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BSI - BS EN 50527-1 - TC

Tracked Changes (Redline) - Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices Part 1: General

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Organization: BSI
Publication Date: 25 February 2020
Status: active
Page Count: 87
ICS Code (Occupational safety. Industrial hygiene): 13.100
ICS Code (Radiation protection): 13.280
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40

Document History

BS EN 50527-1 - TC
February 25, 2020
Tracked Changes (Redline) - Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices Part 1: General
A description is not available for this item.

References

This document references:
EN 45502-2-3 - Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems
Published by CEN on March 1, 2010
This Part 2-3 of EN 45502 specifies requirements that are applicable to those ACTIVE IMPLANTABLE MEDICAL DEVICES that are intended to treat hearing impairment via electrical stimulation of the...
This document references:
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 CEN on May 1, 2015
This part of EN 45502 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 50527-2-2 - Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices - Part 2-2: Specific assessment for workers with cardioverter defibrillators (ICDs)
Published by CENELEC on May 1, 2018
This European Standard provides the procedure for the specific assessment required in EN 50527-1:2016, Annex A, for workers with implanted cardioverter defibrillators (ICDs) and Cardiac...
This document references:
EN 45502-2-2 - Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)
Published by CENELEC on March 1, 2008
This Part 2-2 of EN 45502 specifies requirements that are applicable to IMPLANTABLE CARDIOVERTER DEFIBRILLATORS and the functions of ACTIVE IMPLANTABLE MEDICAL DEVICES intended to treat...
This document references:
EN 45502-2-2 - Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)
Published by CENELEC on March 1, 2008
This Part 2-2 of EN 45502 specifies requirements that are applicable to IMPLANTABLE CARDIOVERTER DEFIBRILLATORS and the functions of ACTIVE IMPLANTABLE MEDICAL DEVICES intended to treat...
This document references:
EN 50527-2-2 - Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices - Part 2-2: Specific assessment for workers with cardioverter defibrillators (ICDs)
Published by CENELEC on May 1, 2018
This European Standard provides the procedure for the specific assessment required in EN 50527-1:2016, Annex A, for workers with implanted cardioverter defibrillators (ICDs) and Cardiac...
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