functional Check-out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 24
Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25
Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25
User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25
Table of Contents 3
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GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC 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
Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3
Archiving and Loading Presets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
Adjusting the Display Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6
System Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7
B Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 11
M Mode Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 15
Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 17
Color Flow Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20
Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23
Probe/Connectors Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24
Using Cine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Backup and Restore Database, Preset Configurations and Images . . . . . . 4 - 26
Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 33
Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 33
Table of Contents 4
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GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
CHAPTER 5
Components and Functions (Theory)
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1
Purpose of Chapter 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1
Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2
System Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2
Software Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 3
Common Service Platform. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4
Table of Contents 5
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GE HEALTHCARE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
CHAPTER 6
Service Adjustments
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1
Purpose of this chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1
Monitor Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
Adjustments Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
6 Table of Contents
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GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
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 Store Key Function . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Setting the Print Key to Screen Capture . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Capturing a Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Reset the Store Key to Customer’s Functionality . . . . . . . . . . . . . . . . . . . . 7 - 6
Common Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 7
Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 7
PC Diagnostics (Non-Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 8
PC Diagnostics (Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 8
Restart LOGIQ F Series After Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 8
Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
Table of Contents 7
Page 24
GE HEALTHCARE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
CHAPTER 8
Replacement Procedures
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Purpose of Chapter 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
DISASSEMBLY/RE-ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Warning and Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Returning/Shipping for repairs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Air filter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 3
Trackball Roller Cleaning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4
Attaching Keyboard Film . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 5
Loading Base Image Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 7
8 Table of Contents
Page 25
GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC 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
Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4
Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 6
Table of Contents 9
Page 26
GE HEALTHCARE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
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
Standard GE Tool Kit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4
Special Tools, Supplies and Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6
Input Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Outlet Test -Wiring Arrangement - USA & Canada . . . . . . . . . . . . . . . . . . . 10 - 8
Grounding Continuity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
Chassis Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 10
Isolated Patient Lead (Source) Leakage–Lead to Lead . . . . . . . . . . . . . . . . 10 - 11
Isolated Patient Lead (Sink) Leakage-Isolation Test . . . . . . . . . . . . . . . . . . 10 - 11
Probe Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13
When There's Too Much Leakage Current... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 15
10 Table of Contents
Page 27
GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
Chapter 1 Introduction

Section 1-1 Overview

1-1-1 Purpose of Chapter 1

This chapter describes important issues related to safely servicing the LOGIQ F Series. The service
provider must read and understand all the information presented in this manual before installing or
servicing a unit.
Table 1-1 Contents in Chapter 1
Section Description Page Number
1-1
1-2
1-3
1-4
1-5
1-6
Overview
Important Conventions
Safety Considerations
EMC, EMI, and ESD
Lockout/Tagout (LOTO) requirements
Customer Assistance

1-1-2 Purpose of Service Manual

This Service Manual provides installation and service information for the LOGIQ F Series and contains
the following chapters:
1.) Chapter 1 - Introduction: Contains a content summary and warnings.
2.) Chapter 2 - Site Preparations: Contains pre-installation requirements for the LOGIQ F Series.
3.) Chapter 3 - System Setup: 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 F Series.
7.) Chapter 7 - Diagnostics/Troubleshooting: Provides procedures for running diagnostic or related routines for the LOGIQ F Series.
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 F Series.
10.)Chapter 10 - Care & Maintenance: Provides periodic maintenance procedures for the LOGIQ F Series.
1-1
1-6
1-8
1-11
1-12
1-13
Section 1-1 - Overview 1 - 1
Page 28
GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL

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

• Service Personnel (installation, maintenance, etc.).
• Hospital’s Service Personnel
• Contractors (Some parts of Chapter 2 - Site Preparation)

1-1-4 Purpose of Operator Manual(s)

The Operator Manual(s) should be fully read and understood before operating the LOGIQ F Series and also kept near the unit for quick reference.
NOTE: Probe information displayed on screen does not necessarily reflect the probes available on your
ultrasound system. Please refer to the probe list for available probes and features.

1-1-5 LOGIQ F Series Models Covered by this Manual

Table 1-2 LOGIQ F3 Model Designations
Part Number Description
5478043 LOGIQ F3 Console for China
5478051 LOGIQ F3 Console (except China)
Table 1-3 LOGIQ F5 Model Designations
Part Number Description
5478049 LOGIQ F5 Console for China (3 Probe Ports)
5478050 LOGIQ F5 Console for China (4 Probe Ports)
Table 1-4 LOGIQ F6 Model Designations
Part Number Description
5478040 LOGIQ F6 Console for Europe and EAGM
5478041 LOGIQ F6 Console for APAC
5478042 LOGIQ F6 Console for India
5478044 LOGIQ F6 Console for Latin America
5478045 LOGIQ F6 Console for China (3 Probe Ports)
5478046 LOGIQ F6 Console for China (4 Probe Ports)
5478047 LOGIQ F6 Console for global (3 Probe Ports)
5478048 LOGIQ F6 Console for global (19” LCD)
Table 1-5 LOGIQ F8 Model Designations
Part Number Description
5478035 LOGIQ F8 Console for China
5478037 LOGIQ F8 Console for Europe and EAGM
5478038 LOGIQ F8 Console for India
5478039 LOGIQ F8 Console for Latin America and APAC
1 - 2 Section 1-1 - Overview
Page 29
GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL

1-1-6 Peripheral List

Table 1-6 LOGIQ F Series Peripheral List
Item Part Name Part Number Replaced By Qty FRU
Printers
8000 Sony UP-D897 Chinese kit 5151262 1 Y
8000A Sony UP-D897 USA kit 5151259 1 Y
8000B Sony UP-D897 European kit 5151261 1 Y
8000C Sony UP-D897 Japanese kit 5151263 1 Y
8000D Sony UP-D897 Brazil kit 5495509 1 Y
8001 Sony UP-D25MD USA kit 5398062 1 Y
8001A Sony UP-D25MD European kit 5398063 1 Y
8001B Sony UP-D25MD Japanese kit 5398064 1 Y
8001C Sony UP-D25MD Chinese kit 5398061 1 Y
8002 Sony UP-D711MD 5449734 1 Y
8003 HP Officejet 100 Chinese kit 5426594 1 Y
8003A HP Officejet 100 European kit 5426595 1 Y
8003B HP Officejet 100 Japanese kit 5426596 1 Y
8003C HP Officejet 100 USA kit 5426597 1 Y
8004 Sony UP-D898MD USA kit 5151259-2 1 Y
8004A Sony UP-D898MD Europe kit 5151261-2 1 Y
8004B Sony UP-D898MD China kit 5151262-2 1 Y
8004C Sony UP-D898MD Japan kit 5151263-2 1 Y
8004D Sony UP-D898MD Brazil kit 5495509-2 1 Y
8005 HP Officejet Pro 8100 NA 1 Y
DVD-RW
8006 LITEON eUAU108 5485883 5653589 1 Y
8007 LITEON eBAU108 5653589 1 Y
Footswitch
8008 MKF 2-MED GP26 (IPx8) 5151236 1 Y
8009 FSU-1000 (IPx8) 5338419 1 Y
USB Stick
8010 SanDisk CRUZER 4G 5168040-4 5168040-5 1 Y
8011 Keeber 4G USB stick 5168040-5 1 Y
8012 1TB mobile USB HDD 5434317-3 5434317-4 1 Y
ECG Module
8013 USB ECG Module (AHA) 5173122 1 N
Section 1-1 - Overview 1 - 3
Page 30
GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
Table 1-6 LOGIQ F Series Peripheral List
Item Part Name Part Number Replaced By Qty FRU
8014 USB ECG Module (IEC) 5173040 1 N
Biopsy Kit
8015 4C-RS biopsy kit 5160703 1 Y
8016 E8C-RS biopsy kit E8385MJ 1 Y
8017 E8C-RS reusable biopsy kit 2398164 1 Y
8019 L6-12-RS reusable biopsy kit 5176499 1 Y
8020 3Sc-RS reusable biopsy kit 5329137 1 Y
8021 RAB2-6-RS reusable biopsy kit KTD106236 1 Y
8022 1TB mobile USB HDD 5434317-4 1 Y
Keyboard Film
8023 Keyboard Film for service 5727997-S 1 Y
1 - 4 Section 1-1 - Overview
Page 31
GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
1-1-6 Peripheral List (cont’d)
Table 1-7 LOGIQ F Series System and Application Software List
Item Part Name Part Number Replaced By Qty FRU
8022
8022A
8022B
8022C
8022D
8022E
8022F
8022G
8022H
8022I
8022J
LOGIQ F Series R1.0.0 System and
Application Software USB
LOGIQ F Series R1.0.1 System and
Application Software USB
LOGIQ F Series R1.0.2 System and
Application Software USB
LOGIQ F Series R1.0.3 System and
Application Software USB
LOGIQ F Series R1.0.3 System and
Application Software USB
LOGIQ F Series R1.0.4 System and
Application Software USB
LOGIQ F Series R1.0.5 System and
Application Software USB
LOGIQ F Series R1.0.6 System and
Application Software USB
LOGIQ F Series R1.0.7 System and
Application Software USB
LOGIQ F Series R1.0.8 System and
Application Software USB
LOGIQ F Series R1.0.9 System and
Application Software USB
5485882-S 5485882-2S 1 Y
5485882-2S 5485882-3S 1 Y
5485882-3S 5495846-4S 1 Y
5485882-4S 5495846-4S 1 Y
5495846-4S 5495846-5S 1 Y
5495846-5S 5495846-6S 1 Y
5495846-6S 5495846-7S 1 Y
5495846-7S 5495846-8S 1 Y
5495846-8S 5495846-9S 1 Y
5495846-9S 5495846-10S 1 Y
5495846-10S 5495846-11S 1 Y
8022K
8022L
8022M
LOGIQ F Series R1.0.10 System and
Application Software USB
LOGIQ F Series R1.0.11 System and
Application Software USB
LOGIQ F Series R1.1.0 System and
Application Software USB (Only for USA)
5495846-11S 5495846-12S 1 Y
5495846-12S 1 Y
5765268-S 1 Y
Section 1-1 - Overview 1 - 5
Page 32
GE LOGIQ F SERIES
DANGER
NOTICE
DIRECTION 5446617-100, REVISION 10 BASIC 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 IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL CAUSE SEVERE PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE IGNORED.
WARNING
WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT CAN CAUSE SEVERE PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED.
CAUTION
NOTE: Notes provide important information about an item or a procedure.
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.
1 - 6 Section 1-2 - Important Conventions
Page 33
GE LOGIQ F SERIES
N
DIRECTION 5446617-100, REVISION 10 BASIC 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 1-8 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 1-9 Standard Icons Indicating a Special Procedure Be Used
AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

1-2-3 Product Icons

Please refer to User Manual (Basic User Manual or User Guide) for the detail Product Icons information.
TAG
&
LOCKOUT
Date
Signed
EYE
PROTECTIO
Section 1-2 - Important Conventions 1 - 7
Page 34
GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC 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

Servicing should be performed by authorized personnel only. Only personnel who have participated in a LOGIQ F Series Training are authorized to service the equipment.

1-3-3 Mechanical Safety

WARNING
WARNING
WARNING
CAUTION
WARNING
WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.
ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT CAN EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN HANDLING AND PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A DAMAGED OR DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS CAN RESULT IN SERIOUS INJURY AND EQUIPMENT DAMAGE.
NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK, IT MAY BE DAMAGED.
The LOGIQ F Series weighs 65 kg or more, depending on installed peripherals, when ready for use. Care must be used when moving it or replacing its parts. Failure to follow the precautions listed could result in injury, uncontrolled motion and costly damage.
ALWAYS:
Be sure the pathway is clear.
Use slow, careful motions.
Use two people when moving on inclines or lifting more than 65 kg (144 lbs).
AFTER UNPLUG POWER CORD, WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO TEST POINTS TO VERIFY ISOLATION.
1 - 8 Section 1-3 - Safety Considerations
Page 35
GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
1-3-3 Mechanical Safety (cont’d)
NOTE: Special care should be taken when transporting the unit in a vehicle:
• Secure the unit in an upright position.
• Lock the wheels (brake)

1-3-4 Electrical Safety

To minimize shock hazard, the equipment chassis must be connected to an electrical ground. The system is equipped with a three-conductor AC power cable. This must be plugged into an approved electrical outlet with safety ground. 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.
WARNING
DO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY CIRCUMSTANCES.

1-3-5 Label Locations

Refer to LOGIQ F Series User Guide Section Warning Label Location in Safety Chapter.
Section 1-3 - Safety Considerations 1 - 9
Page 36
GE LOGIQ F SERIES
DANGER
DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL

1-3-6 Dangerous Procedure Warnings

Warnings, such as the examples below, precede potentially dangerous procedures throughout this manual. Instructions contained in the warnings must be followed.
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.
WARNING
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.
WARNING
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.
WARNING
SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC INVALID MAY CAUSE THE DAMAGE OF SYSTEM FILES.
WARNING
AFTER UNPLUG POWER CORD, WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO TEST POINTS TO VERIFY ISOLATION.

1-3-7 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 USER/SERVICE staff should dispose all the waste properly as per federal, state, and local
waste disposal regulation.
1 - 10 Section 1-3 - Safety Considerations
Page 37
GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC 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 F Series 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

WARNING
DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING THE NECESSARY ESD PRECAUTIONS:
1.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE EQUIPMENT.
Section 1-4 - EMC, EMI, and ESD 1 - 11
Page 38
GE LOGIQ F SERIES
NOTICE
DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL

Section 1-5 Lockout/Tagout (LOTO) requirements

Follow OSHA Lockout/Tagout requirements (USA) or local Lockout/Tagout requirements by ensuring you are in total control of the AC power plug at all times during the service process.
To apply Lockout/Tagout:
1.) Plan and prepare for shutdown.
2.) Shutdown the equipment.
3.) Isolate the equipment.
4.) Apply Lockout/Tagout Devices.
5.) Remove battery.
6.) Control all stored and residual energy.
7.) Verify isolation.
All potentially hazardous stored or residual energy is relieved.
Energy Control and Power Lockout for LOGIQ F Series
WHEN SERVICING PARTS OF THE SYSTEM WHERE THERE IS EXPOSURE TO VOLTAGE GREATER THAN 30 VOLTS:
1. TURN OFF THE SCANNER.
2. UNPLUG THE SYSTEM.
3. MAINTAIN CONTROL OF THE SYSTEM POWER PLUG.
4. WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO TEST POINTS TO VERIFY ISOLATION. THE AMBER LIGHT ON THE OP PANEL ON/OFF BUTTON
TAG
&
LOCKOUT
Date
Signed
WILL TURN OFF.
5. REMOVE THE SYSTEM BATTERY.
Equipment being returned must be clean and free of blood and other infectious substances.
GE Healthcare policy states that body fluids must be properly removed from any part or equipment prior to shipment. GE Healthcare 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 transportation 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.
1 - 12 Section 1-5 - Lockout/Tagout (LOTO) requirements
Page 39
GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL

Section 1-6 Customer Assistance

1-6-1 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 1-10 Phone Numbers for Customer Assistance
Location Phone Number
USA
GE Vingmed Ultrasound
Ultrasound Service Engineering
9900 Innovation Drive
Wauwatosa, WI 53226
Canada 1-800-668-0732
Latin America
Europe (OLC- EMEA)
GE Ultraschall Deutschland GmbH
Beethovenstraße 239
Postfach 11 05 60, D-42655 Solingen
Germany
Online Services Ultrasound Asia
Australia
China
India
Japan
Korea
Singapore
Service: On-site
Service Parts
Application Support
Service
Application Support
OLC - EMEA
Phone: +49 (0)212 2802 - 652
+33 1 3083 1300
Fax: +49 (0) 212 2802 - 431
Phone: +(61) 1-800-647-855
+(86) 800-810-8188
+(91) 1-800-11-4567
+(81) 42-648-2924
+(82) 2620 13585
+(95) 6277-3444
1-800-437-1171
1-800-558-2040
1-800-682-5327 or 1-262-524-5698
1-800-321-7937
1-262-524-5698
Section 1-6 - Customer Assistance 1 - 13
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1-6-2 System Manufacturer

Table 1-11 System Manufacturer
Manufacturer FAX Number
GE Medical Systems (China) Co., Ltd.
No.19, Changjiang Road, Wuxi National Hi-Tech Development Zone, Jiangsu, P.R. China 214028

1-6-3 Factory Site

Table 1-12 Factory Site
GE Medical Systems (China) Co., Ltd.
No.19, Changjiang Road, Wuxi National Hi-Tech Development Zone, Jiangsu, P.R. China 214028
TEL: +86 510-85225888
FAX: +86 510-85226688
Factory Site FAX Number
TEL: +86 510-85225888
FAX: +86 510-85226688
1 - 14 Section 1-6 - Customer Assistance
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GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
Chapter 2 Site Preparations

Section 2-1 Overview

2-1-1 Purpose of chapter 2

This chapter provides the information required to plan and prepare for the installation of LOGIQ F Series.Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit.
Table 2-1 Contents in Chapter 2
Section Description Page Number
2-1
2-2
2-3
Overview
General Console Requirements
Facility Needs
2-1
2-2
2-6
Section 2-1 - Overview 2 - 1
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Section 2-2 General Console Requirements

2-2-1 Console Environmental Requirements

Table 2-2 Environmental Requirements for LOGIQ F Series
Operational Storage Transport
Temperature
Humidity
Pressure
o
3 - 40oC
37 - 104
30 - 80% non-condensing
700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
o
F
-5 - 50
C
o
23 - 122
10 - 90% non-condensing
F
o
-5 - 50
C
o
23 - 122
10 - 90% non-condensing
F
NOTE: Temperature in degrees C. Conversion to Degrees F = (Degrees 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

NOTE: GE Healthcare 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.
NOTE: Please note that image artifacts can occur, if at any time within the facility, the ground from the
main facility's incoming power source to the Ultrasound unit is only a conduit.
2 - 2 Section 2-2 - General Console Requirements
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GE LOGIQ F SERIES DIRECTION 5446617-100, REVISION 10 BASIC SERVICE MANUAL
2-2-2 Electrical Requirements (cont’d)
2-2-2-1 LOGIQ F Series Power Requirements
The following power line parameters should be monitored for one week before installation. We recommend that you use an analyzer Dranetz Model 606-3 or Dranetz Model 626:
Table 2-3 Electrical Specifications for LOGIQ F Series
PARAMETER AREA LIMITS
Voltage Range 100-240V~ 400VA
Power All applications MAX. 400 VA
Line Frequency All applications 50/60Hz
Less than 25% of nominal peak voltage for less than 1 millisecond for any type of
Power Transients All applications
transient, including line frequency, synchronous, asynchronous, or aperiodic transients.
Decaying Oscillation All applications
2-2-2-2 Inrush Current
Inrush Current is not a factor to consider due to the inrush current limiting properties of the power supplies.
2-2-2-3 Site Circuit Breaker
It is recommended that the branch circuit breaker for the machine be ready accessible.
CAUTION
POWER OUTAGE MAY OCCURE.
The LOGIQ F Series requires a dedicated single branch circuit. To avoid circuit overload and possible loss of critical care equipment, make sure you DO NOT have any other equipment operating on the same circuit.
2-2-2-4 Site Power Outlets
A desiccated AC power outlet must be within reach of the unit without extension cords. Other outlets adequate for the external 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.
Less than 15% of peak voltage for less than 1 millisecond.
2-2-2-5 Unit Power Plug
If the unit arrives without the power plug, or with the wrong plug, you must contact your GE dealer or the installation engineer must supply what is locally required.
2-2-2-6 Power Stability Requirements
Voltage drop-out
Max 10 ms.
Power Transients
(All applications) Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including line frequency, synchronous, asynchronous, or aperiodic transients.
Section 2-2 - General Console Requirements 2 - 3
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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 F Series complies with limits as stated on the EMC label. However there is no guarantee that interface will not occur in a particular installation.
Possible EMI sources should be identified before the unit is installed.
Electrical and electronic equipment may produce EMI unintentionally as the result of defect.
These sources include:
• medical lasers,
• scanners,
• cauterizing guns,
•computers,
•monitors,
• fans,
• gel warmers,
• microwave ovens,
• light dimmers,
• portable phones.
The presence of broadcast station or broadcast van may also cause interference. See for EMI Prevention tips.
See Ta bl e 2 -4 for EMI Prevention tips.
Table 2-4 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.
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 interface with the ultrasound signals.
If more than 20% or a pair of fingers on the RF gaskets are broken, replace the gaskets. Do not turn on the unit until any loose metallic part is removed.
Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit RF leakage. Or, if a label has been found in such a position, move the label.
The interconnect cables are grounded and require ferrite beads and other shielding. Also, cable length, material, and routing are all important; do not change from what is specified.
Properly dress peripheral cables
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
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2-2-4 Scan Probe Environmental Requirements

Operation: 3° to 40° C
Storage: -5° to 50° 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.
Section 2-2 - General Console Requirements 2 - 5
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Section 2-3 Facility Needs

2-3-1 Purchaser Responsibilities

The work and materials needed to prepare the site is the responsibility of the purchaser. Delay, confusion, and waste of manpower can be avoided by completing pre installation work before delivery. 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 proof 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
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2-3-2 Required Features

NOTE: GE Medical Systems requires a dedicated power and ground for the proper operation of its
Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the distribution panel to the Ultrasound outlet.
Please note that image artifacts can occur, if at any time within the facility, the ground from the main facility's incoming power source to the Ultrasound unit is only a conduit.
• Dedicated single branch power outlet of adequate amperage meeting all local and national codes which is located less than 2.5 m (8 ft.) from the unit’s proposed location
• Door opening is at least 76 cm (30 in) wide
• Proposed location for unit is at least 0.3 m (1 ft.) from the wall for cooling
• Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with peripheral within 1 m of the unit to connect cables.
Section 2-3 - Facility Needs 2 - 7
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2-3-3 Recommended and Alternate Ultrasound Room Layout

Recommended standard floor plan and a minimal floor plan for ultrasound equipment:
DEDICATED ALALOG TELEPHONE LINE FOR CONNECTION TO INSITE
ROOM,
PROCESSING
FILM
DEDICATED
POWER
RECEPTACLE
18 IN.
(46 CM)
CONSOLE
LINEN SUPPLY
FILM VIEWER
FILM SUPPLIES
FILE
CABINET
SECRETARYS OR DOCTOR’S DESK
SINK
FOOT
SW
STOOL
FILM VIEWER
COUNTER TOP
COUNTER
TOP
SINK
SUCTION LINE
EMERGECY OXYGEN
OVERHEAD LIGHTS DIMMER
A 14 by 17 foot Recommended Floor Plan
LINEN SUPPLY
PROBES/SUPPLIES
EXTERNAL
PERIPHERALS
LOGIQ 5
CONSOLE
DEDICATED POWER OUTLETS
DEDICATED ANALOG TELEPHONE LINE FOR CONNECTION TO INSITE
FOOT
SW
STOOL
EXAMINATION
TABLE
76 IN.
(193 CM)
24 IN.
(61 CM)
PATIENT
TOILET
FACILITY
DOOR
42 IN.
(107 CM)
Scale : Each square equals one square foot
DOOR
30 IN.
(76 CM)
24 IN. (61 CM)
EXAMINARION
TABLE
76 IN. (193 CM)
GE CABINET FOT SOFTWARE AND MANUALS
An 8 by 10 foot Minimal Floor Plan
Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT
2 - 8 Section 2-3 - Facility Needs
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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:
Wire 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 F Series 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 F Series.
• 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 F Series 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.
Section 2-3 - Facility Needs 2 - 9
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2-3-4-4 DICOM Option Pre-installation Requirements (cont’d)
.
LOGIQ F
Host Name
AE Title
ROUTING INFORMATION
ROUTER1
ROUTER2
ROUTER3
DICOM APPLICATION INFORMATION
NAME
Store 1
Store 2
Store 3
Local Port
Destination IP Addresses
...
...
...
MAKE/REVISION IP ADDRESSES PORTAE TITLE
IP Address
Net Mask
Default
...
...
GATEWAY IP Addresses
...
...
...
...
...
...
...
Store 4
Store 5
Store 6
Worklist
Storage Commit
MPPS
...
...
...
...
...
...
Figure 2-2 Worksheet for DICOM Network Information
2 - 10 Section 2-3 - Facility Needs
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Chapter 3 System Setup

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 and external peripherals for electrical safety are included in this procedure. Also included LOGIQ F Series in this section are guidelines for transporting the unit to a new site.
Table 3-1 Contents in Chapter 3
Section Description Page Number
3-1 Overview 3-1
3-2 Setup Reminders 3-2
3-3 Receiving and Unpacking the Equipment 3-5
3-4 Preparing for Installation 3-8
3-5 Completing the Installation 3-5
3-6 System Configuration 3-6
3-7 Software/Option Configuration 3-7
3-8 Connectivity Installation Worksheet 3-8
3-9 Loading Base Image Software 3-9
3-10 Software Version check out 3-10
3-11 Paperwork 3-11
Chapter 3 System Setup 3 - 1
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Section 3-2Setup Reminders

3-2-1 Average Installation Time

Table 3-2 Average Installation Time
Description Average Installation Time Comments
Unpacking the scanner
Scanner wo/options
DICOM Option
0.5 hour
0.5 hour
0.5 hour
Dependant on the configuration that is required
Dependant on the amount of configuration
The LOGIQ F Series has been designed to be installed and checked out by an experienced service technician in approximately 1 hour. LOGIQ F Series consoles with optional equipment may take slightly longer.
3 - 2 Section 3-2 - Setup Reminders
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3-2-2 Installation Warnings

1.) Since the LOGIQ F Series weighs approximately 65 kg without options, preferably two people
should unpack it. Two people are also preferable for installing any additional bulky items.
2.) There are no operator serviceable components. To prevent shock, do not remove any covers or panels. Should problems or malfunctions occur, unplug the power cord. Only qualified service personnel should carry out servicing and troubleshooting.
NOTE: For information regarding packing labels, refer to LABELS ON PACKAGE.
3.) After being transported, the unit may be very cold or hot. If this is the case, allow the unit to acclimate before you turn it on. It requires one hour for each 2.5°C increment it's temperature is below 10°C or above 30°C.
CAUTION
Equipment damage possibility. Turning the system on without acclimation after arriving at site may cause the system to be damaged.
Table 3-3 Acclimation Time
60 55 50 45 40 35 30 25 20 15 10 5 0 -5 -10 -15 -20 -25 -30 -35 -40
°C
140 131 122 113 104 95 86 77 68 59 50 41 32 23 14 5 -4 -13 -22 -31 -40
°F
864200000002468101214161820
hrs
Chapter 3 System Setup 3 - 3
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3-2-3 Safety Reminders

DANGER
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE AC GROUND LINE (I.E., METER’S GROUND SWI TCH IS O PEN), DON’T TOUCH THE UNIT!
Two people should unpack the unit because of its weight. Two people are required whenever a part weighing 19kg (35 lb.) or more must be lifted.
If the unit is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.
To prevent electrical shock, connect the unit to a properly grounded power outlet. Do not use a three to two prong adapter. This defeats safety grounding.
Do NOT wear the ESD wrist strap when you work on live circuits and more than 30 V peak is present.
Do not use a 20 Amp to 15 Amp adapter on the 120 Vac unit’s power cord. This unit requires a dedicated 20 A circuit and can have a 15A plug if the on board peripherals do not cause the unit to draw more than 14.0 amps.
CAUTION
CAUTION
Do not operate this unit unless all board covers and frame panels are securely in place. System performance and cooling require this.
OPERATOR MANUAL(S) The User Manual(s) should be fully read and understood before operating the LOGIQ F Series and kept near the unit for quick reference.
Figure 3-1 Environmental Labels
3 - 4 Section 3-2 - Setup Reminders
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Section 3-3 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.
CAUTION
CAUTION
NOTE: To avoid injury, hold the strap clasp with one hand when cutting the strap.
NOTE: Rotate the inside plastic lock counterclockwise to remove it and then remove the outside lock.
NOTE: There is no clear plastic if the system is transported by sea. Ignore this step if there is no clear
Do not lift the unit by the Keyboard. Equipment damage may result.
The crate with the LOGIQ F Series weighs approximately 75kg. Be prepared for a sudden shift of weight as the unit is removed from its base (pallet)
Unpacking the the equipment
1.) Tear off the "stop open" mark.
2.) Cut off the two packing straps around the crate.
3.) Remove the top cover.
4.) Remove the three plastic locks.
5.) Remove the outside shipping box.
6.) Remove the clear plastic (wrapped around the system) and aluminum foil bag from the unit.
plastic.
NOTE: To avoid damaging the unit, please use a pair of scissors instead of the knife.
7.) Unlock the strap.
8.) Remove the foams beside the LCD monitor and the front wheels.
9.) Unlock the wheels, and then hold the control panel at the front side to move the system until the two front wheels are on the ground.
10.)With one hand holding the control panel and the other hand holding the rear handle, move the whole system down to the ground.
11.)Remove all the covers and foams from the unit.
Chapter 3 System Setup 3 - 5
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Figure 3-2 Open the box
3 - 6 Section 3-3 - Receiving and Unpacking the Equipment
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3-3-1 Moving into Position

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

3-3-2 Product Locator Installation Card

NOTE: The Product Locator Installation Card shown may not be same as the provided Product Locator
card.
Figure 3-3 Product Locator Installation Card
Chapter 3 System Setup 3 - 7
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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 Docking Cart is set to the correct voltage. The Voltage settings for the LOGIQ F Series is found on a label to the right of the Power switch and External I/O, on the rear of the system.
WARNING
3-4-2-2 Video Formats
Connecting a LOGIQ F Series to the wrong voltage level will most likely destroy it.
Check that the video format is set to the locally used video standard, NTSC or PAL.

3-4-3 EMI Protection

This Unit has been designed to minimize the effects of Electro Magnetic Interference (EMI). Many of 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.
3 - 8 Section 3-4 - Preparing for Installation
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Section 3-5 Completing the Installation

3-5-1 Power On / Boot Up

NOTE: After turning off 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
When power is applied to the scanner, power is distributed to the Cooling Unit, Control Panel, LCD, Peripherals and the Back-end Processor.
3-5-1-2 Turn on the system
Press the Power On/Off switch at the front of the system once.
Figure 3-4 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 once.
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3-5-2-1 Back-end Processor Power Down (cont’d)
2.) The System-Exit window is displayed.
Figure 3-5 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 blue.
5.) Disconnect the probes. Clean or disinfect all probes as necessary. Store them in their shipping cases to avoid damage.
3-5-2-2 Scanner Shutdown
Disconnect the Mains Power Cable if necessary. For example: Relocating the scanner.

3-5-3 Transducer Connection

1.) Plug the probe connector into the probe port, then lock the probe.
NOTE: Please ensure that the probe latch is in an unlocked position before you connect the probe to the
system.
NOTE: It is not necessary to turn OFF power to connect or disconnect a probe.
3 - 10 Section 3-5 - Completing the Installation
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Section 3-6 System Configuration

3-6-1 System Specifications

3-6-1-1 Physical Dimensions
The physical dimensions of the LOGIQ F Series unit are summarized in Table 3-4 on page 3-11 . The Size of LOGIQ F Series.
Table 3-4 Physical Dimensions of LOGIQ F Series
Height Width Depth Unit
1450 720 800 mm
57.09 28.35 31.50 inches
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3-6-1-2 Weight
Table 3-5 Weight of LOGIQ F Series With Monitor and Without Other Peripherals
Model Weight [kg] Weight [lb]
LOGIQ F Series Approximately 65 Approximately 144

3-6-2 Electrical Specifications

Table 3-6 Electrical Specifications for LOGIQ F Series
System Voltage Current Frequency
LOGIQ F Series
100 -240 V AC

3-6-3 On-Board Optional Peripherals

Table 3-7 List of Optional Peripherals
B/W Printer SONY UP-D897MD USB
B/W Printer SONY UP-D898MD USB
B/W Printer SONY UP-D711MD USB
HP Printer HP HP Officejet 100 USB
HP Printer HP HP Officejet Pro 8100 USB
USB Memory SanDisk SanDisk 4G USB
1-Pedal Footswitch Whanam FSU1000 USB
3-Pedal Footswitch Whanam MKF 2-MED GP26 USB
USB Hard Disk Seagate USB HDD 1T USB
Color Printer SONY UP-D25MD USB
ECG NORAV ECG -USB1 USB

3-6-4 Connecting Cables

400VA 50/60Hz
WARNING
Equipment damage possibility. Be sure to use the following recommended connecting cables to connect recording devices and a network with LOGIQ F Series console.
3 - 12 Section 3-6 - System Configuration
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3-6-5 Peripherals/Accessories Connector Panel

LOGIQ F Series peripherals and accessories can be properly connected using the side connector panel.
3-6-5-1 Rear Panel Connector
Figure 3-6 Rear Connector Panel
Table 3-8 Peripheral/Accessory Connector Panel
1
2
3
4
5
6
7
8
9
Isolated USB port
VGA port
USB port
Audio
S-Video port
AC Inlet
Ethernet
Composited port
Circuit breaker
For AC Printer ONLY
VGA Video Out
USB 2.0
Audio Line Out
S-Video Out
100-240V
LAN for InSite Connection (RJ45)
Composited Video Out
6.5A
NOTE: The AC printer can be connected to the isolated USB port on the rear panel only.
NOTE: There is only one isolated USB port on the system as shown above.
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3-6-5-2 Pin assignment for each connector
Table 3-9 Pin Assignments of External VGA
Pin No. Signal Pin No. Signal
1RED9 NC
2 GREEN 10 NC
3BLUE11 NC
4NC12NC
5NC13HSY
6 GND 14 VSY
7 GND 15 NC
8GND
Table 3-10 Pin Assignments of USB
Pin No. Signal Pin No. Signal
1 +5 VDC 5 +5 VDC
2DATA6DATA
3DATA7DATA
4GND8GND
Table 3-11 Pin Assignments of Audio
Pin No. Signal Pin No. Signal
1GND4 NC
2L+5R+
3 Speaker L 6 Speaker R
Table 3-12 Pin Assignment of S-Video
Pin No. Output Signal Pin No. Output Signal
1GND3 Y
2GND4 C
Table 3-13 Pin Assignment of Composite Video Out
Pin No. Output Signal Pin No. Output Signal
1 Composite Out 2 GND
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3-6-5-3 Connect Peripherals
A.) Connect B/W printer to the system.
UP-D711MD Printer can be properly connected using USB Ports.
Figure 3-7 Connect B/W printer to the system
Sony UP-D711MD Printer is connected to the LOGIQ F Series system via the USB port on the USB hub under the control panel.
NOTE: The DC printer can only be connected to the system via the DC power port and the USB port
on the rear side of the USB hub as shown below.
Figure 3-8 Power and USB Ports for DC printer
1.) DC Power Port
2.) USB Port
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3-6-5-3 Connect Peripherals (cont’d)
B.) Connect UP-D25MD color printer to the system. UP-D25MD Color Printer can be properly
connected using the isolated USB Port. And connect the power cable of UP-D25MD to the wall outlet.
Figure 3-9 Connect color printer to the system
C.) Connect the B/W printer (Sony UP-897/UP-D898MD)to the system
The B/W printer can be properly connected using the isolated USB Port. And connect the power cable of Sony UP-D897/UP-D898MD to the wall outlet.
Figure 3-10 Connect B/W Printer (Sony UP-897) to the system
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3-6-5-3 Connect Peripherals (cont’d)
D.) Connect Foot Switch to the system.
Foot Switch can be properly connected using USB Ports.
1-Pedal Footswitch
Figure 3-11 Connect Foot Switch to the system
E.) Connect the USB Memory to the system. The USB Memory can be properly connected using USB
ports.
3-Pedal Footswitch
Figure 3-12 USB Memory Connection
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3-6-5-3 Connect Peripherals (cont’d)
F.) ECG can be properly connected using USB ports.
Figure 3-13 ECG Connection
G.) Connect HP Officejet 100 printer to the system. HP Officejet 100 Printer can be properly connected
using the isolated USB Port. And connect the power cable of HP Officejet 100 to the wall outlet.
Figure 3-14 HP Officejet 100 printer to the system
H.) Connect the USB HDD to the system. The USB Harddisk can be properly connected using USB
ports.
Figure 3-15 USB Hard Disk Connection
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3-6-5-4 Digital Printer Setup
There are two steps to do when setting up a digital printer: 1. follow the procedure below for each printer, then 2. set up specific properties for each printer if you need.
Follow this procedure for each printer:
1.) Select Utility--> Connectivity--> Service. Add the Standard Print.
Figure 3-16 Add the Printer
2.) Highlight Standard Print in the Service list. Select the printer from the Printer pull-down Properties menu. For the UP-D897 printer, select “Portrait” as orientation. Type the printer name in the Name field. This name is used on the Button screen. After you select the printer from the Printer pull-down Properties menu again, it turns white. Press Save.
Figure 3-17 Select the Printer
3.) Select Button. Select the appropriate print key (Print1, Print2...) from the Physical Print Buttons section. Select the printer from the MyComputer column and press >> to move it to the Printflow View column. Press Save.
Figure 3-18 Select Button
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3-6-5-5 Digital Printer Instructions
Follow these steps to set up the paper size of the printer, take Sony UP-D897 as an example.
1.) Press Utility-->System-->Peripherals. Select the UP-D897 from the pull-down menu under Standard Printer Properties. Click Properties.
Figure 3-19 Properties
2.) Select Properties from Printer pull-down menu.
Figure 3-20 Properties
3.) Click Printing Preferences at the bottom of Properties Window.
Figure 3-21 Printing Preferences
4.) Select Paper Size. Press Apply. Press OK.
5.) Press Save, then Exit.
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3-6-6 Available Probes

See in specification in the LOGIQ F Series User Reference Manual for Probes and intended use.
Table 3-14 List of Probes on LOGIQ F Series
Probe Name Material of Headshell Area of Using TYPE Catalog Number Part Number
Abdomen
Obstetrics
4C-RS
8C-RS
E8C-RS
3Sc-RS
L6-12-RS VALOX
RAB2-6-RS
NORYL
VALOX
VALOX
VALOX
NORYL
Gynecology
Pediatrics
Urology
Biopsy
Abdomen
Pediatrics
Cardiac
Obstetrics
Gynecology
Urology
Endocaviy
Biopsy
Abdomen
Transcranial
Pediatrics
Cardiac
Biopsy
Small Parts
Vascular
Pediatrics
Musculoskeletal
Biopsy
Abdomen
Obstetrics
Gynecology
Urology
Biopsy
CONVEX H4000SR 5488477
CONVEX H40402LS 5499508
CONVEX 5499516
Sector 47237516
LINEAR 5454332
4D KT2302893

Section 3-7 Software/Option Configuration

Refer to the LOGIQ F Series 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 F Series Basic User Manual, Chapter 16, Customizing Your System.
For information on configuring DICOM Connectivity, Refer to the LOGIQ F Series Basic User Manual, Chapter 16, Customizing Your System.
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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:
Type:
Title
Floor:
Room:
REV:
Phone
Comments:
E-Mail Address
IP Settings
IP Address:
Subnet Mask:
Default Gateway:
Services (Destination Devices)
Device Type
1 2 3 4 5 6 7 8 9 10 11 12
Manufacturer
Name
Remote Archive Setup
Remote Archive IP:
Remote Archive Name:
IP Address
Port
AE Title
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Section 3-9 Loading Base Image Software

Refer to
Section 8-5 "Loading Base Image Software" on page 8-7.
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Section 3-10Software Version check out

3-10-1 Functional Check-out

1.) Power on LOGIQ F Series scanner and wait until system booting to main screen.
2.) Select Utility on control panel or touch panel.
3.) Select About on screen or touch panel.
Figure 3-22 About and Software version
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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 3-23 Product Locator Installation Card
Chapter 3 System Setup 3 - 25
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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 F Series console,
diagnostics by using the built-in service software, and power supply.
Table 4-1 Contents in Chapter 4
Section Description Page Number
4-1 Overview 4-1
4-2 Required Equipment 4-1
4-3 General Procedure 4-2
4-4 Software Configuration Checks 4-33
4-5 Peripheral Checks 4-33

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)
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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.

4-3-1 Power On/Boot Up

After connect the system to the electrical supply, 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
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.
Figure 4-1 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.
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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.
3.) Using the Trackball or Select key, select Shutdown.
4.) The shutdown process takes a few seconds and the power off sequence is complete when the
power status LED is turned amber.
5.) Disconnect the probes.Clean or disinfect all probes as necessary. Store them in their shipping
cases to avoid damage.
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.
Figure 4-2 System Exit Window
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4-3-2-3 Check System Date and Time
A warning message “Please check the system date and time are correct” appears on the screen when the system is powered on. This warning message appears for the possible reasons:
• The system is not boot up for over 14 days.
• The system time has been changed by 24 hours earlier than the current system time of last boot-up.
This warning message is to remind the user to check the system date in case the system date and time is incorrect.
Figure 4-3 Check system date and time message
Move the cursor to OK and press Cursor key on the control panel to select OK. The system enters scanning mode.
Check the system date and time. If it is incorrect, follow below steps to reset the system date and time.
1.) Enter Utility -> System -> General -> Date/Time.
2.) Reset the system date and time.
3.) Select Apply and then select OK.
4.) Select Save.
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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 (or USB memory device) for reloading on the system.
NOTICE
Presets should NOT be saved on the same CD-R disk (or USB memory device) as images. The Archive Menu lists the images but does NOT list the presets stored on a CD-R disk (or USB memory device).
4-3-3-1 Archiving Presets to an CD-R Disk (or USB memory device)
1.) Insert an empty (blank) CD-R disk into the DVD-RW.
2.) Access the Utility Menu, and select System. The Backup sheet will be shown on the LCD display.
Figure 4-4 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.
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4-3-3-2 Loading Presets from an CD-R disk (or USB memory device)
1.) Insert the CD-R disk with the archived Presets into the DVD-RW.
2.) Access to the Utility Menu, and select System. The Restore sheet will be shown on the LCD display.
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.

4-3-4 Adjusting the Display Monitor

Please refer to Section 6-2 "Monitor Adjustments" on page 6-2
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4-3-5 System Features

4-3-5-1 Control Panel

















Figure 4-5 Control Panel Tour



1. Power On/Off
2. Page Up/Down keys
3. Rotary Button
4. TGC
5. User Defined keys
6. Patient key
7. Probe/Preset keys
8. Worksheet key
9. End Exam key
10. Archive key
NOTE: CWD, PDI, 4D, CF and touch panel are not supported on LOGIQ F3.
4-3-5-2 LOGIQ F Series SoftMenu Key Tour
1.) Page Up/Down key: To turn the menu page up and down.
2.) Rotary key: Rotate to adjust the menuMonitor Display
11. A/N Keyboard
12. 4D (option)
13. Scan Coach
14. Mode/Gain/XYZ Controls
15. Trackball
16. Cursor key
17. Clear key
18. Comment key
19. Body Pattern key
20. Measure key
21. Ellipse key
Figure 4-6 SoftMenu Key Tour
22. M/D Cursor key
23. Scan Area key
24. Set/B Pause key
25. Freeze key
26. AO and CHI keys
27. Steer/Zoom/Depth key
28. Left/Right key
29. P1 and P2 keys
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4-3-5-3 Touch Panel (Option)
NOTE: Touch panel is an option, and it is not supported on LOGIQ F3.
Touch Panel contains exam function and mode/function specific controls.
a.) Exam Function Controls
Figure 4-7 Exam Function Controls
1.) Patient: Enters Patient screen
2.) Scan: Enters scanning mode screen
3.) Reports: Activates default report and Touch Panel of report chioces.
4.) End Exam: Activates Image Management and Touch panel with end of exam options.
5.) Utility: Activates system configuration menus.
6.) Model: Selects the application to use.
7.) Probe Indicator: Indicates and selects the probes.
NOTE: Different menus are displayed depending on which touch panel is selected.
At the bottom of the Touch panel, there are five joystick rotaries. The functionality of these rotaries changes, depending upon the currently-displayed menu. Press the button to switch between parameters, activate/disable fucntions or adjust the parameter. Rotate the dial to adjust the parameter.
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4-3-5-3 Touch Panel (Option) (cont’d)
b.) Mode/Function Specific Controls
In general, the key name is indicated at the top of the key. There are different types of Touch panel keys as illustrated below:
Figure 4-8 Mode/Function Specific Controls
1.) Press to toggle control on/off.
2.) Progress/Select keys are used for controls that have three or more choices.
3.) Press to move to the next Touch panel page.
4.) Parameters which can be adjusted by rotaries knobs.
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4-3-5-4 Monitor Display
Figure 4-9 Monitor Display Tour
1. Institution/Hospital Name, Date, Time, Operator Identification.
2. Patient Name, Patient Identification.
3. Power Output Readout.
4. Probe Identifier. Exam Preset.
5. Imaging Parameters by Mode.
6. Cine Gauge.
7. Active Images screen.
8. Delete Image.
9. Save As Menu.
10. Number of Images in Exam.
11. Page Indication.
12. Trackball Functionality Status.
13. Current date and time, Caps Lock: (lit when on), network connection indicator (PC=connected, PC with X=not connected), system messages display, InSite status, InSite controls. Image Preview
14. Image Preview.
15. Measurement Summary Window.
16. Worksheet/Direct Report.
17. Probe Orientation Marker.
18. Image.
19. Region of interest.
20. Gray/Color Bar.
21. Measurement Results Window.
22. Image Clipboard.
23. Measurement Calipers.
24. TGC.
25. Depth Scale.
26. Focal Zone Indicator.
27. Body Pattern.
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4-3-6 B Mode Checks

4-3-6-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-21, in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
B Mode Menu
TGC
Depth/Zoom
Figure 4-10 Controls available in B Mode
B Mode
Scan Area
Freeze
Figure 4-11 B Mode Screen Picture Example
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4-3-6-2 B Mode OP Panel Controls
Table 4-2 B Mode Controls
Description/Benefit
Control Possible Bioeffect
Depth Yes Depth controls the distance over which the B-Mode
images anatomy. To visualize deeper structures, increase the depth. If there is a large part of the display which is unused at the bottom, decrease the depth.
Gain No B-Mode Gain increases or decreases the amount of echo
information displayed in an image. It may have the effect of brightening or darkening the image if sufficient echo information is generated.
Focus Yes Increases the number of focal zones, moves the focal
Auto Optimize No Auto Optimize (Auto) lets you optimize the image based
Mode Cursor No Displays the M/D-Mode cursor on the B-Mode image.
CrossXBeam Yes CrossXBeam is the process of combining three or more
Tissue Harmonic Imaging (THI)
Frequency Yes Multi Frequency mode lets you downshift to the probe's
Steer Yes You can slant the B-Mode or Color Flow linear image left
Virtual Convex Yes On Linear and Sector probes, Virtual Convex provides a
TGC No TGC amplifies returning signals to correct for the
Yes Enhances image resolution and improved small parts
zone(s) and change the zone width 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.
upon a the actual B Mode image data (Auto Tissue Optimize, ATO). The preset levels (Low, Medium, and High) allow you to pick a preference for the contrast enhancement in the resulting image. Low does the least amount of contrast enhancement, high does the most. Auto is available in single or multi image, on live, frozen or CINE images (in B-Mode only), and while in zoom and in Spectral Doppler. Auto in PW Doppler Mode(ASO) optimizes the spectral data. Auto adjusts the Velocity Scale/PRF (live imaging only), baseline shift, dynamic range, and invert (if preset). Upon deactivation, the spectrum is still optimized.
frames from different steering angles into a single frame. CrossXBeam is available on Convex and Linear probes. CrossXBeam combines multiple co-planar images from different view angles into a single image at real-time frame rates, using bi-cubic interpolation.
imaging.
next lower frequency or shift up to a higher frequency.
or right to get more information without moving the probe. The angle steer function only applies to linear probes.
larger field of view in the far field.
attenuation caused by tissues at increasing depths. TGC slide pots are spaced proportionately to the depth. The area each pot amplifies varies as well. A TGC curve may appear on the display (if preset), matching the controls that you have set (except during zoom). You can choose to deactivate the TGC curve on the image.
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Table 4-2 B Mode Controls
Description/Benefit
Control Possible Bioeffect
Width Ye s You can widen or narrow the size of the sector angle to
Tilt Yes You can steer the sector angle to get more information
Reverse No Flips the image 180 degrees left/right.
Dynamic Range No Dynamic Range controls how echo intensities are
Line Density Yes Optimizes B-Mode frame rate or spatial resolution for the
Map No The system supplies B, M, and Doppler Mode system
Frame Average No Temporal filter that averages frames together, thereby
Colorize No Colorize is the colorization of a conventional B-Mode
Edge Enhance No Edge Enhance brings out subtle tissue differences and
Rotation No You can flip the image up/down.
Rejection No Selects a level below which echoes will not be amplified
Suppression No Suppresses the noise in the image.
maximize the image's region of interest (ROI).
without moving the probe while in B-Mode, M-Mode, Doppler Mode, and Color Flow Mode.
converted to shades of gray, thereby increasing the adjustable range of contrast.
best possible image.
maps.
using more pixels to make up one image. This has the effect of presenting a smoother, softer image.
image or Doppler Spectrum to enhance the user's ability to discern B, M, and Doppler Mode intensity valuations. Colorize is NOT a Doppler Mode. NOTE: You can colorize realtime or CINE images or Timeline CINE. Colorizes the gray scale image to enhance the eye's discrimination capability. Spectrum Colorize colorizes the spectrum as a function of power using the inverse of the Colorize map for the signal intensity in each Doppler line. Colorize enhances the visibility of the spectrum's characteristics and enhances your ability to identify spectral broadening and the edge contours of the spectrum used to define the peak frequency/velocity. The colorize bar displays while Colorize is activated.
boundaries by enhancing the gray scale differences corresponding to the edges of structures.
CAUTION: When reading an rotated image, be careful to observe the probe orientation to avoid possible confusion over scan direction or left/right image reversal.
(an echo must have a certain minimum amplitude before it will be processed).
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Table 4-2 B Mode Controls
Description/Benefit
Control Possible Bioeffect
SRI-HD No SRI-HD (Speckle Reduction Imaging High Definition) is an
LOGIQView (Option) No LOGIQView provides the ability to construct and view a
adaptive algorithm to reduce the unwanted effects of speckle in the ultrasound image. Image speckle usually appears as a grainy texture in otherwise uniform areas of tissue. Its appearance is related to image system characteristics, rather than tissue characteristics, so that changes in system settings, such as probe type, frequency, depth, and others, can change the appearance of the speckle. Too much speckle can impair image quality and make it difficult to see the desired detail in the image. Likewise, too much filtering of speckle can mask or obscure desired image detail. Extra care must be taken to select the optimal SRI-HD level. SRI-HD is available in 2D imaging and may be used with any transducer or clinical application when image speckle appears to interfere with the desired image detail.
static 2D image which is wider than the field of view of a given transducer. This feature allows viewing and measurements of anatomy that is larger than what would fit in a single image. Examples include scanning of vascular structures and connective tissues in the arms and legs. LOGIQView constructs the extended image from individual image frames as the operator slides the transducer along the surface of the skin in the direction of the scan plane. The quality of the resulting image is somewhat user-dependent and requires some additional skill and practice to develop proper technique and become fully proficient. LOGIQView is not available for the following: Multi Image, Timeline Modes, Color Flow Mode or PDI Mode.
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4-3-7 M Mode Controls

4-3-7-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-21, in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
M-Mode Menu
TGC
M-Mode/Gain
Figure 4-12 Controls available in M Mode
M/D Cursor
Figure 4-13 M Mode Screen Picture Example
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4-3-7-2 M Mode Controls
Table 4-3 M Mode Controls
Control Possible Bioeffect Description/Benefit
Sweep Speed
Anatomical M-Mode (option)
No Changes the speed at which the timeline is swept.
Available in M-Mode, Doppler Mode and M Color Flow Mode.
Yes Anatomical M-Mode gives you the ability to manipulate
the cursor at different angles and positions. The M-Mode display changes according to a motion of the M cursor.
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4-3-8 Doppler Mode Checks

4-3-8-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-21, in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
Primary Menu
TGC
PW-Mode/Gain
Figure 4-14 Controls available in Doppler Mode
M/D Cursor
Set/B Pause Cursor
Figure 4-15 Doppler Mode Screen Picture Example
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4-3-8-2 Doppler Mode Controls
Table 4-4 Doppler Mode Controls
Control Possible Bioeffect Description/Benefit
Auto Spectral Optimize [ASO] (Auto)
Update Yes Toggles between simultaneous and update
Doppler sample volume gate position (Trackball)
Doppler sample volume length
Scale (Velocity Scale)
Angle Correct No Estimates the flow velocity in a direction at an angle to
Quick Angle No Quickly adjusts the angle by 60 degrees.
Wall Filter No Insulates the Doppler signal from excessive noise
Baseline No Adjusts the baseline to accommodate faster or slower
Mode Cursor No Displays the Doppler Mode cursor on the B-Mode
Steer and Fine Steer Ye s You can slant the ROI of the Color Flow linear image
Volum e No Controls audio output.
Invert No Vertically inverts the spectral trace without affecting the
Compression No Dynamic range controls how echo intensities are
Trace Method No Traces the average mean and peak velocities in
Cycles to Average No The average value over a number of cycles (from 1-5).
Trace Sensitivity No Adjust the trace to follow the waveform for signal
Trace Direction No Specifies trace direction.
Yes Auto in Doppler Mode optimizes the spectral data. Auto
adjusts the Velocity Scale/PRF (on live images only), baseline shift, Dynamic Range and invert (if preset). The benefit of Auto can be found in reduced optimization time and a more consistent and accurate optimization process.
presentation while viewing the timeline.
Yes Moves the sample volume gate on the B-Mode's
Doppler Mode cursor. The gate is positioned over a specific position within the vessel.
Yes Sizes the sample volume gate.
Yes Adjusts the velocity scale to accommodate faster/
slower blood flow velocities. Velocity scale determines pulse repetition frequency. If the sample volume gate range exceeds single gate Scale capability, the system automatically switches to high PRF mode. Multiple gates appear, and HPRF is indicated on the display.
the Doppler vector by computing the angle between the Doppler vector and the flow to be measured.
NOTE: When the Doppler Mode Cursor and angle correct indicator are aligned (the angle is O), you cannot see the angle correct indicator.
caused from vessel movement.
blood flows to eliminate aliasing.
image.
left or right to get more information without moving the probe. The angle steer function only applies to linear probes.
baseline position.
converted to shades of gray, thereby increasing the range of contrast you can adjust.
realtime or frozen images.
strength.
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Table 4-4 Doppler Mode Controls
Control Possible Bioeffect Description/Benefit
Display Format No Changes the horizontal/vertical layout between B-Mode
and M-Mode, or timeline only.
Modify Auto Calcs No Activates the menu to select which calculations are
automatically calculated.
Auto Calcs No Activates the calculation automatically which you select
Simultaneous Yes Simultaneous allows two modes or three modes to be
in the Modify Auto Calculation when the system is in a state of freeze or live.
active at the same time. For example, both B-Mode and PW Modes are active, or B-Mode, PW Mode, and CF Doppler Modes are active.
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4-3-9 Color Flow Mode Checks

NOTE: Color Flow Mode only support by LOGIQ C5 Premium
4-3-9-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-21, in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
Primary Menu
TGC
Figure 4-16 Controls available in Color Flow Mode
CF Mode/Gain
Figure 4-17 CFM Mode Screen Picture Example
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4-3-9-2 Color Flow Mode Controls
Table 4-5 Color Flow Mode Controls
Control Possible Bioeffect Description/Benefit
Flow Selection No In the Lower Extremity Vein (LEV) and Abdominal
applications, you can quickly select the flow state via a shortcut on the Color Flow Mode menu.
Gain No Gain amplifies the overall strength of echoes processed in
the Color Flow window or spectral Doppler timeline.
Scale (Velocity Scale)
Wall Filter No Filters out low flow velocity signals. It helps get rid of
Size/Position Ye s Adjust size and position of the color window.
Invert (Color Invert) No Lets you view blood flow from a different perspective, e.g.,
Baseline No Changes the Color Flow or Doppler spectrum baseline to
Angle Steer Yes You can slant the ROI of the Color Flow linear image left
Accumulation No Accumulation enhances the flow in an image.
Color Flow Line Density
Map No Allows you to select a specific color map. After you have
Map Compress No Change the gradation of color map.
Threshold No Threshold assigns the gray scale level at which color
Frame Average No Averages color frames.
Transparency Map No Brings out the tissue behind the color map.
Spatial Filter No Smooths out the color, makes it look less pixely.
Flash Suppression No Activates/deactivates Flash Suppression, a motion artifact
Packet Size Ye s Controls the number of samples gathered for a single
Sample Volume Yes Adjusts the size of the color flow doppler transmit wave (or
Yes Increases/decreases the Scale on the color bar.
motion artifacts caused from breathing and other patient motion.
red away (negative velocities) and blue toward (positive velocities). You can invert a real-time or frozen image.
NOTE: Invert reverses the color map, NOT the color PRF.
accommodate higher velocity blood flow. Minimizes aliasing by displaying a greater range of forward flow with respect to reverse flow, or vice versa. Baseline adjusts the alias point. The default baseline is at the midpoint of the color display and at the midpoint of the color bar reference display.
or right to get more information without moving the probe. The Angle Steer function only applies to linear probes.
Available in Color Flow, PDI, and B Flow.
Yes Optimizes the Color Flow frame rate or spatial resolution
for the best possible color image.
made your selection, the color bar displays the resultant map.
information stops.
elimination process.
color flow vector.
pulse) and size (or length). Lower setting gives better flow resolution and a higher setting increases sensitivity.
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Table 4-5 Color Flow Mode Controls
Control Possible Bioeffect Description/Benefit
CF/PDI Auto Sample Volume
CF/PDI Focus Depth
CF/PDI Frequency Yes
CF/PDI Auto Frequency
CF/PDI Center Depth
PDI Yes Power Doppler Imaging (PDI) is a color flow mapping
TVI (Option) Yes Tissue Velocity Imaging (TVI) calculates and color-codes
TVD Yes TVD: Tissue Velocity Doppler: basing on TVI mode,
Yes Set the default value at Utility -> Imaging -> CF Mode.
Yes
Yes
Yes
technique used to map the strength of the Doppler signal coming from the tissue rather than the frequency shift of the signal. Using this technique, the ultrasound system plots color flow based on the number of reflectors that are moving, regardless of their velocity. PDI does not map velocity, therefore it is not subject to aliasing.
the velocities in tissue. The tissue velocity information is acquired by sampling of tissue Doppler velocity values at discrete points.The information is stored in a combined format with gray scale imaging during one or several cardiac cycles with high temporal resolution.
activate a sample volume of PW ventricular wall to get the spectral information of the sample section.
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4-3-10 Basic Measurements

NOTE: The following instructions assume that you first scan the patient and then press Freeze.
4-3-10-1 Distance and Tissue Depth Measurements
1.) Press Measure once, an active caliper displays.
2.) To position the active caliper at the start point (distance) or the most anterior point (tissue depth), move the Trackball.
3.) To fix the start point, press Set. The system fixes the first caliper and displays a second active caliper.
4.) To position the second active caliper at the end point (distance) or the most posterior point (tissue depth), move the Trackball.
5.) To complete the measurement, press Set. The system displays the distance or tissue depth value in the measurement results window.
Before you complete a measurement:
To toggle between active calipers, press Cursor Select.
To erase the second caliper and the current data measured and start the measurement again, press Clear once.
NOTE: To rotate through and activate previously fixed calipers, adjust Cursor Select.
NOTE: After you complete the measurement, to erase all data that has been measured to this point,
but not data entered onto worksheets, select Clear.
4-3-10-2 Circumference/Area (Ellipse) Measurement
1.) Press MEASURE once; an active caliper displays.
2.) To position the active caliper, move the TRACKBALL.
3.) To fix the start point, press SET. The system fixes the first caliper and displays a second active caliper.
4.) To position the second caliper, move the TRACKBALL.
5.) Adjust the ELLIPSE; an ellipse with an initial circle shape appears.
NOTE: Be careful not to press the Ellipse control as this activates the Body Pattern.
6.) To position the ellipse and to size the measured axes (move the calipers), move the TRACKBALL.
7.) To increase the size, adjust the ELLIPSE upward button. To decrease the size, adjust the ELLIPSE downward button.
8.) To toggle between active calipers, press MEASURE.
9.) To complete the measurement, press SET. The system displays the circumference and area in the measurement results window.
Before you complete a measurement:
- To erase the ellipse and the current data measured, press CLEAR once. The original caliper
is displayed to restart the measurement.
- To exit the measurement function without completing the measurement, press CLEAR a
second time.
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4-3-10-3 Worksheets
Measurement/Calculation worksheets are available to display and edit measurements and calculations. There are generic worksheets as well as Application specific worksheets. The worksheets are selected from the Measurement Touch Panel.
4-3-10-4 Report Pages
Measurements/Calculations that are included on the worksheet can also be displayed on Report Pages. Report Pages can be customized to meet the appropriate needs of the user.

4-3-11 Probe/Connectors Usage

4-3-11-1 Connecting a probe
1.) Place the probe's carrying case on a stable surface and open the case.
2.) Carefully remove the probe and unwrap the probe cable.
3.) DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable damage.
4.) Align the connector with the probe port and carefully push into place.
5.) Lock the probe.
6.) Carefully position the probe cord so it is free to move and is not resting on the floor.
4-3-11-2 Activating the probe
The probe activates in the currently-selected operating mode. The probe's default settings for the mode and selected exam are used automatically.
4-3-11-3 Deactivating the probe
1.) Press the Freeze key.
2.) Gently wipe the excess gel from the face of the probe. (Refer to the Basic User Manual for complete probe cleaning instructions.)
3.) Carefully slide the probe around the right side of the keyboard, toward the probe holder. Ensure that the probe is placed gently in the probe holder.
4-3-11-4 Disconnecting the probe
Probes can be disconnected at any time. However, the probe should not be selected as the active probe.
1.) Unlock the probe.
2.) Pull the probe and connector straight out of the probe port.
3.) Carefully slide the probe and connector away from the probe port and around the right side of the keyboard.
4.) Ensure the cable is free.
5.) Be sure that the probe head is clean before placing the probe in its storage box.
WARNIN
Take the following precautions with the probe cables: Do not bend, be sure to keep probe cables free from the wheels.
4 - 24 Section 4-3 - General Procedure
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