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ISO/IEC TR 20017

Information technology - Radio frequency identification for item management - Electromagnetic interference impact of ISO/IEC 18000 interrogator emitters on implantable pacemakers and implantable cardioverter defibrillators

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Organization: ISO
Publication Date: 15 December 2011
Status: active
Page Count: 64
ICS Code (Information coding): 35.040
scope:

This Technical Report presents a test method and results for the evaluation of ISO/IEC 18000 radio frequency identification (RFID) interrogator electromagnetic interference (EMI) on implantable pacemakers and implantable cardioverter defibrillators.

Document History

ISO/IEC TR 20017
December 15, 2011
Information technology - Radio frequency identification for item management - Electromagnetic interference impact of ISO/IEC 18000 interrogator emitters on implantable pacemakers and implantable cardioverter defibrillators
This Technical Report presents a test method and results for the evaluation of ISO/IEC 18000 radio frequency identification (RFID) interrogator electromagnetic interference (EMI) on implantable...

References

This document references:
AAMI 60601-1-2 - MEDICAL ELECTRICAL EQUIPMENT – Part 1-2: General requirements for basic safety and essential performance – Collateral Standard: Electromagnetic disturbances – Requirements and tests
Published by AAMI on January 1, 2014
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document references:
EN 50371 - Generic Standard to Demonstrate the Compliance of Low Power Electronic and Electrical Apparatus with the Basic Restrictions Related to Human Exposure to Electromagnetic Fields (10 MHz - 300 GHz) - General Public
Published by CENELEC on March 1, 2002
A description is not available for this item.
This document references:
ISO 14708-1 - Implants for Surgery - Active Implantable Medical Devices - Part 1: General Requirements for Safety, Marking and for Information to be Provided by the Manufacturer
Published by ISO on August 15, 2014
This part of ISO 14708 specifies requirements that are generally applicable to active implantable medical devices. NOTE 1 For particular types of active implantable medical devices, these general...
This document references:
EN 50392 - Generic standard to demonstrate the compliance of electronic and electrical apparatus with the basic restrictions related to human exposure to electromagnetic fields (0 Hz - 300 GHz)
Published by CENELEC on January 1, 2004
A description is not available for this item.
This document references:
EN 50357 - Evaluation of Human Exposure to Electromagnetic Fields from Devices Used in Electronic Article Surveillance (EAS), Radio Frequency Identification (RFID) and Similar Applications
Published by CENELEC on October 1, 2001
A description is not available for this item.
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