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I.S. EN 50527-2-3:2021

Current
Current

The latest, up-to-date edition.

Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices - Part 2-3: Specific assessment for workers with implantable neurostimulators
Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

15-11-2021

Preview

For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.

Only cited Standards give presumption of conformance to New Approach Directives/Regulations.

European foreword
1 Scope
2 Normative references
3 Terms and definitions
4 Specific assessment
5 Documentation
Annex A (normative) Device specific replacement of EN 50527-1:2016,Table 1
Annex B (informative) Rationale
Annex C (informative) Nerve Stimulation for SCS
Annex D (informative) Selection of Conductivity Values for SCS Modelling
Annex E (informative) Modelling Nerve Stimulation for SCS
Annex F (informative) Electrode factor for non-isotropic tissue
Bibliography

This document provides the procedure for the specific assessment required in EN 50527-1:2016, Annex A, for workers with implanted neurostimulator systems (NS), specifically of the type used for spinal cord stimulation (SCS).

Committee
TC 106X
DocumentType
Standard
Pages
112
ProductNote
The date of any NSAI previous adoption may not match the date of its original CEN/CENELEC document. THIS STANDARD IS ALSO REFERES TO EN 62226-3-1, EN 60118-4<br>
PublisherName
National Standards Authority of Ireland
Status
Current

Standards Relationship
EN 50527-2-3:2021 Identical

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