GE LOGIQ P5 BT11 SERVICE MANUAL_SM_5394141_1 Operating Manual For Model e360S-US

Technical
Publication

Direction 5394141
Revision 1

GE Healthcare

GE Healthcare

LOGIQ™P5 Service Manual

Operating Documentation

Copyright© 2010 by General Electric Co.

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Page 1-2 -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Table of Contents

CHAPTER 1

Introduction

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-1

Purpose of Chapter 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-1

Purpose of Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-1

Typical Users of the Basic Service Manual . . . . . . . . . . . . . . . . . . . . . . . . .1-2

LOGIQ™ P5 Models Covered by this Manual . . . . . . . . . . . . . . . . . . . . . . .1-2

Purpose of Operator Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-2

Important Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3

Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3

Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-4

Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-5

WEEE Label . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-7

Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-12

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-12

Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-12

Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-12

Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-13

Label Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-14

Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-16

Lockout/Tagout Requirements (For USA Only) . . . . . . . . . . . . . . . . . . . . . .1-16

EMC, EMI, and ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-17

Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-17

CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-17

Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . .1-17

Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-18

Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-18

System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-19

Table of Contents 3

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

CHAPTER 2

Pre-Installation

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-1

Purpose of chapter 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-1

General Console Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-2

Console Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-2

Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3

EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-5

Scan Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . .2-6

Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7

Purchaser Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7

Required Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8

Desirable Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8

Recommended and Alternate Ultrasound Room Layout . . . . . . . . . . . . . . .2-9

Networking Pre-installation Requirements . . . . . . . . . . . . . . . . . . . . . . . . . .2-10

4 -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

CHAPTER 3

Installation

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1

Purpose of chapter 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1

Installation Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

Average Installation Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

Installation Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3

Receiving and Unpacking the Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4

Moving into Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9

Adjusting System Clock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9

Product Locator Installation Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9

Preparing for Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10

Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10

EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10

Completing the Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11

Power On/Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11

Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-14

Transducer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-15

System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-16

System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-16

Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-18

On-Board Optional Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-18

External I/O Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-19

Video Specification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-21

Setting VCR (Mitsubishi MD3000) USB Interface . . . . . . . . . . . . . . . . . . . . 3-22

Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-23

Software/Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-23

Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-24

Insite IP Address Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-25

Loading Base System Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-25

Loading Base system Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-25

- 5

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-25

Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-25

Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-26

Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-26

User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-26

6 -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

CHAPTER 4

Functional Checks

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1

Purpose of Chapter 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1

Required Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1

General Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2

Power On/Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2

Power Off / Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4

System Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5

System B/M-Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8

System CFM and PWD Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9

Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10

Probe/Connectors Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12

Using Cine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-13

Image Management (QG) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14

Using the DVD-R . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-15

Backup and Restore Database, Preset Configurations and Images . . . . . 4-19

ECG Check Out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-25

Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-25

Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-26

Monitor Function Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-27

15" LCDMON II Assy & LCD Panel with filter Function Validation Procedure 4-27

15" OSD Key Assy Function Validation Procedure . . . . . . . . . . . . . . . . . . . 4-28

Keyboard Function Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-29

Main Keyboard Assy Function Validation Procedure . . . . . . . . . . . . . . . . . 4-29

Sub Keyboard Assy Function Validation Procedure . . . . . . . . . . . . . . . . . . 4-32

Trackball Assy validation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-32

A/N Key assy validation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-32

Freeze key validation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-32

TGC key assay / TGC Knob Set validation . . . . . . . . . . . . . . . . . . . . . . . . . 4-33

Sub Keyboard Encoder Knob Set validation . . . . . . . . . . . . . . . . . . . . . . . . 4-33

Mechanical Function Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-34

Cover Parts Function Validation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-34

LCD plastic filter Function Validation Procedure . . . . . . . . . . . . . . . . . . . . 4-35

- 7

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Air filter set Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . . .4-35

TGC key assy/TGC Knob Set, Sub keyboard encoder Knob Set, Keycap set, Main

Keyboard Encoder Knob set Function Validation Procedure . . . . . . . . . . . .4-36

Cup holder Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . . .4-37

Front caster/Rear caster Function Validation Procedure . . . . . . . . . . . . . . .4-38

Probe holder Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . .4-39

Flexible LCD Arm Function Validation Procedure . . . . . . . . . . . . . . . . . . . .4-40

Board Function Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-41

CL1TRX Assy / BL1TRX Assy Function Validation Procedure . . . . . . . . . .4-41

ACWD Assy Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . .4-42

Probe Assessment Diagnostic Test Validation Procedure . . . . . . . . . . . . . .4-45

SYSCONML Assy Function Validation Procedure . . . . . . . . . . . . . . . . . . . .4-47

APS/APS Pro Assy PCB Function Validation Procedure . . . . . . . . . . . . . . .4-48

P3RLY,P2RLY and P2RLY with Dummy Assy function check procedure . .4-49

SOM Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-50

ASIG Assy Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . .4-50

BackPlane Assy Function Validation Procedure . . . . . . . . . . . . . . . . . . . . .4-51

Nest fan Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-52

Transbox Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . .4-52

ACPC Assy set Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . .4-52

Transbox Assy Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . .4-53

Fuse set Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . .4-53

ARP Assy Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . .4-53

ASIG ASSY Function Validation Procedure . . . . . . . . . . . . . . . . . . . . . . . . .4-53

Site Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-54

8 -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

CHAPTER 5

Components and Functions (Theory)

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1

Purpose of Chapter 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2

Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3

LOGIQ™ P5 Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3

LOGIQ™ A5/A5Pro Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6

Main Board Detail . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9

P3RLY and P2RLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11

CL1TRX and BL1TRX . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-12

SYSCONPM(SYSCONCM) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16

SOM Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-19

Top Console . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-26

Keyboard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-26

LOGIQ™ P5 Monitor II and LOGIQ™ A5/A5Pro Monitor II . . . . . . . . . . . . 5-28

ARP (Rear Panel) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-30

Input/Output Signals for peripheral . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-31

Power Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-32

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-32

TRANSBOX(AC Power) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-32

APS/APS Pro (LV Power & HV Power) . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-33

AC Power Outlet for Peripheral . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-34

Cable Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-35

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-35

Internal Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-35

Peripherals and Cable connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-36

Filters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-39

Filters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-39

Fans . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-39

Service Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-40

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-40

Global Service User Interface (GSUI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-41

Service Home Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-42

- 9

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Error Logs Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-43

Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-45

Image Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-46

Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-46

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-47

Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-49

Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-50

PM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-50

Remote Software/Option Installation and Updates . . . . . . . . . . . . . . . . . . .5-51

RFS (Service For Request) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-52

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-52

System Checkout Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-52

Sending RFS Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-54

Machine RFS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-56

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-56

Enabling MRFS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-56

Fast Polling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-59

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-59

Enabling Fast Polling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-59

10 -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

CHAPTER 6

Service Adjustments

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-1

Purpose of this chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-1

Regulatory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-1

Monitor Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2

Rotate and tilt the monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2

Brightness and Contrast . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3

LCD Plastic filter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4

Flexible LCD arm - locking mechanism . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6

Trackball Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7

- 11

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 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 4

Check and Record the P2 Key Function . . . . . . . . . . . . . . . . . . . . . . . . . . .7-4

Setting the P2 Key to Screen Capture . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-5

Capturing a Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-6

Reset the P2 Key to Customer’s Functionality . . . . . . . . . . . . . . . . . . . . . . .7-7

Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-8

Common Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-9

Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-9

PC Diagnostics (Non-Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-10

PC Diagnostics (Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-14

FRU Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-16

LED Descriptions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-20

CL1TRX/BL1TRX Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-20

P3RLY/P2RLY Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-20

SYSCONPM/SYSCONCM Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-20

APS/APS Pro Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-21

Trouble Shooting Tree . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-22

System Does Not Power On / Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-22

System Does Not Boot . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-23

Noise in Image . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-26

Unable to Scan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-27

Trackball . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-28

Monitor Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-29

Unable to Record to VCR . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-31

Printer Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-32

DVD-RW Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-34

Network Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-35

12 -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

CHAPTER 8

Replacement Procedures

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-1

Purpose of Chapter 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-1

DISASSEMBLY/RE-ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2

LCD Plastic filter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3

Monitor cover set . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5

OSD button and lamp set, LCD Plastic Filter . . . . . . . . . . . . . . . . . . . . . . . 8-9

LCD Std Arm with Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10

Monitor Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-12

Flexible LCD Arm Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-13

Main Keyboard Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-37

Sub Keyboard Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-40

Trackball Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-42

English, Greek, Russian, Swedish, Norwegian A/N Key assy . . . . . . . . . . 8-43

Freeze key assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-45

TGC key assy / TGC Knob Set . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-47

Sub Keyboard Encoder Knob Set . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-49

Keycap set, Main Keyboard Encoder Knob set . . . . . . . . . . . . . . . . . . . . . 8-50

Side Left Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-51

Side Right Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-52

Front Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-53

Rear Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-55

Middle Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-57

Top Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-59

Top Bottom Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-60

Pole Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-61

Neck Front . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-62

Neck Rear . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-64

Dummy Cover L / R . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-66

EMI Cover L . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-68

EMI Cover R . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-69

APS/APS Pro Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-70

CL1TRX Assy / BL1TRX Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-73

P3RLY / P2RLY Assy & P2RLY with Dummy . . . . . . . . . . . . . . . . . . . . . . . 8-75

Backplane Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-77

ACWD Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-79

SYSCON PM Assy/SYSCON CM Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-81

PM SOM Assy with 1G/ CM SOM Assy with 512M . . . . . . . . . . . . . . . . . . 8-84

ASIG Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-86

- 13

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Battery on SYSCONPM/CM Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-87

Front Caster / Rear Caster . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-89

Rear Handle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-91

Rear Hook . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-92

Probe Holder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-94

Cup Holder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-95

ECG Cable Hook . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-96

Air Filter Set . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-97

DVD R/W Drive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-98

Nest Fan Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-100

ARP Assy 110V/220V . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-102

SATA HDD Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-104

ACPC Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-107

Transbox Assy 110V/220V . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-109

Fuse Set . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-112

Read and Write Serial Info . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-113

Software Loading Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-117

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-117

Parts Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-117

TimeRequired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-117

Software Loading Steering Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-118

Before Starting Software Loading . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-119

Software Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-129

Installing Base Image Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-129

Verifying Base Image Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-134

Installing Application Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-141

Standard Confirmation & Functional Checks . . . . . . . . . . . . . . . . . . . . . . . .8-144

Full Backup / Restore Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-159

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-159

Parts Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-159

Full Backup Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-159

Restore procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-162

Software Reloading . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-163

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-163

Software Reloading Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-163

Mechanical Option Installation instruction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-172

Endo Probe Holder Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-174

Microphone Option fixture Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-175

14 -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Drawer Option installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-176

Cable Arm Hook installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-177

BW Printer Fixture Keyboard installation . . . . . . . . . . . . . . . . . . . . . . . . . . 8-178

BW printer Fixture Middle installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-181

Color Printer Fixture Middle installation - UP23MD Printer . . . . . . . . . . . . . 8-183

Color Printer Fixture Middle installation - UP-D25MD Printer . . . . . . . . . . . 8-185

Printer VCR DVD Fixture Top installation - UP23MD Printer . . . . . . . . . . . 8-187

Color Printer Fixture Top Installation - UP-D25MD Printer . . . . . . . . . . . . . 8-189

Printer VCR DVD fixture Top installation - CP900 Printer . . . . . . . . . . . . . 8-192

Printer VCR DVD Fixture Top Installation (MD-3000) . . . . . . . . . . . . . . . . 8-195

Printer VCR DVD Fixture Top Installation (MD-800) . . . . . . . . . . . . . . . . . 8-200

Rear Handle installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-203

Additional Task Lamp installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-205

Protect Cover Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-207

Swivel Lock Caster Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-208

LOGIQ A5 Rear Swivel Caster Installation . . . . . . . . . . . . . . . . . . . . . . . . . 8-209

BT11 Drawer Option Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-210

MTZ PROBE HOLDER Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-213

DVR Fixture Top Installation - SONY DVO-1000MD DVD Recorder . . . . . 8-214

- 15

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

CHAPTER 9

Renewal Parts

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-1

List of Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-2

MONITOR . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-3

KEYBOARD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-5

COVERS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-7

PCB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-9

BODY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-11

POWER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-14

Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-16

Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-20

Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-21

Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-22

Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-23

16 -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 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

System Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-7

Preliminary Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-7

Functional Checks (See Also Chapter 4) . . . . . . . . . . . . . . . . . . . . . . . . . . 10-8

System Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-8

Peripheral/Option Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-9

Input Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-9

Mains Cable Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-9

Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-9

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-10

Optional Diagnostic Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-11

Probe Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-11

Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-12

Safety Test Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-12

GEMS Leakage Current Limits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-13

Outlet Test - Wiring Arrangement - USA & Canada . . . . . . . . . . . . . . . . . . 10-14

Grounding Continuity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-15

Chassis Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-17

Isolated Patient Lead (Source) Leakage–Lead to Ground . . . . . . . . . . . . . 10-19

Isolated Patient Lead (Source) Leakage–Lead to Lead . . . . . . . . . . . . . . . 10-22

Isolated Patient Lead (Sink) Leakage-Isolation Test . . . . . . . . . . . . . . . . . 10-22

Probe Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-24

When There's Too Much Leakage Current... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-28

- 17

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

18 -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

Important Precautions

• THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER
THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE
TRANSLATION SERVICES.

WARNING

(EN)

AVERTISSEMENT

(FR)

• DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE
MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD.

• FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE
PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, MECHANICAL
OR OTHER HAZARDS.

• CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.

• SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE AUTRE
LANGUE QUE L’ANGLAIS, C’EST AU CLIENT QU’IL INCOMBE DE LE FAIRE
TRADUIRE.

• NE PAS TENTER D’INTERVENTION SUR LES éQUIPEMENTS TANT QUE LE
MANUEL SERVICE N’A PAS éTé CONSULTé ET COMPRIS.

• LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAîNER CHEZ LE
TECHNICIEN, L’OPéRATEUR OU LE PATIENT DES BLESSURES DUES à DES
DANGERS éLECTRIQUES, Mé CANIQUES OU AUTRES.

WARNUNG

(DE)

• DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER
SPRACHE.

• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENö TIGT,
IST ES AUFGABE DES KUNDEN FüR EINE ENTSPRECHENDE ÜBERSETZUNG
ZU SORGEN.

• VERSUCHEN SIE NICHT, DAS GERä T ZU REPARIEREN, BEVOR DIESES
KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN
WURDE.

• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN
DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN
DURCH ELEKTRISCHE SCHLä GE, MECHANISCHE ODER SONSTIGE
GEFAHREN KOMMEN.

- i

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

• ESTE MANUAL DE SERVICIO Só LO EXISTE EN INGLéS.

• SI ALGúN PROVEEDOR DE SERVICIOS AJENO A GEHC SOLICITA UN IDIOMA
QUE NO SEA EL INGLéS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN
SERVICIO DE TRADUCCIó N.

AVISO

(ES)

• NO SE DEBERá DAR SERVICIO Té CNICO AL EQUIPO, SIN HABER
CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.

• LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL
PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN
LESIONES PROVOCADAS POR CAUSAS ELéCTRICAS, MECá NICAS O DE
OTRA NATURALEZA.

• ESTE MANUAL DE ASSISTêNCIA Té CNICA Só SE ENCONTRA DISPONíVEL EM
INGLêS.

• SE QUALQUER OUTRO SERVIç O DE ASSISTêNCIA TéCNICA, QUE Nã O A
GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, é DA

ATENÇÃO

(PT)

RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIç OS DE TRADUç ã O.

• Nã O TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTêNCIA Té CNICA.

• O Nã O CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANç A
DO TéCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELéTRICOS,
MECâ NICOS OU OUTROS.

AVVERTENZA

(IT)

HOIATUS

(ET)

• IL PRESENTE MANUALE DI MANUTENZIONE è DISPONIBILE SOLTANTO IN
INGLESE.

• SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEHC RICHIEDE IL
MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE è TENUTO A PROVVEDERE
DIRETTAMENTE ALLA TRADUZIONE.

• SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO
AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL
CONTENUTO.

• NON TENERE CONTO DELLA PRESENTE AVVERTENZA POTREBBE FAR
COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI ALL’ADDETTO ALLA
MANUTENZIONE, ALL’UTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE
ELETTRICA, PER URTI MECCANICI OD ALTRI RISCHI.

• KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.

• KUI KLIENDITEENINDUSE OSUTAJA Nõ UAB JUHENDIT INGLISE KEELEST
ERINEVAS KEELES, VASTUTAB KLIENT Tõ LKETEENUSE OSUTAMISE EEST.

• ä RGE ü RITAGE SEADMEID TEENINDADA ENNE EELNEVALT Kä ESOLEVA
TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU SAAMIST.

• Kä ESOLEVA HOIATUSE EIRAMINE Võ IB Põ HJUSTADA TEENUSEOSUTAJA,
OPERAATORI Võ I PATSIENDI VIGASTAMIST ELEKTRILö ö GI, MEHAANILISE
Võ I MUU OHU TAGAJä RJEL.

ii -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

• TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.

• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN
ENGLANNINKIELISTä MATERIAALIA, TARVITTAVAN Kä ä NNö KSEN
HANKKIMINEN ON ASIAKKAAN VASTUULLA.

VAROITUS

(FI)

• ä Lä YRITä KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT
JA YMMä RTä NYT Tä Mä N HUOLTO-OHJEEN.

• MIKä LI Tä Tä VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA
PALVELUNTARJOAJAN, LAITTEISTON Kä YTTä Jä N TAI POTILAAN
VAHINGOITTUMINEN Sä HKö ISKUN, MEKAANISEN VIAN TAI MUUN
VAARATILANTEEN VUOKSI.

• ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ ∆ΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.

• ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ

ΕΓΧΕΙΡΙ∆ΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ, ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ
ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ.

ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ

(EL)

• ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ

ΕΚΤΟΣ ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ

ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ

ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ.

• ΕΑΝ ∆Ε ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝ∆ΕΧΕΤΑΙ ΝΑ
ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή
ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝ∆ΥΝΟΥΣ.

FIGYELMEZTETÉS

(HU)

VIÐVÖRUN

(IS)

• EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHETŐ
EL.

• HA A VEVŐ SZOLGÁLTATÓJA ANGOLTÓL ELTÉRŐ NYELVRE TART IGÉNYT,
AKKOR A VEVŐ FELELŐSSÉGE A FORDÍTÁS ELKÉSZÍTTETÉSE.

• NE PRÓBÁLJA ELKEZDENI HASZNÁLNI A BERENDEZÉST, AMÍG A
KARBANTARTÁSI KÉZIKÖNYVBEN LEÍRTAKAT NEM ÉRTELMEZTÉK.

• EZEN FIGYELMEZTETÉS FIGYELMEN KÍVÜL HAGYÁSA A SZOLGÁLTATÓ,
MŰKÖDTETŐ VAGY A BETEG ÁRAMÜTÉS, MECHANIKAI VAGY EGYÉB
VESZÉLYHELYZET MIATTI SÉRÜLÉSÉT EREDMÉNYEZHETI.

• ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.

• EF ÞJÓNUSTUAÐILI VIÐSKIPTAMANNS ÞARFNAST ANNARS TUNGUMÁLS EN
ENSKU, ER ÞAÐ Á ÁBYRGÐ VIÐSKIPTAMANNS AÐ ÚTVEGA ÞÝÐINGU.

• REYNIÐ EKKI AÐ ÞJÓNUSTA TÆKIÐ NEMA EFTIR AÐ HAFA SKOÐAÐ OG
SKILIÐ ÞESSA ÞJÓNUSTUHANDBÓK.

• EF EKKI ER FARIÐ AÐ ÞESSARI VIÐVÖRUN GETUR ÞAÐ VALDIÐ MEIÐSLUM
ÞJÓNUSTUVEITANDA, STJÓRNANDA EÐA SJÚKLINGS VEGNA RAFLOSTS,
VÉLRÆNNAR EÐA ANNARRAR HÆTTU.

- iii

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

• TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKéM JAZYCE.

•VPř íPADě , ŽE POSKYTOVATEL SLUŽEB ZÁKAZNÍKŮM POTř EBUJE Ná VOD
V JINéM JAZYCE, JE ZAJIšTěNí Př EKLADU DO ODPOVíDAJíCíHO JAZYKA
úKOLEM Zá KAZNíKA.

• NEPROVÁDĚJTE úDRŽBU TOHOTO ZAř íZENí, ANIŽ BYSTE SI Př Eč ETLI

VÝSTRAHA

(CS)

TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.

•VPř íPADě NEDODRŽOVá Ní TéTO VýSTRAHY Mů ŽE DOJíT ÚRAZU
ELEKTRICKÁM PROUDEM PRACOVNíKA POSKYTOVATELE SLUŽEB,
OBSLUŽNéHO PERSONá LU NEBO PACIENTů VLIVEM ELEKTRICKé HOP
PROUDU, RESPEKTIVE VLIVEM K RIZIKU MECHANICKÉHO POŠKOZENÍ NEBO
JINÉMU RIZIKU.

• DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.

• HVIS EN KUNDES TEKNIKER HAR BRUG FOR ET ANDET SPROG END
ENGELSK, ER DET KUNDENS ANSVAR AT SØRGE FOR OVERSÆTTELSE.

ADVARSEL

(DA)

• FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE
DENNE SERVICEMANUAL ER BLEVET LÆST OG FORSTÅET.

• MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDFØRE SKADE
PÅ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR
TEKNIKEREN, OPERATØREN ELLER PATIENTEN.

WAARSCHUWING

(NL)

BRĪDINĀJUMS

(LV)

• DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS
VERKRIJGBAAR.

• ALS HET ONDERHOUDSPERSONEEL EEN ANDERE TAAL VEREIST, DAN IS DE
KLANT VERANTWOORDELIJK VOOR DE VERTALING ERVAN.

• PROBEER DE APPARATUUR NIET TE ONDERHOUDEN VOORDAT DEZE
ONDERHOUDSHANDLEIDING WERD GERAADPLEEGD EN BEGREPEN IS.

• INDIEN DEZE WAARSCHUWING NIET WORDT OPGEVOLGD, ZOU HET
ONDERHOUDSPERSONEEL, DE OPERATOR OF EEN PATIËNT GEWOND
KUNNEN RAKEN ALS GEVOLG VAN EEN ELEKTRISCHE SCHOK,
MECHANISCHE OF ANDERE GEVAREN.

•šĪ APKALPES ROKASGRĀMATA IR PIEEJAMA TIKAI ANGĻU VALODĀ.

• JA KLIENTA APKALPES SNIEDZĒJAM NEPIECIEŠAMA INFORMĀCIJA CITĀ
VALODĀ, NEVIS ANGĻU, KLIENTA PIENĀKUMS IR NODROŠINĀT TULKOŠANU.

• NEVEICIET APRĪKOJUMA APKALPI BEZ APKALPES ROKASGRĀMATAS
IZLASĪŠANAS UN SAPRAŠANAS.

•ŠĪ BRĪDINĀJUMA NEIEVĒROŠANA VAR RADĪT ELEKTRISK

ĀS STRĀVAS
TRIECIENA, MEHĀNISKU VAI CITU RISKU IZRAISĪTU TRAUMU APKALPES
SNIEDZĒJAM, OPERATORAM VAI PACIENTAM.

iv -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

• ŠIS EKSPLOATAVIMO VADOVAS YRA IŠLEISTAS TIK ANGLŲ KALBA.

• JEI KLIENTO PASLAUGŲ TEIKĖJUI REIKIA VADOVO KITA KALBA – NE ANGLŲ,
VERTIMU PASIRŪPINTI TURI KLIENTAS.

ĮSPĖJIMAS

(LT)

•NEMĖGINKITE ATLIKTI ĮRANGOS TECHNINĖS PRIEŽIŪROS DARBŲ, NEBENT
VADOVAUTUMĖTĖS ŠIUO EKSPLOATAVIMO VADOVU IR JĮ SUPRASTUMĖTE

• NEPAISANT ŠIO PERSPĖJIMO, PASLAUGŲ TEIKĖJAS, OPERATORIUS AR
PACIENTAS GALI BŪTI SUŽEISTAS DĖL ELEKTROS SMŪGIO, MECHANINIŲ AR
KITŲ PAVOJŲ.

• DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.

• HVIS KUNDENS SERVICELEVERANDØR TRENGER ET ANNET SPRÅK, ER DET
KUNDENS ANSVAR Å SØRGE FOR OVERSETTELSE.

ADVARSEL

(NO)

• IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE
SERVICEHÅNDBOKEN ER LEST OG FORSTÅTT.

• MANGLENDE HENSYN TIL DENNE ADVARSELEN KAN FØRE TIL AT
SERVICELEVERANDØREN, OPERATØREN ELLER PASIENTEN SKADES PÅ
GRUNN AV ELEKTRISK STØT, MEKANISKE ELLER ANDRE FARER.

OSTRZEŻENIE

(PL)

ATE NŢIE

(RO)

• NINIEJSZY PODRĘCZNIK SERWISOWY DOSTĘPNY JEST JEDYNIE W JĘZYKU
ANGIELSKIM.

•JEśLI FIRMA śWIADCZĄCA KLIENTOWI USłUGI SERWISOWE WYMAGA
UDOSTęPNIENIA PODRę CZNIKA W JęZYKU INNYM NIŻ ANGIELSKI,
OBOWIĄZEK ZAPEWNIENIA STOSOWNEGO TłUMACZENIA SPOCZYWA NA
KLIENCIE.

• NIE PRó BOWAć SERWISOWAć NINIEJSZEGO SPRZęTU BEZ UPRZEDNIEGO
ZAPOZNANIA SIę Z PODRęCZNIKIEM SERWISOWYM.

• NIEZASTOSOWANIE SIę DO TEGO OSTRZEŻENIA MOżE GROZIć
OBRAŻENIAMI CIAłA SERWISANTA, OPERATORA LUB PACJENTA W WYNIKU
PORAŻENIA PRĄDEM, URAZU MECHANICZNEGO LUB INNEGO RODZAJU
ZAGROŻEń.

• ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZĂ.

• DACĂ UN FURNIZOR DE SERVICII PENTRU CLIENŢI NECESITĂ O ALTĂ LIMBĂ
DECÂT CEA ENGLEZĂ, ESTE DE DATORIA CLIENTULUI SĂ FURNIZEZE O
TRADUCERE.

• NU ÎNCERCAŢI SĂ REPARAŢI ECHIPAMENTUL DECÂT ULTERIOR
CONSULTĂRII ŞI ÎNŢELEGERII ACESTUI MANUAL DE SERVICE.

• IGNORAREA ACESTUI AVERTISMENT AR PUTEA DUCE LA RĂNIREA
DEPANATORULUI, OPERATORULUI SAU PACIENTULUI ÎN URMA
PERICOLELOR DE ELECTROCUTARE, MECANICE SAU DE ALTĂ NATURĂ.

- v

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

• Данное руко во дс тво по обслуживанию ПРЕДОСТАВЛЯЕТСЯ
только на английском Язык е.

• Ес ли сервисноМУ ПЕРСОНАЛУ клиента необходимо руко в о дс тв о

не на английском ЯЗЫКЕ, клиенту следует самостоЯтельно
ОБЕСПЕЧИТЬ перевод.

ОСТОРОЖНО!

(RU)

• ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО ОБРАТИТЕСЬ
К ДАННОМУ РУКОВОДСТВУ И ПОЙМИТЕ ИЗЛОЖЕННЫЕ В НЕМ СВЕДЕНИЯ.

• НЕСОБЛЮДЕНИЕ УКАЗАННЫХ ТРЕБОВАНИЙ МОЖЕТ ПРИВЕСТИ К ТОМУ,
ЧТО СПЕЦИАЛИСТ ПО ТЕХОБСЛУЖИВАНИЮ

, ОПЕРАТОР ИЛИ ПАЦИЕНТ

ПОЛУЧАТ УДАР ЗЛЕКТРИЧЕСКИМ ТОКОМ, МЕХАНИЧЕСКУЮ ТРАВМУ ИЛИ
ДРУГОЕ ПОВРЕЖДЕНИЕ.

• TÁTO SERVISNÁ PRÍRUČKA JE K DISPOZíCII LEN V ANGLIČTINE.

• AK ZÁKAZNÍKOV POSKYTOVATEĽ SLUŽIEB VYŽADUJE INÝ JAZYK AKO
ANGLIČTINU, POSKYTNUTIE PREKLADATEĽSKÝCH SLUŽIEB JE
ZODPOVEDNOSŤOU ZÁKAZNÍKA.

UPOZORNENIE

(SK)

• NEPOKÚŠAJTE SA VYKONÁVAŤ SERVIS ZARIADENIA SKÔR, AKO SI
NEPREČÍTATE SERVISNÚ PRÍRUČKU A NEPOROZUMIETE JEJ.

• ZANEDBANIE TOHTO UPOZORNENIA Mô ŽE VYÚSTIŤ DO ZRANENIA
POSKYTOVATEĽA SLUŽIEB, OBSLUHUJúCEJ OSOBY ALEBO PACIENTA
ELEKTRICKýM PRúDOM, PRÍPADNE DO MECHANICKé HO ALEBO INéHO
NEBEZPEč ENSTVA.

VARNING

(SV)

DİKKAT

(TR)

• DEN HÄR SERVICEHANDBOKEN FINNS BARA TILLGÄNGLIG PÅ ENGELSKA.

• OM EN KUNDS SERVICETEKNIKER HAR BEHOV AV ETT ANNAT SPRÅK ÄN
ENGELSKA ANSVARAR KUNDEN FÖR ATT TILLHANDAHÅLLA
ÖVERSÄTTNINGSTJÄNSTER.

• FÖRSÖK INTE UTFÖRA SERVICE PÅ UTRUSTNINGEN OM DU INTE HAR LÄST
OCH FÖRSTÅR DEN HÄR SERVICEHANDBOKEN.

• OM DU INTE TAR HÄNSYN TILL DEN HÄR VARNINGEN KAN DET RESULTERA I
SKADOR PÅ SERVICETEKNIKERN, OPERATÖREN ELLER PATIENTEN TILL
FÖLJD AV ELEKTRISKA STÖTAR, MEKANISKA FAROR ELLER ANDRA FAROR.

• BU SERVİS KILAVUZU YALNIZCA İNGİLİZCE OLARAK SAĞLANMIŞTIR.

•EĞER MÜŞTERİ TEKNİSYENİ KILAVUZUN İNGİLİZCE DIŞINDAKİ B

İR DİLDE
OLMASINI İSTERSE, KILAVUZU TERCÜME ETTİRMEK MÜŞTERİNİN
SORUMLULUĞUNDADIR.

•SERVİS KILAVUZUNU OKUYUP ANLAMADAN EKİPMANLARA MÜDAHALE
ETMEYİNİZ.

• BU UYARININ GÖZ ARDI EDİLMESİ, ELEKTRİK ÇARPMASI YA DA MEKANİK
VEYA DİĞER TÜRDEN KAZALAR SONUCUNDA TEKNİSYENİN, OPERATÖRÜN
YA DA HASTANIN YARALANMASINA YOL AÇABİLİR.

vi -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

(JA)

(ZH-CN)

(KO)

- vii

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

DAMAGE IN TRANSPORTATION

All packages should be closely examined at time of delivery. If damage is apparent write “Damage In
Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for” by
a GE representative or hospital receiving agent. Whether noted or concealed, damage MUST be
reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the
contents and containers held for inspection by the carrier. A transportation company will not pay a claim
for damage if an inspection is not requested within this 14 day period.

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY

All electrical Installations that are preliminary to 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 Healthcare 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 Healthcare 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, 9900 Innovation Drive (RP-2123), Wauwatosa, WI 53226, USA.

GE Healthcare employees should use the iTrak System to report all documentation errors or omissions.

SERVICE SAFETY CONSIDERATIONS

DANGER

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN
THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND
ADJUSTING.

WARNINGWARNING

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.

viii -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

LEGAL NOTES

The contents of this publication may not be copied or duplicated in any form, in whole or in part, without
prior written permission of GE Healthcare.

GE Healthcare may revise this publication from time to time without written notice.

TRADEMARKS

All products and their name brands are trademarks of their respective holders.

COPYRIGHTS

All Material Copyright© 2004 and 2008 by General Electric Company Inc. All Rights Reserved.

- ix

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

Revision History

Revision Date Reason for change

1 May 3, 2010 Initial Release

List of Effected Pages(LOEP)

Pages Revision Pages Revision Pages Revision

Title Page 1 4-1 to 4-55 1 10-1 to 10-30 1

Warnings i to -x 1 5-1 to 5-60 1 Index-1 to Index-4 1

TOC vii to 1 6-1 to 6-8 1 Back Cover N/A

1-1 to 1-19 1 7-1 to 7-36 1

2-1 to 2-12 1 8-1 to 8-210 1

3-1 to 3-26 1 9-1 to 9-23 1

x -

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE 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™ P5 scanner. The
service provider must read and understand all the information presented in this manual before installing
or servicing a unit.

Table 1-1 Contents in Chapter 1

Section Description Page Number

1-1

1-2

1-3

1-4

1-5

Overview

Important Conventions

Safety Considerations

EMC, EMI, and ESD

Customer Assistance

1-1-2 Purpose of Service Manual

This Service Manual provides installation and service information for the LOGIQ™ P5 Ultrasound
Scanning System and contains the following chapters:

1.) Chapter 1 - Introduction: Contains a content summary and warnings.

2.) Chapter 2 - Pre-Installation: Contains pre-installation requirements for the LOGIQ™ P5.

3.) Chapter 3 - Installation : Contains installation procedures.

4.) Chapter 4 - Functional Checks: Contains functional checks that are recommended as part of the

installation, or as required during servicing and periodic maintenance.

5.) Chapter 5 - Components and Functions (Theory) : Contains block diagrams and functional

explanations of the electronics.

6.) Chapter 6 - Service Adjustments : Contains instructions on how to make available adjustments

to the LOGIQ™ P5.

7.) Chapter 7 - Diagnostics/Troubleshooting : Provides procedures for running diagnostic or related

routines for the LOGIQ™ P5.

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™ P5.

10.)Chapter 10 - Care & Maintenance : Provides periodic maintenance procedures for the LOGIQ™

P5.

1-1

1-3

1-12

1-17

1-18

Section 1-1 - Overview 1-1

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

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

• Service Personnel (installation, maintenance, etc.)

• Hospital’s Service Personnel

• Contractors (Some parts of Chapter 2 - Pre-Installation)

1-1-4 LOGIQ™ P5 Models Covered by this Manual

Table 1-2 LOGIQ™ P5 Model Designation

Hcat# Description

H44662LD LP5 BT11 FOR USA

H44662LE LP5 PRO BT11 FOR ASIA110V

H44662LF LP5 PRO BT11 FOR KOREA

H44662LN LOGIQ P5 OB KOREA

H44662LP LP5 PRO BT11 FOR EUROPE

H44662LR LP5 ADVANCED BT11 JAPAN

H44662LT LP5 ADVANCED BT11 LATIN220

H44662LY LP5 PREMIUM BT11 EUROPE

H44662LZ LP5 PREMIUM BT11 FOR ASIA

H44672LA LP5 PREMIUM BT11 ASEAN 220

H44672LB LP5 PREMIUM BT11 ANZ 220

H44672LD LP5 PREMIUM BT11 LATIN220

H44672LE LP5 PREMIUM BT11 LATIN110

H44672LF LP5 PREMIUM BT11 FOR USA

H44672LL LOGIQ P5 OB for Japan

H44672LH LOGIQ P5 OB for EMEA

H44672LJ LOGIQ P5 Basic OB

H44672LK LOGIQ P5 Premium OB

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

The Operator Manual(s) should be fully read and understood before operating the LOGIQ™ P5 and
also kept near the unit for quick reference.

1-2 Section 1-1 - Overview

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

Section 1-2 Important Conventions

1-2-1 Conventions Used in Book

Icons

Pictures, or icons, are used wherever they reinforce the printed message. The icons, labels and
conventions used on the product and in the service information are described in this chapter.

Safety Precaution Messages

Various levels of safety precaution messages may be found on the equipment and in the service
information. The different levels of concern are identified by a flag word that precedes the precautionary
message. Known or potential hazards are labeled in one of following ways:

DANGER

DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL
CAUSE SEVERE PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE
IGNORED.

WARNINGWARNING

CAUTION

NOTICE

NOTE: Notes provide important information about an item or a procedure.

WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT CAN CAUSE
SEVERE PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE
IGNORED.

Caution is used to indicate the presence of a hazard that will or can cause minor personal injury
and property damage if instructions are ignored.

Equipment Damage Possible
Notice is used when a hazard is present that can cause property damage but has absolutely no

personal injury risk.

Example: Disk drive will crash.

Information contained in a NOTE can often save you time or effort.

Section 1-2 - Important Conventions 1-3

GE HEALTHCARE

N

DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

1-2-2 Standard Hazard Icons

Important information will always be preceded by the exclamation point contained within a triangle, as
seen throughout this chapter. In addition to text, several different graphical icons (symbols) may be
used to make you aware of specific types of hazards that could cause harm.

Table 1-3 Standard Hazard Icons

ELECTRICAL MECHANICAL RADIATION

LASER HEAT PINCH

LASER

LIGHT

Other hazard icons make you aware of specific procedures that should be followed.

Table 1-4 Standard Icons Indicating a Special Procedure Be Used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

TAG

&

LOCKOUT

Date

Signed

EYE

PROTECTIO

1-4 Section 1-2 - Important Conventions

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

1-2-3 Product Icons

The following table describes the purpose and location of safety labels and other important information
provided on the equipment.

Table 1-5 Product Icons

LABEL/SYMBOL PURPOSE/MEANING LOCATION

Identification and Rating Plate

Device Listing/Certification Labels

Type/Class Label

IP Code (IPX8)

Manufacturer's name and address
Date of manufacture
Model and serial numbers
Electrical ratings

Laboratory logo or labels denoting
conformance with industry safety standards
such as UL or IEC.

Used to indicate the degree of safety or protection.

Indicates the degree of protection provided by
the enclosure per IEC 529. IPX8 indicates drip
proof.

Equipment Type CF (heart in the box symbol)
IEC 878-02-05 indicates equipment having a
high degree of protection suitable for direct
cardiac contact.

IEC60601-2-27

"CAUTION" The equilateral triangle is usually
used in combination with other symbols to
advise or warn the user.

Rear of console near power inlet
Under monitor
On each probe

Rear of console
Under front of monitor

Footswitch

ECG connector
Surgical probes
Defibrillator

Various

ATTENTION - Consult accompanying
documents " is intended to alert the user to
refer to the operator manual or other
instructions when complete information cannot
be provided on the label.

"CAUTION - Dangerous voltage" (the lightning
flash with arrowhead in equilateral triangle) is
used to indicate electric shock hazards.

"Mains OFF" Indicates the power off position of
the mains power switch.

Various

Various

Rear of system adjacent to mains switch

Section 1-2 - Important Conventions 1-5

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

Table 1-5 Product Icons

LABEL/SYMBOL PURPOSE/MEANING LOCATION

"OFF/Standby" Indicates the power off/
standby position of the power switch.

CAUTION
This Power Switch DOES NOT ISOLATE
Mains Supply

"Mains ON" Indicates the power on position of
the mains power switch.

"ON" Indicates the power on position of the
power switch.

CAUTION
This Power Switch DOES NOT ISOLATE

Mains Supply

Adjacent to On-Off/Standby Switch

Front Panel Switch

"Protective Earth" Indicates the protective
earth (grounding) terminal.

Indicates an earth GROUND potential

Internal

Product schematics
Peripherals

1-6 Section 1-2 - Important Conventions

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

1-2-4 WEEE Label

The following table describes the meaning of WEEE label and its translation provided on the equipment.

Table 1-6 WEEE Label

LABEL/SYMBOL LANGUAGE PURPOSE/MEANING

This symbol indicates that the waste of electrical and electronic equipment must

English

Czech (CZE)

not be disposed as unsorted municipal waste and must be collected separately.
Please contact an authorized representative of the manufacturer for information
concerning the decommissioning of your equipment.

Tento symbol znamená, že díly elektrických nebo elektronických zařízení
nesmí být likvidovány do netříděného odpadu, ale musí být likvidovány
samostatně. Obraťte se prosím na autorizovaného představitele výrobce,
který poskytne informace týkající se likvidace vašeho přístroje.

Danish (DAN)

Dutch (DUT)

Catalan (CAT)

Chinese (CHN)

Dette symbol angiver, at elektrisk og elektronisk affald ikke må
bortskaffes som usorteret brændbart affald, men skal indsamles særskilt.
Kontakt venligst en autoriseret repræsentant for producenten for at få
oplysninger om, hvordan dit udstyr skal bortskaffes.

Dit symbool geeft aan dat het afval van elektrische en elektronische
apparatuur niet ongescheiden mag worden meegegeven met het
huisvuil, maar apart moet worden ingeleverd. Neem contact op met een
erkende vertegenwoordiger van de fabrikant voor informatie over het
inleveren van uw apparatuur.

Aquest símbol indica que els residus dels equips elèctrics i electrònics
s'han d'abocar per separat, no com a residus municipals no classificats.
Contacteu amb un representant autoritzat del fabricant per obtenir
informació sobre com desfer-vos del vostre equip.

Estonian (EST)

See märk näitab, et tarbetuks muutunud elektri- ja elektroonikaseadmeid
ei tohi ära visata sortimata olmejäätmetena, vaid need tuleb eraldi kokku
koguda. Seadmete käitlemise kohta küsige lisateavet tootja volitatud
esindajalt.

Section 1-2 - Important Conventions 1-7

GE HEALTHCARE

µ

p

DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

Table 1-6 WEEE Label

LABEL/SYMBOL LANGUAGE PURPOSE/MEANING

Tämä kuvatunnus ilmaisee, että sillä merkittyä sähkö- ja

Finnish (FIN)

elektroniikkalaitetta ei saa hävittää lajittelemattomana yhdyskuntajätteenä
vaan se on kerättävä talteen erikseen. Ota yhteyttä tuotteen valmistajan
valtuuttamaan myyntiedustajaan ja kysy lisätietoja laitteen käytöstä
poistosta.

Ce symbole indique que les déchets relatifs à l'équipement électrique et

French- France
(FRA)

électronique ne doivent pas être jetés comme les ordures ménagères
non-triées et doivent être collectés séparément. Contactez un repré
sentant agréé du fabricant pour obtenir des informations sur la mise au
rebut de votre équipement.

Dieses Symbol kennzeichnet elektrische und elektronische Geräte, die
nicht mit dem gewöhnlichen, unsortierten Hausmüll entsorgt werden dü

German (GER)

rfen, sondern separat behandelt werden müssen. Bitte nehmen Sie
Kontakt mit einem autorisierten Beauftragten des Herstellers auf, um
Informationen hinsichtlich der Entsorgung Ihres Gerätes zu erhalten.

Greek (GRE)

Hungarian
(HUN)

Icelandic (ICE)

Αυτό το σύµβολο υποδηλώνει ότι τα απόβλητα ηλεκτρικού και ηλεκτρονικού εξ
οπλισµού δεν πρέπει να απορρίπτονται ως κοινά απορρίµατα, αλλά να συλλέγον
ται ξεχωριστά. Παρακαλούµε επικοινωνήστε µε έναν εξουσιοδοτηµένο αντιπρό
σωπο του κατασκευαστή για πληροφορίες σχετικά µε την απόρριψη του εξοπλισ

ού.

A szimbólum azt jelzi, hogy az elektromos és elektronikus készülék hulladékát
tilos nem szelektív lakossági hulladékként kezelni, hanem elkülönítve kell gyű
jteni. Kérjük, a berendezés leselejtezését illetőleg lépjen kapcsolatba a gyártó
hivatalos ké

viseletével.

Merki þetta táknar að rafeindatækjum skal eytt á sérstakan máta, ekki m
á losa rafeindatæki í hefðbundin sorphirðuílát sem óflokkað sorp.
Vinsamlega hafið samband við umboðsmann framleiðanda fyrir upplý
singar um hvernig tækinu skal eytt.

1-8 Section 1-2 - Important Conventions

GE HEALTHCARE

pp

DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

Table 1-6 WEEE Label

LABEL/SYMBOL LANGUAGE PURPOSE/MEANING

Questo simbolo indica che i rifiuti derivanti da apparecchiature elettriche ed

Italian (ITA)

elettroniche non devono essere smaltiti come rifiuti municipali indifferenziati e
devono invece essere raccolti separatamente. Per informazioni relative alle
modalità di smantellamento delle apparecchiature fuori uso, contattare un
ra

resentante autorizzato del fabbricante.

Japanese
(JPN)

Šis apzīmējums norāda, ka no elektriskā un elektroniskā aprīkojuma

Latvian (LAT)

atkritumiem nedrīkst atbrīvoties kā no nešķirotiem mājsaimniecības
atkritumiem un tie ir jāsavāc atsevišķi. Lūdzu, sazinieties ar pilnvarotu raž
otāja pārstāvi, lai saņemtu informāciju par aprīkojuma ekspluatācijas pā
rtraukšanu.

Lithuanian
(LIT)

Norwegian
(NOR)

Polish (POL)

Portuguese­Brazilian (POB)

Šis simbolis nurodo, kad elektros ir elektroninės įrangos atliekos turi būti
surenkamos atskirai ir negali būti šalinamos kaip nerūšiuotos savivaldybė
s tvarkomos atliekos. Informacijos apie įrangos veikimo sustabdymą
kreipkitės į įgaliotąjį gamintojo atstovą.

Dette symbolet angir at elektrisk og elektronisk utstyr ikke skal kastes
som restavfall, men må leveres inn separat. Ta kontakt med en autorisert
representant for produsenten hvis du vil ha informasjon om hvordan
utstyret skal avhendes.

Ten symbol oznacza, iż składowanie zużytych urządzeń elektrycznych i
elektronicznych wraz z ogólnymi odpadami miejskimi jest zabronione.
Informacji na temat miejsc składowania tego typu odpadów udziela
producent sprzętu.

Este símbolo indica que os resíduos do equipamento elétrico e eletrônico
não devem ser descartados no sistema de coleta de lixo municipal, e sim
coletados separadamente. Favor entrar em contato com um
representante autorizado do fabricante para obter informações sobre
como descartar seu equipamento.

Section 1-2 - Important Conventions 1-9

GE HEALTHCARE

j

g

DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

Table 1-6 WEEE Label

LABEL/SYMBOL LANGUAGE PURPOSE/MEANING

Acest simbol indică faptul că deşeurile de echipamente electrice şi

Romanian
(ROM)

electronice nu au voie să fie aruncate nediferenţiat ca gunoi menajer şi c
ă ele trebuie colectate separat. Vă rugăm să luaţi legătura cu un
reprezentant autorizat al producătorului pentru a obţine informaţii
referitoare la eliminarea ecologică a echipamentului dumneavoastră.

Символ обозначает: недопустимо выбрасывать электрическое и эле

Russian (RUS)

ктронное оборудование с неотсортированным бытовым мусором. Он
о должно собираться отдельно. Для получения сведений об утилиза
ции оборудования обратитесь к авторизованному представителю ко
мпании-производителя.

Ovaj simbol označava da se otpad električne i elektronske opreme ne

Serbian (SCC)

sme odlagati zajedno sa običnim gradskim smećem, već se mora
pokupiti posebno. Molimo vas da kontaktirate ovlašćenog predstavnika
proizvođača svoje opreme, kako bi ste se informisali o njenom pravilnom
rashodu.

Slovakian
(SLK)

Slovenian
(SLN)

Spanish-Spain
(SPA)

Swedish
(SWE)

Tento symbol označuje, že odpad elektrického a elektronického materiá
lu sa nesmie vyhadzovať do netriedeného komunálneho odpadu, ale mus
í sa likvidovať oddelene. Viac informácií o likvidácii vášho zariadenia vám
poskytne poverený zástupca výrobcu.

Ta simbol obeležava da se elektronski otpad in elektronska oprema ne sme
odlagati skup z navadnim mesnim otpadom, ter se mora pobrat posebej. Prosimo
vas da kontaktirate pooblaščenega prodajalca opreme, kako bi se informirali o
n

enem pravilnem rashodu.

Este símbolo indica que el equipo eléctrico y electrónico no debe tirarse
con los desechos domésticos y debe tratarse por separado. Contacte
con el representante local del fabricante para obtener más información
sobre la forma de desechar el equipo.

Denna symbol anger att elektriska och elektroniska utrustningar inte får avyttras
som osorterat hushållsavfall och måste samlas in separat. Var god kontakta en
auktoriserad tillverkarrepresentant för information angående avyttring av
utrustnin

en.

1-10 Section 1-2 - Important Conventions

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

Table 1-6 WEEE Label

LABEL/SYMBOL LANGUAGE PURPOSE/MEANING

Bu sembol, elektrikli ve elektronik ekipmanların sınıflandırılmamış çöp

Turkish (TUR)

olarak atılmaması ve ayrı olarak toplanması gerektiğini belirtir. Lütfen
ekipmanınızın imhasıyla ilgili olarak üreticinin yetkili temsilcisine baş
vurun.

The symbol is affixed to a battery to advise the user or owner that it must be recycled or disposed of
in accordance with local, state, or country laws.

English

The letter below indicates the toxic element (Pb=Lead, Cd=Cadmium, Hg=Mercury) that is contained
in the battery that may require special recycling or disposal method, Please contact a GEHC
representative to facilitate servicing, removal and disposal options.

Section 1-2 - Important Conventions 1-11

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

Section 1-3 Safety Considerations

1-3-1 Introduction

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

1-3-2 Human Safety

Operating personnel must not remove the system covers.
Servicing should be performed by authorized personnel only.
Only personnel who have participated in a LOGIQ™ P5 Training are authorized to service the
equipment.

1-3-3 Mechanical Safety

WARNINGWARNING

WARNINGWARNING

WARNINGWARNING

CAUTION

CAUTION

WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE
EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.

ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT
CAN EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN
HANDLING AND PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A
DAMAGED OR DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS
CAN RESULT IN SERIOUS INJURY AND EQUIPMENT DAMAGE.

NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK,
IT MAY BE DAMAGED.

Always lower and center the Operator I/O Panel before moving the scanner.

The LOGIQ™ P5 weighs 75 kg or more, depending on installed peripherals, (165 lbs., or
more) when ready for use. Care must be used when moving it or replacing its parts. Failure
to follow the precautions listed could result in injury, uncontrolled motion and costly
damage.

ALWAYS:
Be sure the pathway is clear.
Use slow, careful motions.
Use two people when moving on inclines or lifting more than 16 kg (35 lbs).

CAUTION

1-12 Section 1-3 - Safety Considerations

There is a pinch point in LCD monitor. Need care for injury on hands or fingers in flipping
down the LCD monitor.

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE 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)

• DO NOT use the Control Panel as an anchor point.

• Place the probes in their carrying case.

• Eject DVD media from the system.

CAUTION

Keep the heat venting holes on the monitor unobstructed to avoid overheating of the
monitor.

1-3-4 Electrical Safety

To minimize shock hazard, the equipment chassis must be connected to an electrical ground. The
system is equipped with a three-conductor AC power cable. This must be plugged into an approved
electrical outlet with safety ground. If an extension cord is used with the system, make sure that the total
current rating of the system does not exceed the extension cord rating.

The power outlet used for this equipment should not be shared with other types of equipment.

Both the system power cable and the power connector meet international electrical standards.

WARNINGWARNING

DO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY
CIRCUMSTANCES.

Section 1-3 - Safety Considerations 1-13

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

1-3-5 Label Locations

Figure 1-1 OUTSIDE MARKINGS OF LOGIQ™ P5 (Rear)

1.) Identification and Rating Plate - USA/Asia 120V Console

2.) Identification and Rating Plate - Europe/Asia/Latin America 220V Console

3.) Identification and Rating Plate - Japan 100V Console

4.) Identification and Rating Plate - Korea 220V Console

5.) Identification and Rating Plate - China 220V Console

6.) UL Label

1-14 Section 1-3 - Safety Considerations

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

1-3-5 Label Locations (cont’d)

Figure 1-2 OUTSIDE MARKINGS OF LOGIQ™ P5

1.) Possible Shock Hazard

2.) Label -”Do not use the following devices near this equipment.”

3.) Label - “The equipment weighs approximately 75kg.

4.) Prescription Devices

5.) CE Mark Label (Left), WEEE Label (Right)

6.) CISPR Label

7.) Grounding reliability Label

8.) Voltage Range Indication and Power indication Label

9.) Standard LCD Arm & flexible LCD Arm Option Label & Mercury Label

10.)LCD Arm Rotation Label

Section 1-3 - Safety Considerations 1-15

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE 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.

DANGER

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT
IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.

WARNINGWARNING

WARNINGWARNING

EXPLOSION WARNING

DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE.
OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT
CONSTITUTES A DEFINITE SAFETY HAZARD.

DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT
BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT

INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION
OF THE EQUIPMENT.

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

Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the electrical Mains
plug.

1-16 Section 1-3 - Safety Considerations

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE 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™ P5 unit conforms to all applicable conducted and radiated emission limits and to immunity
from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line transient
requirements.

For applicable standards refer to the Safety Chapter in the Basic User Manual.

NOTE: For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh, clamps, are in

good condition, installed tightly without skew or stress. Proper installation following all
comments noted in this service manual is required in order to achieve full EMC performance.

1-4-3 Electrostatic Discharge (ESD) Prevention

WARNINGWARNING

DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING
THE NECESSARY ESD PRECAUTIONS:

1.ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP, TO THE ADVISED

ESD CONNECTION POINT LOCATED ON THE REAR OF THE SCANNER (TO THE
RIGHT OF THE POWER CONNECTOR).

2.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC

SENSITIVE EQUIPMENT.

Section 1-4 - EMC, EMI, and ESD 1-17

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

Section 1-5 Customer Assistance

1-5-1 Contact Information

If this equipment does not work as indicated in this service manual or in the User Manual, or if you
require additional assistance, please contact the local distributor or appropriate support resource, as
listed below.

Prepare the following information before you call:

- System ID serial number.

- Software version.

Table 1-7 Phone Numbers for Customer Assistance

Location Phone Number

1-800–437–1171
USA/ Canada
GE Medical Systems
Ultrasound Service Engineering
4855 W. Electric Avenue
Milwaukee, WI 53219

1-800-682-5327
Customer Answer Center

1-262-524-5698

Fax: [phone]

Latin America
GE Medical Systems
Ultrasound Service Engineering
4855 W. Electric Avenue
Milwaukee, WI 53219

Customer Answer Center

Europe
GE Ultraschall Deutschland GmbH& Co. KG
BeethovenstraBe 239
Postfach 11 05 60, D-42665 Solingen
Germany

Asia (Singapore/ Japan)
GE Ultrasound Asia
Service Department - Ultrasound
298 Tiong Bahru Road #15-01/06
Central Plaza
Singapore 169730

1-262-524-5300

1-262-524-5698

Fax: [phone]

Tel: [phone]

[phone]

Fax: [phone]

Tel: [phone]

[phone]

Fax: [phone]

[phone]

1-18 Section 1-5 - Customer Assistance

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

1-5-2 System Manufacturer

Table 1-8 System Manufacturer

Manufacturer FAX Number

GE Ultrasound Korea
462-120 65-1, Sangdaewon-dong, Joong-won-Gu,
Seongnam-Si, Gyeonggi-do,
Korea

82-31-740-6436

Section 1-5 - Customer Assistance 1-19

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SEVICE MANUAL

1-20 Section 1-5 - Customer Assistance

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Chapter 2
Pre-Installation

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 a LOGIQ™ P5/
A5/A5Pro. Included are descriptions of the facility and electrical needs to be met by the purchaser of the
unit. A checklist is also provided at the end of this section to help determine whether the proper planning
and preparation is accomplished before the actual equipment installation is scheduled.

Table 2-1 Contents in Chapter 2

Section Description Page Number

2-1

2-2

2-3

Overview

General Console Requirements

Facility Needs

2-1

2-2

2-7

Section 2-1 - Overview 2 - 1

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 2-2 General Console Requirements

2-2-1 Console Environmental Requirements

Table 2-2 Environmental Requirements for LOGIQ™ P5/A5/A5Pro Scanners

Operational Storage Transport

Temperature

Humidity

Pressure

o

10 - 30 oC
50 - 104

30 - 85%
non-condensing

700 - 1060hPa 700 - 1060hPa 700 - 1060hPa

o

F

-10 - 60
14 - 140

30 - 90%
non-condensing

C

o

F

o

-40 - 60

-40 - 140

30 - 90%
non-condensing

Table 2-3 Environmental Requirements for an Ultrasound Room

Item Values

Power Source

Current Rating

Radiation Shielding

Temperature

Humidity

Heat Dissipation

Floor Landing

Floor Condition

Weight

refer to Table 2-4 on page 2-3.

7.5A (100V-120V); 3.5A (220-240V)

NONE REQUIRED for ULTRASOUND ENERGY

20-26 DEG. C (68-79 DEG F) for PATIENT COMFORT

50% to 70% for PATIENT COMFORT

2000 BTU/Hr.

Approximately 680 - 800 kg/m2 without Accessories

Gradient: WITHIN 5 degrees

75 kg (165lbs) without Accessories

C

o

F

2-2-1-1 Cooling

The cooling requirement for the LOGIQ™ P5/A5/A5Pro is 2000 BTU/hr. This figure does not include
cooling needed for lights, people, or other equipment in the room. Each person in the room places an
additional 300 BTU/hr. demand on the cooling system.

2-2-1-2 Lighting

Bright light is needed for system installation, updates and repairs. However, operator and patient
comfort may be optimized if the room light is subdued and indirect. Therefore a combination lighting
system (dim/bright) is recommended. Keep in mind that lighting controls and diameters can be a source
of EMI which could degrade image quality. These controls should be selected to minimize possible
interface.

2 - 2 Section 2-2 - General Console Requirements

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

2-2-2 Electrical Requirements

NOTE: GE Medical Systems requires a dedicated power and ground for the proper operation of its

Ultrasound equipment. This dedicated power shall originate at the last distribution panel before
the system.

Sites with a mains power system with defined Neutral and Live:

The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size ground wire from the distribution panel to the Ultrasound outlet.

Sites with a mains power system without a defined Neutral:

The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full
size ground wire from the distribution panel to the Ultrasound outlet.

NOTE: Please note that image artifacts can occur, if at any time within the facility, the ground from the

main facility's incoming power source to the Ultrasound unit is only a conduit.

2-2-2-1 LOGIQ™ P5/A5/A5Pro 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 2-4 Electrical Specifications for LOGIQ™ P5/A5/A5Pro

PARAMETER AREA LIMITS

Voltage Range

Power All applications MAX. 750 VA

Line Frequency All applications 50/60Hz (±2Hz)

Power Transients All applications

Decaying Oscillation All applications

2-2-2-2 Inrush Current

Inrush Current is not a factor to consider due to the inrush current limiting properties of the power
supplies.

2-2-2-3 Site Circuit Breaker

It is recommended that the branch circuit breaker for the machine be ready accessible.

100~120V 100~120 VAC ±10% (90-132 VAC)

220~240V 220-240 VAC ±10% (198-264 VAC)

Less than 25% of nominal peak voltage
for less than 1 millisecond for any type of
transient, including line frequency,
synchronous, asynchronous, or
aperiodic transients.

Less than 15% of peak voltage for less
than 1 millisecond.

CAUTION

POWER OUTAGE MAY OCCURE.
The LOGIQ™ P5/A5/A5Pro 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.

Section 2-2 - General Console Requirements 2 - 3

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

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.

2-2-2-5 Unit Power Plug

If the unit arrives without the power plug, or with the wrong plug, you must contact your GE dealer or
the installation engineer must supply what is locally required.

2-2-2-6 Power Stability Requirements

Voltage drop-out

Max 10 ms.

Power Transients

(All applications)
Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including
line frequency, synchronous, asynchronous, or aperiodic transients.

2 - 4 Section 2-2 - General Console Requirements

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

2-2-3 EMI Limitations

Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies,
magnetic fields, and transient in the air wiring. They also generate EMI. The LOGIQ™ P5/A5/A5Pro
complies with limits as stated on the EMC label. However there is no guarantee that interface will not
occur in a particular installation.

Possible EMI sources should be identified before the unit is installed.

Electrical and electronic equipment may produce EMI unintentionally as the result of defect.

These sources include:

• medical lasers,

• scanners,

• cauterizing guns,

•computers,

•monitors,

• fans,

• gel warmers,

• microwave ovens,

• light dimmers,

• portable phones.
The presence of broadcast station or broadcast van may also cause interference. See for EMI

Prevention tips.

See Table 2-5 for EMI Prevention tips.

Table 2-5 EMI Prevention/abatement

EMI Rule Details

Keep the unit at least 5 meters or 15 feet away from other EMI sources. Special shielding

Be aware of RF sources

Ground the unit

Replace all screws, RF
gaskets, covers, cores

Replace broken RF gaskets

Do not place labels where RF
gaskets touch metal

Use GE specified harnesses
and peripherals

Take care with cellular phones Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.

Properly dress peripheral
cables

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.

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.

Section 2-2 - General Console Requirements 2 - 5

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

2-2-4 Scan Probe Environmental Requirements

Operation:10° to 30° C

Storage:--10° to 60° C

NOTE: Temperature in degrees C. Conversion to Degrees F = (Degrees C * 9/5) + 32).

NOTICE

SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES
OF -10 TO + 60 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE
PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.

2 - 6 Section 2-2 - General Console Requirements

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

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.

Section 2-3 - Facility Needs 2 - 7

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

2-3-2 Required Features

NOTE: GE Medical Systems requires a dedicated power and ground for the proper operation of its

Ultrasound equipment. This dedicated power shall originate at the last distribution panel before
the system.

Sites with a mains power system with defined Neutral and Live:

The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size ground wire from the distribution panel to the Ultrasound outlet.

Sites with a mains power system without a defined Neutral:

The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full
size ground wire from the distribution panel to the Ultrasound outlet.

Please note that image artifacts can occur, if at any time within the facility, the ground from the main
facility's incoming power source to the Ultrasound unit is only a conduit.

• Dedicated single branch power outlet of adequate amperage meeting all local and national codes
which is located less than 2.5 m (8 ft.) from the unit’s proposed location

• Door opening is at least 76 cm (30 in) wide

• Proposed location for unit is at least 0.3 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.

NOTE: The LOGIQ™ P5/A5/A5Pro has two outlets outside the unit. Both are for on board peripherals.

• Clean and protected space to store transducers (in their cases or on a rack)

• Material to safely clean probes (done with a plastic container, never metal)

2-3-3 Desirable Features

• Door is at least 92 cm (3 ft.) wide

• Circuit breaker for dedicated power outlet is easily accessible

• Sink with hot and cold water

• Receptacle for bio–hazardous waste, like used probe sheaths

• Emergency oxygen supply

• Storage for linens and equipment

• Nearby waiting room, lavatory, and dressing room

• Dual level lighting (bright and dim)

• Lockable cabinet ordered by GE for its software and proprietary manuals.

2 - 8 Section 2-3 - Facility Needs

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

2-3-4 Recommended and Alternate Ultrasound Room Layout

Recommended standard floor plan and a minimal floor plan for ultrasound equipment:

DEDICATED ALALOG TELEPHONE
LINE FOR CONNECTION TO INSITE

ROOM,

PROCESSING

FILM

DEDICATED

POWER

RECEPTACLE

18 IN.

(46 CM)

CONSOLE

LINEN SUPPLY

FILM VIEWER

FILM SUPPLIES

FILE

CABINET

SECRETARYS OR
DOCTOR’S DESK

SINK

FILM VIEWER

COUNTER TOP

COUNTER

TOP

SINK

SUCTION LINE

EMERGECY
OXYGEN

OVERHEAD
LIGHTS DIMMER

A 14 by 17 foot Recommended Floor Plan

LINEN SUPPLY

PROBES/SUPPLIES

FOOT

SW

STOOL

EXAMINATION

TABLE

76 IN.

(193 CM)

24 IN.

(61 CM)

PATIENT

TOILET

FACILITY

DOOR

42 IN.

(107 CM)

Scale : Each square equals one square foot

STOOL

EXAMINARION

DOOR

30 IN.

(76 CM)

24 IN.
(61 CM)

An 8 by 10 foot Minimal Floor Plan

Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT

EXTERNAL

PERIPHERALS

DEDICATED POWER

FOOT

SW

TABLE

LOGIQ 5

CONSOLE

76 IN.
(193 CM)

OUTLETS

DEDICATED ANALOG TELEPHONE
LINE FOR CONNECTION TO INSITE

GE CABINET
FOT SOFTWARE
AND MANUALS

Section 2-3 - Facility Needs 2 - 9

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

2-3-5 Networking Pre-installation Requirements

2-3-5-1 Purpose of DICOM Network Function

DICOM services provide the operator with clinically useful features for moving images and patient
information over a hospital network. Examples of DICOM services include the transfer of images to
workstations for viewing or transferring images to remote printers. As an added benefit, transferring
images in this manner 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.

2-3-5-2 DICOM Option Pre-installation Requirements

To configure the LOGIQ™ P5/A5/A5Pro 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™ P5/A5/A5Pro.

• 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™ P5/A5/A5Pro for DICOM APPLICATION INFORMATION. A field for the make

(manufacturer) and the revision of the device, is also included. This information may be useful for
solving errors.

2 - 10 Section 2-3 - Facility Needs

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

2-3-5-2 DICOM Option Pre-installation Requirements (cont’d)

.

.

LOGIQ™

Host Name

Local Port

IP Address

..

.

AE Title

ROUTING INFORMATION

ROUTER1
ROUTER2
ROUTER3

DICOM APPLICATION INFORMATION

NAME

Store 1

Store 2

Store 3

Store 4

Destination
IP Addresses

...
...
...

MAKE/REVISION IP ADDRESSES PORTAE TITLE

Net Mask

Default

...

GATEWAY IP Addresses

...

...
...
...

...

...

...

...

Store 5

Store 6

Worklist

Storage
Commit

MPPS

...

...

...

...

...

Figure 2-2 Worksheet for DICOM Network Information

Section 2-3 - Facility Needs 2 - 11

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

This page was intentionally left blank.

2 - 12 Section 2-3 - Facility Needs

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Chapter 3
Installation

Section 3-1 Overview

3-1-1 Purpose of Chapter 3

This chapter contains information needed to install the unit. Included are references to a procedure that
describes how to receive and unpack the equipment and how to file a damage or loss claim.
How to prepare the facility and unit of the actual installation, and how to check and test the unit, probes,
and external peripherals for electrical safety are included in this procedure. Also included in this section
are guidelines for transporting the unit to a new site.

Table 3-1 Contents in Chapter 3

Section Description Page Number

3-1 Overview 3-1

3-2 Installation Reminders 3-2

3-3 Receiving and Unpacking the Equipment 3-4

3-4 Preparing for Installation 3-10

3-5 Completing the Installation 3-11

3-6 System Configuration 3-16

3-7 Available Probes 3-23

3-8 Software/Option Configuration 3-23

3-9 Connectivity Installation Worksheet 3-24

3-10 Insite IP Address Configuration 3-25

3-11 Loading Base System Software 3-25

3-12 Warnings 3-25

3-13 Paperwork 3-26

Section 3-1 - Overview 3-1

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-2 Installation Reminders

3-2-1 Average Installation Time

Table 3-2 Average Installation Time

Description Average Installation Time Comments

Unpacking the scanner

Scanner wo/options

DICOM Option

InSite Option

0.5 hour

0.5 hour

0.5 hour

0.5 hour

Dependant on the configuration that is required

Dependant on the amount of configuration

The LOGIQ™ P5/A5/A5Pro has been designed to be installed and checked out by an experienced
service technician in approximately four hours. LOGIQ™ P5/A5/A5Pro consoles with optional
equipment may take slightly longer.

3-2-2 Installation Warnings

1.) Since the LOGIQ™ P5/A5/A5Pro weighs approximately 75 kg.(165 lb.) without options, preferably

two people should unpack it. Two people are also preferable for installing any additional bulky items.

2.) There are no operator serviceable components. To prevent shock, do not remove any covers or
panels. Should problems or malfunctions occur, unplug the power cord. Only qualified service
personnel should carry out servicing and troubleshooting.

NOTE: For information regarding packing labels, refer to LABELS ON PACKAGE.

3.) After being transported, the unit may be very cold or hot. If this is the case, allow the unit to
acclimate before you turn it on. It requires one hour for each 2.5°C increment 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 96 86 77 68 59 50 41 32 23 14 5 -4 -13 -22 -31 -40

°F

864200000002468101214161820

hrs

3-2 Section 3-1 - Overview

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-2-3 Safety Reminders

DANGER

CAUTION

CAUTION

CAUTION

CAUTION

CAUTION

CAUTION

CAUTION

WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE
AC GROUND LINE (I.E., METER’S GROUND S WIT CH I S OPEN), 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.

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™ P5/
A5/A5Pro and kept near the unit for quick reference.

CAUTION

ACOUSTIC OUTPUT HAZARD
Although the ultrasound energy transmitted from the LOGIQ™ P5/A5/A5Pro probe is within
FDA limits, avoid unnecessary exposure. Ultrasound energy can produce heat and
mechanical damage.

Figure 3-1 Environmental Labels

Section 3-1 - Overview 3-3

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

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

Do not lift the unit by the Keyboard. Equipment damage may result.

The crate with the LOGIQ™ P5/A5/A5Pro weighs approximately 75 kg. (165 lb.) Be prepared for
a sudden shift of weight as the unit is removed from its base (pallet)

1.) Cut the three PLASTIC BANDs.

Plastic Bands

Figure 3-2 Cutting the Plastic Bands.

3-4 Section 3-1 - Overview

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-3 Receiving and Unpacking the Equipment (cont’d)

2.) Lift the TOP COVER up and off.

Top Cover

Figure 3-3 Removing the top Cover

Section 3-1 - Overview 3-5

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-3 Receiving and Unpacking the Equipment (cont’d)

3.) Remove the Top Plate up and off..

Top Plate

Figure 3-4 Removing the Top Plate

3-6 Section 3-1 - Overview

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-3 Receiving and Unpacking the Equipment (cont’d)

4.) Remove the three PLASTIC JOINTs from the OUTER SLEEVE.

5.) Remove the OUTER SLEEVE.

Plastic Joint

Figure 3-5 Removing Plastic Joints and Sleeves

Outer Sleeve

Palette Assy

Section 3-1 - Overview 3-7

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-3 Receiving and Unpacking the Equipment (cont’d)

6.) Remove the MONITOR SUPPORTER and Option Box.

7.) Remove the PLASTIC BAG.

8.) Unlock the front caster and carefully put the console off the PALETTE.

Monitor Pad

Figure 3-6 Moving the LOGIQ™ P5/A5/A5Pro from the crate

3-8 Section 3-1 - Overview

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-3-1 Moving into Position

CAUTION

CAUTION

Do not lift the unit by the Keyboard.
Do not tilt the unit more than 5 degrees to avoid tipping it over.
To avoid injury by tipping over. Set the monitor to the lowest position before moving.

Equipment Damage Possibility. Lifting the console by holding covers may damage the covers.
Do not lift the console by holding any covers.

In general, a single adult can move the LOGIQ™ P5/A5/A5Pro 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™ P5/A5/A5Pro is a compact and mobile machine, two people should move it over
rough surfaces or up and down grades.

3-3-2 Adjusting System Clock

Set the system clock for the LOGIQ™ P5/A5/A5Pro to the local time. For procedure of adjusting the
system clock, refer to section 3-6-1-1 on page 16.

Fill out proper customer Information the Product Locator Installation Card. Mail this Installation Card
“Product Locator” to the address corresponding to your pole.

3-3-3 Product Locator Installation Card

NOTE: The Product Locator Installation Card shown may not be same as the provided Product Locator

card.

Figure 3-7 Product Locator Installation Card

Section 3-1 - Overview 3-9

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-4 Preparing for Installation

3-4-1 Verify Customer Order

Compare items received by the customer to that which is listed on the delivery order. Report any items
that are missing, back ordered or damaged.

3-4-2 Physical Inspection

3-4-2-1 System Voltage Settings

Verify that the scanner is set to the correct voltage.
The Voltage settings for the LOGIQ™ P5/A5/A5Pro Scanner is found on a label to the right of the Power
switch and External I/O, on the rear of the system.

WARNINGWARNING

Connecting a LOGIQ™ P5/A5/A5Pro scanner to the wrong voltage level will most likely
destroy the scanner.

3-4-2-2 Video Formats

Check that the video format for VCR playback 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.

3-10 Section 3-4 - Preparing for Installation

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-5Completing the Installation

3-5-1 Power On/Boot Up

NOTE: After turning off the system, wait at least ten seconds before turning it on again. The system

may not be able to boot if power is recycled too quickly.

3-5-1-1 Scanner Power On

1.) Connect the Main Power Cable at the rear of the System.

WARNINGWARNING

Protective earth must be taken when connecting AC power cable (200V) without its plug
to wall outlet.

2.) Connect the Main Power cable to an appropriate mains power outlet.

3.) Switch ON the Main Circuit Breaker at the rear of the System.

Figure 3-8 Circuit Breaker

When power is applied to the Scanner, and the Rear Circuit breaker is turned ON, Power is distributed
to the DC Power supply unit and power control assy in the AC power assy. When the Power ON/OFF
key is pressed once, the DC power supply is enabled and feed each DC power to board assemblies.
and system run the software.

4.) Press the ON/OFF

key at the front of the System once.

Section 3-4 - Preparing for Installation 3-11

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-5-1-1 Scanner Power On (cont’d)

Figure 3-9 Power On/Off Switch Location

3-12 Section 3-4 - Preparing for Installation

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-5-1-2 Power Up Sequence

1.) The Start Up Screen will be shown on the Monitor display when the system is turned ON.

Figure 3-10 Start Up Screen Display

2.) After initialization is complete, all lighted buttons on the Control Panel light and the default B-Mode
screen or Patient screen (no probes are connected) is displayed on the monitor display.

3-5-1-3 Power Up Sequence

NOTE: To enter the Maintenance Mode, select Maintenance button.

NOTE: Figure 3-11 on page 3-13 displays when Service Dongle inserted in Rear Panel.

Figure 3-11 Start Application Window

NOTE: Start is selected automatically when it time out.

NOTE: In case the system is locked with task manager, use arirang as a password to unlock the

system.

Section 3-4 - Preparing for Installation 3-13

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-5-2 Power Off/ Shutdown

NOTE: After turning off a system, wait at least ten seconds before turning it on again. The system may

not be able to boot if power is recycled too quickly.

3-5-2-1 Power Shutdown

1.) Press the ON/OFF

2.) Click the shutdown icon in the shutdown dialog box and wait until the system shutdown.

3.) Switch OFF the Main Circuit Breaker at the rear of the system refer to Figure 3-8 on page 3-11 .

4.) Disconnect the Main Power Cable is necessary. For example : Relocating the scanner.

key at the front of the System. refer to Figure 3-9 on page 3-12 .

3-14 Section 3-4 - Preparing for Installation

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-5-3 Transducer Connection

1.) Connect a transducer to one of the three rightmost transducer receptacle as follows:

A.) Ensure that the transducer twist lock lever to the horizontal position.
B.) Insert the transducer connector on the receptacle guide pin until it touches the receptacle

mating surface.

C.) Twist the transducer twist lock lever to horizontal position to lock it in place. Twist the lever

to the vertical position to disconnect the transducer.

NOTE: It is not necessary to turn OFF power to connect or disconnect a transducer.

Section 3-4 - Preparing for Installation 3-15

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-6 System Configuration

3-6-1 System Specifications

3-6-1-1 System Settings

Table 3-1 System Configuration

Configuration Category Description

Enables the user or service personnel to set the

Settings

1.) Press Insert key on the A/N keyboard to enter the utility menu.

2.) Select Utility > System > General.

3.) Set the Hospital name, Department, Date and Time, Language, and Units.

date, time, unit, language, basic information about
the organization such as the institution name and
department.

Figure 3-12 Setting Display

4.) Click on Exit to terminate the utility function.

3-16 Section 3-4 - Preparing for Installation

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-6-1-2 Physical Dimensions

The physical dimensions of the LOGIQ™ P5/A5/A5Pro unit are summarized in Table 3-2 on page 3-17 .
The Size of LOGIQ™ P5/A5/A5Pro, with monitor and peripherals

Table 3-2 Physical Dimensions of LOGIQ™ P5/A5/A5Pro

Height Width Depth Unit

135/141 43.0 64.0 cm

53.15 - 55.50 16.97 25.2 inches

WEIGHT : 75Kg (165bs)

including Monitor

NOTE : Length is in mm

Variation +/- 10%

430

1350 / 1410

640

840 / 900

Figure 3-13 Overall Dimensions

Section 3-4 - Preparing for Installation 3-17

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-6-1-3 Weight without Monitor and Peripherals

Table 3-3 Weight of LOGIQ™ P5/A5/A5Pro With Monitor and Without Other Peripherals

Model Weight [kg] Weight [lbs]

LOGIQ™ P5/A5/

A5Pro

Approximately 75 Approximately 165

3-6-1-4 Acoustic Noise Output:

Less than 70dB (A) according to DIN 45635 - 19 - 01 - KL2.

3-6-2 Electrical Specifications

Table 3-4 Electrical Specifications for LOGIQ™ P5/A5/A5Pro

System Voltage Current Frequency

1 110 ~ 120 VAC 7 ~ 9A 50~60Hz

2 220 ~ 240 VAC 3.5 ~ 4.5A 50~60Hz

3-6-3 On-Board Optional Peripherals

Table 3-5 List of Recording Devices

Device Manufacturer Model Video Signal

B/W Video Printer SONY UP-D897MD N/A (* USB Interface)

Video Cassette Recorder Mistubishi

DVD Video Recorder Panasonic LQ-MD800 NTSC/PAL (USB Interface)

A6 Color Video Printer SONY UP-D23MD N/A (* USB Interface)

HS-MD3000U
HS-MD3000E

NTSC/PAL (USB Interface)

See each option installation instructions for installation and connection procedures.

NOTE: There are no external peripheral options for the LOGIQ™ P5/A5/A5Pro.

3-18 Section 3-4 - Preparing for Installation

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-6-4 External I/O Connector Panel

Located on the rear panel are video input and output connectors, audio input and output, USB,
footswitch connector power connector and control connections for VCR or DVD Recorder, printer, and
service tools.

This section indicates the pin assignment for each connector.

Figure 3-14 Rear Connector Panel

NOTE: Each outer (case) ground line of peripheral/accessory connectors are protectively grounded.

Signal ground lines are not isolated, except the Service port (3). All of signal lines (include signal
GND) of the Service port are isolated.

Section 3-4 - Preparing for Installation 3-19

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-6-4-1 External I/O Pin Outs

Pin No. Signal Pin No. Signal

1RED9 N/A

2 GREEN 10 SGND

3BLUE11 N/A

4N/A12N/A

5 GND 13 HSYNC

6 RGND 14 VSYNC

7 GGND 15 N/A

8BGND

Table 3-6 Pin Assignments of DB15 connector for External VGA

Pin No. Signal Pin No. Signal

1+5 VDC3DATA +

2 DATA - 4 GND

Table 3-7 Pin Assignments of USB

Pin No. Signal Pin No. Signal

1TX+5 NC

2 TX- 6 RX-

3RX+7 NC

4NC8NC

Table 3-8 Pin Assignments of Ethernet

3-20 Section 3-4 - Preparing for Installation

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-6-5 Video Specification

Video specifications may be needed to be able to connect the VCR or DVD Video Recorder to the
LOGIQ™ P5/A5/A5Pro.

Table 3-9 Video Specifications

640x480

Timing Parameter NTSC PAL

Horizontal Rate [kHz] 60.02 31.25 31.47 37.88 46.88 48.36

Horizontal Period [µs] 16.66 32.00 31.78 26.40 21.33 20.68

Pixel Clock [MHz] 78.75 29.50 24.55 40.00 49.50 65.00

H Blank Width [µs] 3.66 5.97 5.70 6.40 5.17 4.92

H Sync Width [µs] 1.22 2.34 2.36 3.20 1.62 2.09

H Front Porch [µs] 0.20 0.75 0.73 1.00 0.32 0.37

Active Horizontal Period [µs] 13.00 26.03 26.07 20.00 16.16 15.75

Vertical Rate [Hz] 75.03 50.00 59.94 60.32 75.00 60.00

Vertical Period [ms] 13.33 20.00 16.68 16.58 13.33 16.67

V Sync Width [lines=ms] 32=0.53 49=1.57 45=1.43 28=0.74 25=0.53 38=0.79

V Front Porch [lines=µs] 3=50.00 5=160.00 6=190.70 4=105.60 3=64.00 6=124.10

Equalization Gate [lines=µs] 1=16.66 5=160.0 6=190.7 1=26.4 1=21.3 3=62.00

Lines: Field/Frame 800 625/625 525/525 628 625 806

Active Lines/Frame 768 576 480 600 600 768

60Hz

800x600

60Hz

800x600

75Hz

1024x768

60Hz

Section 3-4 - Preparing for Installation 3-21

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

3-6-6 Setting VCR (Mitsubishi MD3000) USB Interface

1.) Turn off the Power of the VCR.

2.) Open the rear panel of the VCR.

3.) Set dip switches. Off 1~6 pins, On 7 pin, and Off 8 pin.

NOTE: 7 Pin ON = USB Interface, OFF = RS232C Interface.

Figure 3-15 Setting VCR USB Interface

3-22 Section 3-4 - Preparing for Installation

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-7 Available Probes

See Specifications in the LOGIQ™ P5/A5/A5Pro User Manual for probes and intended use.

See Chapter 9, for part numbers to be used when ordering new or replacement probes.

Section 3-8 Software/Option Configuration

refer to the LOGIQ™ P5/A5/A5Pro 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™ P5/A5/A5Pro Basic User
Manual, Chapter 16, Customizing Your System.

For information on configuring DICOM Connectivity, refer to the LOGIQ™ P5/A5/A5Pro Basic User
Manual, Chapter 16, Customizing Your System.

Section 3-8 - Software/Option Configuration 3-23

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-9 Connectivity Installation Worksheet

Site System Information

Site:

Dept:

LOGIQ SN:

CONTACT INFORMATION

Name

TCP/IP Settings

Name - AE Title:

Type:

Title

Floor:

Room:

REV:

Phone

Comments:

E-Mail Address

IP Settings

IP Address:

Subnet Mask:

Default Gateway:

Services (Destination Devices)

Device Type

1
2
3
4
5
6
7
8
9
10
11
12

Manufacturer

Name

Remote Archive Setup

Remote Archive IP:

Remote Archive Name:

IP Address

Port

AE Title

3-24 Section 3-8 - Software/Option Configuration

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-10 Insite IP Address Configuration

This information needed to facilitate the OnLine Center engineers in connecting to the system is found
in the InSite Installation Manual.

Section 3-11 Loading Base System Software

3-11-1 Loading Base system Software

For more information on loading base system software, refer to Chapter 8.

Section 3-12 Warnings

3-12-1 Warnings

3-12-1-1 USB HDD

External USB type Hard drive may be used to back up the data. But not all kinds of USB type can
be supported.

Never use USB types which require additional power source.

3-12-1-2 Starting Echoloader in Maintenance mode

If Echoloader never started once, starting Echoloader in the maintenance mode will not work. In
other words, in order to be able to start Echoloader in maintenace mode, Echoloader should have
been started at least once.

Section 3-11 - Loading Base System Software 3-25

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 3-13 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.

3-13-1 Product Locator Installation

NOTE: The Product Locator Installation Card shown may not be same as the provided Product Locator

card.

Figure 3-16 Product Locator Installation Card

3-13-2 User Manual(s)

Check that the correct User Manual(s) for the system and software revision, is included with the
installation. Specific language versions of the User Manual may also be available. Check with your GE
Sales Representative for availability.

3-13-2-1 Reference off-board peripherals and options

None.

3-26 Section 3-12 - Warnings

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Chapter 4
Functional Checks

Section 4-1 Overview

4-1-1 Purpose of Chapter 4

This chapter provides procedures for quickly checking major functions of the LOGIQ™ P5/A5/A5Pro
scanner diagnostics by using the built-in service software, and power supply adjustments.

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 4-25

4-5 Peripheral Checks 4-26

4-6 Monitor Function Checks 4-27

4-7 Keyboard Function Checks 4-29

4-8 Mechanical Function Checks 4-34

4-9 Board Function Checks 4-41

4-10 Site Log 4-54

Section 4-2 Required Equipment

• An empty (blank) DVD-R or CD-R Disk.

• At least one transducer.

Section 4-1 - Overview 4 - 1

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

Section 4-3 General Procedure

CAUTION

SYSTEM REQUIRES ALL COVERS
Operate this unit only when all board covers and frame panels are securely in place. The
covers are required for safe operation, good system performance and cooling purposes.

NOTICE

Lockout/Tagout Requirements (For USA only)
Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the Power Cable

on the system.

TAG

&

LOCKOUT

Date

Signed

4-3-1 Power On/Boot Up

NOTE: After turning off the system, wait at least ten seconds before turning it on again. The system

may not be able to boot if power is recycled too quickly.

4-3-1-1 Scanner Power On

1.) Connect the Main Power cable to an appropriate mains power outlet.

2.) Switch ON the Main Circuit Breaker at the rear of the System.

Figure 4-1 Circuit Breaker

When power is applied to the Scanner, and the Rear Circuit breaker is turned ON, Power is distributed
to the DC Power supply unit and power control assy in the AC power assy. When the Power ON/OFF
key is pressed once, the DC power supply is enabled and feed each DC power to board assemblies.
and system run the software

4 - 2 Section 4-2 - Required Equipment

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-1-1 Scanner Power On (cont’d)

3.) Press the ON/OFF

key at the front of the System once.

Figure 4-2 Power On/Off Standby Switch Location

Section 4-2 - Required Equipment 4 - 3

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-2 Power Off / Shutdown

NOTE: After turning off a system, wait at least ten seconds before turning it on again. The system may not be

able to boot if power is recycled too quickly.

4-3-2-1 Scanner Shutdown

1.) Press the On/Off Key at the front of the System once to display the SYSTEM - EXIT menu.

2.) Select Shutdown from the SYSTEM - EXIT menu.

Figure 4-3 System Exit Menu for Power Down

4-3-2-2 Switch off the System

1.) Switch OFF the Circuit Breaker at the back of the scanner.

2.) Unplug the power cord if necessary. For example : Servicing or relocating the scanner.

4 - 4 Section 4-2 - Required Equipment

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-3 System Features

4-3-3-1 Control Panel for LOGIQ™ P5

10

1

2

3

9

4

5

Figure 4-4 Control Panel Tour LOGIQ™ P5

1.) Power on/off switch

2.) Alpha Numeric key

3.) Patient Key

4.) TGC

5.) Track Ball

6.) Function Select key

7.) Freeze Key

8.) Gain Knob

9.) User Define Key

8

7

6

Section 4-2 - Required Equipment 4 - 5

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-3-2 Control Panel for LOGIQ™ A5/LOGIQ™ A5Pro

Figure 4-5 Control Panel Tour LOGIQ™ A5/ LOGIQ™ A5Pro

1.) Power on/off switch

2.) Alpha Numeric key

3.) Patient Key

4.) TGC

5.) Track Ball

6.) Function Select key

7.) Freeze Key

8.) Gain Knob

9.) User Define Key

NOTE: If the LOGIQ™ A5 have been upgrade with Color Upgrade kit, LOGIQ™ A5 have same keyboard as

LOGIQ™ P5.

NOTE: LOGIQ™ A5Pro has the same control panel of LOGIQ™ A5, but PW Mode button is not

enabled.

4 - 6 Section 4-2 - Required Equipment

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-3-3 Monitor Display for LOGIQ™ P5

12

4

5

6

7

8

9

10

11

3

12

22

13

14

15

16

17

18

19 20

Figure 4-6 P5 Monitor Display Tour

1. Institution/Hospital Name, Date, Time,

Operator Identification.

2. Patient Name, Patient Identification.

3. Power Output Readout

4. GE Symbol: Probe Orientation Marker.

5. Image Preview.

6. Gray/Color Bar.

7. Cine Gauge.

8. Measurement Summary Window.

9. Image.

10. Measurement Calipers.

11. Measurement Results Window.

12. Probe Identifier. Exam Preset.

21

13. Imaging Parameters by Mode.

14. Focal Zone Indicator.

15. TGC.

16. Body Pattern.

17. Depth Scale.

18. Top Menu

19. Caps Lock: Lit when On.

20. Service Interface icon (wrench), iLinq
icon, and system messages display
(not shown on image)

21. Trackball Functionality Status: Scroll,
M&A (Measurement and Analysis),
Position, Size, Scan Area Width and
Tilt.

22. Sub Menu

Section 4-2 - Required Equipment 4 - 7

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-4 System B/M-Mode Checks

For a basic functional check of the system’s different modes, the Quick Guide will familiarize you with
image optimization for B-Mode, M-Mode, Color Flow, and Doppler.

Table 4-2 B/M-Mode Functions

Power Output (Acoustic Power)

Dynamic Range

Focus Number and Position

Rejection

Edge Enhance

Frame Average

Colorize

Gray Map

Rotation (Up/Down) Rotates the image by selecting the value from the pop up menu.

Optimizes image quality and allows user to reduce beam
intensity. 2% increments between 0-100%.

Dynamic Range controls how echo intensities are converted to
shades of gray, thereby increasing the adjustable range of
contrast.

Increases the number of transmit focal zones or moves the
focal zone(s) so that you can tighten up the beam for a specific
area. A graphic caret corresponding to the focal zone
position(s) appears on the right edge of the image.

Selects a level below which echoes will not be amplified (an
echo must have a certain minimum amplitude before it will be
processed).

Edge Enhance brings out subtle tissue differences and
boundaries by enhancing the gray scale differences
corresponding to the edges of structures. Adjustments to M
Mode's edge enhancement affects the M Mode only.

Temporal filter that averages frames together. This has the
effect of presenting a smoother, softer image.

Enables gray scale image colorization. To deactivate, reselect
a Gray Map.

Determines how the echo intensity levels received are
presented as shades of gray.

Multi Frequency mode lets you

Frequency

Frame Rate/Resolution

B Flow

Sensitivity/PRI Adjusts the sample rate for the flow signal.

Background On/Off

Sweep Speed Changes the speed at which the timeline is swept.

downshift to the probe's next lower
frequency or shift up to a higher
frequency.

Optimizes B Mode frame rate or spatial resolution for the best
possible image.

Provides intuitive representation of non-quantitative
hemodynamics in vascular structures.

Background On lets you view the anatomy roadmap;
Background Off lets you view just flow information.

4 - 8 Section 4-2 - Required Equipment

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-5 System CFM and PWD Checks

Table 4-3 CFM and PWD Functions

Baseline

PRF/Wall Filter

Angle Correct

Threshold

Map

Invert

Packet Size

Quick Angle Correct Quickly adjusts the angle by 60 degrees

Doppler Display Formats

Adjusts the baseline to accommodate faster or slower blood
flows to eliminate aliasing.

Velocity scale determines pulse repetition frequency. If the
sample volume gate range exceeds single gate PRF capability,
the system automatically switches to high PRF mode. Multiple
gates appear, and HPRF is indicated on the display.

Estimates the flow velocity in a direction at an angle to the
Doppler vector by computing the angle between the Doppler
vector and the flow to be measured

Threshold assigns the gray scale level at which color
information stops.

Allows a specific color map to be selected. After a selection has
been made, the color bar displays the resultant map.

Allows blood flow to be viewed from a different perspective, i.e.
red away (negative velocities) and blue toward (positive
velocities). The real-time or frozen image can be inverted.

Controls the number of samples gathered for a single color flow
vector.

Display layout can be preset to have B-Mode and Time-motion
side-by-side or over-under.

In the side-by-side layout, there are three display alternatives
defined: equal priority, time-motion priority or time-motion with
B-Mode reference.

In the over-under layout, there are three display alternatives
defined: time-motion priority, B Mode priority or equal priority.

Sample Volume Gate Length Sizes the sample volume gate

Scan Area

Slants the B-Mode or Color Flow linear image left or right to get
more information without moving the probe

Section 4-2 - Required Equipment 4 - 9

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-6 Basic Measurements

NOTE: The following instructions assume that you first scan the patient and then press Freeze.

4-3-6-1 Distance and Tissue Depth Measurements

1.) Press MEASURE

2.) To position the active caliper at the start point (distance) or the most anterior point (tissue

depth), move the TRACKBALL

3.) To fix the start point, press Set. The system fixes the first caliper and displays a 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
value in the measurement results window.

Before you complete a measurement:

To toggle between active calipers, press MEASURE

To erase the second caliper and the current data measured and start the measurement again, press

CLEAR

NOTE: To rotate through and activate previously fixed calipers, turn CURSOR SELECT

NOTE: After you complete the measurement, to erase all data that has been measured to this point,

but not data entered onto worksheets, press CLEAR

4-3-6-2 Circumference/Area (Ellipse) Measurement

1.) Press MEASURE

2.) To position the active caliper, move the TRACKBALL

3.) To fix the start point, press SET

4.) To position the second caliper, move the TRACKBALL

5.) Turn the ELLIPSE

once.

caliper.

once an active caliper displays.

.

.

. The system displays the distance or tissue depth

.

.

.

once; an active caliper displays.

.

. The system fixes the first caliper and displays a second active

.

control; an ellipse with an initial circle shape appears.

NOTE: Be careful not to press the Ellipse control as this activates the Body Pattern.

6.) To position the ellipse and to size the measured axes (move the calipers), move the

TRACKBALL

7.) To increase the size, turn the ELLIPSE
turn the ELLIPSE

8.) To toggle between active calipers, press MEASURE

9.) To complete the measurement, press SET
in the measurement results window.

Before you complete a measurement:

- To erase the ellipse and the current data measured, press CLEAR

is displayed to restart the measurement.

- To exit the measurement function without completing the measurement, press CLEAR

second time.

4 - 10 Section 4-2 - Required Equipment

.

control in a clockwise direction. To decrease the size,

control in a counterclockwise direction.

.

. The system displays the circumference and area

once. The original caliper

a

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-6-3 Worksheets

Measurement/Calculation worksheets are available to display and edit measurements and calculations.
There are generic worksheets as well as Application specific worksheets.

Section 4-2 - Required Equipment 4 - 11

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-7 Probe/Connectors Usage

4-3-7-1 Connecting a probe

1.) Place the probe's carrying case on a stable surface and open the case.

2.) Carefully remove the probe and unwrap the probe cable.

3.) DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable
damage.

4.) Turn the connector locking handle counterclockwise.

5.) Align the connector with the probe port and carefully push into place.

6.) Turn the connector locking handle clockwise to secure the probe connector.

7.) Carefully position the probe cable in the probe cord holder spot so it is free to move, but not
resting on the floor.

4-3-7-2 Activating the probe

Select the appropriate probe from the probe indicators on the monitor screen. The probe selection
screen will be come up when the application key is enabled.

The probe activates in the currently-selected operating mode. The probe's default settings for the mode
and selected exam are used automatically.

4-3-7-3 Deactivating the probe

When deactivating the probe, the probe is automatically placed in standby mode.

1.) Press the Freeze key.

2.) Gently wipe the excess gel from the face of the probe. (refer to the Basic User Manual for
complete probe cleaning instructions.)

3.) Carefully slide the probe around the right side of the keyboard, toward the probe holder.
Ensure that the probe is placed gently in the probe holder.

4-3-7-4 Disconnecting the probe

Probes can be disconnected at any time. However, the probe should not be selected as the active
probe.

1.) Move the probe locking handle counterclockwise. Pull the probe and connector straight out of
the probe port.

2.) Carefully slide the probe and connector away from the probe port and around the right side of
the keyboard. Ensure the cable is free.

3.) Be sure that the probe head is clean before placing the probe in its storage box.

4 - 12 Section 4-2 - Required Equipment

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-8 Using Cine

4-3-8-1 Activating CINE

Press FREEZE
Stop. To stop CINE Loop playback. press Run/Stop.

4-3-8-2 Quickly Move to Start/End Frame

Press FIRST

4-3-8-3 Start Frame/End Frame

Turn the START FRAME
right to move forward through the CINE Loop.

, then roll the TRACKBALL to activate CINE. To start CINE Loop playback, press Run/

to move to the first CINE frame; press LAST to move to the last CINE frame.

dial to the left to move to the beginning of the CINE Loop. Turn the dial to the

Turn the END FRAME
move backward through the CINE Loop.

4-3-8-4 Adjusting the CINE Loop Playback Speed

Turn the LOOP SPEED

4-3-8-5 Disconnecting B-Mode CINE from Timeline CINE

To review the B-Mode CINE Loop only, press CINE MODE SELECTION

To review the Timeline CINE Loop only, press CINE MODE SELECTION

To return to linked B-Mode and Timeline CINE Loop review, press CINE MODE SELECTION
B/TL

.

4-3-8-6 Moving through a CINE Loop Frame By Frame

Turn FRAME BY FRAME

dial to the right to move to the end of the CINE Loop. Turn the dial to the left to

dial right/left to increase/decrease the CINE Loop playback speed.

to move through CINE memory one frame at a time.

and select B ONLY.

and select TL ONLY.

and select

Section 4-2 - Required Equipment 4 - 13

GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL

4-3-9 Image Management (QG)

For Image Management functionality refer to the LOGIQ™ P5/A5/A5Pro Quick Guide. It talks about
several topics:

• Clipboard

• Printing Images

• Browsing and Managing an Exam’s Stored Image

• Connectivity, and Dataflow Concept and Creation

• Starting an Exam

• Configuring Connectivity

•TCP/IP

• Services (Destinations)

• Buttons

• Views
Verifying and Pinging a Device

4 - 14 Section 4-2 - Required Equipment