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CENELEC - EN 50061

Safety of Implantable Cardiac Pacemakers

inactive, Most Current
Organization: CENELEC
Publication Date: 1 May 1988
Status: inactive
Page Count: 36
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40

Document History

EN 50061
May 1, 1988
Safety of Implantable Cardiac Pacemakers
A description is not available for this item.

References

This document is referenced by:
ISO 14117 - Active implantable medical devices — Electromagnetic compatibility — EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
Published by ISO on September 1, 2019
This document specifies test methodologies for the evaluation of the electromagnetic compatibility (EMC) of active implantable cardiovascular devices that provide one or more therapies for...
This document is referenced by:
AAMI 14117 - Active implantable medical devices—Electromagnetic compatibility—EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
Published by AAMI on January 1, 2019
This document specifies test methodologies for the evaluation of the electromagnetic compatibility (EMC) of active implantable cardiovascular devices that provide one or more therapies for...
This document is referenced by:
IEC 60601-2-31 - Medical electrical equipment – Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source
Published by IEC on January 1, 2020
This part of IEC 60601 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of EXTERNAL PACEMAKERS powered by an INTERNAL ELECTRICAL POWER SOURCE, hereafter referred to as ME EQUIPMENT. This...
This document is referenced by:
60601-2-33 INT 1 - MEDICAL ELECTRICAL EQUIPMENT – Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
Published by IEC on May 1, 2023
A description is not available for this item.
This document is referenced by:
BS EN 45502-1 - 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 BSI on June 30, 2015
A description is not available for this item.
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