CSA ISO/IEC TR 20017:14 (R2019)
Current
The latest, up-to-date edition.
Information technology - Radio frequency identification for item management - Electromagnetic interference impact of ISO/IEC 18000 interrogator emitters on implantable pacemakers and implantable cardioverter defibrillators (Adopted ISO/IEC TR 20017:2011, first edition, 2011-12-15)
Hardcopy , PDF
English
01-01-2014
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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Abbreviated terms
5 The need for EMC between RFID and implanted medical devices
6 EMI studies
7 Differences in results
8 Need for comprehensive test methodologies
Annex A (informative) - JAISA/Hokkaido-University study
Bibliography
CSA Preface Standards development within the Information Technology sector is harmonized with international standards development. Through the CSA Technical Committee on Information Technology (TCIT), Canadians serve as the Canadian Advisory Committee (CAC) on ISO/IEC Joint Technical Committee 1 on Information Technology (ISO/IEC JTC1) for the Standards Council of Canada (SCC), the ISO member body for Canada and sponsor of the Canadian National Committee of the IEC. Also, as a member of the International Telecommunication Union (ITU), Canada participates in the International Telegraph and Telephone Consultative Committee (ITU-T). For brevity, this Standard will be referred to as \"CAN/CSA-ISO/IEC TR 20017\" throughout. This Standard has been formally approved, without modification, by the Technical Committee and has been approved as a National Standard of Canada by the Standards Council of Canada. 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.
| DocumentType |
Standard
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| ISBN |
978-1-77139-491-8
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| Pages |
0
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| ProductNote |
THIS STANDARD ALSO REFERS TO IEC, PT62334, 62369, 62311, 62479: 2009, under development
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| PublisherName |
Canadian Standards Association
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| Status |
Current
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CSA Preface Standards development within the Information Technology sector is harmonized with international standards development. Through the CSA Technical Committee on Information Technology (TCIT), Canadians serve as the Canadian Advisory Committee (CAC) on ISO/IEC Joint Technical Committee 1 on Information Technology (ISO/IEC JTC1) for the Standards Council of Canada (SCC), the ISO member body for Canada and sponsor of the Canadian National Committee of the IEC. Also, as a member of the International Telecommunication Union (ITU), Canada participates in the International Telegraph and Telephone Consultative Committee (ITU-T). For brevity, this Standard will be referred to as \"CAN/CSA-ISO/IEC TR 20017\" throughout. This Standard has been formally approved, without modification, by the Technical Committee and has been approved as a National Standard of Canada by the Standards Council of Canada. 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.
| Standards | Relationship |
| ISO/IEC TR 20017:2011 | Identical |
| AAMI PC69 : 2007 | |
| IEC 62209-2:2010 | Human exposure to radio frequency fields from hand-held and body-mounted wireless communication devices - Human models, instrumentation, and procedures - Part 2: Procedure to determine the specific absorption rate (SAR) for wireless communication devices used in close proximity to the human body (frequency range of 30 MHz to 6 GHz) |
| EN 50392:2004 | 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) |
| EN 62311:2008 | Assessment of electronic and electrical equipment related to human exposure restrictions for electromagnetic fields (0 Hz - 300 GHz) |
| ISO/IEC 19762-3:2008 | Information technology Automatic identification and data capture (AIDC) techniques Harmonized vocabulary Part 3: Radio frequency identification (RFID) |
| ISO/IEC 19762-4:2008 | Information technology Automatic identification and data capture (AIDC) techniques Harmonized vocabulary Part 4: General terms relating to radio communications |
| IEC 62479:2010 | Assessment of the compliance of low-power electronic and electrical equipment with the basic restrictions related to human exposure to electromagnetic fields (10 MHz to 300 GHz) |
| ISO/IEC 18000-6:2013 | Information technology — Radio frequency identification for item management — Part 6: Parameters for air interface communications at 860 MHz to 960 MHz General |
| CFR 48(CH1 PTS52-99) : OCT 2017 | FEDERAL ACQUISITION REGULATIONS SYSTEM |
| EN 50061 : 88 AMD 1 95 | SAFETY OF IMPLANTABLE CARDIAC PACEMAKERS |
| ISO/IEC 29160:2012 | Information technology Radio frequency identification for item management RFID Emblem |
| CFR 48(CH1 PTS1-51) : OCT 2017 | FEDERAL ACQUISITIONS REGULATIONS SYSTEM |
| ISO/IEC 18000-7:2014 | Information technology Radio frequency identification for item management Part 7: Parameters for active air interface communications at 433 MHz |
| EN 50357:2001 | Evaluation of human exposure to electromagnetic fields from devices used in Electronic Article Surveillance (EAS), Radio Frequency Identification (RFID) and similar applications |
| IEC 60601-1-2:2014 | Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
| AAMI TIR18:2010 | GUIDANCE ON ELECTROMAGNETIC COMPATIBILITY OF MEDICAL DEVICES IN HEALTHCARE FACILITIES |
| ISO 14708-2:2012 | Implants for surgery Active implantable medical devices Part 2: Cardiac pacemakers |
| ISO/IEC 19762-1:2008 | Information technology Automatic identification and data capture (AIDC) techniques Harmonized vocabulary Part 1: General terms relating to AIDC |
| ISO 14708-1:2014 | Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer |
| ISO/IEC 18000-2:2009 | Information technology — Radio frequency identification for item management — Part 2: Parameters for air interface communications below 135 kHz |
| ISO/IEC 18000-4:2015 | Information technology Radio frequency identification for item management Part 4: Parameters for air interface communications at 2,45 GHz |
| IEEE C95.1-2005 | IEEE Standard for Safety Levels with Respect to Human Exposure to Radio Frequency Electromagnetic Fields, 3 kHz to 300 GHz |
| IEC 62311:2007 | Assessment of electronic and electrical equipment related to human exposure restrictions for electromagnetic fields (0 Hz - 300 GHz) |
| IEC 62369-1:2008 | Evaluation of human exposure to electromagnetic fields from short range devices (SRDs) in various applications over the frequency range 0 GHz to 300 GHz - Part 1: Fields produced by devices used for electronic article surveillance, radio frequency identification and similar systems |
| EN 50371:2002 | 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 |
| ISO/IEC 18000-1:2008 | Information technology Radio frequency identification for item management Part 1: Reference architecture and definition of parameters to be standardized |
| ISO/IEC 18000-3:2010 | Information technology — Radio frequency identification for item management — Part 3: Parameters for air interface communications at 13,56 MHz |
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