GE Healthcare
Technical
Publications
Direction 5118586-100
Rev. 2
LOGIQ e Basic User Manual
Operating Documentation
Copyright 2006 By General Electric Co.
Regulatory Requirements
This product complies with regulatory requirements of the following European Directive 93/42/EEC concerning medical devices.
This manual is a reference for the LOGIQ e. It applies to all versions of the R4.x.x software for the LOGIQ e ultrasound system.
GE Healthcare
GE Healthcare: Telex 3797371
P. O. Box 414, Milwaukee, Wisconsin 53201 USA
(Asia, Pacific, Latin America, North America)
GE Ultraschall TEL: 49 212.28.02.208
Deutschland GmbH & Co. KG FAX: 49 212.28.02.431
Beethovenstrasse 239
Postfach 11 05 60
D-42655 Solingen GERMANY
Revision History
List of Effective Pages
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April 7, 2006 |
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August 1, 2006 |
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Title Page |
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Revision History |
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Chapter 10 |
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Regulatory Requirements |
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Chapter 11 |
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Table of Contents |
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Chapter 12 |
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Chapter 1 |
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Chapter 13 |
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Chapter 2 |
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Chapter 14 |
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Chapter 3 |
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Chapter 4 |
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Chapter 5 |
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Chapter 17 |
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Chapter 6 |
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Chapter 7 |
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Index |
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Chapter 8 |
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Please verify that you are using the latest revision of this document. Information pertaining to this document is maintained on ePDM (GE Medical Systems 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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Regulatory Requirements
Conformance Standards
The following classifications are in accordance with the IEC/
EN 60601-1:6.8.1:
•According to 93/42/EEC Medical Device Directive, this is Class IIa Medical Device.
•According to IEC/EN 60601-1, Equipment is Class I, Type B with BF or CF Applied Parts.
•According to CISPR 11, this is Group 1, Class A ISM Equipment.
•According to IEC 60529, the footswitch rate is IPx1 (FSU2001) or IPx8 (MKF 2-MED GP26).
This product complies with the regulatory requirement of the following:
•Council Directive 93/42/EEC concerning medical devices: the CE label affixed to the product testifies compliance to the Directive.
The location of the CE marking is shown in Chapter 2 of this manual.
European registered place of business: GE Medical Systems Europe
Quality Assurance and safety Regulatory Manager BP 34
F 78533 Buc Cedex, France Tel: +33 (0) 1 30 70 4040
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Conformance Standards (continued)
•International Electrotechnical Commission (IEC).
•IEC/EN 60601-1 Medical Electrical Eqiupment, Part 1 General Requirements for Safety.
•IEC/EN 60601-1-1 Safety requirements for medical electrical systems.
•IEC/EN 60601-1-2 Electromagnetic compatibility — Requirements and tests.
•IEC/EN 60601-1-4 Programmable electrical medical systems.
•IEC 60601-2-37 Medical electrical equipment. Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment.
•IEC 61157 Declaration of acoustic output parameters.
•International Organization of Standards (ISO)
•ISO 10993-1 Biological evaluation of medical devices.
•Underwriters’ Laboratories, Inc. (UL), an independent testing laboratory.
•UL 2601-1 Medical Electrical Equipment, Part 1 General Requirements for Safety.
•Canadian Standards Association (CSA).
•CSA 22.2, 601.1 Medical Electrical Equipment, Part 1 General Requirements for Safety.
•NEMA/AIUM Acoustic Output Display Standard (NEMA US-3, 1998).
•Medical Device Good Manufacturing Practice Manual issued by the FDA (Food and Drug Administration, Department of Health, USA).
Certifications
•General Electric Medical Systems is ISO 9001 and ISO 13485 certified.
Original Documentation
•The original document was written in English.
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Country-specific Approval
•Japan
MHLW Certified Number: 218ABBZX00060000
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Table of Contents
Conformance Standards — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — i-3 Certifications — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — i-4 Original Documentation — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — i-4 Country-specific Approval — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — i-5
Table of Contents Chapter 1 — Introduction
System Overview
Attention — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 1-2 Documentation — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 1-3 Principles of Operation — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 1-4 Indications for Use — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 1-5 Contraindication — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 1-6 Prescription Device — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 1-6
Contact Information
Contacting GE Medical Systems Ultrasound — — — — — — — — — — — — — — — — — — — — 1-7 Manufacturer — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 1-11
Chapter 2 — Safety
Safety Precautions
Precaution Levels — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 2-2 Hazard Symbols — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 2-3 Patient Safety- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 2-5 Device Labels- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 2-11 EMC (Electromagnetic Compatibility) — — — — — — — — — — — — — — — — — — — — — — — — 2-14 Patient Environmental Devices- — — — — — — — — — — — — — — — — — — — — — — — — — — — — 2-23 Acoustic Output — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 2-25 Warning Label Locations — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 2-28
Chapter 3 — Preparing the System for Use
Site Requirements
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-2 Before the system arrives — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-3 Environmental Requirements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-4 Acclimation Time — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-4
Console Overview
Console graphics — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-5 Peripheral/Accessory Connection- — — — — — — — — — — — — — — — — — — — — — — — — — — 3-12
System Positioning/Transporting
Moving the System — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-20 When moving the system — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-21
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Transporting the System — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-22 Attaching the Security Cable — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-23
Powering the System
Connecting and Using the System — — — — — — — — — — — — — — — — — — — — — — — — — — 3-24
Adjusting the Display Monitor
Rotate the LCD monitor- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-30 Brightness — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-31 Speakers — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-31
Probes
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-32 Selecting probes- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-32 Connecting the Probe — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-33 Cable Handling — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-34 Deactivating the Probe — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-35 Disconnecting the Probe — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-36 Transporting Probes — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-37 Storing the Probe — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-37
Operator Controls
Control Panel Map — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-38 Keyboard — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-39 Top/Sub Menu — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-40 Mode, Display and Record- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-41 Measurement and Annotation — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-42
Monitor Display
Monitor Display- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 3-44
Chapter 4 — Preparing for an Exam
Beginning an Exam
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 4-2 Beginning a New Patient — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 4-3 Retrieving and editing archived information — — — — — — — — — — — — — — — — — — — — 4-17 Selecting an Application Preset and a probe — — — — — — — — — — — — — — — — — — — 4-26 Ending a Patient Exam — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 4-30
Chapter 5 — Optimizing the Image
Optimizing B-Mode
Intended Uses — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-2 B-Mode Top/Sub Menu — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-4 Dual Purpose Controls — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-4 B-Mode Scanning Hints- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-5 Depth — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-6 Gain — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-7 Focus — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-8 Auto Optimize (Auto)- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-9 CrossBeam (Compounding)- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-10 M/D Cursor — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-12 Harmonics — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-13 Frequency — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-14 Virtual Convex — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-15
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TGC — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-15 Scan Area — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-16 Tilt- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-16 Angle Steer — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-17 Reverse — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-17 Dynamic Range (Compression) — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-18 Line Density — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-19 Map- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-20 Frame Average- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-22 Colorize — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-23 Edge Enhance — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-24 Rotation — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-24 Rejection — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-25 B Softener — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-25
Optimizing M-Mode
Intended Use — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-26 Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-26 Typical exam protocol — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-26 M-Mode Display — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-27 M-Mode Top/Sub Menu- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-28 Dual Purpose Controls — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-28 Scanning Hints — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-29 Sweep Speed- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-29 Anatomical M-Mode — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-30
Optimizing Color Flow
Intended Use — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-32 Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-32 Activating Color Flow — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-33 Exiting Color Flow- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-34 Color Flow and Power Doppler Scanning Hints — — — — — — — — — — — — — — — — — 5-34 Color Flow Mode Top/Sub Menu — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-35 Dual Purpose Controls — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-35 Gain — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-36 PRF (Pulse Repetition Frequency) — — — — — — — — — — — — — — — — — — — — — — — — — — 5-36 Wall Filter- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-37 Color Scan Area — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-37 Invert (Color Invert) — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-38 Baseline- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-38 Color Flow Line Density- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-39 Angle Steer — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-40 Map- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-41 Threshold- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-42 Frame Average- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-42 Transparency Map — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-43 Spatial Filter — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-43 Duplex/Triplex — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-43 Packet Size — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-44 Power Doppler Imaging (PDI) — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-45
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Optimizing M Color Flow
M Color Flow Mode- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-48
Optimizing Spectral Doppler
Intended Use — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-50 Spectral Doppler Display — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-53 Doppler Mode Display — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-54 Dual Purpose Controls — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-55 Doppler Mode Scanning Hints — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-56 Doppler Mode Top/Sub Menu — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-57 B Pause- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-58 Doppler Sample Volume Gate Position (Trackball)- — — — — — — — — — — — — — — 5-58 Doppler Sample Volume Length- — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-59 PRF- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-60 Angle Correct — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-62 Quick Angle — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-62 Wall Filter- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-63 Baseline- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-63 M/D Cursor — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-64 Invert — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-64 Cycles to Average- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-65 Dynamic Range (Compression)- — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-66 Spectral Trace (Trace Method)- — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-66 Trace Sensitivity — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-67 PW/CF Ratio — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-67 Trace Direction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-67 Full Timeline- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-68 Display Format — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-69 Time Resolution — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-69 Spectral Average — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-69 Modify Auto Calcs- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-70 Auto Calcs — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-70 Continuous Wave Doppler (CWD) — — — — — — — — — — — — — — — — — — — — — — — — — — 5-71
Using 3D
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-73 3D Acquisition — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 5-74
Chapter 6 — Scanning/Display Functions
Zooming an Image
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-2 Zoom- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-2
Split Screen
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-3
Freezing an Image
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-4 Freezing an image — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-4 Post processing — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-6
Using CINE
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-7
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i-10 |
LOGIQ e Basic User Manual |
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Direction 5118586-100 Rev. 2 |
Activating CINE — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-7 CINE and Monitor Display — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-8 Using CINE — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-8
Annotating an Image
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-10 Adding Comments to an Image — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-12 Body Patterns- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-16
Electronic Documentation
Documentation Distribution — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-20 Using Online Help Via F1 — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-21 Electronic media — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 6-27
Chapter 7 — General Measurements and Calculations
Introduction
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-2 Location of Measurement Controls — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-5 General Instructions — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-8
Measurement and Calculation Setup
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Starting Study and Measurement SetUp — — — — — — — — — — — — — — — — — — — — — |
7-15 |
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Specifying Which Measurements Go in a Study or Folder- — — — — — — — — — |
7-25 |
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Changing Measurements- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — |
7-27 |
|
Adding Folders and Measurements — — — — — — — — — — — — — — — — — — — — — — — — — |
7-29 |
|
M&A Advanced Preset — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — |
7-45 |
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Manual Calcs Presets — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — |
7-47 |
Mode Measurements
B-Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-49 Doppler Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-55 M-Mode Measurements- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-59 Viewing and Editing Worksheets — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-61 Transferring Patient Data to a PC- — — — — — — — — — — — — — — — — — — — — — — — — — — 7-66
Generic Measurements
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-67 B-Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-68 M-Mode Measurements- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-77 Doppler Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-80 Helpful hints — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 7-89
Chapter 8 — Abdomen and Small Parts
Abdomen/Small Parts Exam Preparation
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 8-2 General Guidelines — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 8-2
Abdomen
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 8-3 B-Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 8-4 M-Mode Measurements- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 8-6 Doppler Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 8-7
Small Parts
B-Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 8-11 M-Mode Measurements- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 8-15
|
LOGIQ e Basic User Manual |
i-11 |
|
Direction 5118586-100 Rev. 2 |
Doppler Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 8-16
Chapter 9 — OB/GYN
OB Exam
Exam Preparation — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-2 Acoustic Output Considerations — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-3 To Start an Obstetrics Exam — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-4
OB Measurements and Calculations
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-8 B-Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-10 M-Mode Measurements- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-38 Doppler Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-39 OB Worksheet — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-44
Anatomical Survey
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-48
OB Graphs
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-51 To View OB Graphs — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-52
OB-Multigestational
Using other OB studies — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-63 Multiple Fetus- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-65
OB Table Editor
OB Table Settings Menu — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-71 OB Table Templates — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-74 OB Table Edit Menu — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-80 EFW for OB User Table/Formula Editor — — — — — — — — — — — — — — — — — — — — — — 9-83
GYN Measurements
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-88 To Start a Gynecology Exam — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-89 B-Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-90 M-Mode Measurements- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-97 Doppler Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 9-98
Chapter 10 — Cardiology
Cardiology Exam Preparation
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-2 General Guidelines — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-2
Cardiology Measurements
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-3 Naming Format for Cardiac Measurements — — — — — — — — — — — — — — — — — — — — 10-4 Cardiac Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-8 B-Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-9 M-Mode Measurements- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-28 Doppler Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-41 Color Flow Mode — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-68 Combination Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — 10-72 Cardiac Worksheet — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-76 Setting up and Organizing Measurements and Calculations — — — — — — — 10-80 Generic Study — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-81
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i-12 |
LOGIQ e Basic User Manual |
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Direction 5118586-100 Rev. 2 |
ECG Option
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-84 ECG Top/Sub Menu — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 10-85
Chapter 11 — Vascular
Vascular Exam Preparation
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-2 General Guidelines — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-2
Vascular Measurements
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-3 B-Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-5 M-Mode Measurements- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-6 Doppler Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-7
Vascular Worksheet
To view the Vascular Worksheet — — — — — — — — — — — — — — — — — — — — — — — — — — 11-23 Worksheet Display Top/Sub Menu — — — — — — — — — — — — — — — — — — — — — — — — — 11-25 To edit a worksheet- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-26 Examiner’s Comments — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-30 Intravessel ratio — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-31 Vessel Summary — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-33 Recording Worksheet — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 11-36
Chapter 12 — Urology
Urology Exam Preparation
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 12-2 General Guidelines — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 12-2
Urology Calculations
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 12-3 Urology B-Mode Measurements — — — — — — — — — — — — — — — — — — — — — — — — — — — — 12-4
Chapter 13 — Pediatrics
Pediatrics Exam Preparation
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 13-2 General Guidelines — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 13-2
Pediatrics Calculations
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 13-3 Pediatrics- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 13-4
Chapter 14 — ReportWriter
Chapter 15 — Recording Images
Getting Set Up to Record Images
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-2 Adding Devices — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-4 Adding a Dataflow- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-4 Adding Devices to a Print Button — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-4 Formatting Removable Media — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-4 Using the DICOM Spooler — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-5 Troubleshooting — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-5
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LOGIQ e Basic User Manual |
i-13 |
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Direction 5118586-100 Rev. 2 |
Image/Data Management
Reviewing Patient Images — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-6 Clipboard — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-6 Storing an Image — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-9 Using the Monitor Display Controls to Manage Images- — — — — — — — — — — 15-10 Image Management Guide — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-12 Save As (Saving Images to the media to View on a Windows PC)- — — 15-13 USB Flash Drive — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-16 EZBackup/EZMove — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-18 Data Transfer — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-19 Send To (Send the image to the DICOM Device) — — — — — — — — — — — — — — — 15-26 Daily Maintenance — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-28 Notes- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-30
Other Printing Options
Connecting to a Standard Computer Printer — — — — — — — — — — — — — — — — — — 15-31 Setting up the Off-Line Paper Printer — — — — — — — — — — — — — — — — — — — — — — — 15-32 Setting up Digital Peripherals — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 15-36
Transferring Patient Data to a PC
Transferring OB/GYN Patient Data to a PC — — — — — — — — — — — — — — — — — — — 15-41
Portable Exam
Chapter 16 — Customizing Your System
Presets
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-2
System Presets
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-3 Changing system parameters — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-3 System/General Preset Menu — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-4 System/System Imaging Preset Menu — — — — — — — — — — — — — — — — — — — — — — 16-12 System/System Measure Preset Menu — — — — — — — — — — — — — — — — — — — — — — 16-14 System/Backup and Restore Preset Menu — — — — — — — — — — — — — — — — — — — 16-16 System/Peripherals Preset Menu — — — — — — — — — — — — — — — — — — — — — — — — — — 16-35 System/About Preset Menu — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-36
Imaging Presets
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-37 Changing imaging presets — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-38 Imaging Presets — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-39
Comments Libraries Presets
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-43 Comments Libraries/Libraries Preset Menu — — — — — — — — — — — — — — — — — — — 16-43 Comments Libraries/Comments Preset Menu — — — — — — — — — — — — — — — — — 16-46 Comments Libraries/Applications Preset Menu — — — — — — — — — — — — — — — — 16-48
Body Patterns Presets
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-51 Body Pattern Libraries/Libraries Preset Menu — — — — — — — — — — — — — — — — — 16-51 Body Pattern Libraries/Body Patterns Preset Menu — — — — — — — — — — — — — 16-54 Body Pattern Libraries/Applications Preset Menu- — — — — — — — — — — — — — — 16-55
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i-14 |
LOGIQ e Basic User Manual |
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Direction 5118586-100 Rev. 2 |
Application Presets
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-58
Test Patterns
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-61
Configuring Connectivity
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-63 Structured Reporting — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-63 Connectivity Functions — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-64 TCPIP — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-65 Device — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-67 Service — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-68 Dataflow — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-87 Button — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-88 Removable Media- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-90 Miscellaneous — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-92
Measure
System Administration
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-96 System Admin — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-97 Users- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-98 Logon — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-100 Function Keys — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 16-101
Service
Search
Chapter 17 — Probes and Biopsy
Probe Overview
Ergonomics — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-2 Cable handling — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-2 Probe orientation — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-3 Labeling- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-3 LOGIQ e Applications — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-6 LOGIQ e Features — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-6 Specifications — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-7 Probe Usage — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-8 Care and Maintenance — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-8 Probe Safety — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-9 Special handling instructions — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-11 Probe handling and infection control — — — — — — — — — — — — — — — — — — — — — — — — 17-13 Probe Cleaning Process — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-14
Probe Discussion
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-22 LOGIQ e Convex Probes- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-23 LOGIQ e Linear Probes- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-24 Sector Probes — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-24
Biopsy Special Concerns
Precautions Concerning the Use of Biopsy Procedures — — — — — — — — — — 17-25
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Preparing for a Biopsy
Displaying the Guidezone — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-27 Preparing the Biopsy Guide Attachment — — — — — — — — — — — — — — — — — — — — — 17-30 Biopsy Needle Path Verification — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-42 The Biopsy Procedure- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-43 Post Biopsy — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 17-44
Surgery/Intra-operative Use
Preparing for Surgery/Intra-operative Procedures — — — — — — — — — — — — — — 17-45
Chapter 18 — User Maintenance
System Data
Features/Specifications — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-2 Clinical Measurement Accuracy — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-6
System Care and Maintenance
Overview — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-9 Inspecting the System — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-9 Weekly Maintenance- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-10 Cleaning the system — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-11 Other Maintenance — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-14
Quality Assurance
Introduction — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-15 Typical Tests to Perform — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-16 Baselines — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-19 Periodic Checks — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-19 Results — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-20 System Setup- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-21 Test Procedures — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-21 Setting up a Record Keeping System — — — — — — — — — — — — — — — — — — — — — — — 18-30 Ultrasound Quality Assurance Checklist — — — — — — — — — — — — — — — — — — — — — 18-31
Supplies/Accessories
Peripherals- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-32 Console — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-33 Probes- — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-33 Gel — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-34 Disinfectant — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — 18-34 Ultrasound Probe and Cord Sheath Sets- — — — — — — — — — — — — — — — — — — — — 18-35
Index
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Chapter 1
Introduction
This chapter consists of information concerning indications for use/contraindications, contact information and how this documentation is organized.
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Introduction
System Overview
Attention
This manual contains necessary and sufficient information to operate the system safely. Advanced equipment training may be provided by a factory trained Applications Specialist for the agreed-upon time period.
Read and understand all instructions in this manual before attempting to use the LOGIQ e system.
Keep this manual with the equipment at all times. Periodically review the procedures for operation and safety precautions.
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System Overview
Documentation
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LOGIQ e documentation consists of three manuals: |
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• The Basic User Manual (TRANSLATED) and Online Help |
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(TRANSLATED) provides information needed by the user to |
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operate the system safely. It describes the basic functions of |
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the system, safety features, operating modes, |
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measurements/calculations, probes, and user care and |
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maintenance. |
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NOTE: |
Probe information displayed on screen examples does not |
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necessarily reflect the probes available on your ultrasound |
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system. Please refer to the Probes chapter for a listing of |
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available probes and features. |
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• The Advanced Reference Manual (ENGLISH ONLY) |
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contains data tables, such as OB and Acoustic Output |
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tables. |
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• The Quick Guide (TRANSLATED) provides descriptions of |
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basic system features and operation. It is intended to be |
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used in conjunction with the Basic User Manual in order to |
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provide the information necessary to operate the system |
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safely. Quick Cards may also be provided with additional |
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feature information. |
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• The User Guide is a condensed user instruction guide |
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(translated into Swedish, Danish, Russian, Greek, Dutch, |
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Finnish, Norwegian, and Polish). |
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• AIUM Booklet |
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NOTE: |
The documentation kit provides the Quick Guide and Release |
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Notes on paper and electronically and the Basic User Manual |
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and Advanced Reference Manual are only provided in electronic |
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format. The media includes English and all translations. Paper |
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documentation may be ordered by using a form in the Quick |
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Guide. |
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The LOGIQ e manuals are written for users who are familiar with |
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basic ultrasound principles and techniques. They do not include |
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sonographic training or detailed clinical procedures. |
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Introduction
Principles of Operation
Medical ultrasound images are created by computer and digital memory from the transmission and reception of mechanical high-frequency waves applied through a transducer. The mechanical ultrasound waves spread through the body, producing an echo where density changes occur. For example, in the case of human tissue, an echo is created where a signal passes from an adipose tissue (fat) region to a muscular tissue region. The echoes return to the transducer where they are converted back into electrical signals.
These echo signals are highly amplified and processed by several analog and digital circuits having filters with many frequency and time response options, transforming the highfrequency electrical signals into a series of digital image signals which are stored in memory. Once in memory, the image can be displayed in real-time on the image monitor. All signal transmission, reception and processing characteristics are controlled by the main computer. By selection from the system control panel, the user can alter the characteristics and features of the system, allowing a wide range of uses, from obstetrics to peripheral vascular examinations.
Transducers are accurate, solid-state devices, providing multiple image formats. The digital design and use of solid-state components provides highly stable and consistent imaging performance with minimal required maintenance. Sophisticated design with computer control offers a system with extensive features and functions which is user-friendly and easy to use.
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System Overview
Indications for Use
The LOGIQ e is intended for use by a qualified physician for ultrasound evaluation. Specific clinical applications and exam types include:
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• |
Fetal/Obstetrics |
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• |
Abdominal (including GYN) |
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• |
Pediatric |
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• Small Organ (including breast, testes, thyroid) |
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• |
Neonatal Cephalic |
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• |
Adult Cephalic |
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• Cardiac (adult and pediatric) |
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• |
Peripheral Vascular |
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• Intraoperative (abdominal, thoracic and peripheral) |
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• Musculo-skeletal Conventional |
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• |
Urology (including prostate) |
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• |
Transrectal |
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• |
Transvaginal |
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CAUTION |
This machine should be used in compliance with law. Some |
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jurisdictions restrict certain uses, such as gender |
determination.
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Introduction
Contraindication
The LOGIQ e ultrasound system is not intended for ophthalmic use or any use causing the acoustic beam to pass through the eye.
Prescription Device
CAUTION: United States law restricts this device to sale or use by, or on the order of a physician.
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Contact Information
Contact Information
Contacting GE Medical Systems Ultrasound
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For additional information or assistance, please contact your |
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local distributor or the appropriate support resource listed on the |
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following pages: |
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INTERNET |
http://www.gehealthcare.com |
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http://www.gehealthcare.com/usen/ultrasound/products/ |
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probe_care.html |
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USA |
GE Healthcare TEL: (1) 800-437-1171 |
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Ultrasound Service Engineering FAX: (1) 414-721-3865 |
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P.O. Box 414 |
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Milwaukee, WI 53201 |
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Clinical Questions |
For information in the United States, Canada, Mexico and parts |
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of the Caribbean, call the Customer Answer Center |
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TEL: (1) 800-682-5327 or (1) 262-524-5698 |
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In other locations, contact your local Applications, Sales or |
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Service Representative. |
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Service Questions |
For service in the United States, call GE CARES |
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TEL: (1) 800-437-1171 |
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In other locations, contact your local Service Representative. |
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Accessories |
To request the latest GE Accessories catalog or equipment |
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Catalog Requests |
brochures in the United States, call the Response Center |
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TEL: (1) 800-643-6439 |
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In other locations, contact your local Applications, Sales or |
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Service Representative. |
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Introduction
Contacting GE Medical Systems Ultrasound (continued)
Placing an Order To place an order, order supplies or ask an accesory-related question in the United States, call the GE Access Center
TEL: (1) 800-472-3666
In other locations, contact your local Applications, Sales or Service Representative.
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CANADA |
GE Medical Systems |
TEL: (1) 800-664-0732 |
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Ultrasound Service Engineering |
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9900 Innovation Drive |
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Wauwatosa, WI 53226 |
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Customer Answer Center |
TEL: (1) 262-524-5698 |
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LATIN & SOUTH |
GE Medical Systems |
TEL: (1) 262-524-5300 |
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AMERICA |
Ultrasound Service Engineering |
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9900 Innovation Drive |
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Wauwatosa, WI 53226 |
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Customer Answer Center |
TEL: (1) 262-524-5698 |
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EUROPE |
GE Ultraschall |
TEL: 0130 81 6370 toll free |
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Deutschland GmbH & Co. KG TEL: (33) 130.831.300 |
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Beethovenstrasse 239 |
FAX: (49) 212.28.02.431 |
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Postfach 11 05 60 |
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D-42655 Solingen |
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ASIA |
GE Ultrasound Asia (Singapore) |
TEL: 65-291 8528 |
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Service Department — Ultrasound |
FAX: 65-272-3997 |
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298 Tiong Bahru Road #15-01/06 |
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Central Plaza |
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Singapore 169730 |
JAPAN
GE Yokogawa Medical Systems TEL: (81) 426-48-2950
Customer Service Center FAX: (81) 426-48-2902
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Contact Information
Contacting GE Medical Systems Ultrasound (continued)
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ARGENTINA |
GEME S.A. TEL: (1) 639-1619 |
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Miranda 5237 FAX: (1) 567-2678 |
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Buenos Aires — 1407 |
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AUSTRIA |
GE GesmbH Medical Systems Austria TEL: 0660 8459 toll free |
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Prinz Eugen Strasse 8/8 FAX: +43 1 505 38 74 |
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A-1040 WIEN TLX: 136314 |
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BELGIUM |
GE Medical Systems Benelux TEL: 0 800 11733 toll free |
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Gulkenrodestraat 3 FAX: +32 0 3 320 12 59 |
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B-2160 WOMMELGEM TLX: 72722 |
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BRAZIL |
GE Sistemas Medicos |
TEL: 0800-122345 |
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Av Nove de Julho 5229 FAX: (011) 3067-8298 |
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01407-907 Sao Paulo SP |
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DENMARK |
GE Medical Systems |
TEL: +45 4348 5400 |
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Fabriksparken 20 FAX: +45 4348 5399 |
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DK-2600 GLOSTRUP |
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FRANCE |
GE Medical Systems |
TEL: 05 49 33 71 toll free |
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738 rue Yves Carmen |
FAX: +33 1 46 10 01 20 |
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F-92658 BOULOGNE CEDEX |
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GERMANY |
GE Ultraschall TEL: 0130 81 6370 toll free |
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Deutschland GmbH & Co. KG TEL: (49) 212.28.02.207 |
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Beethovenstrasse 239 |
FAX: (49) 212.28.02.431 |
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Postfach 11 05 60 |
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D-42655 Solingen |
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GREECE |
GE Medical Systems Hellas |
TEL: +30 1 93 24 582 |
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41, Nikolaou Plastira Street |
FAX: +30 1 93 58 414 |
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G-171 21 NEA SMYRNI |
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ITALY |
GE Medical Systems Italia |
TEL: 1678 744 73 toll free |
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Via Monte Albenza 9 |
FAX: +39 39 73 37 86 |
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I-20052 MONZA TLX: 3333 28 |
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LUXEMBOURG |
TEL: 0800 2603 toll free |
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Introduction
Contacting GE Medical Systems Ultrasound (continued)
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MEXICO |
GE Sistemas Medicos de Mexico S.A. de C.V. |
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Rio Lerma #302, 1° y 2° Pisos TEL: (5) 228-9600 |
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Colonia Cuauhtemoc FAX: (5) 211-4631 |
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06500-Mexico, D.F. |
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NETHERLANDS |
GE Medical Systems Nederland B.V. TEL: 06 022 3797 toll free |
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Atoomweg 512 FAX: +31 304 11702 |
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NL-3542 AB UTRECHT |
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POLAND |
GE Medical Systems Polska TEL: +48 2 625 59 62 |
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Krzywickiego 34 FAX: +48 2 615 59 66 |
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P-02-078 WARSZAWA |
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PORTUGAL |
GE Medical Systems Portuguesa S.A. |
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TEL: 05 05 33 7313 toll free |
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Rua Sa da Bandeira, 585 FAX: +351 2 2084494 |
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Apartado 4094 TLX: 22804 |
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P-4002 PORTO CODEX |
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RUSSIA |
GE VNIIEM TEL: +7 095 956 7037 |
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Mantulinskaya UI. 5A FAX: +7 502 220 32 59 |
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123100 MOSCOW TLX: 613020 GEMED SU |
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SPAIN |
GE Medical Systems Espana TEL: 900 95 3349 toll free |
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Hierro 1 Arturo Gimeno FAX: +34 1 675 3364 |
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Poligono Industrial I TLX: 22384 A/B GEMDE |
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E-28850 TORREJON DE ARDOZ |
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SWEDEN |
GE Medical Systems TEL: 020 795 433 toll free |
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PO-BOX 1243 FAX: +46 87 51 30 90 |
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S-16428 KISTA TLX: 12228 CGRSWES |
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SWITZERLAND |
GE Medical Systems (Schweiz) AG TEL: 155 5306 toll free |
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Sternmattweg 1 FAX: +41 41 421859 |
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CH-6010 KRIENS |
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TURKEY |
GE Medical Systems Turkiye A.S. TEL: +90 212 75 5552 |
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Mevluk Pehliran Sodak FAX: +90 212 211 2571 |
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Yilmaz Han, No 24 Kat 1 |
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Gayretteppe |
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ISTANBUL |
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Contact Information
Contacting GE Medical Systems Ultrasound (continued)
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UNITED KINGDOM |
GE Medical Systems TEL: 0800 89 7905 toll free |
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Coolidge House FAX: +44 753 696067 |
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352 Buckingham Avenue |
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SLOUGH |
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Berkshire SL1 4ER |
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OTHER |
NO TOLL FREE TEL: international code + 33 1 39 20 0007 |
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COUNTRIES |
Manufacturer
GE Medical System (China) Co., Ltd.
No. 19, Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu, P.R. China 214028
TEL: +86 510 85225888; FAX: +86 510 85226688
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Chapter 2
Safety
Describes the safety and regulatory information pertinent for operating this ultrasound system.
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Safety
Safety Precautions
Precaution Levels
Icon description
Various levels of safety precautions may be found on the equipment and different levels of concern are identified by one of the following flag words and icons which precede the precautionary statement.
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DANGER |
Indicates that a specific hazard is known to exist which through |
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inappropriate conditions or actions will cause: |
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• Severe or fatal personal injury |
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• |
Substantial property damage. |
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WARNING |
Indicates that a specific hazard is known to exist which through |
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inappropriate conditions or actions may cause: |
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• |
Severe personal injury |
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• |
Substantial property damage. |
Indicates that a potential hazard may exist which through inappropriate conditions or actions will or can cause:
•Minor injury
•Property damage.
Indicates precautions or recommendations that should be used in the operation of the ultrasound system, specifically:
•Maintaining an optimum system environment
•Using this Manual
•Notes to emphasize or clarify a point.
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Hazard Symbols
Icon Description
Potential hazards are indicated by the following icons:
Table 2-1: Potential Hazards
|
Icon |
Potential Hazard |
Usage |
Source |
|
• Patient/user infection due to |
• Cleaning and care |
ISO 7000 |
|
|
contaminated equipment. |
instructions |
No. 0659 |
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• Sheath and glove |
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guidelines |
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• Electrical micro-shock to patient, e.g., |
• Probes |
||
|
ventricular |
• ECG, if applicable |
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• Connections to back |
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panel |
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• Patient injury or tissue damage from |
• ALARA, the use of |
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ultrasound radiation. |
Power Output following |
||
|
the ‘as low as |
|||
|
reasonably achievable’ |
|||
|
principle |
|||
|
• Risk of explosion if used in the |
• Flammable anesthetic |
||
|
presence of flammable anesthetics. |
|||
|
• Patient/user injury or adverse reaction |
• Replacing fuses |
||
|
from fire or smoke. |
• Outlet guidelines |
||
|
• Patient/user injury from explosion and |
|||
|
fire. |
|||
|
LOGIQ e Basic User Manual |
2-3 |
|
Direction 5118586-100 Rev. 2 |
Safety
Important Safety Considerations
|
The following topic headings (Patient Safety, and Equipment |
|
|
and Personnel Safety) are intended to make the equipment user |
|
|
aware of particular hazards associated with the use of this |
|
|
equipment and the extent to which injury can occur if |
|
|
precautions are not observed. Additional precautions may be |
|
|
provided throughout the manual. |
|
|
CAUTION |
Improper use can result in serious injury. The user must be |
|
thoroughly familiar with the instructions and potential hazards |
|
|
involving ultrasound examination before attempting to use the |
|
|
device. Training assistance is available from GE Medical |
|
|
Systems if needed. |
|
|
The equipment user is obligated to be familiar with these |
|
|
concerns and avoid conditions that could result in injury. |
|
2-4 |
LOGIQ e Basic User Manual |
|
Direction 5118586-100 Rev. 2 |
Safety Precautions
Patient Safety
Related Hazards
WARNING
Patient identification
The concerns listed can seriously affect the safety of patients undergoing a diagnostic ultrasound examination.
Always include proper identification with all patient data and verify the accuracy of the patient’s name and ID numbers when entering such data. Make sure correct patient ID is provided on all recorded data and hard copy prints. Identification errors could result in an incorrect diagnosis.
Diagnostic Equipment malfunction or incorrect settings can result in information measurement errors or failure to detect details within the image.
The equipment user must become thoroughly familiar with the equipment operation in order to optimize its performance and recognize possible malfunctions. Applications training is available through the local GE representative. Added confidence in the equipment operation can be gained by establishing a quality assurance program.
|
LOGIQ e Basic User Manual |
2-5 |
|
Direction 5118586-100 Rev. 2 |
Safety
Related Hazards (continued)
Mechanical
hazards
Electrical
Hazard
The use of damaged probes can result in injury or increased risk of infection. Inspect probes often for sharp, pointed, or rough surface damage that could cause injury or tear protective barriers. Become familiar with all instructions and precautions provided with special purpose probes.
A damaged probe can also increase the risk of electric shock if conductive solutions come in contact with internal live parts. Inspect probes often for cracks or openings in the housing and holes in and around the acoustic lens or other damage that could allow liquid entry. Become familiar with the probe’s use and care precautions outlined in Probes and Biopsy.
|
CAUTION |
Ultrasound transducers are sensitive instruments which can |
|
easily be damaged by rough handling. Take extra care not to |
|
|
drop transducers and avoid contact with sharp or abrasive |
|
|
surfaces. A damaged housing, lens or cable can result in |
|
|
patient injury or serious impairment or operation. |
|
|
CAUTION |
Ultrasound can produce harmful effects in tissue and |
|
potentially result in patient injury. Always minimize exposure |
|
|
time and keep ultrasound levels low when there is no medical |
|
|
benefit. Use the principle of ALARA (As Low As Reasonably |
|
|
Achievable), increasing output only when needed to obtain |
|
|
diagnostic image quality. Observe the acoustic output display |
|
|
and be familiar with all controls affecting the output level. See |
|
|
the Bioeffects section of the Acoustic Output chapter in the |
|
|
Advanced Reference Manual for more information. |
|
2-6 |
LOGIQ e Basic User Manual |
|
Direction 5118586-100 Rev. 2 |
Safety Precautions
Related Hazards (continued)
Training It is recommended that all users receive proper training in applications before performing them in a clinical setting. Please contact the local GE representative for training assistance.
ALARA training is provided by GE Application Specialists. The ALARA education program for the clinical end-user covers basic ultrasound principles, possible biological effects, the derivation and meaning of the indices, ALARA principles, and examples of specific applications of the ALARA principle.
|
LOGIQ e Basic User Manual |
2-7 |
|
Direction 5118586-100 Rev. 2 |
Safety
Equipment and Personnel Safety
Related Hazards
WARNING
WARNING
DANGER
This equipment contains dangerous voltages that are capable of serious injury or death.
If any defects are observed or malfunctions occur, stop operating the equipment and perform the proper action for the patient. Inform a qualified service person and contact a Service Representative for information.
There are no user serviceable components inside the console. Refer all servicing to qualified service personnel only.
Only approved and recommended peripherals and accessories should be used.
All peripherals and accessories must be securely mounted to the LOGIQ e.
The concerns listed below can seriously affect the safety of equipment and personnel during a diagnostic ultrasound examination.
|
Explosion |
Risk of explosion if used in the presence of flammable |
|
Hazard |
anesthetics. |
|
2-8 |
LOGIQ e Basic User Manual |
|
Direction 5118586-100 Rev. 2 |
Safety Precautions
Related Hazards
(continued)
Electrical
Hazard
To avoid injury:
•Do not remove protective covers. No user serviceable parts are inside. Refer servicing to qualified service personnel.
•To assure adequate grounding, connect the attachment plug to a reliable (hospital grade) grounding outlet (having equalization conductor 
).
•Never use any adaptor or converter of a three-prong-to- two-prong type to connect with a mains power plug. The protective earth connection will loosen.
•Do not place liquids on or above the console. Spilled liquid may contact live parts and increase the risk of shock.
CAUTION
Smoke &
Fire Hazard
Biological
Hazard
Do not use this equipment if a safety problem is known to exist. Have the unit repaired and performance verified by qualified service personnel before returning to use.
The system must be supplied from an adequately rated electrical circuit. The capacity of the supply circuit must be as specified.
For patient and personnel safety, be aware of biological hazards while performing invasive procedures. To avoid the risk of disease transmission:
•Use protective barriers (gloves and probe sheaths) whenever possible. Follow sterile procedures when appropriate.
•Thoroughly clean probes and reusable accessories after each patient examination and disinfect or sterilize as needed. Refer to Probes and Biopsy for probe use and care instructions.
•Follow all infection control policies established by your office, department or institution as they apply to personnel and equipment.
|
LOGIQ e Basic User Manual |
2-9 |
|
Direction 5118586-100 Rev. 2 |
Safety
Related Hazards
(continued)
CAUTION
Contact with natural rubber latex may cause a severe anaphylactic reaction in persons sensitive to the natural latex protein. Sensitive users and patients must avoid contact with these items. Refer to package labeling to determine latex content and FDA’s March 29, 1991 Medical Alert on latex products.
|
CAUTION |
Archived data is managed at the individual sites. Performing |
|
data backup (to any device) is recommended. |
|
CAUTION |
DO NOT use high-frequency surgical equipment with the |
|
LOGIQ e. |
|
2-10 |
LOGIQ e Basic User Manual |
|
Direction 5118586-100 Rev. 2 |
Safety Precautions
Device Labels
Label Icon Description
The following table describes the purpose and location of safety labels and other important information provided on the equipment.
Table 2-2: Label Icons
|
Label/Icon |
Purpose/Meaning |
Location |
|
Identification and Rating Plate |
• Manufacture’s name and address |
See Figure 2-3/Figure 2-4 for |
|
• Date of manufacture |
location information. AC |
|
|
• Model and serial numbers |
Adapter Label. |
|
|
• Electrical ratings (Volts, Amps, |
||
|
phase, and frequency) |
||
|
Type/Class Label |
Used to indicate the degree of safety |
|
|
or protection. |
||
|
IP Code (IPX1 or IPX8) |
Indicates the degree of protection |
Bottom of Footswitch |
|
IPX1: FSU-2001 |
provided by the enclosure per IEC60 |
|
|
IPX8: MKF 2-MED GP26 |
529. |
|
|
IPX1 cannot be used in an operating |
||
|
room environment. |
||
|
IPX8 can be used in an operating |
||
|
room environment. |
||
|
Type BF Applied Part (man in the box) |
Beside the probe connector |
|
|
symbol is in accordance with IEC 878- |
||
|
02-03. |
||
|
Type CF Applied Part (heart in the |
ECG marked Type CF or |
|
|
box) symbol is in accordance with IEC |
probes |
|
|
60878-02-03. |
||
|
“ATTENTION” — Consult |
Various |
|
|
accompanying documents” is intended |
||
|
to alert the user to refer to the operator |
||
|
manual or other instructions when |
||
|
complete information cannot be |
||
|
provided on the label. |
||
|
“CAUTION” — Dangerous voltage” (the |
Various |
|
|
lightning flash with arrowhead) is used |
||
|
to indicate electric shock hazards. |
||
|
“ON” indicates the power on position |
See the Console Overview |
|
|
of the power switch. |
section for location |
|
|
CAUTION: This Power Switch DOES |
information. |
|
|
NOT ISOLATE Mains Supply. |
||
|
LOGIQ e Basic User Manual |
2-11 |
|
Direction 5118586-100 Rev. 2 |
Safety
Table 2-2: Label Icons
|
Label/Icon |
Purpose/Meaning |
Location |
|
“Protective Earth” indicates the |
Inside of AC adapter |
|
|
protective earth (grounding) terminal. |
||
|
NRTL Listing and Certification Mark is |
Bottom |
|
|
used to designate conformance to |
||
|
nationally recognized product safety |
||
|
standards. The Mark bears the name |
||
|
and/or logo of the testing laboratory, |
||
|
product category, safety standard to |
||
|
which conformity is assessed and a |
||
|
control number. |
||
|
Type CF Defib-Proof Applied Part |
ECG Module |
|
|
(heart in the box with paddle) symbol |
||
|
is in accordance with IEC 60878-02- |
||
|
06. |
||
|
This symbol indicates that waste |
Bottom |
|
|
electrical and electronic equipment |
||
|
must not be disposed of as unsorted |
||
|
municipal waste and must be collected |
||
|
separately. Please contact an |
||
|
authorized representative of the |
||
|
manufacturer for information |
||
|
concerning the decommissioning of |
||
|
your equipment. |
||
|
When closing the LCD cover, use |
Bottom |
|
|
caution to avoid injuring hands or |
||
|
fingers as there is a closing |
||
|
mechanism which allows the LCD |
||
|
cover to automatically close. |
||
|
2-12 |
LOGIQ e Basic User Manual |
|
Direction 5118586-100 Rev. 2 |
Safety Precautions
Label Icon Description (continued)
|
Classifications |
Type of protection against electric shock |
|
• Class I Equipment—LOGIQ e Console with AC Adapter (*1) |
|
|
Degree of protection against electric shock |
•Type BF Applied part (*2)
•Type CF Applied part (*3)
(for Probes marked with BF symbol)
(for ECG marked with CF symbol)
Continuous Operation
System is Ordinary Equipment (IPX0)
Footswitch is IPX1 (FSU-2001) or IPX8 (MKF 2-MED GP26)
*1. Class I Equipment
EQUIPMENT in which protection against electric shock does not rely on BASIC INSULATION only, but includes a protective earth ground. This additional safety precaution prevents exposed metal parts from becoming LIVE in the event of an insulation failure.
*2. Type BF Applied Part
TYPE BF APPLIED PART providing a specified degree of protection against electric shock, with particular regard to allowable LEAKAGE CURRENT.
Table 2-3: Type BF Equipment
|
Normal Mode |
Single fault condition |
||
|
Patient leakage current |
Less than 100 microA |
Less than 500 microA |
|
|
*3. Type CF Applied Part |
|||
|
TYPE CF APPLIED PART providing a degree of protection |
|||
|
higher than that for Type BF Applied Part against electric shock |
|||
|
particularly regarding allowable LEAKAGE CURRENTS. |
|||
|
Table 2-4: Type CF Equipment |
|||
|
Normal Mode |
Single fault condition |
||
|
Patient leakage current |
Less than 10 microA |
Less than 50 microA |
|
|
LOGIQ e Basic User Manual |
2-13 |
|
Direction 5118586-100 Rev. 2 |
Safety
EMC (Electromagnetic Compatibility)
|
NOTE: |
This equipment generates, uses and can radiate radio |
|
frequency energy. The equipment may cause radio frequency |
|
|
interference to other medical and non-medical devices and radio |
|
|
communications. To provide reasonable protection against such |
|
|
interference, this product complies with emissions limits for a |
|
|
Group 1, Class A Medical Devices Directive as stated in EN |
|
|
60601-1-2. However, there is no guarantee that interference will |
|
|
not occur in a particular installation. |
|
|
NOTE: |
If this equipment is found to cause interference (which may be |
|
determined by turning the equipment on and off), the user (or |
|
|
qualified service personnel) should attempt to correct the |
|
|
problem by one or more of the following measure(s): |
|
|
• reorient or relocate the affected device(s) |
|
|
• increase the separation between the equipment and the |
|
|
affected device |
|
|
• power the equipment from a source different from that of the |
|
|
affected device |
|
|
• consult the point of purchase or service representative for |
|
|
further suggestions. |
|
|
NOTE: |
The manufacturer is not responsible for any interference caused |
|
by using other than recommended interconnect cables or by |
|
|
unauthorized changes or modifications to this equipment. |
|
|
Unauthorized changes or modifications could void the users’ |
|
|
authority to operate the equipment. |
|
|
NOTE: |
To comply with the regulations on electromagnetic interference |
|
for a Class A FCC Device, all interconnect cables to peripheral |
|
|
devices must be shielded and properly grounded. Use of cables |
|
|
not properly shielded and grounded may result in the equipment |
|
|
causing radio frequency interference in violation of the FCC |
|
|
regulations. |
EMC Performance
All types of electronic equipment may characteristically cause electromagnetic interference with other equipment, either transmitted through air or connecting cables. The term EMC (Electromagnetic Compatibility) indicates the capability of equipment to curb electromagnetic influence from other equipment and at the same time not affect other equipment with similar electromagnetic radiation from itself.
|
2-14 |
LOGIQ e Basic User Manual |
|
Direction 5118586-100 Rev. 2 |
Safety Precautions
EMC Performance (continued)
|
Proper installation following the service manual is required in |
|
|
order to achieve the full EMC performance of the product. |
|
|
The product must be installed as stipulated in 4.2, Notice upon |
|
|
Installation of Product. |
|
|
In case of issues related to EMC, please call your service |
|
|
personnel. |
|
|
The manufacturer is not responsible for any interference caused |
|
|
by using other than recommended interconnect cables or by |
|
|
unauthorized changes or modifications to this equipment. |
|
|
Unauthorized changes or modifications could void the users’ |
|
|
authority to operate the equipment. |
|
|
CAUTION |
Do not use devices which intentionally transmit RF signals |
|
(cellular phones, transceivers, or radio controlled products), |
|
|
other than those supplied by GE (wireless microphone, |
|
|
broadband over power lines, for example) unless intended for |
|
|
use with this system, in the vicinity of this equipment as it may |
|
|
cause performance outside the published specifications. |
|
|
Keep power to these devices turned off when near this |
|
|
equipment. |
|
|
Medical staff in charge of this equipment is required to instruct |
|
|
technicians, patients and other people who may be around this |
|
|
equipment to fully comply with the above regulation. |
|
LOGIQ e Basic User Manual |
2-15 |
|
Direction 5118586-100 Rev. 2 |
Safety
EMC Performance (continued)
Portable and mobile radio communications equipment (e.g. twoway radio, cellular/cordless telephones and similar equipment) should be used no closer to any part of this system, including cables, than determined according to the following method:
|
Table 2-5: |
Portable and mobile radio communications equipment distance |
|||
|
requirements |
||||
|
Frequency Range: |
150 kHz — 80 MHz |
80 MHz — 800 MHz |
800 MHz — 2.5 GHz |
|
|
Calculation Method: |
d=[3.5/V1] square root |
d = [3.5/E1] square root |
d = [7/E1] square root of |
|
|
of P |
of P |
P |
||
|
Where: d= separation distance in meters, P = rated power of the transmitter, V1=compliance value for |
||||
|
conducted RF, E1 = compliance value for radiated RF |
||||
|
If the maximum |
The separation distance in meters should be |
|||
|
transmitter power in |
||||
|
watts is rated |
||||
|
5 |
2.6 |
2.6 |
5.2 |
|
|
20 |
5.2 |
5.2 |
10.5 |
|
|
100 |
12.0 |
12.0 |
24.0 |
|
|
2-16 |
LOGIQ e Basic User Manual |
|
Direction 5118586-100 Rev. 2 |
Safety Precautions
Notice upon Installation of Product
Separation distance and effect from fixed radio communications equipment: field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast transmitter cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the ultrasound system is used exceeds the applicable RF compliance level as stated in the immunity declaration, the ultrasound system should be observed to verify normal operation. If abnormal operation is observed, additional measures may be necessary, such as re-orienting or relocating the ultrasound system or using an RF shielded examination room may be necessary.
1.Use either power supply cords provided by GE Medical Systems or ones designated by GE Medical Systems. Products equipped with a power source plug should be plugged into the fixed power socket which has the protective grounding conductor. Never use any adaptor or converter to connect with a power source plug (e.g. three-prong-to-two- prong converter).
2.Locate the equipment as far away as possible from other electronic equipment.
3.Be sure to use only the cables provided by or designated by GE Medical Systems. Connect these cables following the installation procedures (e.g. wire power cables separately from signal cables).
4.Lay out the main equipment and other peripherals following the installation procedures described in the Option Installation manuals.
|
LOGIQ e Basic User Manual |
2-17 |
|
Direction 5118586-100 Rev. 2 |
Safety
General Notice
1.Designation of Peripheral Equipment Connectable to This Product.
The equipment indicated in Chapter 18 can be hooked up to the product without compromising its EMC performance.
Avoid using equipment not designated in the list. Failure to comply with this instruction may result in poor EMC performance of the product.
2.Notice against User Modification
The user should never modify this product. User modifications may cause degradation in EMC performance. Modification of the product includes changes in:
a.Cables (length, material, wiring, etc.)
b.System installation/layout
c.System configuration/components
d.Securing system parts (cover open/close, cover screwing)
|
2-18 |
LOGIQ e Basic User Manual |
|
Direction 5118586-100 Rev. 2 |
Safety Precautions
Peripheral Update for EC countries
|
The following is intended to provide the users in EC countries |
|
|
with updated information concerning the connection of the |
|
|
LOGIQ e to image recording and other devices or |
|
|
communication networks. |
|
|
Peripheral used in |
The LOGIQ e has been verified for overall safety, compatibility |
|
the patient |
and compliance with the following on-board image recording |
|
environment |
devices: |
|
• Sony UP-D897MD B/W Printer |
|
|
• Sony UP-D23MD Color Printer |
|
|
The LOGIQ e may also be used safely while connected to |
|
|
devices other than those recommended above if the devices |
|
|
and their specifications, installation, and interconnection with the |
|
|
system conform to the requirements of IEC/EN 60601-1-1. |
|
|
CAUTION |
The connection of equipment or transmission networks other |
|
than as specified in the user instructions can result in an |
|
|
electric shock hazard or equipment malfunction. Substitute or |
|
|
alternate equipment and connections requires verification of |
|
|
compatibility and conformity to IEC/EN 60601-1-1 by the |
|
|
installer. Equipment modifications and possible resulting |
|
|
malfunctions and electromagnetic interference are the |
|
|
responsibility of the owner. |
|
|
General precautions for installing an alternate off-board, remote |
|
|
device or a network would include: |
|
|
1. The added device(s) must have appropriate safety standard |
|
|
conformance and CE Marking. |
|
|
2. There must be adequate mechanical mounting of the device |
|
|
and stability of the combination. |
|
|
3. Risk and leakage current of the combination must comply |
|
|
with IEC/EN 60601-1. |
|
|
4. Electromagnetic emissions and immunity of the combination |
|
|
must conform to IEC/EN 60601-1-2. |
|
LOGIQ e Basic User Manual |
2-19 |
|
Direction 5118586-100 Rev. 2 |
Safety
Peripheral Update for EC countries (continued)
|
Peripheral used in |
The LOGIQ e has also been verified for compatibility, and |
|
the non-patient |
compliance for connection to a local area network (LAN) via a |
|
environment |
wireless LAN, provided the LAN components are IEC/EN 60950 |
|
compliant. |
|
|
The LOGIQ e has also been verified for compatibility, and |
|
|
compliance for connection to a DVD-RW via the system USB |
|
|
port, provided the DVD-RW is IEC/EN 60950 compliant. |
|
|
General precautions for installing an alternate off-board, remote |
|
|
device or a network would include: |
|
|
1. The added device(s) must have appropriate safety standard |
|
|
conformance and CE Marking. |
|
|
2. The added device(s) must be used for their intended |
|
|
purpose having a compatible interface. |
|
2-20 |
LOGIQ e Basic User Manual |
|
Direction 5118586-100 Rev. 2 |
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