Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices - Specific assessment for workers with cardioverter defibrillators (ICDs) Ingestion-build-279162 ISO 30422 supersedes PD 76006:2017

ISO 30422 supersedes PD 76006:2017

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BS EN 61021-1 guideline specifies the dimensions

Note 4: It is the responsibility of the user of BS EN 12606 to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use

Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices - Specific assessment for workers with cardioverter defibrillators (ICDs) Ingestion-build-279162 ISO 30422 supersedes PD 76006:20171 Scope 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 Resynchronization Therapy devices with associated defibrillation functions (CRT D). Only devices of this type equipped with leads implanted transvenously are considered. It offers different approaches for doing the risk assessment. NOTE 1 If the worker has