MDCG 2019-6: Q&A: Requirements relating to notified bodies

MDCG Guidance MDCG 2025-02 rev.5
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Summary

MDCG 2019-6 — Q&A: Requirements relating to notified bodies

Revision: rev.5

This is a guidance document endorsed by the Medical Device Coordination Group (MDCG) under the EU Medical Device Regulation (MDR 2017/745) and/or In Vitro Diagnostic Regulation (IVDR 2017/746).

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Document Details

Document IDMDCG 2019-6
TypeMDCG Guidance
AuthorityMDCG
Publication Date2025-02
Revisionrev.5

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TypeMDCG Guidance
Published ByMDCG
Date2025-02

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