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CSA 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: CSA
Publication Date: 1 January 2014
Status: active
Page Count: 75
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

CSA ISO/IEC TR 20017
January 1, 2014
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...
CAN/CSA-ISO/IEC TR 20017:14
January 1, 2014
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:
PC69 ERTA - Active implantable medical devices – Electromagnetic compatibility – EMC test protocols for implantable cardiac pacemakers and implantable cardioverter
Published by AAMI on January 1, 2008
A description is not available for this item.
This document references:
AAMI TIR18 - Guidance on electromagnetic compatibility of medical devices in healthcare facilities
Published by AAMI on January 1, 2010
Introduction and scope Because the performance of electronic medical devices can be disrupted by electromagnetic (EM) energy, patient safety can potentially be put at increased risk because of the...
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:
ISO 14708-2 - Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
Published by ISO on September 1, 2019
This document specifies requirements that are applicable to those active implantable medical devices intended to treat bradyarrhythmias and devices that provide therapies for cardiac...
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