General Electric VIVID E80_E90_E95 SERVICE MANUAL_SM_GC091052_3 VividTM E95 Version 202 Basic Service Manual Direction Number: GC091542

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Technical Publication

Vivid™ E80 / Vivid™ E90 / Vivid™ E95

Version 201

Service Manual Direction Number: GC091052

Rev. 3

BASIC SERVICE DOCUMENTATION. COPYRIGHT GENERAL ELECTRIC COMPANY.

This manual is a reference for the Vivid E80, Vivid E90 and Vivid E95 ultrasound systems (Hereafter listed as Vivid E80/E90/E95). All information provided in this manual is relevant for all three systems unless otherwise specified.

Manufacturer:

GE VINGMED ULTRASOUND AS Strandpromenaden 45 NO-3191 Horten, Norway Tel:(+47) 3302 1100 Fax: (+47) 3302 1350 www.gehealthcare.com

Change history

Revision History

Date

Revision

2 2014-12-12 Initial release of manual.

(YYYY-MM-DD)

Reason for change

3 2015-11-19 • Update per change of CE notified body to TUV, CE

0123.

• Updated ‘Translation Policy’ (language disclaimers).

• Added new spare parts in Chapter 9.

List of Effective Pages (LOEP)

Pages Revision Pages Revision

Front Rev. 3 Chapter 6 Rev. 3 Front matter Rev. 3 Chapter 7 Rev. 3 TOC Rev. 3 Chapter 8 Rev. 3 Chapter 1 Rev. 3 Chapter 9 Rev. 3 Chapter 2 Rev. 3 Chapter 10 Rev. 3 Chapter 3 Rev. 3 Index Rev. 3 Chapter 4 Rev. 3 Rear Cover Rev. 3 Chapter 5 Rev. 3

Please verify that you are using the latest revision of this document. Information pertaining to this document is maintained on ePDM (GE Healthcare electronic Product Data Management). If you need to know the latest revision , cont a ct your distri butor, local GE Sales Representative or in the USA call the GE Ultrasound Clinical Answer Center at 1 800 6825327 or 1 262 524 5698.

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Important precautions

Translation policy

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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 transport ation company will not pay a claim for damage if an inspection is not requested within this 14 day period.

Certified electrical contractor statement - For USA Only

All electrical installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations, and testing shall be performed by qualified GE personnel. In per for m ing 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 field engineers, personnel of third-party service companies with equivalent training, or licensed electricians) to perform electrical servicing on the equipment.

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Omission and errors

If there are any omissions, errors or sugges t ion s for imp ro vin g this documentation, contact the GE Global Documentation Group with specific information listing the system typ e, m an ual title, part number or direction number, revision number, page number and suggestion details.

Mail the

information to:

GE Vingmed Ultrasound AS Service Documentation P.O.Box 141 NO-3191 HORTEN NORWAY

GE employees should use TrackWise to report service documentation issues.

These issues will then be in the internal problem reporting tool and communicated to the writer.

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WARNING

Service Safety Considerations

DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH,

ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and kneeling pads, to reduce the risk of injury.

For a complete review of all safety requirements, see: ‘Safety considerations’ on page 1-8.

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Legal notes

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

GE makes no representations or warranties with respect to the information herein. In addition, the information is subject to change without notice. Every precaution has been taken in the preparation of this document. Nevertheless, GE assumes no responsibility for errors, omissions, or any damages, including special or consequential, resulting from the use of this information. GE will issue updates to this information periodically, as needed. If there are any questions regarding the information contained in this manual, please contact your GE Representative.

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Trademarks

Copyrights

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

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THIS P A GE WAS INTENTIONALLY LEFT BLANK

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Translation policy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-2 Damage in transportation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-15 Certified electrical contractor statement - For USA Only - - - - - - - - - - - - i-15 Omission and errors - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-16 Service Safety Considerations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-17 Legal notes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-18 Trademarks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-19 Copyrights - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-19

Table of Contents Chapter 1 — Introduction

Manual Overview

Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-2 Vivid E80/E90/E95 models covered by this manual - - - - - - - - - - - - - - - 1-2 Product description - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3

Important conventions

Conventions used in book - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-4 Standard hazard icons - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-6 Product icons - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-7

Safety considerations

Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-8 Human Safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-8 Mechanical safety- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-11 Electrical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-14

Dangerous procedure warnings Lockout/Tagout (LOTO) requirements Returning probes and repair parts Electromagnetic compatibility (EMC)

What is EMC? - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-19 Compliance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-19 Electrostatic discharge (ESD) prevention - - - - - - - - - - - - - - - - - - - - - 1-20

Customer assistance

Contact information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-21 Phone numbers for Customer Assistance - - - - - - - - - - - - - - - - - - - - - 1-22 System manufacturer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-23

Chapter 2 — Site Preparations

General Ultrasound system requirements

Ultrasound system environmental requirements- - - - - - - - - - - - - - - - - - 2-2 Electrical requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-4 EMI limitations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-7

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EMI prevention/abatement- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-8 Probes environmental requirements - - - - - - - - - - - - - - - - - - - - - - - - - - 2-9

Facility needs

Purchaser responsibilities - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-10 Required facility needs - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-12 Desirable features- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-13 Minimal floor plan suggestion- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-13 Recommended floor plan suggestion - - - - - - - - - - - - - - - - - - - - - - - - 2-14 Suggested floor plan, Ultrasound system, and EchoPAC PC in same room -

2-15

Networking setup requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-15

Environmental Dangers

Patient Vicinity UL60601-1 (USA)- - - - - - - - - - - - - - - - - - - - - - - - - - - 2-18 Patient Environment IEC60601-1 (IEC60601-1-1) and ANSI AAMI

ES60601-1- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-19

Chapter 3 — System Setup

Setup reminders

Setup warnings- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-2

Receiving and unpacking the equipment

Warnings for receiving and unpacking - - - - - - - - - - - - - - - - - - - - - - - - 3-4 The Tilt and Shock indicators- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-5 Receiving the Vivid E80/E90/E95 - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-8 Unpacking the Vivid E80/E90/E95 - - - - - - - - - - - - - - - - - - - - - - - - - - 3-11

Packing materials - recycling information Preparing for setup

Verify customer order - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17 Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17 EMI protection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17

Completing the setup

System specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-18 Electrical specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19 Connections on the I/O Rear Panel - - - - - - - - - - - - - - - - - - - - - - - - - 3-20 Connections on the Patient I/O panel - - - - - - - - - - - - - - - - - - - - - - - - 3-21 Connecting probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-22

Configuration

Vivid E80/E90/E95 configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-25 Service Screen setup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-32 Optional peripherals/peripheral connection - - - - - - - - - - - - - - - - - - - - 3-36 Software Options configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-37

Connectivity overview

Physical connection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-39

Connectivity setup

Compatibility - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-41 Select TCP/IP Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-42 Changing the AE Title and/or Port Number (Port No.) - - - - - - - - - - - - 3-43 DHCP setup- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-44 Set the Remote Archive’s Network Information - - - - - - - - - - - - - - - - - 3-47

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Product Locator Installation Card

Chapter 4 — General Procedures and Functional Checks

General procedures

Power ON/Boot Up - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2 Power shut down - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-5 Complete power down - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-7 Creating presets - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-8

Functional checks

2D Mode (B mode) checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-9 M Mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13 Color Mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-17 PW/CW Doppler Mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-21 Tissue Velocity Imaging (TVI) Checks- - - - - - - - - - - - - - - - - - - - - - - - 4-25 Probe/Connectors Checks- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-29 ECG Check - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-30 Cineloop Check - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-31 Back End Processor checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-32 Operating Panel Test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-33 Peripheral checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-33 Mechanical Functions Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-35

Chapter 5 — Components and Functions (Theory)

Software overview

System software- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-2 Application software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-2

InSite ExC

Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3 InSite ExC Icon- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3 InSite ExC Status - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4 InSite ExC Definitions - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5 Initiating a Request for Service (RFS)- - - - - - - - - - - - - - - - - - - - - - - - - 5-6 Exiting InSite ExC- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-9

Vivid E80/E90/E95 overview

Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-10 Note regarding USB ports - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-10 Related information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-10 Vivid E80/E90/E95 block diagram- - - - - - - - - - - - - - - - - - - - - - - - - - - 5-11 Signal flow overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-12 System configuration and software- - - - - - - - - - - - - - - - - - - - - - - - - - 5-12 Operating Panel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-12 The electronics- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-12 Operating modes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-13

Top Console with LCD monitor and Operating Panel

Top Console description - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-14 Operating Panel (Control Panel)- - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-19

Main Console

Main Console description - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-21

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Air Flow control

Air Flow components- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-22 Software control - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-22 Location- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-23

Casters and brakes

Casters and brakes description - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-24

Front End Processor (FEP)

Front End Card Rack general description - - - - - - - - - - - - - - - - - - - - - 5-25 Transmitter board (GTX) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-26 Relay board (GRLY) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-28 CRX board- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-30 Front Plane boards (XD BUS) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-32 cSound Power Module (CPM) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-33

Back End Processor (BEP)

Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-34 Signal flow and processing - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-34 Location of the Back End Processor (BEP) - - - - - - - - - - - - - - - - - - - - 5-34 BEP description - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-34 BEP’s side connectors - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-35 BEP’s top connectors - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-36 BEP’s rear connectors- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-36 Inside the BEP - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-36 LEDs- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-37 BEP Power Supply - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-38 Graphics adapters - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-38 Internal storage devices - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-38

Power distribution

Main Power Supply- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-39 cSound Power Module (CPM) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-42

Input and Output (I/O) modules

Patient I/O (Physio)- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-43 BEP I/O Board - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-45

Restart Vivid E80/E90/E95 after diagnostics

Chapter 6 — Service Adjustments

LCD Monitor adjustments

Cautions and Warnings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2 LCD backlight adjustment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-3

Chapter 7 — Diagnostics/Troubleshooting

Service safety considerations Gathering Troubleshooting Data

Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3 Collect Vital System Information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3 Collect a ‘trouble image’ with logs- - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-4

Screen captures

Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-6 Ctrl+PrintScreen shortcut - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-6 Capture a screen image using the shortcut - - - - - - - - - - - - - - - - - - - - - 7-7

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Troubleshooting

XY Lock is not working - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-8 Related information: - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-8 XY Brake Motors Troubleshooting - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-8 Z Movement fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-8 Motor controller test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-10

Chapter 8 — Replacement Procedures

Warnings and important information

Warnings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-2 Returning/shipping probes and repair parts - - - - - - - - - - - - - - - - - - - - - 8-3 Manpower - When two persons are needed - - - - - - - - - - - - - - - - - - - - 8-5 Tools needed for servicing Vivid E80/E90/E95- - - - - - - - - - - - - - - - - - - 8-5

Loading the software

Loading the software from Usb Flash Drive (UFD) - - - - - - - - - - - - - - - - 8-7 Setup after software loading - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-8

Replacing covers and bumpers

Side covers replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-9 Top Cover replacement- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-11 Foot rest bumper replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-14 Front cover replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-16 Plate connectors Filter cover and filter replacement- - - - - - - - - - - - - - - - - - - - - - - - - - - 8-21 Rear cover replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-23 Rear bumper replacement- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-25 Rear handle replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-27

LCD Monitor and LCD Arm parts replacement

Replacing the 19” LCD Monitor assembly - - - - - - - - - - - - - - - - - - - - - 8-29 Replacing the LCD Arm assembly - - - - - - - - - - - - - - - - - - - - - - - - - - 8-31 LCD Z-Lock replacement- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-33

Upper OP Panel/Touch Panel Assembly replacement

Read and follow - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-35 Preparations- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-35 Remove the Upper OP Panel/Touch Panel Assembly - - - - - - - - - - - - 8-36 Install the Upper OP Panel/Touch Panel Assembly - - - - - - - - - - - - - - 8-36 Verification- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-37

Lower Operating Panel Parts replacement

Knobs for Encoders and Slidepots replacement- - - - - - - - - - - - - - - - - 8-38 Replacing the Operating Panel, Lower - - - - - - - - - - - - - - - - - - - - - - - 8-39 Replacing the Trackball- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-42

A/N Keyboard parts replacement

Replacing the Alpha-Numeric (A/N) Keyboard Assembly - - - - - - - - - - 8-45 Wagon AN Drawer Sheet Met. Assembly replacement- - - - - - - - - - - - 8-48

Other Top Console Parts replacement

Replacing the Speaker Assembly- - - - - - - - - - - - - - - - - - - - - - - - - - - 8-51 Replacing the Bulkhead Board- - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-53 Bulkhead, Plate, Extended replacement - - - - - - - - - - - - - - - - - - - - - - 8-54 Handle, Left Top / Handle Right Top, replacement- - - - - - - - - - - - - - - 8-56

/guide replacement - - - - - - - - - - - - - - - - - - - - - - - 8-19

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Palm Rest ASSY replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-58 Up-Down Button Board (Buttons Frame UI Assy) replacement - - - - - - 8-59 Button IF Board Assy replacement - - - - - - - - - - - - - - - - - - - - - - - - - - 8-61

Replacing XYZ Parts

XY Mechanism replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-63 Z-Mechanism replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-65 XYZ Control Assembly replacement - - - - - - - - - - - - - - - - - - - - - - - - - 8-67

Main Console parts replacement

Fan Assembly replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-69 Main Cable replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-70

Casters and Brakes replacement

Rear Casters replacement- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-73 Front Casters replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-76 Pedal Mechanism replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-79 Brake Pedal replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-83 Pedal Release replacement- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-83 Pedal Dir Lock replacement- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-84

Front End Processor (FEP) / Card Cage parts replacement

Front End parts overview- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-85 Front End cover replacement- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-86 Relay Board (RLY) replacement- - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-88 Transmitter Board (GTX) replacement - - - - - - - - - - - - - - - - - - - - - - - 8-91 cSound Receiver Board (CRX) replacement - - - - - - - - - - - - - - - - - - - 8-93 cSound Power Module (CPM) replacement- - - - - - - - - - - - - - - - - - - - 8-95

Back End Processor (BEP) parts replacement

Back End Processor (BEP) replacement- - - - - - - - - - - - - - - - - - - - - - 8-97 Hard Disk Drive (HDD) replacement- - - - - - - - - - - - - - - - - - - - - - - - 8-101

Main Power Supply replacement

Preparations- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-105 Main Power Supply removal procedure- - - - - - - - - - - - - - - - - - - - - - 8-105 Main Power Supply installation procedure- - - - - - - - - - - - - - - - - - - - 8-105

Patient I/O assembly replacement

Read and follow - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-107 Preparations- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-107 Patient I/O module removal procedure - - - - - - - - - - - - - - - - - - - - - - 8-107 Patient I/O installation procedure - - - - - - - - - - - - - - - - - - - - - - - - - - 8-108 Verification- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-108

Peripherals replacement

DVD R/W drive replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-109 Black & White Digital Graphic Printer replacement- - - - - - - - - - - - - - 8-110

Cables replacement

TwinAx PCIe cable replacement- - - - - - - - - - - - - - - - - - - - - - - - - - - 8-112

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Chapter 9 — Renewal Parts

List of Abbreviations Software for Vivid E80/E90/E95 Covers and Bumpers Top Console parts

Main Monitor and LCD Arm parts - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-9 Operating Panel (OP) parts - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-11 Alphanumeric (AN) Keyboard parts - - - - - - - - - - - - - - - - - - - - - - - - - 9-12 Speaker and Bulkhead parts - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-13

XYZ parts Main Console parts Casters (wheels) parts Front End Processor (FEP) Card Rack parts Back End Processor (BEP) parts Main Power Supply I/O modules parts Peripherals for use with Vivid E80/E90/E95

DVD drive - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-21 Internal printer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-21 External printers - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-22 Digital Video Stream Recorder (external) - - - - - - - - - - - - - - - - - - - - - 9-22 3D Monitor - external- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-23

Mains power cables - Vivid E80/E90/E95 Internal Cables - Vivid E80/E90/E95 ECG cables - Vivid E80/E90/E95 Physio TX parts Probes for Vivid E80/E90/E95

Phased Array Sector probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-31 Linear Array probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-31 Curved Array (Convex) probes- - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-32 Doppler probes- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-32 Transesophageal Phased Array probes - - - - - - - - - - - - - - - - - - - - - - 9-33 Intra-operative probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-33

Options - Vivid E80/E90/E95

Chapter 10 — Care and Maintenance

Overview

Periodic maintenance inspections - - - - - - - - - - - - - - - - - - - - - - - - - - 10-2

Why do maintenance

Quality assurance- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-3

Maintenance task schedule

How often should maintenance tasks be performed? - - - - - - - - - - - - - 10-4

Index

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Chapter 1 Introduction

This chapter describes important issues related to safely servicing the Vivid E80/E90/E95. The service provider must read and understand all the information presented here before installing or servicing the Vivid E80/E90/E95.

Vivid E80/E90/E95 – Service Manual 1-1 GC091052 Rev. 3

Introduction

Manual Overview

Introduction

This manual provides installation and service info rmation for the Vivid E80/E90/E95.

Vivid E80/E90/E95 models covered by this manual

Table 1-1: Vivid E80/E90/E95 models and software compatibility

Model Number

GC000220 Vivid E95 v200.0 v201.0 v201.x GC000230 Vivid E90 v200.0 v201.0 v201.x GC000240 Vivid E80 v200.0 v201.0 v201.x

Description System SWAppl.

NOTE: Unless otherwise specified, the content of this manual applies to

all Vivid E80/E90/E95 models.

Can be upgraded to

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Manual Overview

Product description

Overview of the Vivid E80/E90/E95 Ultrasound system

This Vivid E80/E90/E95 is a high performance digit al ultras ound imaging system with total data management.

The Ultrasound system provides image generation in 2D, Color Doppler, Power Doppler, M-Mode, Color M-Mode, PW and 4D, Tissue Velocity imaging, and Contrast applications.

The fully digital architecture of the Vivid E80/E90/E95 allows optimal usage of all scanning modes and probe types throughout the full spectrum of operating frequencies.

Signal flows from the Probe Connector Panel to the Front End, and then over to the Back End Processor and finally to the monitor and peripherals.

System configuration is stored on the Vivid E80/E90/E95. All necessary software is loaded from the hard drive on power

up.

Purpose of the operator manual(s)

The operator manuals should be fully read and understood before operating the Vivid E80/E90/E95.

The online versions of the operator manuals are available via the Help function on Vivid E80/E90/E95’s Operating Panel.

The translated user manuals are available as PDF files on the Usb Flash Drive (UFD) delivered with the Vivid E80/E90/E95.

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Introduction

DANGER

Important conventions

Conventions used in book

Important conventions, used in this document, are described below.

Model designations

This manual covers the Ultrasound systems listed in: ‘Vivid E80/E90/E95 models covered by this ma nual’ on

page 1-2.

Icons

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

Safety precaution messages

Various levels of safety precaution me ss ag e s ma y be fo und on the equipment and in the service informatio n . The different levels of concern are identified by a flag word that precedes the precautionary message. Known or potential hazards to personnel are labeled in one of three ways:

• DANGER

• WARNING

• CAUTION

Danger is used to indicate the presence of a hazard that will cause severe personal injury or death, or substantial property damage if the instructions are ignored.

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Important conventions

WARNING

CAUTION

Warning is used to indicate the presence of a hazard that may cause severe personal injury or substantial property damage if instructions are ignored.

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

NOTE: Notes are used to provide important information about an item

or a procedure.

NOTE: Be sure to read the notes; the information contained in a note

can often save you time or effort.

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Introduction

Standard hazard icons

Important information will always be preceded by either the exclamation point (!) contained within a triangle, or the symbols for “Danger”, “Warning” or “Caution” , 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 possibly cause harm. Even if a symbol isn’t used in this manual, it may be included for your reference.

Table 1-2: Standard hazard icons

ELECTRICAL

MECHANICAL

RADIATION

LASER

HEAT

PINCH

NOTE: Even if a symbol isn’t used on the product or in this manual, it

may be included for your reference.

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Important conventions

Standard Icons that indicate that a special procedure is to be used

Some others icons make you aware of specific procedures that should be followed.

Table 1-3: Standard Icons that indicates that a special procedure is to be used

Avoid Static Electricity Tag and Lock Out Wear Eye Protection

Hand Protection Foot Protection Wear Eye Protection

Product icons

Refer to the Device labels in the Safety chapter in the User Manual.

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Introduction

WARNING

Safety considerations

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.

Human Safety

• Operating personnel must not remove the Ultrasound system covers.

• Servicing should be performed by authorized personnel only .

Only personnel who have participated in a Vivid E80/E90/ E95 Training Seminar are authorized to service the equipment.

NOTE: Local laws may restrict this device for sale or use by or on the

order of a physician.

NOTE: For Vivid E80/E90/E95 Vet, local laws may restrict this device

for sale or use by or on the order of a veterinarian.

DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH,

ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

If the covers are removed from an operating Vivid E80/E90/ E95, some metal surfaces may be warm enough to pose a potential heat hazard if touched, even while in shutdown mode.

Because of the limited access to cabinets and equipment in the field, placing people in awkward positions, GE has limited the lifting weight for one person in the field to 16 KG (35 LBS). Anything over 16 KG (35 LBS) requires 2 people.

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Safety considerations

WARNING

Have two people available to deliver and unpack the Vivid E80/ E90/E95.

Attempts to move the Vivid E80/E90/E95 considerable distances or on an incline by one person could result in injury or damage or both.

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, ONLY

install GE approved part s. DO NOT perform any unauthorized modification of the equipment.

Tilting the console requires two people in order to avoid injury to service personnel and damage to the equipment.

Ensure that the Ultrasound system is turned off and unplugged Wait for at least 20 seconds for capacitors to discharge as

there are no test points to verify isolation. The amber light on the OP panel ON/OFF button will turn off.

Ultrasound system components may be energized. Always refer to the Ultrasound system's Proprietary Ser vice Manual for LOTO warnings and cautions

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Introduction

WARNING

When the top console is in its locked position, the gas shock is compressed and stores mechanical energy. During normal operation the top console, the weight of the monitor and the mechanical force of the gas shock are in balance. Take care if/ when you activate this gas shock. Personal injury can occur after the panel is removed and the shock pressure is released. Take care when you repair the e levation assembly.

Risk of electrical shock, Ultrasound system must be turned off and disconnected from power source. Cord must be controlled at all times.

Wait for at least 20 seconds for capacitors to discharge as there are no test points to verify isolation. The amber light on the OP panel on/off button will turn off.

Ultrasound System components may be energized. Always refer to the Ultrasound system's Proprietary Ser vice Manual for LOTO warnings and cautions.

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.

Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and kneeling pads, to reduce the risk of injury.

Beware of possible sharp edges on all mechanical parts. If sharp edges are encountered, the appropriate PPE should be used to reduce the risk of injury.

Wear all PPE including gloves as indicated in the chemical MSDS.

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Safety considerations

WARNING

Mechanical safety

While the software install procedure is designed to preserve data, you should save any patien t data, images, system setup s to removable media or hardcopy before doing a software upgrade.

Ultrasound probes are highly sensitive medical instruments that can easily be damaged by improper handling. Use care when handling and protect from damage when not in use. Do not use a damaged or defective probe. Failure to follow these precautions can result in serious injury and equipment damage.

Never use a probe that has fallen to the floor. Even if it looks OK, it may be damaged.

The Ultrasound system should not be moved with the Operator I/O Panel extended. Move the operator i/o panel to its ce ntered and locked position. Lower the Operator I/O Panel as much as possible before moving the Ultrasound system.

Prior to elevating Ultrasound system:

• verify that the floating Operating Panel is locked in its lowest, parking position.

• verify that the front brake is locked and the Ultrasound system is unable to swivel.

• verify that the rear brakes are in the locked position.

When the Ultrasound system is raised for a repair or moved along any incline, use extreme caution since it may become unstable and tip over.

Remember: If the front caster swivel lock is engaged for transportation, pressing the release pedal once disengages the swivel lock. You must depress the release pedal a second time to engage the brake.

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Introduction

CAUTION

Before you move or transport the Ultrasound system, make sure to lock the LCD monitor arm firmly and flip down the monitor to prevent damage to the Ultrasound system.

Always lock the Top Console (Operating Panel) in its parking (locked) position before moving the Ultrasound system around.

Do not move the Ultrasound system if the Operating Panel is in unlocked position.

To avoid injury when you move the LCD monitor and the monitor arm, do not put your finger, hand, or object on the joint of the monitor or the monitor arm.

Ensure that nobody touches the console arm/frogleg when moving the Operating Panel.

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

Vivid E80/E90/E95 weighs 128 kg (283 lb.) or more, depending on installed peripherals, when ready for use. Care must be used when moving it or replacing its parts.

Failure to follow the precautions listed below 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)

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Safety considerations

CAUTION

Do not transport Vivid E80/E90/E95 in a vehicle without locking the casters (wheels) and securing it as described in chapter 4.

Use protective glasses during drilling, filing smooth surfaces, and during all other work where ey es ne e d protection.

Use protective gloves when working with sharp edges or when directed to wear PPE during a removal/ replacement procedure.

Use safety shoes when doing work where there is any chance of foot injury.

Be careful not to pinch any of the cables.

NOTE: Special care should be taken when transporting the Ultrasound

system in a vehicle:

• Before transporting, place the Ultrasound system in its special storage case.

• Ensure that the Ultrasound system is firmly secured while inside the vehicle.

• Secure Ultrasound system with straps or as directed otherwise to prevent motion during transport.

• Prevent vibration damage by driving cautiously. Avoid unpaved roads, excessive speeds, and erratic stops or starts.

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Introduction

WARNING

Electrical safety

Safe practices

Follow these guidelines to minimize shock hazards whenever you are using the Vivid E80/E90/E95:

• To minimize shock hazard, the equipment chassis must be connected to an electrical ground.

• The Vivid E80/E90/E95 is equipped with a three-conductor AC power cable. This must be plugged into an approved electrical outlet with safety ground.

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

• Both the Vivid E80/E90/E95 power cable and the power connector must meet international electrical standards

Connecting a Vivid E80/E90/E95 to the wrong voltage level will most likely destroy it.

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Safety considerations

Probes

Follow these guidelines before connecting a probe to the Ultrasound system:

• Inspect the probe prior to each use for damage or degradation to the:

• housing

• cable strain relief

• lens

• seal

• connector pins

• locking mechanism

• Do not use a damaged or defective probe.

• Never immerse the probe connector or adapter into any liquid.

• The Vivid E80/E90/E95 has more than one type of probe port. Use the appropriate probe port designed for the probe you are connecting.

Peripherals

Refer to the Patient Safety Environment section of the User’s Manual for peripheral isolation information.

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Introduction

DANGER

WARNING

Dangerous procedure warnings

Warnings, such as the example below, precede potentially dangerous procedures throughout this manual. Instructions contained in the warnings must be followed.

DANGEROUS VOL T AGES, CAPABLE OF CAUSING DEA TH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

If the covers are removed from an operating Vivid E80/E90/ E95, some metal surfaces may be warm enough to pose a potential heat hazard if touched, even while in shutdown mode.

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, ONLY

install GE approved part s. DO NOT perform any unauthorized modification of the equipment.

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Lockout/Tagout (LOTO) requirements

WARNING

Lockout/Tagout (LOTO)

requirements

Follow Lockout/T agout requirements by ensuring you are in total control of the AC power plug at all times during the service process.

To apply Lockout/Tagout (LOTO):

1. Plan and prepare for shutdown.

2. Shutdown the equipment.

3. Isolate the equipment.

4. Apply Lockout/Tagout Devices.

5. Control all stored and residual energy.

6. Verify isolation.

All potentially hazardous stored or residual energy is relieved.

Energy Control and Power Lockout for Vivid E80/E90/E95. When servicing parts of the Ultrasound system where there is

exposure to voltage greater than 30 volts:

1. Follow LOCK OUT/TAG OUT procedures.

2. Turn off the breaker.

3. Unplug the Ultrasound system.

4. Maintain control of the Ultrasound system power plug.

5. Wait at least 30 seconds for capacitors to discharge as there are no test points to verify isolation.

Ultrasound System components may be energized.

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Introduction

Returning probes and repair parts

Equipment being returned must be clean and free of blood and other infectious substances. GE policy states that body fluids must be prop er ly re moved from a ny part or equipment prior to shipment. GE employees, as well as customers, are responsible for ensuring that parts/equipment have been properly decontaminated prior to shipment. Under no circumstance should a part or equipment with visible body fluids be taken or shipped from a clinic or site (for example, body coils or an ultrasou nd probe).

The purpose of the regulation is to protect employees in the transporta tion industry, as well as the people who will receive or open this package.

NOTE: The US Depar tment of Transportation (DOT) has ruled that

“items that were saturated and/or dripping with human blood that are now caked with dried blood; or which were used or intended for use in patient care” are “regulated medical waste” for transportation purposes and must be transported as a hazardous material.

NOTE: The USER/SERVICE staff should dispose of all the waste

properly , per federal, st ate, and local waste disposal regulation s.

The Vivid E80/E90/E95 is not meant to be used for long-term storage of patient data or images. The user is responsible for the data on the Vivid E80/E90/E95 and a regular backup is highly recommended.

If the Vivid E80/E90/E95 is sent for repair, please ensure tha t any patient information is backed up and erased from the Vivid E80/E90/E95 before shipping. It is always possible during system failure and repair to lose patient dat a. GE is not responsible for the loss of this data.

If PHI (Patient Healthcare Information) data needs to be sent to GE employees for service purposes, GE will ascertain agreement from the customer. Patient information shall only be transferred by approved service processes, tools and devices restricting access, protecting or encrypting data where required, and providing traceability in the form of paper or electronic documents at each stage of the procedure while maintaining compliance with cross-border restrictions of patient information transfers.

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Electromagnetic compatibility (EMC)

What is 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 to 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.

Compliance

Vivid E80/E90/E95 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 of the Ultrasound system’s User’s 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.

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Introduction

WARNING

Electrostatic discharge (ESD) prevention

DO NOT touch any boards with integrated circuits prior to taking the necessary ESD precautions.

Always connect yourself, via an arm-wrist strap, to the advised ESD connection point located on the rear of the Ultrasound system (near the power connector).

Follow general guidelines for handling of electrostatic sensitive equipment.

Risk of electrical shock, Ultrasound system must be turned off. Avoid all contact with electrical contacts, conductors and components. Always use non-conductive handles designed for the removal and replacement of ESD sensitive parts. All parts that have the potential for storing energy must be discharged or isolated before making contact.

If the covers are removed from an operating Vivid E80/E90/ E95, some metal surfaces may be warm enough to pose a potential heat hazard if touched, even while in shutdown mode.

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Customer assistance

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.

Before you call, identify the following information, and acquire image (Alt+D) to send to the Customer Care team:

1. Ultrasound system ID serial number.

2. Software version.

3. Date and time of occurrence.

4. Sequence of events leading to issue.

5. Is the issue repeatable?

6. Imaging mode, probe, preset/application.

7. Media brand, speed, capacity, type.

8. Save secondary image capture, cine loop, 4D multi-volume loop.

9. Detailed description of any problem encountered .

10. Where applicable, s ave the appropriate log files. Remember to save the log files for each day on a separate

media, labelled accordingly.

NOTE: Restart the application before resuming clinical scanning.

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Introduction

Phone numbers for Customer Assistance

Table 1-4: Phone Numbers for Customer Assistance

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Customer assistance

System manufacturer

Table 1-5: System manufacturer

MANUFACTURER PHONE NUMBER FAX NUMBER

GE VINGMED ULTRASOUND A/S STRANDPROMENADEN 45 P.O. BOX 141 NO-3191 HORTEN NORWAY

+47 3302 1100 +47 3302 1350

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Introduction

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Chapter 2 Site Preparations

This chapter provides the information required to plan and prepare for the setup of an Ultrasound system. Included are descriptions of the facility and electrical needs to be met by the purchaser of the Ultrasound system.

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Site Preparations

CAUTION

General Ultrasound system

requirements

Ultrasound system environmental requirements

If the Ultrasound system is very cold or hot

When unpacking the Ultrasound system, allow the temperature of the Ultrasound system to stabilize before powering up. The following table describes guidelines for reaching operational temperatures from storage or transport temperatures.

If the Ultrasound system is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.

Table 2-1: Ultrasound system acclimate time

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General Ultrasound system requirements

Vivid E80/E90/E95 environmental specifications

Table 2-2: Environmental specifications for Vivid E80/E90/E95 systems

T emperature

Conditions

Operation: 10 to 35 °C

Storage and transport:

(50-95 °F)

-20 to +60 °C (-4 to +140 °F)

Cooling

NOTE: Each person in the room places an additional 300 BTU/h

Lighting

Air pressure

limits

Humidity limits

30 - 85% non-condensing

30 - 95% non-condensing

limits

700-1060 hPa 2390 BTU/h

700-1060 hPa N/A

Heat dissipation

The cooling requirement for the Vivid E80/E90/E95 with monitor and on board peripherals, is up to 2390 BTU/h. This figure d oes not include cooling needed for lights, people, or other equipment in the room.

demand on the cooling system.

Bright light is needed for Ultrasound 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 dimmers can be a source of EMI which could degrade image quality. These controls should be selected to minimize possible interference.

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Site Preparations

Electrical requirements

General requirements

NOTE: GE 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 Ultrasound system.

The Vivid E80/E90/E95 will function on voltages from 100-240 Volts and 5 0 or 60 Hz. However, if using 220 volt power in North America, then a center tapped power source is required.

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 system is only a conduit.

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General Ultrasound system requirements

CAUTION

Electrical requirements for the Vivid E80/E90/E95

In the table below, the electrical specifications for the Vivid E80/ E90/E95 includes monitor and on-board peripherals.

The specifications apply for the following models:

• GC000220 - Vivid E95

• GC000230 - Vivid E90

• GC000240 - Vivid E80

Table 2-3: Electrical specifications

VOLTAGE TOLERANCES POWER

CONSUMPTION

100-240 VAC ±10% 700 W / 770 VA 50/60 Hz

The current drain will vary depending on the mains voltage.

• At 230 VAC the current may be up to 3 A.

• At 100 VAC the current may be up to 7 A.

FREQUENCY

Site circuit breaker

Power outage may occur. The Vivid E80/E90/E95 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.

It is recommended that the branch circuit breaker for the Ultrasound system be readily accessible.

Site power outlets

A dedicated AC power outlet must be within reach of the Ultrasound system without extension cords. Other outlets adequate for the external peripherals, medical and test equipment needed to support this Ultrasound system must also be present within 1 m (3.2 ft.) of the Ultrasound system. Electrical installation must meet all current local, state, and national electrical codes.

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Site Preparations

Power plug

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

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.

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General Ultrasound system requirements

EMI limitations

Ultrasound systems are susceptible to Electromagnetic Interference (EMI) from radio frequencies, magnetic fields, and transients in the air or wiring. They also generate EMI. The Ultrasound system complies with limits as stated on the EMC label. However there is no guarantee that interference will not occur in a particular installation.

Possible EMI sources should be identified before the Ultrasound system is installed.

Electrical and electronic equipment may produce EMI unintentionally as the result of a defect. Some of these sources include:

• medical lasers

• scanners

• cauterizing guns

• computers

• monitors

• fans

• gel warmers

• microwave ovens

• light dimmers

• mobile phones

• in-house wireless phones (DECT phones)

• wireless computer keyboard and mouse

• air conditioning system

• High Frequency (HF) surgery equipment

• general AC/DC adapters

The presence of a broadcast station or broadcast van may also cause interference.

See: ‘EMI prevention/abatement’ on page 2-8 for EMI prevention tips.

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Site Preparations

EMI prevention/abatement

Table 2-4: EMI prevention/abatement

EMI RULE DETAILS

Be aware of Radio Frequency sources

Ground the Ultrasound system

Replace all screws, Radio Frequency gaskets, covers, cores

Replace broken Radio Frequency gaskets

Do not place labels where Radio Frequency gaskets touch metal

• Keep the Ultrasound system at least 5 meters (15 feet) away from other EMI sources.

• Special shielding may be required to eliminate interference problems caused by high frequency, high powered radio or video broadcast signals.

Poor grounding is the most likely reason an Ultrasound system will have noisy images. Check grounding of the power cord and power outlet.

• After you finish repairing or updating the Ultrasound system, replace all covers and tighten all screws.

• Any cable with an external connection requires a magnet wrap at each end.

• Install all covers. Loose or missing covers or Radio Frequency gaskets allow radio frequencies to interfere with the ultrasound signals.

If more than 20% or a pair of the fingers on an Radio Frequency gasket are broken, replace the gasket. Do not turn on the Ultrasound system until any loose metallic part is removed.

Where applicable, never place a label where Radio Frequency gaskets meet the Ultrasound system. Otherwise, the gap created will permit Radio Frequency leakage. Or, if a label has been found in such a position, move the label.

Use GE specified harnesses and peripherals

Take care with cellular phones

Properly route peripheral cables

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.

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

Where applicable, do not allow cables to lie across the top of the Card Rack 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.

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General Ultrasound system requirements

CAUTION

Probes environmental requirements

Operation and storage temperatures for probes

Table 2-5: Operation and storage temperatures for probes

Conditions Electronic PAMPTE

Operation: 10 to 40 ºC (50 to 104 ºF) 5 to 42.7 ºC (41 to 108,9 ºF) Storage: -20 to 50 ºC (-4 to 122 ºF) -20 to 60 ºC (-4 to 140 ºF) Temperature in degrees Celsius (ºC) conversion to degrees F (ºF):

(ºF) = (ºC * 9/5) + 32

PAMPTE probes are designed for storage temperatures of -20 to +60 degrees C (-4 to +140 degrees F).

Electronic probes are designed for storage temperatures of -20 to +50 degrees C (-4 to +122 degrees F).

When exposed to large temperature variations, the product should be kept at room temperature th e ne ed e d tim e to stabilize its temperature before use.

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Site Preparations

Facility needs

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. Purchaser responsibility includes:

• Procuring the materials required

• Completing the preparations before delivery of the Ultrasound system

• Paying the costs for any alterations and modifications not specifically provided in the sales contract

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Facility needs

Purchaser responsibilities (continued)

NOTE: All electrical installations 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, calibrations, and testing must also be performed by qualified personnel. The products involved (and the accompanying electrical installations) are highly sophisticated and special engineering competence is required. All electrical work on these products 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 Ultrasound 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 (preferably prior to the purchase).

The ultrasound suite must be clean prior to delivery of the Ultrasound system. Carpet is not recommended because it collects dust and creates static. Potential sources of EMI (electromagnetic interference) shou ld als o be inve stig at ed before delivery. Dirt, static, and EMI can negatively impact Ultrasound system reliability.

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Site Preparations

Required facility needs

NOTE: GE 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 Ultrasound system.

The Ultrasound system will function on voltages from 100-240 Volts and 5 0 or 60 Hz. However, if using 220 volt power in North America, then a center tapped power source is required.

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.

• 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 Ultrasound system’s proposed location

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

• Proposed location for Ultrasound system is at least 0.5 m (1.5 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 Ultrasound system to connect cables.

• Power outlets for other medical equipment

• Power outlets for test equipment within 1 m (3.2 ft.) of Ultrasound system

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

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

For the amperage requirements, see: ‘Electrical requirements’ on page 2-4.

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Facility needs

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

Minimal floor plan suggestion

Scale:

Each square equals one square foot (app. 31 x 31 cm)

1. Sink

2. Linens

3. Probes / supplies

4. Ethernet Connector

5. Power outlet

6. Stool

7. Ultrasound system

8. GE cabinet for software and manuals (optional)

9. Examination table

10. Door (76 cm)

Figure 2-1. Minimal floor plan, 2.5 m x 3 m (8 by 10 foot)

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Site Preparations

13 14

Recommended floor plan suggestion

Scale: Each square equals one square foot (app. 31 x 31 cm)

1. Secretaries or Doctors Desk

2. File Cabinet

3. Film Viewer

4. Counter Top

5. Counter Top and Sink with hot and cold water

6. Overhead Lights Dimmer Dual Level Lighting (bright and dim)

7. Emergency Oxygen

8. Suction Line

9. Ultrasound system

10. Dedicated Power Outlet Circuit Breaker protected and easily accessible

11. Network Interface

12. 457 mm (18 inches) distance of Ultrasound system from wall or objects

13. Stool

14. Footswitch

15. Storage for Linens and Equipment

16. Examination Table – 1930 x 610 mm (76 x 24 inches)

17. Lavatory and Dressing Room

18. Door – at least 762 mm (30 inches)

Figure 2-2. Recommended floor plan, 4.27 x 5.18 m (14 x 17 foot)

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Facility needs

Suggested floor plan, Ultrasound system, and EchoPAC PC in same room

1. EchoPAC workstation parts

2. UPS

3. Ethernet network wall outlet

4. 3x mains power outlets

5. Hot and Cold water

6. Dedicated mains power outlet

7. Ethernet network wall outlet

Figure 2-3. Suggested Room with EchoPAC workstation and Ultrasound system

Networking setup requirements

Stand alone Ultrasound system (without network connection)

None.

Ultrasound system connected to hospital’s network

Supported networks:

10/100/1000 Mbit Ethernet/DICOM network (option)

InSite requirements

InSite requires an Ethernet connection either via:

• 10/100 Mbit or 10/100/1000 Mbit Interface

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Site Preparations

Purpose of the 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.

DICOM option setup requirements

To configure the Ultrasound system to work with other network connections, the site’s network administrator must provide information to complete the form “Worksheet for DICOM Network Information”. Ensure that there ar e no spaces in any field of the form.

Entries must include:

• A host name, local port number, AE Title, IP address and Net Mask for the Ultrasound system.

• 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 Ultrasound system 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 error solving.

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Facility needs

Figure 2-4. Worksheet for DICOM Network Information

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Site Preparations

Environmental Dangers

Commercial devices such as laser cameras, printers, VCRs and external monitors, usually exceed allowable leakage current limits and, when plugged into separate AC outlets, are in violation of patient safety stand ar ds. Suitable electrical isolation of such external AC outlets, or providing the device with extra protective earth, will be required in order to meet UL60601-1 and IEC60601-1 / IEC60601-1-1 standards for electrical leakage.

Patient Vicinity UL60601-1 (USA)

2.12.20DV (UL60601-1:2003)

In area in which patients are normally cared for, the patient vicinity is the space with surfaces likely to be contacted by the patient or attendant who can touch the patient. This encloses a space within the room 1.83 m (6 ft.) beyond the perimeter of the bed (examination table, dental chair, treatment booth, and the like) in its intended location, and extending vertically 2.29 m (7.5 ft.) above the floor.

1. Patient environment

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Environmental Dangers

Patient Environment IEC60601-1 (IEC60601-1-1) and ANSI AAMI ES60601-1

Sub Clause 2.202 and figure 201 (IEC60601-1-1:2000) Sub Clause 3.79 and figure A.9 (IEC60601-1:2005 and ANSI AAMI

ES60601-1:2005)

Such an area is an environment in which medical diagnosis, monitoring or treatment is carried out. It is very difficult to attach unique dimensions to the PATIENT ENVIROMENT.

In practice a distance of 2,5 m (8.2 ft.) above the floor on which the medical personnel stand and a horizontal distance of 1,5 m (4.9 ft.) have justified themselves as indicative of the dimensions of the Patient Environment.

The patient environment/vicinity will be depicted as a dashed line in this procedure. See example below.

1. Patient environment

Figure 2-5. Patient environment

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Site Preparations

THIS P A GE WAS INTENTIONALLY LEFT BLANK

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Chapter 3 System Setup

This chapter contains information needed to install Vivid E80/E90/E95.

Included is 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 Ultrasound system of the actual installation, and how to check and test the Ultrasound system, probes, and external peripherals for electrical safety are also included in this procedure.

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System Setup

DANGER

CAUTION

Setup reminders

Setup warnings

WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DON’T TOUCH THE ULTRASOUND SYSTEM!

To prevent electrical shock, connect the Ultrasound system to a properly grounded power outlet. Do not us e a thr ee 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 operate this Ultrasound system unless all boar d co ve rs and frame panels are securely in place. System performa n ce and cooling require this.

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Setup reminders

CAUTION

Setup warnings (continued)

If the Ultrasound system is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.

The following table describes guidelines for rea ching operational temperatures from storage or transport temperatures.

Operator Manual(s) The User Manual(s) should be fully read and understood

before operating the Vivid E80/E90/E95 and kept near the Ultrasound system for quick reference.

Acoustic Output Hazard Although the ultrasound energy transmitted from the Vivid E80/

E90/E95 probe is within AIUM/NEMA standards, avoid unnecessary exposure. ultrasound energy can produce heat and mechanical damage.

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System Setup

CAUTION

Receiving and unpacking the

equipment

Warnings for receiving and unpacking

Two people are needed to unpack the Ultrasound system because of its weight. Attempts to move the Ultrasound system considerable distances or on an incline by one person could result in injury or damage or both.

Two people are required whenever a part weighing 16 KG (35 LBS) or more must be lifted.

Remember to use relevant personal pr ot ec tin g eq uip m en t (PPE) during packing and unpacking. Check with your local EHS representative.

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Receiving and unpacking the equipment

The Tilt and Shock indicators

Overview

Improper handling during transportation may harm the equipment inside the package even if the package itself is undamaged.

To make it easier to detect if the handling during transportation has been improper, a set of Tilt & Shock indicators have been attached to the transportation box.

Table 3-1: Shock and Tilt Watch

Description Illustration

ShockWatch

Tilt Watch

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System Setup

If Shock Indicator has triggered or is missing

Table 3-2: Shock Indicator has triggered or is missing

Step Task

If the Shock Indicator is missing:

Note on the shipping papers at the time of receipt that the Shock Indicator label is missing.

If the Shock Indicator has triggered:

Note on the shipping papers at the time of receipt that the Shock Indicator label was activated.

Inspect the product for possible concealed damage.

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Receiving and unpacking the equipment

If Tilt Indicator has triggered or is missing

An activated tilt indicator label does not indicate whether the package was simply “Tipped” (laid down with no impact shock) or “Tipped Over” (free fall, with an impact shock). Using both shock indicator labels and tilt indicator labels will help identify whether a Tip Over impact shock occurred.

Table 3-3: Tilt Indicator has triggered or is missing

Step Task

If the Tilt Indicator is missing:

Note on the shipping papers at the time of receipt that the Tilt Indicator label is missing.

If the Tilt Indicator has triggered:

Note on the shipping papers at the time of receipt that the Tilt Indicator label was activated.

Inspect the product for possible concealed damage.

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System Setup

Receiving the Vivid E80/E90/E95

Examine all packages

Examine package closely at time of delivery, as described in the procedure below.

Table 3-4: Examine all packages

Step Task Illustrations

Is damage apparent?

• If YES; continue with the instructions in ‘Damage in transportation’ on page 3-10.

• If NO; continue with the next step.

Is the Shock Indicator colored red inside the middle of the indicator?

• If YES: The Shock Indicator has been activated. Continue with the instructions in ‘Damage in transportation’ on page 3-10, then continue with the next step.

• If NO: continue with the next step.

1 - Red Color

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Table 3-4: Examine all packages (Cont'd)

Step Task Illustrations

Is the Tilt Indicator red colored inside the middle of the indicator?

• If YES: The Tilt Indicator has been activated. Continue with the instructions in ‘Damage in transportation’ on page 3-10 before you continue with the next step.

• If NO: continue with the next step.

1 - Red Color

Continue with the instructions in ‘Unpacking the Vivid E80/E90/E95’ on page 3-11.

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System Setup

Damage in transportation

Follow this procedure if damage is apparent:

1. 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.

2. Report the damage to the carrier.

• 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 conten ts 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.

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Unpacking the Vivid E80/E90/E95

This procedure describes how to unpack the Vivid E80/E90/E95 from the cardboard box.

Before cutting the straps, check Shock and Tilt Tags to make sure they have not been triggered. If damaged, report it to the carrier. If not, continue with the procedure below.

Table 3-5: Uncrating the Vivid E80/E90/E95

Step Task Illustration

Cut the straps around the crate.

Remove the Top Cover.

Remove the Complete Column Left and Complete Column Right.

Remove the Box For Accessories.

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Table 3-5: Uncrating the Vivid E80/E90/E95 (Cont'd)

Step Task Illustration

Remove the two Frames (sides) and the two Exit Ramp Bases.

Install the two Exit Ramp Bases on the Complete Exit Ramp (the rear plate).

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Table 3-5: Uncrating the Vivid E80/E90/E95 (Cont'd)

Step Task Illustration

Remove the Support For Monitor.

Remove the Complete Front Protection.

Remove the plastic bag from the Vivid E80/E90/E95.

10.

Remove the Inlay UI Top.

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Table 3-5: Uncrating the Vivid E80/E90/E95 (Cont'd)

Step Task Illustration

11.

12.

Fold down the assembled Exit Ramp.

Unlock the Front Brakes on the Vivid E80/E90/E95, but keep direction lock activated. The direction lock keeps the front wheels in position, and secures the direction stability when the system is rolled down the ramp from the pallet.

Unlock the Rear Brakes.

1. Direction (Dir) Lock

2. Release Dir Lock and Front Brakes

3. Front Brakes

4. Rear Brakes

Carefully move the Vivid E80/E90/ E95 down the ramp, with rear end first.

Assemble the empty transportation box and place all of the filling inside the box before you close it.

Close the box, and store it for possible future use.

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Packing materials - recycling information

Packing materials - recycling

information

The packing materials for Vivid E80/E90/E95 are recyclable:

Table 3-6: Packaging parts for Vivid E80/E90/E95

Item Description Qty. Material *) Illustration

Export pallet 1200 x 800 1 D

Complete base 1 A

Complete column left and right

Support for monitor 1 C

Inlay UI Top 1 C

Complete front protection 1 B

Vivid E80/E90/E95 – Service Manual 3-15 GC091052 Rev. 3

System Setup

Table 3-6: Packaging parts for Vivid E80/E90/E95 (Cont'd)

Item Description Qty. Material *) Illustration

10.

11.

Exit ramp 1 A

Frame 2 A

Exit ramp base 2 A

Box for accessories 1 A

Top cover 1140 x 755 x 150 1 A

12.

Support plate, used to keep

1A Front Protection in place if there are few or none probes included.

13.

Protectors for Top Cover 2 A

*) Material type: A:

BB34bc with varnish C9068 BB27c with varnish C9068 PE foam, Stratocell Wood ISPM15

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Preparing for setup

Verify customer order

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

Physical inspection

Verify that the Vivid E80/E90/E95 arrived intact (visual inspection).

If the Vivid E80/E90/E95 has been damaged, please refer to ‘Damage in transportation’ on page i-15 in the beginning of this manual.

EMI protection

The Vivid E80/E90/E95 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 Vivid E80/E90/E95 from image artifacts caused by this interference. For this reason, it is imperative that all covers and hardware are installed and secured before the Vivid E80/E90/ E95 is put into operation.

See ‘EMI limitations’ on page 2-7 for more information about EMI protection.

Vivid E80/E90/E95 – Service Manual 3-17 GC091052 Rev. 3

System Setup

Completing the setup

System specifications

System requirements verification

• Verify that the site meets the requirements listed in Chapter 2.

(See: ‘Facility needs’ on page 2-10.)

• Verify that the specifications below do not conflict with any on-site conditions.

Physical dimensions

Table 3-7: Physical dimensions of Vivid E80/E90/E95 with

monitor and peripherals - in transportation position

Height Width Depth Unit

141.0 58.5 83.0 cm

55.5 23 32.7 Inches

Mass with monitor and peripherals

Table 3-8: Mass of Vivid E80/E90/E95 with monitor, without

Model Mass [KG] Mass [LBS] Vivid E80/E90/

E95

probes and peripherals

128 283

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Completing the setup

WARNING

Electrical specifications

Connecting a Vivid E80/E90/E95 to the wrong voltage level will most likely destroy it.

Verification of the Vivid E80/E90/E95’s voltage setting

Verify that the mains voltage specified fo r the Vivid E80/E90/E95 is available on-site.

The voltage setting for the Vivid E80/E90/E95 is fou nd on a label near the Mains Power Circuit Breaker on the rear of the Vivid E80/E90/E95.

Electrical specifications for Vivid E80/E90/E95

In the table below, the electrical specifications for Vivid E80/E90/ E95 includes monitor and on board peripherals.

Table 3-9: Elec tric al sp ecif ica tio ns fo r all Vivid E80/E90/E95

models

Voltage 100-240 VAC ±10% Power Consumption 700W / 770 VA Frequency 50/60 Hz

Vivid E80/E90/E95 – Service Manual 3-19 GC091052 Rev. 3

System Setup

Connections on the I/O Rear Panel

NOTE: Accessory equipment connected to the analog and digital

interfaces must be certified according to the respective IEC standards (e.g. IEC60950 for data processing equipment and IEC60601-1 for medical equipment). Furthermore, all complete configurations shall comply with the valid version of the system standard IEC60601-1-1. Everybody who connects additional equipment to the signal input part or signal output part of Vivid E80/E90/E95, configures a medical system, and is therefore responsible that the Ultrasound system complies with the requirements of the valid version of IEC60601-1-1. If in doubt, consult the technical service department or your local representative for GE.

Connect Ethernet

Connect the network cable to the Ethernet connector on the I/O Rear Panel.

The connector is located on the rear side of Vivid E80/E90/E95.

Connect USB Flash Card

NOTE: Only approved USB Flash Cards must be used. USB Flash

Cards approved for Vivid E80/E90/E95 are verified for EMC performance according to EN55011 class B. The use of any other USB Flash Cards will compromise this verification, and may cause interference on Vivid E80/E90/E95 itself, or on other electronic devices.

For approved models, please refer to Chapter 9. Install the USB Flash Card in one of the USB ports on the Vivid

E80/E90/E95.

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Completing the setup

Connections on the Patient I/O panel

The Patient I/O panel is located on the front of Vivid E80/E90/ E95.

1. PHONO

2. ECG

3. AUX (PRESSURE/PULSE)

Figure 3-1. Patient I/O Panel

Connect ECG

Connect the ECG cable to the ECG connector on the Patient I/O panel.

Connect Heart Microphone (Phono)

The Heart Microphone has its corresponding Phono adapter. Connect the Heart Microphone via the corresponding Phono

Adapter to the Phono input on the Patient I/O panel.

1. MA-300

2. PHONO ADAPTER

Figure 3-2. Heart Microphone (Phono)

Vivid E80/E90/E95 – Service Manual 3-21 GC091052 Rev. 3

System Setup

Connecting probes

Introduction to ‘Connecting probes’

The Vivid E80/E90/E95 has three types of probe ports; one PD probe port, three PDT probe ports and one Doppler probe port.

Probes can be connected at any time, whether the Vivid E80/ E90/E95 is On or Off.

The Vivid E80/E90/E95 has three types of probe ports; one PD probe port, three PDT probe ports and one Doppler probe port.

• The PD probe port is compatible with the Vivid 7 probe connectors.

• The three PDT probe ports are specific to the Vivid E80/ E90/E95 probe connectors.

• The Doppler probe port is used for CW Doppler probes (non-sector-probes), sometimes called PEDOF probes.

1. PD PROBE PORT: FOR VIVID 7 COMPATIBLE PROBE CONNECTORS

2. PDT PROBE PORT: FOR Vivid E9 SPECIFIC PROBE CONNECTORS

NOTE! The DOPPLER probe connector is not illustrated in this figure.

Figure 3-3. Probe connectors

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Completing the setup

CAUTION

Connect a probe

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

probe.

Do not allow the probe head to hang freely. Excessive impact to the probe will result in irreparable damage.

To prevent probe connector pins damage, or PCB board damage, do not use excessive force when connecting the probes.

Keep the probe cables away from the wheels. Do not bend the probe cables. Do not cross cables between probes.

Follow these steps to connect a probe:

1. Before connecting the probe: a. Do a visual check of the probe pins and Ultrasound

system sockets. b. Remove any dust or foam remains from the probe pins. c. Inspect the probe and the probe cable for any visual

damage.

2. Hold the probe connector vertically with the cabl e po int ing upward.

3. Turn the connector locking handle counter-clockwise to the horizontal position.

4. Align the connector with the probe port and carefully push into place.

5. Turn the locking handle clockwise to the full vertical position to lock in place.

6. Position the probe cable so that it is not resting on the floor.

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System Setup

Disconnect a probe

Follow these steps to disconnect a probe:

1. Rotate the lock handle counter-clockwise to the horizontal position to unlock the connector.

2. Remove the connector from the port.

3. Ensure that the probe head is clean before placing the probe in its storage case.

For cleaning instructions, see the User Manual.

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Configuration

Vivid E80/E90/E95 configuration

Select System Settings screen

1. Select Config (F2) and log on as adm.

2. Select System and then select Settings, if needed. The Settings screen is displayed.

Figure 3-4. Settings screen

Vivid E80/E90/E95 – Service Manual 3-25 GC091052 Rev. 3

System Setup

Enter location

1. Settings

2. Location

3. System

Figure 3-5. Enter loc at ion

Table 3-10: Enter location

STEP TASK EXPECTED RESULT(S)

Select the Hospital field and type the name of the hospital (max 64 characters).

After restart:

• The 24 first characters of this name are displayed on the scanning screen’s title bar.

• All 64 are displayed on the image properties on saved images.

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General Electric VIVID E80_E90_E95 SERVICE MANUAL_SM_GC091052_3 VividTM E95 Version 202 Basic Service Manual Direction Number: GC091542

Specifications and Main Features

Frequently Asked Questions

User Manual

Vivid™ E80 / Vivid™ E90 / Vivid™ E95

Translation policy

Damage in transportation

Certified electrical contractor statement - For USA Only

Omission and errors

Service Safety Considerations

Legal notes

Trademarks

Copyrights

Table of Contents

Chapter 1

Introduction

Manual Overview

Introduction

Vivid E80/E90/E95 models covered by this manual

Product description

Overview of the Vivid E80/E90/E95 Ultrasound system

Purpose of the operator manual(s)

Important conventions

Conventions used in book

Model designations

Icons

Safety precaution messages

Standard hazard icons

Standard Icons that indicate that a special procedure is to be used

Product icons

Safety considerations

Introduction

Human Safety

Mechanical safety

Electrical safety

Safe practices

Probes

Peripherals

Dangerous procedure warnings

Lockout/Tagout (LOTO) requirements

Returning probes and repair parts

Electromagnetic compatibility (EMC)

What is EMC?

Compliance

Electrostatic discharge (ESD) prevention

Customer assistance

Contact information

Phone numbers for Customer Assistance

System manufacturer

Chapter 2

Site Preparations

Ultrasound system environmental requirements

If the Ultrasound system is very cold or hot

Vivid E80/E90/E95 environmental specifications

Cooling

Lighting

Electrical requirements

General requirements

Electrical requirements for the Vivid E80/E90/E95

Site circuit breaker

Site power outlets

Power plug

Power stability requirements

EMI limitations

EMI prevention/abatement

Probes environmental requirements

Operation and storage temperatures for probes

Facility needs

Purchaser responsibilities

Required facility needs

Desirable features

Minimal floor plan suggestion

Recommended floor plan suggestion

Suggested floor plan, Ultrasound system, and EchoPAC PC in same room

Networking setup requirements

Stand alone Ultrasound system (without network connection)

Ultrasound system connected to hospital’s network

InSite requirements

Purpose of the DICOM network function

DICOM option setup requirements