GE Versana Premier Basic Service Manual_SM_5789130-100_5 LOGIQt α200 Service Manual

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GE
Technical Publication
Versana Premier
Basic Service Manual Direction Number: 5789130-100 English
Rev.5
ADVANCED SERVICE DOCUMENTATION. PROPERTY OF GE HEALTHCARE. USE OF THESE MATERIALS LIMITED TO AGENTS AND EMPLOYEES OF GE HEALTHCARE OR OTHER PARTIES EXPRESSLY LICENSED BY GE HEALTHCARE. UNLICENSED USE IS STRICTLY PROHIBITED.
All Material Copyright © 2018-2019 by General Electric Company Inc. All Rights Reserved.
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Product Information
This Manual covers the software version of R1.x.x for Versana Premier ultrasound system.
GE
Copyright © 2018-2019, General Electric Company. GE Medical Systems, a General Electric Company, going to market as GE
Manufacturer:
GE Medical Systems (China) Co., Ltd. No. 19, Changjiang Road WuXi National Hi-Tech Dev. Zone 214028 Jiangsu, China TEL: +86 510 85225888; FAX: +86 510 85226688 www.gehealthcare.com
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Revision History
Revision History
DATE
REV
(YYYY/MM/DD) REASON FOR CHANGE
Rev.1
Rev.2 2018/08/30 Update Common Service Desktop
Rev.3 2018/09/16 Update Probe Part Number
Rev.4 2019/01/16 Update Peripherals Installation Procedure
Rev.5 2019/05/20 Update FRU List
2018/03/09
Initial Release
List of Effected Pages (LOEP)
REVISION
CHAPTER NUMBER
Front Rev.5 Chapter 6 Rev.5
Front matter Rev.5 Chapter 7 Rev.5
TOC Rev.5 Chapter 8 Rev.5
Chapter 1 Rev.5 Chapter 9 Rev.5
Chapter 2 Rev.5 Chapter 10 Rev.5
Chapter 3 Rev.5 Index Rev.5
Chapter 4 Rev.5 Rear Cover Rev.5
Chapter 5 Rev.5
NUMBER CHAPTER NUMBER
REVISION
NUMBER
Please verify that you are using the latest revision of this document. Information pertaining to this document is maintained on MyWorkshop/ePDM (GE electronic Product Data Management). If you need to know the latest revision, contact your distributor, local GE Sales Representative or in the USA call the GE Ultrasound Clinical Answer Center at 1 800 682 5327 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 transportation company will not pay a claim for damage if an inspection is not requested within this 14 day period.

Certified electrical contractor statement - For USA Only

All electrical Installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE personnel. In performing all electrical work on these products, GE will use its own specially trained field engineers. All of GE’s electrical work on these products will comply with the requirements of the applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers, personnel of third-party service companies with equivalent training, or licensed electricians) to perform electrical servicing on the equipment.
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Omission and errors

WARNING
If there are any omissions, errors or suggestions for improving this documentation, contact the GE Global Documentation Group with specific information listing the system type, manual title, part number, revision number, page number and suggestion details.
Mail the
information to:
GE Medical Systems (China) Co., Ltd. No. 19 Changjiang Road Wuxi National Hi-Tech Dev. Zone 214028 Jiangsu, China TEL: +86 510 85225888; FAX: +86 510 85226688
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.

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 pad, to reduce the risk of injury.
For a complete review of all safety requirements, refer to Chapter 1 in the Service Manual.
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Legal notes

Proprietary to GE

The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE.
GE may revise this publication from time to time without written notice.
Permission to use this Advanced Service Software and related documentation (herein called the material) by persons other than GE employees is provided only under an Advanced Service Package License relating specifically to this Proprietary Material. This is a different agreement from the one under which operating and basic service software is licensed. A license to use operating or basic service software does not extend to or cover this software or related documentation.
If you are a GE employee or a customer who has entered into such a license agreement with GE to use this proprietary software, you are authorized to use this Material according to the conditions stated in your license agreement.
However, you do not have the permission of GE to alter, decompose or reverse-assemble the software, and unless you are a GE employee, you may not copy the Material. The Material is protected by Copyright and Trade Secret laws; the violation of which can result in civil damages and criminal prosecution.
If you are not party to such a license agreement or a GE Employee, you must exit this Material now.

Trademarks

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

Copyrights

All Material Copyright © 2018-2019 by General Electric Company Inc. All Rights Reserved.
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Translation policy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-2 Damage in transportation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14 Certified electrical contractor statement - For USA Only - - - - - - - - - - - - i-14 Omission and errors - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-15 Service Safety Considerations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-15 Legal notes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-16 Proprietary to GE - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-16 Trademarks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-16 Copyrights - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-16
Table of Contents Chapter 1 — Introduction
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-2
Manual Overview
Contents in this manual - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3 Typical users of the Proprietary Service Manual - - - - - - - - - - - - - - - - - 1-4 Purpose of Operator Manual(s) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-4 Versana Premier models covered by this manual- - - - - - - - - - - - - - - - - 1-5 Smart Manual Function - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-6
Important conventions
Conventions used in book - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-7 Standard hazard icons - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-9
Product icons Labels locations
Rating Plate Location - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-12
Safety considerations
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-14 Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-14 Human Safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-14 Mechanical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-17 Electrical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-20
Dangerous procedure warnings Lockout/Tagout (LOTO) requirements Returning probes and repair parts EMC, EMI and ESD
Electromagnetic Compatibility (EMC) - - - - - - - - - - - - - - - - - - - - - - - - 1-25 CE Compliance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-25 Electrostatic discharge (ESD) prevention - - - - - - - - - - - - - - - - - - - - - 1-26

Table of Contents

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Customer assistance
Contact information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-27 Phone numbers for Customer Assistance - - - - - - - - - - - - - - - - - - - - - 1-28 System manufacturer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-28 Authorized Representative- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-29 Factory Site - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-29
Chapter 2 — Site Preparations
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-2
General Ultrasound system requirements
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-3 Ultrasound system environmental requirements- - - - - - - - - - - - - - - - - - 2-3 Electrical requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-6 EMI limitations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-9 Probes environmental requirements - - - - - - - - - - - - - - - - - - - - - - - - - 2-11 Time and manpower requirements - - - - - - - - - - - - - - - - - - - - - - - - - - 2-11
Facility needs
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-12 Purchaser responsibilities - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-13 Required facility needs - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-14 Desirable features- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-15 Minimal floor plan suggestion- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-16 Recommended floor plan suggestion - - - - - - - - - - - - - - - - - - - - - - - - 2-17 Suggested floor plan, Ultrasound system,
and EchoPAC PC in same room - - - - - - - - - - - - - - - - - - - - - - - - 2-18
Networking setup requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-18
Environmental Dangers
Patient Vicinity UL60601-1 (USA) - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-21 Patient Environment IEC60601-1 and ANSI AAMI ES60601-1 - - - - - - 2-22
Chapter 3 — System Setup
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-2
Setup reminders
Average setup time - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3 Setup warnings- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3
Receiving and unpacking the equipment
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6 Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6 Warnings for receiving and unpacking - - - - - - - - - - - - - - - - - - - - - - - - 3-6 The Tilt indicator - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-7 Receiving the Versana Premier - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-8 Unpacking the Versana Premier - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-14 Packing the Equipment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17
Packing materials - recycling information Preparing for setup
Verify customer order - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19 Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19
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EMI protection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19
Completing the setup
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-20 Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-20 System specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-20 Electrical specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-21 Peripherals/Accessories Connector Panel- - - - - - - - - - - - - - - - - - - - - 3-22 Connections on the I/O Rear Panel - - - - - - - - - - - - - - - - - - - - - - - - - 3-24 Connecting probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-24 Powering the system - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-24
System Configuration
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-25 Versana Premier configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-25
Peripherals Installation
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-28 Furnished materials - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-29 Peripherals Installation Instructions - - - - - - - - - - - - - - - - - - - - - - - - - 3-31
Connectivity setup
EZ configuration Wizard - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-67 TCP/IP Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-77 Network setup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-78 Setup connection to a DICOM server - - - - - - - - - - - - - - - - - - - - - - - - 3-79 How to get the Versana Premier to recognize
another Device on the Network - - - - - - - - - - - - - - - - - - - - - - - - - 3-81 How to Setup and Use a DICOM Image Storage Service - - - - - - - - - - 3-82 Dataflow - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-83 Button - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-84 Removable Media - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-86 Miscellaneous - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-88 Bluetooth - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-92 Tricefy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-93
Option Setup
Software Option Installation Procedure - - - - - - - - - - - - - - - - - - - - - - - 3-96
Paperwork after setup
Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-99 User’s Manual(s) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-99 Product Locator Installation Card - - - - - - - - - - - - - - - - - - - - - - - - - - 3-100
Chapter 4 — General Procedures and Functional Checks
Overview
Purpose of this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2 Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2 Special Equipment required - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2
General procedures
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-4 Power ON/Boot Up - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-5 Power off - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-8 Check System Date and Time - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-10
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Logging on to Versana Premier as “ADM” - - - - - - - - - - - - - - - - - - - - - 4-11 Service Key (SSA) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-12 Exit to Windows Desktop from the Versana Premier
application software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13 Removable media - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13 Backup and Restore Database, Preset Configurations and Images - - - 4-13 Data Management - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-23 Backup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-23 Restore the factory defaults - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-23 Installation and Setup Procedure for Peripherals - - - - - - - - - - - - - - - - 4-23 Where are the User Manuals and the Service Manual? - - - - - - - - - - - 4-24 How to display or print the PDF files from the Manual CD? - - - - - - - - - 4-24 Cleaning the Trackball- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-25 Cleaning the air filters - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-27 Monitor - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-29 Operator Control Panel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-29
Disk Encryption/Decryption
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-30 Disk Encryption - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-31 Pause Encryption - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-34 Resume Encryption- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-35 Change Password - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-36 Change Recovery Key - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-38 Unlock with user entered key & recovery key- - - - - - - - - - - - - - - - - - - 4-39 Emergency Scanning - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-40 Disk Decryption - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-41
Functional checks
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-42 Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-42 Preparation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-42 Basic Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-43 Control Panel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-43 Versana Premier SoftMenu Key Tour - - - - - - - - - - - - - - - - - - - - - - - - 4-44 Control Panel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-45 Performance Tests - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-46 B Mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-50 B Mode Screen Example - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-50 Preparations- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-50 Adjust the B mode controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-50 M Mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-51 M-Mode Screen Example - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-51 Preparations- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-51 Adjust the M Mode controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-51 Color Mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-52 Select Color 2D Mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-52 Adjust the Color Mode controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-53 Select Color M Mode- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-54 PW Doppler Mode Checks- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-56
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Adjust the PW Doppler Mode controls- - - - - - - - - - - - - - - - - - - - - - - - 4-57 Tissue Velocity Imaging (TVI) Checks- - - - - - - - - - - - - - - - - - - - - - - - 4-58 Adjust the TVI Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-59 Basic Measurements- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-60 Probe/Connectors Check- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-61 ECG Check - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-63 Cineloop Check - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-64 Preparation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-64 Adjust the Cineloop controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-64 Back End Processor checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-64 Operator Panel Test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-65 Peripheral checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-65 Turn OFF Power to Versana Premier - - - - - - - - - - - - - - - - - - - - - - - - 4-65 Mechanical Functions Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-65
Power supply test & adjustments
Power Supply Test Procedure - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-67 Power Supply Adjustment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-67
Application Turnover Check List
Software Configuration Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-68
Site Log My Trainer
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-70
Chapter 5 — Components and Functions (Theory)
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-2
Block Diagram and Theory
General Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3 Top Console- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3
Common Service Desktop
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-6
Chapter 6 — Service Adjustments
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2
Preset Region
Region presetting procedure - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-4
Monitor Adjustments
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-6 Monitor Adjustments - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-6 Brightness and Contrast - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-7
Chapter 7 — Diagnostics/Troubleshooting
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-2
Gathering Trouble Data
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3 Collect Vital System Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3 Collect a Trouble Image with Logs - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-4
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Screen Capture
Capturing a Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-6 Capturing a Screen with Service Dongle - - - - - - - - - - - - - - - - - - - - - - - 7-8 Capturing a Screen by physical print buttons - - - - - - - - - - - - - - - - - - - 7-10
System Warning/Error and Logs
Temperature warning - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-11 Temperature exceeds threshold- - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-11 System voltage failure- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-12 Hardware configuration error - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-12 System error - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-13
Common Service Desktop
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-14 Disruptive mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-15 Color statuses - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-16 Licenses - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-16 Home - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-18
Network and Common Diagnostics
Network Configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-37 Remote Access - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-41 Service Diagnostics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-45
Troubleshooting
Console Troubleshooting - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-51
Chapter 8 — Replacement Procedures
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-2
Warnings and important information
Warnings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-3 Returning/shipping probes and repair parts - - - - - - - - - - - - - - - - - - - - - 8-4
Disassembly/Re-assembly
Warning and Caution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-5 Tools needed for servicing Versana Premier - - - - - - - - - - - - - - - - - - - - 8-6 Overview of Versana Premier - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-7
Loading the software
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-9 Customer provided prerequisite - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-9 Data Management - moving all images - - - - - - - - - - - - - - - - - - - - - - - - 8-9 Backing up the Patient Archive and System Configurations - - - - - - - - 8-10 Restoring up the Patient Archive and System Configurations - - - - - - - 8-10 Recording important settings and parameters - - - - - - - - - - - - - - - - - - 8-11 Loading the System Software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-12
Chapter 9 — Renewal Parts
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-2
List of Abbreviations Renewal Parts Lists
Operator Console Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-4 Probe - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-6
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Peripheral - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-6 Power Cord - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-8 Manuals- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-9
Chapter 10 — Care and Maintenance
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-2
Warnings Why do maintenance
Preventive maintenance inspections- - - - - - - - - - - - - - - - - - - - - - - - - 10-4 Quality assurance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-5
Maintenance task schedule
How often should maintenance tasks be performed? - - - - - - - - - - - - - 10-6
Tools required
Standard GE tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-8 GE-2 tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-10 Special tools, supplies and equipment used for maintenance - - - - - - 10-11
System maintenance
Preliminary checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-12 Functional checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-13 Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-16 Optional Diagnostic Checks- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-16 Probe maintenance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-18
Electrical safety tests
Safety test overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-24 Leakage current limits - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-26 Outlet test - wiring arrangement - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-28 Grounding continuity - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-29 Chassis leakage current test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-30 Probe leakage current test- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-32
When there's too much leakage current …
AC/DC Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-35 Chassis Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-35 Probe Fails- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-36 Peripheral Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-36 Still Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-36 New Unit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-36 ECG Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-36
Inspection Paperwork
Ultrasound Inspection Forms - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-37
Electrical Safety Tests Log
Index
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Chapter 1

Introduction
This chapter describes important issues related to safely servicing the Ultrasound system. The service provider must read and understand all the information presented here before installing or servicing the units.
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Introduction

1-1-1 Contents in this chapter

1-1 ‘Overview’ on page 1-2
1-2 ‘Manual Overview’ on page 1-3
1-3 ‘Important conventions’ on page 1-7
1-4 ‘Product icons’ on page 1-11
1-5 ‘Labels locations’ on page 1-12
1-6 ‘Safety considerations’ on page 1-14
1-7 ‘Dangerous procedure warnings’ on page 1-22
1-8 ‘Lockout/Tagout (LOTO) requirements’ on page 1-23
1-9 ‘Returning probes and repair parts’ on page 1-24
1-10 ‘EMC, EMI and ESD’ on page 1-25
1-11 ‘Customer assistance’ on page 1-27

1-1 Overview

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This manual provides installation and service information for the Versana Premier Ultrasound system. It is divided in ten chapters as shown below.

1-2-1 Contents in this manual

The manual is divided into ten chapters.
In the beginning of the manual, before chapter 1, you will find the Revision overview, the Important precautions including
Translation policy, Damage in transportation, Certified electrical contractor statement, Omission & errors, Service safety considerations and Legal notes, and the Table of Contents (TOC).
Manual Overview

1-2 Manual Overview

Chapter number
1.
2.
3.
4.
5.
6.
An Index has been included after Chapter 10.
Table 1-1: Contents in this manual
Chapter title Description
Introduction Contains a content summary and warnings.
Site preparations Contains pre-setup requirements for the Versana
Premier.
System Setup Contains setup procedure with procedure
checklist for the system.
General Procedures and Functional Checks
Components and Functions (Theory)
Service Adjustments Contains instructions on how to make any
Contains functional checks that must be performed as part of the installation, or as required during servicing and periodic maintenance.
Contains block diagrams and functional explanations of the electronics.
available adjustments to the Versana Premier.
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Introduction
Table 1-1: Contents in this manual (Continued)
Chapter
Chapter title Description
number
7.
8.
9.
Diagnostics/ Troubleshooting
Replacement procedures
Provides procedures for running diagnostic or related routines for the Versana Premier.
Provides disassembly procedures and reassembly procedures for all changeable FRU.
Renewal Parts Contains a complete list of replacement parts for
Versana Premier.
10.
Care & Maintenance Provides periodic maintenance procedures for
Versana Premier.
N/A
Index A quick way to the topic you’re looking for.

1-2-2 Typical users of the Proprietary Service Manual

GEHC Service Personnel (setup, maintenance, etc.)
GEHC Online Center Personnel
Licensed Hospital’s Service Providers

1-2-3 Purpose of Operator Manual(s)

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

1-2-4 Versana Premier models covered by this manual

Table 1-2: Versana Premier Model Designations
Model Name System SW
Versana Premier VA R1.x.x
Versana Premier VS R1.x.x
NOTE: When not otherwise specified, the contents of this manual
applies to all Versana Premier models.
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Introduction

1-2-5 Smart Manual Function

On each page of this Proprietary Service Manual, there is a smart manual icon to bring you back to Overview of Versana Premier. By clicking on the system overview list, you can be brought to the FRU list directly.
Figure 1-1. Smart Manual Icon
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1-3 Important conventions

1-3-1 Conventions used in book

Important conventions, used in this document, are described next.
1-3-1-1 Model designations
This manual covers the Versana Premier Ultrasound systems listed in:
1-2-4 ‘Versana Premier models covered by this manual’ on
page 1-5.
1-3-1-2 Icons
Important conventions
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 described in this chapter.
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Introduction
DANGER
WARNING
CAUTION
1-3-1-3 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 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 if the instructions are ignored.
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.
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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1-3-2 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.
Important conventions
Table 1-3: 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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Introduction
1-3-2-1 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 1-4: 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
Be sure to read the notes; the information contained in a note can often save you time or effort.
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Product icons

1-4 Product icons

It is important to refer to the current revision of the Ultrasound system’s Basic User Manual for a full list of product labels prior to servicing the system.
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Introduction
It is important to refer to the current revision of the Ultrasound system’s Basic User Manual for a full list of product labels prior to servicing the system.

1-5-1 Rating Plate Location

Versana Premier labels are provided in English.
The labels are at the rear of the system. The label content may be different for different regions. Please refer to the labels on the system for the actual content.

1-5 Labels locations

Figure 1-2. Versana Premier Label Location
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1-5-1 Rating Plate Location(continued)
1. Rating Plate
Table 1-5: Label Icons
Label/Icon Purpose/Meaning Location
Labels locations
Every system has a unique marking for identification, the Unique Device Identification (UDI) Label. The UDI label consists of a series of alpha-numeric characters and barcode which uniquely identify the Versana Premier system as a medical device manufactured by General Electric. Scan or enter the UDI information into the patient health record as required by country-specific laws.
Serial Number.
Rating plate
Rating plate
NOTE: If the new label is needed during the service activities, please
click “Ask an Expert” to submit the case in the support central: http://supportcentral.ge.com/products/sup_products.asp?prod_ id=44177.
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Introduction

1-6 Safety considerations

1-6-1 Contents in this section

1-6-2 ‘Introduction’ on page 1-14
1-6-3 ‘Human Safety’ on page 1-14
1-6-4 ‘Mechanical safety’ on page 1-17
1-6-5 ‘Electrical safety’ on page 1-20

1-6-2 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.

1-6-3 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 Versana Premier Training Seminar are authorized to service the equipment.
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1-6-3 Human Safety(continued)
WARNING
WARNING
WARNING
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.
Have two people available to deliver and unpack the Versana Premier.
Attempts to move the Ultrasound system considerable distances or on an incline by one person could result in injury or damage or both.
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.
Safety considerations
Ultrasound system components may be energized. Always refer to the Ultrasound system's Proprietary Service Manual for LOTO warnings and cautions.
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Introduction
WARNING
WARNING
WARNING
WARNING
1-6-3 Human Safety(continued)
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 Service Manual for LOTO warnings and cautions
Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and kneeling pad, 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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1-6-4 Mechanical safety

WARNING
WARNING
WARNING
WARNING
CAUTION
CAUTION
While the software install procedure is designed to preserve data, you should save any patient data, images, system setups 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.
Safety considerations
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.
Take extra care when moving the system.
The Versana Premier weighs approximately 70 kg (140 lbs) or more, depending on installed peripherals, when ready for use. To avoid possible injury and equipment damage when transporting from one area of use to another:
Be sure the pathway is clear.
Limit movement to a slow careful walk.
Use two or more persons to move the equipment on inclines or long distance.
Before you move or transport the Ultrasound system, make sure to lock the monitor arm firmly and flip down the monitor to prevent damage to the Ultrasound system.
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Introduction
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
1-6-4 Mechanical safety(continued)
To avoid injury when you move the 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 when moving the operator panel.
Do not move the Ultrasound system if the Operator Panel is in unlocked position.
Do not transport Versana Premier 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 eyes need protection.
Use safety shoes when doing work where there is any chance of foot injury.
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1-6-4 Mechanical safety(continued)
CAUTION
CAUTION
Use protective gloves when working with sharp edges or when directed to wear PPE during a removal/replacement procedure.
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 system in its special storage case.
Lock the wheels (brake).
Ensure that the system is firmly secured while inside the vehicle.
Secure system with straps or as directed otherwise to prevent motion during transport.
Prevent vibration damage by driving cautiously. Avoid unpaved roads, excessive speeds, and erratic stops or starts.
Safety considerations
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Introduction
WARNING
WARNING

1-6-5 Electrical safety

1-6-5-1 Safe practices
Follow these guidelines to minimize shock hazards whenever you are using the Ultrasound system:
To minimize shock hazard, the equipment chassis must be
The Ultrasound system is equipped with a three-conductor
The power outlet used for this equipment should not be
Both the system power cable and the power connector must
Connecting a Versana Premier to the wrong voltage level will most likely destroy it.
connected to an electrical ground.
AC power cable. This must be plugged into an approved electrical outlet with safety ground.
shared with other types of equipment.
meet international electrical standards.
DO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY CIRCUMSTANCES.
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1-6-5-2 Probes
Safety considerations
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 system has more than one type of probe port. Use the appropriate probe port designed for the probe you are connecting.
1-6-5-3 Peripherals
Refer to the Patient Safety Environment section of the User’s Manual for peripheral isolation information.
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Introduction
DANGER
WARNING
WARNING
WARNING
WARNING
WARNING

1-7 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 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 Versana Premier, 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 parts. DO NOT perform any unauthorized modification of the equipment.
SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC INVALID MAY CAUSE THE DAMAGE OF SYSTEM FILES.
AFTER UNPLUG POWER CORD, WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO TEST POINTS TO VERIFY ISOLATION.
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Lockout/Tagout (LOTO) requirements

WARNING
1-8 Lockout/Tagout (LOTO)
requirements
Follow Lockout/Tagout requirements by ensuring you are in total control of the AC power plug at all times during the service process.
To apply Lockout/Tagout (LOTO):
1. Plan and prepare for shutdown.
2. Shutdown the equipment.
3. Isolate the equipment.
4. Remove/disconnect the battery, if present.
5. Apply Lockout/Tagout Devices.
6. Control all stored and residual energy.
7. Verify isolation.
All potentially hazardous stored or residual energy is relieved.
Energy Control and Power Lockout for Versana Premier.
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 for 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
1-9 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 properly removed from any 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 ultrasound probe).
The purpose of the regulation is to protect employees in the transportation industry, as well as the people who will receive or open this package.
NOTE: The US Department of Transportation (DOT) has ruled that
“items that were saturated and/or dripping with human blood that are now caked with dried blood; or which were used or intended for use in patient care” are “regulated medical waste” for transportation purposes and must be transported as a hazardous material.
NOTE: The USER/SERVICE staff should dispose of all the waste
properly, per federal, state, and local waste disposal regulations.
The Ultrasound system is not meant to be used for long-term storage of patient data or images. The user is responsible for the data on the system and a regular backup is highly recommended.
If the system is sent for repair, please ensure that any patient information is backed up and erased from the system before shipping. It is always possible during system failure and repair to lose patient data. 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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1-10 EMC, EMI and ESD

1-10-1 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.
EMC, EMI and ESD

1-10-2 CE Compliance

Versana Premier 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 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
WARNING

1-10-3 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.
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1-11 Customer assistance

1-11-1 Contact information

If this equipment does not work as indicated in this service manual or in the basic 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 log (Alt+D) to send to the Customer Care team:
1. 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.
Customer assistance
NOTE: Restart the application before resuming clinical scanning.
NOTE: The serial number can be found at the rear of the system.
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Introduction

1-11-2 Phone numbers for Customer Assistance

Table 1-6: Phone numbers for Customer Assistance
LOCATION PHONE NUMBER
USA GE Healthcare - GE Medical Systems Ultrasound Service Engineering 9900 Innovation Drive Wauwatosa, WI 53226
Canada Phone: 1-800-668-0732
Latin America Service
Europe (OLC-EMEA) GE Ultraschall Deutschland Gmbh & Co. KG Beethovenstraße 239 Postfach 11 05 60, D-42655 Solingen Germany
Online Services Ultrasound Asia Phone:
Service: On-site 1-800-437-1171
Service Parts 1-800-558-2040
Application Support 1-800-682-5327 or
1-262-524-5698
Application Support
OLC - EMEA Phone:
Fax: +49 (0) 2122-8024-31
• Australia
• China
• India
• Japan
• Korea
• Singapore
1-800-321-7937 1-262-524-5698
+49 (0) 212 2802 - 652 +33 1 3083 1300
+(61) 1-800-647-855 +(86) 800-810-8188 +(91) 1800-425-8025 +(81) 42-648-2940 +(82) 2620 13585 +(95) 6277-3444

1-11-3 System manufacturer

Table 1-7: System manufacturer
MANUFACTURER PHONE NUMBER FAX NUMBER
GE Medical Systems (China) Co., Ltd. No.19 Changjiang Road WuXi National Hi-Tech Dev.Zone 214028 Jiangsu China
+86 510 85225888 +86 510 85226688
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1-11-4 Authorized Representative

Table 1-8: Authorized Representative
AUTHORIZED REPRESENTATIVE
The location of the CE marking is shown in the Safety chapter of the Basic User Manual.
Authorized EU Representative: GE Medical Systems SCS 283 rue de la Minière 78530 BUC, France

1-11-5 Factory Site

Table 1-9: Factory Site
Factory Site
Customer assistance
TELEPHONE / FAX
NUMBER
TELEPHONE / FAX
NUMBER
GE Medical Systems (China) Co., Ltd. No.19, Changjiang Road, Wuxi National Hi-Tech Dev.Zone, 214028 Jiangsu, China
TEL: +86 510-85225888 FAX: +86 510-85226688
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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 the descriptions of the facility and electrical needs to be met by the purchaser of the units.
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Site Preparations

2-1-1 Contents in this chapter

2-1 ‘Overview’ on page 2-2
2-2 ‘General Ultrasound system requirements’ on page 2-3
2-3 ‘Facility needs’ on page 2-12
2-4 ‘Environmental Dangers’ on page 2-21

2-1 Overview

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2-2 General Ultrasound system
CAUTION

2-2-1 Contents in this section

2-2-2 ‘Ultrasound system environmental requirements’ on
page 2-3
2-2-3 ‘Electrical requirements’ on page 2-6
2-2-4 ‘EMI limitations’ on page 2-9
2-2-5 ‘Probes environmental requirements’ on page 2-11
2-2-6 ‘Time and manpower requirements’ on page 2-11

General Ultrasound system requirements

requirements

2-2-2 Ultrasound system environmental requirements

2-2-2-1 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: System Acclimation Time Chart
Degree C -4.5 -2 0.5 3 40 42.5 45 47.5 50 55 60
Degree F 23.9 28.4 32.9 37.4 104 108.5 113 117.5 122 131 140
hours
3
2
1
0 0 1 23 468
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Site Preparations
CAUTION
CAUTION
2-2-2-2 Environmental specifications for Ultrasound system
The system should be operated, stored, or transported within the parameters outlined below. Either its operational environment must be constantly maintained or the unit must be turned off.
Table 2-2: System Environmental Requirements
Temperature
Humidity
Pressure
Operational (Versana Premier with probe)
3- 40° C (without battery)
Storage (Versana Premier)
-5 - 50° C
23 - 122° F
Transport (Versana Premier)
-5 - 50° C
23 - 122° F
37.4 - 104° F
10 - 30° C (with battery)
50 - 86° F
30 - 80% non-condensing
10 - 90% non-condensing
10 - 90% non-condensing
700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
Ensure that the probe face temperature does not exceed the normal operation temperature range.
The Versana Premier system and probe connector is not waterproof. Do not expose the device to water or any kind of liquid.
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2-2-2-3 Cooling
NOTE: Each person in the room places an additional 300 BTU/h
2-2-2-4 Lighting
General Ultrasound system requirements
The cooling requirement for a console Ultrasound system with monitor and on board peripherals, is up to 3800 BTU/h. This figure does 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

2-2-3 Electrical requirements

2-2-3-1 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.
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.
2-2-3-2 Electrical requirements for the Ultrasound system
In the table below, the electrical specifications for the Ultrasound system includes monitor and on board peripherals.
Table 2-3: Electrical Specifications for Versana Premier system
Vol tag e
100-240 VAC ±10% Max. 450VA 50/ 60HZ
Toleranc e Power Consumption Frequency
:
:
2-2-3-3 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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2-2-3-4 Site circuit breaker
CAUTION
It is recommended that the branch circuit breaker for the Ultrasound system be readily accessible.
POWER OUTAGE MAY OCCURE.
The Versana Premier requires a dedicated single branch circuit. To avoid circuit overload and possible loss of critical care equipment, make sure you DO NOT have any other equipment operating on the same circuit.
2-2-3-5 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.
General Ultrasound system requirements
2-2-3-6 Unit 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.
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2-2-3-7 Power stability requirement
Table 2-4: Power stability requirement
IEC 61000-4-11
Voltage dips, short interruptions and voltage variations on mains supply
< 5%T (> 95% dip) for
0.5 cycle;
40%T (60% dip) for 5 cycles;
70%T (30 dip) for 25 cycles;
< 5%T (>95% dip) for 5 sec
< 5%T (> 95% dip) for
0.5 cycle;
40%T (60% dip) for 5 cycles;
70%T (30 dip) for 25 cycles;
< 5%T (>95% dip) for 5 sec
Mains power quality should be that of a typical commercial or hospital environment.
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2-2-4 EMI limitations

General Ultrasound system requirements
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
• portable phones
The presence of a broadcast station or broadcast van may also cause interference.
See: 2-2-4-1 ‘EMI prevention/abatement’ on page 2-10 for EMI prevention tips.
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2-2-4-1 EMI prevention/abatement
Table 2-5: 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
Use GE specified harnesses and peripherals
Take care with cellular phones
Properly route peripheral cables
• 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.
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
CAUTION
CAUTION

2-2-5 Probes environmental requirements

2-2-5-1 Operation, storage and transport temperatures for probes
Probes should be operated, stored, or transported within the parameters outlined below.
Ensure that the probe face temperature does not exceed the normal operation temperature range.
Table 2-6: Probe Environmental Requirements
Operational Storage Transport
Temperature 10° - 40° C
50° - 104° F
Humidity 30- 80%
non-condensing
Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
-5° - 50° C 23° - 122° F
10 - 90% non-condensing
-5° - 50° C 23° - 122° F
10 - 90% non-condensing
Check the room temperature before you use the probe.
Ensure that the probe face temperature does not exceed the normal operation temperature range.
NOTE: Refer to Table 2-1 on page 2-3 to determine the needed
settlement time.

2-2-6 Time and manpower requirements

Site preparation takes time. Begin site preparation checks as soon as possible, if possible, six weeks before delivery, to allow enough time to make any changes.
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Site Preparations

2-3-1 Contents in this section

2-3-2 ‘Purchaser responsibilities’ on page 2-13
2-3-3 ‘Required facility needs’ on page 2-14
2-3-4 ‘Desirable features’ on page 2-15
2-3-5 ‘Minimal floor plan suggestion’ on page 2-16
2-3-6 ‘Recommended floor plan suggestion’ on page 2-17
2-3-7 ‘Suggested floor plan, Ultrasound system, and
EchoPAC PC in same room’ on page 2-18
2-3-8 ‘Networking setup requirements’ on page 2-18

2-3 Facility needs

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2-3-2 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
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.
Facility needs
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) should also be investigated before delivery. Dirt, static, and EMI can negatively impact Ultrasound system reliability.
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2-3-3 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.
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.
:
:
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2-3-3 Required facility needs(continued)
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.
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 0.5m (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 unit 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)
Facility needs
For the amperage requirements, see: 2-2-3 ‘Electrical
requirements’ on page 2-6.

2-3-4 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
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Site Preparations
4
1
3
11
6
13
8
10
5
7
9
12
14
2

2-3-5 Minimal floor plan suggestion

CSI 8x10
Scale: Each square equals one square foot (app. 31 x 31 cm)
1. Door – at least 762 mm (30 inches)
2. Film Viewer
3. Counter Top, Sink with hot and cold water and Supplies Storage
4. Linen Supply
5. Probes/Supplies
6. Examination Table – 1930 x 610 mm (76 x 24 inches)
7. Footswitch
8. Stool
9. Ultrasound system
10. External Peripherals
11. Dedicated Power Outlet ­Circuit Breaker protected and easily accessible
12. Network Interface
13. 457 mm (18 inches) distance of Ultrasound system from wall or objects
14. GE Cabinet for Software and Manuals
Figure 2-1. Minimal floor plan, 2.5 m x 3 m (8 by 10 foot)
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2-3-6 Recommended floor plan suggestion

CSI 14x17
Facility needs
10
11
12
15
9
2
3
4
5
13 14
16
8
7
1
17
6
18
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. A 14 by 17 foot recommended floor plan
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2-3-7 Suggested floor plan, Ultrasound system, and EchoPAC PC in
same room
1. EchoPAC PC 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 PC workstation and Ultrasound Scanner

2-3-8 Networking setup requirements

2-3-8-1 Stand alone Ultrasound system (without network connection)
None.
2-3-8-2 Scanner connected to hospital’s network
Supported networks:
100/1000 Mbit Ethernet/DICOM network (option)
2-3-8-3 InSite requirements
InSite requires an Ethernet connection via:
100/1000 Mbit Interface
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2-3-8-4 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.
Facility needs
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Site Preparations
2-3-8-5 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 are no spaces in any field of the form.
See:
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.
Figure 2-4. Worksheet for DICOM Network Information
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Environmental Dangers

2-4 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 standards. 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.

2-4-1 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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2-4-2 Patient Environment IEC60601-1 and ANSI AAMI ES60601-1

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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Chapter 3

System Setup
This chapter contains information needed to install Versana Premier system.
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 unit of the actual installation, and how to check and test the unit, probes, and external peripherals for electrical safety are also included in this procedure.
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3-1-1 Contents in this chapter

3-1 ‘Overview’ on page 3-2
3-2 ‘Setup reminders’ on page 3-3
3-3 ‘Receiving and unpacking the equipment’ on page 3-6
3-5 ‘Preparing for setup’ on page 3-19
3-6 ‘Completing the setup’ on page 3-20
3-7 ‘System Configuration’ on page 3-25
3-8-3 ‘Peripherals Installation Instructions’ on page 3-31
3-9 ‘Connectivity setup’ on page 3-67
3-11 ‘Paperwork after setup’ on page 3-99

3-1 Overview

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3-2-1 Average setup time

DANGER
CAUTION
CAUTION
CAUTION
Unpacking the Versana Premier: 30 minutes
Set up Versana Premier options: 30 minutes
DICOM Network Configuration: 30 minutes or more, depending on the configuration
Install Insite: 0.5 hour
The Versana Premier installation and functional checkout will take approximately 1 hour. Versana Premier consoles with optional equipment may take slightly longer.

3-2-2 Setup warnings

Setup reminders

3-2 Setup reminders

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 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 operate this unit unless all board covers and frame panels are securely in place. System performance and cooling require this.
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DANGER
CAUTION
3-2-2 Setup warnings(continued)
1. There are no operator serviceable components. To prevent shock, do not remove any covers or panels. Should problems or malfunctions occur, unplug the power cord. Only qualified service personnel should carry out servicing.
NOTE: For information regarding packing labels, refer to LABELS
ON PACKAGE.
2. 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 3°C or above 40°C.
Equipment damage possibility. Turning the system on without acclimation after arriving at site may cause the system to be damaged.
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.
Degree C
Degree F
hours
The following table describes guidelines for reaching operational temperatures from storage or transport temperatures.
Table 3-1: System Acclimation Time Chart
50 45 40 35 30 25 20 15 10 5 0 -5
122 113 104 95 86 77 68 59 50 41 23 23
420000000246
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3-2-2 Setup warnings(continued)
CAUTION
CAUTION
Operator Manual(s)
The User Manual(s) should be fully read and understood before operating the Versana Premier and kept near the Ultrasound system for quick reference.
Acoustic Output Hazard
Although the ultrasound energy transmitted from the Versana Premier probe is within AIUM/NEMA standards, avoid unnecessary exposure. ultrasound energy can produce heat and mechanical damage.
Setup reminders
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CAUTION
CAUTION
3-3 Receiving and unpacking the

3-3-1 Purpose of this section

This section describes how to receive and unpack Versana Premier.

3-3-2 Contents in this section

3-3-3 ‘Warnings for receiving and unpacking’ on page 3-6
3-3-4 ‘The Tilt indicator’ on page 3-7
3-3-5 ‘Receiving the Versana Premier’ on page 3-8
3-3-6 ‘Unpacking the Versana Premier’ on page 3-14
equipment

3-3-3 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 protecting equipment (PPE) during packing and unpacking. Check with your local EHS representative.
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Receiving and unpacking the equipment

3-3-4 The Tilt indicator

3-3-4-1 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 indicator has been attached to the transportation box.
Table 3-2: Tilt Watch
Description Illustration
Tilt Watch
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3-3-5 Receiving the Versana Premier

3-3-5-1 Examine all packages
Examine package closely at time of delivery, as described in the procedure below.
Table 3-3: Examine all packages
Step Task Illustrations
1. Is damage apparent?
• If YES; continue with the instructions in
3-3-5-4 ‘Damage in transportation’ on
page 3-11.
• If NO; continue with the next step.
2. 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
3-3-5-4 ‘Damage in transportation’ on
page 3-11 before you continue with the next
step.
• If NO: continue with the next step.
3. Continue with the instructions in
3-3-6 ‘Unpacking the Versana Premier’ on
page 3-14.
1 - Red Color
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3-3-5-2 Position of the Tilt indicator
The Tilt indicator has been attached to the transportation box as illustrated in the figure below.
Receiving and unpacking the equipment
Figure 3-1. Tilt indicator
1. Tilt Indicator
NOTE: Before cutting the straps, check Tilt Tag
been triggered. If damaged, report it to the carrier. If not, then cut the straps around the crate.
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System Setup
3-3-5-3 If Tilt Indicator has triggered or is missing
The purpose of the tilt indicator label is to alert people handling a product that it is sensitive to tipping and it must remain upright at all times. It is basically an active "Up Arrow" that changes color if the package is tipped 89 degrees or more from horizontal. These labels can be false activated if tipped less than 89 degrees, and shocked or vibrated at the same time. This event does occur, but is considered uncommon. If a package is received with an activated tilt indicator label, there is high degree of certainty it tipped 89 degrees or more from horizontal during shipment.
An activated tilt indicator label does not indicate if 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 if a Tip Over impact shock occurred.
Table 3-4: Tilt Indicator has triggered or is missing
Step Task
1.
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.
2.
Inspect the product for possible concealed damage.
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Receiving and unpacking the equipment
3-3-5-4 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 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.
3-3-5-5 Versana Premier transportation box label
The Versana Premier transportation box label is located at the front of the transportation box.
Figure 3-2. Versana Premier transportation box label 1
Figure 3-3. Versana Premier transportation box label 2
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3-3-5-5 Versana Premier transportation box label(continued)
Table 3-5: Package Label Icons
Label/Icon Purpose/Meaning Location
Keep this way up. Package
Fragile. Package
Package
Keep it away from rain.
2 levels at most. Package
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Receiving and unpacking the equipment
Table 3-5: Package Label Icons
Label/Icon Purpose/Meaning Location
Humidity Limitation Package
Temperature Limitation Package
Pressure Limitation Package
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CAUTION
CAUTION
CAUTION

3-3-6 Unpacking the Versana Premier

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.
Please carefully unpack the system, and do not dispose the package of Versana Premier, so that it can be reused for service.
Do not lift the unit by the Keyboard. Equipment damage may result.
The crate with the Versana Premier weighs approximately 50kg. Be prepared for a sudden shift of weight as the unit is removed from its base (pallet).
NOTE: Please check the Versana Premier console is well assembly
after unpacking the system.
Table 3-6: Unpacking the Versana Premier
Step Description Corresponding Graphic
1 Tear off the "stop open" mark.
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Receiving and unpacking the equipment
Table 3-6: Unpacking the Versana Premier
Step Description Corresponding Graphic
2 Cut off the two packing straps around the crate.
Note: To avoid injury, hold the strap clasp with one hand when cutting the strap.
3 Remove the top cover.
4 Remove the three plastic locks.
Note: Rotate the inside plastic lock
counterclockwise to remove it and then remove the outside lock.
5 Remove the outside shipping box.
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Table 3-6: Unpacking the Versana Premier
Step Description Corresponding Graphic
6 Remove the 2 foams beside the system.
Note: There is no foam if the system is transported by air. Ignore this step if there is no foam.
7 Remove the clear plastic (wrapped around the
8 Cut the cable ties around the four wheels.
Versana Premier) from the unit.
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Receiving and unpacking the equipment
Table 3-6: Unpacking the Versana Premier
Step Description Corresponding Graphic
9 Remove the barrier bag from the unit.
Note: Remove the PE bag if the system is transported by air.
10 Remove the foams beside the monitor.
11 Remove any additional packing material
surrounding the system.
12 Unlock the wheels, and then hold the control
panel at the front side to move the system until the front two wheels on the ground and then slowly move the whole system on the ground.
3-3-6-1 Moving into Position
Please refer to Basic User Manual on how to move the system.

3-3-7 Packing the Equipment

Please pack Versana Premier in the reverse order of unpacking.
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3-4 Packing materials - recycling
information
The packing materials for Versana Premier are recyclable:
The Transportation Box is made of spruce or similar material. (“PHYTOSANITARY CERTIFICATE” included in all shipments to The People's Republic of China.)
Lever lockings (hinges) are made of zinc plated steel.
The inner reinforcements are made of Ethafoam (Polyethylene foam).
The plastic foil is made of LDPE (Low Density Polyethylene).
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3-5 Preparing for setup

3-5-1 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.

3-5-2 Physical inspection

Verify that the system arrived intact (visual inspection).
If the system has been damaged, please refer to ‘Damage in
transportation’ on page i-14 in the beginning of this manual.
Preparing for setup

3-5-3 EMI protection

The Versana Premier 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.
See 2-2-4 ‘EMI limitations’ on page 2-9 for more information about EMI protection.
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3-6 Completing the setup

3-6-1 Purpose of this section

This section describes how to complete the installation of Versana Premier.

3-6-2 Contents in this section

3-6-3 ‘System specifications’ on page 3-20
3-6-4 ‘Electrical specifications’ on page 3-21
3-6-6 ‘Connections on the I/O Rear Panel’ on page 3-24
3-6-7 ‘Connecting probes’ on page 3-24
3-6-8 ‘Powering the system’ on page 3-24

3-6-3 System specifications

3-6-3-1 System requirements verification
Verify that the site meets the requirements listed in Chapter 2.
(See: 2-3 ‘Facility needs’ on page 2-12.)
Verify that the specifications below don’t conflict with any on-site conditions.
3-6-3-2 Physical dimensions
Table 3-7: Physical dimensions of Versana Premier
Height Width Depth Unit
less than 1780 less than 620 less than 810 mm
less than 70 less than 24.4 less than 31.8 Inches
3-6-3-3 Console Weight
Weight: approx. 70 kg (154.3 lbs)
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3-6-4 Electrical specifications

WARNING
Connecting a Versana Premier to the wrong voltage level will most likely destroy it.
3-6-4-1 Verification of the system’s voltage setting
Verify that the mains voltage specified for the Versana Premier is available on-site.
Refer to the latest revision of the Basic User Manual for a full list of product labels prior to serving the system.
3-6-4-2 Electrical specifications for Versana Premier
In the table below, the electrical specifications for Versana Premier includes monitor and on board peripherals.
Table 3-8: Electrical specifications for Versana Premier
Completing the setup
Model Name Vol tag e Tolerances
Versana Premier VA
100-240V ±10% Max.450VA 50/60 Hz
Versana Premier VS
Power
consumption Frequency
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3-6-5 Peripherals/Accessories Connector Panel

Versana Premier peripherals and accessories can be properly connected using the side connector panel.
Figure 3-4. Rear Connector Panel
1. Power out port DC 12V 1.5A Out (Only for Digital Box in China)
2. Diagnostic LED Diagnostic LED 1, Diagnostic LED 2, Diagnostic LED 3
3. Dual USB port USB for use
4. Ethernet 10/100MBase-T for LAN connectivity
5. USB port USB 3.0 Port for use
6. HDMI port For video port (Resolution 1920x1080)
7. VGA VGA Video Out
8. Audio Line Out Audio Line Out
9. S-Video S-Video Out
10. Composite Out Composited Video Out
11. Circuit breaker Circuit breaker
12. AC Inlet 100-240V
13. GND Ground terminal
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