MDCG 2022-7: Q&A on the Unique Device Identification system under MDR and IVDR

MDCG Guidance MDCG 2022-05
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MDCG 2022-7 — Q&A on the Unique Device Identification system under MDR and IVDR

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 2022-7
TypeMDCG Guidance
AuthorityMDCG
Publication Date2022-05

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TypeMDCG Guidance
Published ByMDCG
Date2022-05

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