MDCG 2025-10: Guidance on post-market surveillance of medical devices and IVDs

MDCG Guidance MDCG 2025-12
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Summary

MDCG 2025-10 — Guidance on post-market surveillance of medical devices and IVDs

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 2025-10
TypeMDCG Guidance
AuthorityMDCG
Publication Date2025-12

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Quick Info

TypeMDCG Guidance
Published ByMDCG
Date2025-12

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