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BSI - BS EN 50527-1

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: 31 May 2010
Status: inactive
Page Count: 44
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
January 31, 2017
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.
BS EN 50527-1
May 31, 2010
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:
EEC/89/391 - Council Directive on the Introduction of Measures to Encourage Improvements in the Safety and Health of Workers at work
Published by EEC on January 1, 1989
A description is not available for this item.
This document references:
90/385/EEC - Commission Communication in the Framework of the Implementation of Council Directive in Relation to Active Implantable Medical Devices (1), and Council Directive 93/42/EEC of 14 June 1993 in Relation to Medical Devices (2)
Published by EU on June 20, 1990
A description is not available for this item.
This document references:
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.
This document references:
BS EN 45502-2-3 - Active implantable medical devices Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems
Published by BSI on March 31, 2010
A description is not available for this item.
This document references:
EN 45502-2-1 - Active implantable medical devices Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
Published by CENELEC on December 1, 2003
This Part 2-1 specifies requirements that are applicable to those ACTIVE IMPLANTABLE MEDICAL DEVICES intended to treat bradyarrhythmias. The tests that are specified in EN 45502 are type tests, and...
This document is referenced by:
BS EN 50527-2-1 - Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices Part 2-1: Specific assessment for workers with cardiac pacemakers
Published by BSI on January 31, 2017
A description is not available for this item.
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