Vivid S60 and S70 Basic Service Manual Rev 1 Feb 2019

P R E L I M I N A R Y

© 2019 General Electric Company. Manufacturer: GE Medical Systems, Israel Ltd. Nativ Ha'or Street no. 1 3508510 Haifa ISRAEL Tel: (+972) 4851 9555 Fax: (+972) 4851 9500

29.JAN.2019 VS60-VS70_FRNT_CVR.FM

DIRECTION BC291740-1EN, REVISION 1

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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.

OMISSIONS & ERRORS If there are any omissions, errors or suggestions for improving this documentation, please contact the GE Global Documentation Group with specific information listing the system type, manual title, part number or direction number, revision number, page number and suggestion details. Mail the information to: Service Documentation, GE Vingmed Ultrasound AS P.O.Box: 141 3191 HORTEN NORWAY GE employees should use Post-Market Quality Management (PQM) to report service documentation issues.

SERVICE SAFETY CONSIDERATIONS DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN

THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING. WARNING WARNING Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety

glasses, and kneeling pad, to reduce the risk of injury. For a complete review of all safety requirements, see the Chapter 1 Safety Considerations section in the Service Manual.

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LEGAL NOTES The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE. GE makes no representations or warranties with respect to the information herein. In addition, the information is subject to change without notice. Every precaution has been taken in the preparation of this document. Nevertheless, GE assumes no responsibility for errors, omissions, or any damages, including special or consequential, resulting from the use of this information. GE will issue updates to this information periodically, as needed. If there are any questions regarding the information contained in this manual, please contact your GE Representative.'

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

COPYRIGHTS © 2019 by General Electric Company Inc. All Rights Reserved.

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Revision History Revision

Date (DD.MM.YYYY)

1

25.02.2019

Reason for change Initial release of Basic Service Manual for systems updated to v203.

List of Effected Pages (LOEP) Pages

Revision

Pages

Revision

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Title Page

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4-1 to 4-46

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10-1 to 10-36

Important Precautions -i to -xvi

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5-1 to 5-32

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Back Cover

TOC

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6-1 to 6-4

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1-1 to 1-32

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7-1 to 7-30

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2-1 to 2-16

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8-1 to 8-154

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3-1 to 3-76

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9-1 to 9-32

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CHAPTER 1 Introduction Overview...1 - 1 Purpose of Chapter 1... 1 - 1 Contents in this Chapter... 1 - 1 Service Manual Overview... 1 - 2 Contents in this Service Manual... 1 - 2 Typical Users of the Basic Service Manual... 1 - 3 Vivid™ S60/Vivid™ S70 Models Covered in this Manual... 1 - 4 Product Description... 1 - 5 Important Conventions... 1 - 6 Conventions Used in this Manual... 1 - 6 Standard Hazard Icons... 1 - 7 Safety Considerations... 1 - 8 Introduction... 1 - 8 Human Safety... 1 - 8 Mechanical Safety... 1 - 10 Electrical Safety... 1 - 12 Vivid™ S60/Vivid™ S70 Battery Safety (part of Power Supply)... 1 - 14 Patient Data Safety... 1 - 14 Dangerous Procedure Warnings... 1 - 15 Lockout/Tagout (LOTO) Requirements... 1 - 16 Product Labels and Icons... 1 - 17 Universal Product Labels... 1 - 17 Label Descriptions... 1 - 21 Vivid™ S60/Vivid™ S70 External Labels... 1 - 25 Returning/Shipping Probes and Repair Parts...1 - 26 EMC, EMI, and ESD... 1 - 27 Electromagnetic Compatibility (EMC)... 1 - 27 CE Compliance... 1 - 27 Electrostatic Discharge (ESD) Prevention... 1 - 28 General Caution... 1 - 28 Customer Assistance... 1 - 29 Table of Contents

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Contact Information... 1 - 29

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CHAPTER 2 Site Preparations Overview...2 - 1 Purpose of Chapter 2... 2 - 1 Console Requirements...2 - 2 Unit Environmental Requirements... 2 - 2 Cooling Requirements... 2 - 2 Lighting Requirements... 2 - 2 Time and Manpower Requirements... 2 - 2 Electrical Requirements... 2 - 3 EMI Limitations... 2 - 4 EMI Prevention/Abatement... 2 - 5 Probe Environmental Requirements... 2 - 5 Facility Needs...2 - 6 Purchaser Responsibilities... 2 - 6 Mandatory Site Requirements... 2 - 7 Site Recommendations... 2 - 7 Networking Pre-Installation Requirements... 2 - 12 Connectivity Installation Worksheet...2 - 13

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CHAPTER 3 System Setup Overview... 3 - 1 Purpose of Chapter 3... 3 - 1 Setup Reminders... 3 - 2 Average Setup Time... 3 - 2 Setup Warnings... 3 - 2 Safety Reminders... 3 - 4 Receiving and Unpacking the Equipment... 3 - 5 Warnings for Receiving and Unpacking the Equipment... 3 - 5 Overview... 3 - 5 Additional labels on the Shipping Carton... 3 - 9 Unpacking the Vivid™ S60/Vivid™ S70... 3 - 10 Physical Inspection... 3 - 20 EMI Protection... 3 - 20 Preparing for Setup... Verifying Customer Order... Physical Inspection... Component Inspection... EMI Protection...

3 - 21 3 - 21 3 - 21 3 - 21 3 - 25

Completing the Setup... 3 - 26 Purpose of this Section... 3 - 26 System Specifications... 3 - 26 Electrical Specifications... 3 - 28 Connections on the I/O Rear Panel... 3 - 28 Connections on the Patient I/O Panel... 3 - 29 Connecting Probes... 3 - 30 Power on/Boot up... 3 - 32 Power Shut Down... 3 - 32 Complete Power Down... 3 - 32 Configuration... 3 - 33 Purpose of this Section... 3 - 33 Ultrasound System Configuration... 3 - 33 Service Screen Setup... 3 - 39 Optional Peripherals/Peripheral Connection... 3 - 42 Software Options Configuration... 3 - 44 -iv

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Connectivity Overview... 3 - 45 Physical Connection... 3 - 45 Stand-alone ultrasound system... 3 - 45 “Sneaker Net” Environment... 3 - 45 Wired Ethernet from ultrasound system to a Workstation... 3 - 45 Connection from ultrasound system to a DICOM Server on a Network... 3 - 45 Connectivity Setup... 3 - 46 Introduction... 3 - 46 Compatibility... 3 - 46 Select TCP/IP Screen... 3 - 47 Changing the AE Title and/or Port Number (Port No.)... 3 - 48 Set the Remote Archive’s Network Information... 3 - 48 Save the New Settings... 3 - 49 Wireless Network Configuration... 3 - 50 Options Setup... 3 - 51 Overview... 3 - 51 Software Options... 3 - 51 Color Video Printer Setup... 3 - 51 USB Flash Card Setup... 3 - 51 Tricefy™... 3 - 52 Wireless Network Configuration... 3 - 53 Installation and set up of the View-X function... 3 - 68 CARTO interface installation overview... 3 - 69 Verifying/Installing SW option keys... 3 - 72 External Monitor Output Resolution Adjustment... 3 - 74 Paperwork After Setup... 3 - 75 Installation Acceptance Test Criteria... 3 - 75 User’s Manual(s)... 3 - 75 Product Locator Installation Card... 3 - 75

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CHAPTER 4 General Procedures and Functional Checks Overview... 4 - 1 Purpose of Chapter 4... 4 - 1 Special Equipment Required... 4 - 1 General Procedures... 4 - 2 Overview... 4 - 2 Power On-Off... 4 - 3 Logging On to the Vivid™ S60/Vivid™ S70 as “ADM”... 4 - 9 Install the On-board User Manuals... 4 - 10 Changing Passwords... 4 - 11 Security setup... 4 - 12 Data Management... 4 - 13 Deleting Patient Information (PHI)... 4 - 14 LCD Monitor Position Adjustment... 4 - 15 Moving and Transporting the Vivid S60/Vivid S70 Ultrasound Scanner... 4 - 16 Cleaning the Trackball... 4 - 19 Functional Checks... 4 - 20 Overview... 4 - 20 Performance Checks... 4 - 20 2D Mode (B Mode) Checks... 4 - 21 M Mode Checks... 4 - 24 Color Mode Checks... 4 - 27 PW/CW Doppler Mode Checks... 4 - 32 Tissue Velocity Imaging (TVI) Checks... 4 - 35 Probe/Connectors Check... 4 - 38 ECG Check... 4 - 39 Cineloop Check... 4 - 40 Back End Processor Checks... 4 - 41 Operating Panel Check... 4 - 41 Main OLED/LCD Screen Check... 4 - 42 External Monitor Check... 4 - 42 Peripheral Checks... 4 - 42 Mechanical Functions Checks... 4 - 44

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CHAPTER 5 Components and Function (Theory) Overview...5 - 1 Purpose of Chapter 5... 5 - 1 General Information...5 - 2 Introduction... 5 - 2 Vivid™ S60/Vivid™ S70 System Design...5 - 4 User Interface Section... 5 - 5 Main Scanner Section... 5 - 5 Power Supply Section... 5 - 5 Vivid™ S60/Vivid™ S70 Ultrasound Scanner - Positioning Capabilities...5 - 6 System Up and Down Positions... 5 - 6 Upper Section - Positioning Control... 5 - 7 Main Display - Articulated Arm... 5 - 8 Main Display - Positioning Capabilities... 5 - 9 System Positioning for Transportation... 5 - 10 Vivid™ S60/Vivid™ S70 Ultrasound Scanner - Electronic Cage (v203)... 5 - 11 Scanner Electronic Cage - Main Assemblies (v203)... 5 - 11 Service Access to the Vivid™ S60/Vivid™ S70 System Modules...5 - 14 Modules Accessed from the Front (v203)... 5 - 14 Modules Accessed from the Rear... 5 - 15 Top Console with Monitor, Operator Control Panel and Touch Screen...5 - 16 Monitor (Main Display)... 5 - 16 Operator Control Panel and Speakers... 5 - 16 Touch Screen... 5 - 19 Internal and External Input/Output...5 - 20 Front End Unit...5 - 21 General Information... 5 - 21 Components in the Electronic Cage Assembly... 5 - 22 Front End Power Supply (FEPS)... 5 - 23 Front End (cFE) Board... 5 - 23 Probe Selection Board (PSB)... 5 - 24 Patient I/O Module... 5 - 24 Table of Contents

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Back End Unit... 5 - 25 Introduction... 5 - 25 System Power Distribution... 5 - 26 Introduction... 5 - 26 System Power Management... 5 - 27 Rechargeable Battery Pack... 5 - 27 Cooling System... 5 - 29 General Information... 5 - 29 Peripherals... 5 - 30 Internal Peripheral... 5 - 30 External Peripherals... 5 - 30 Service Desktop - v203... 5 - 31

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