MDCG 2024-13: Regulatory status of ethylene oxide (EtO) for sterilisation of medical devices

MDCG Guidance MDCG 2024-10
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MDCG 2024-13 — Regulatory status of ethylene oxide (EtO) for sterilisation of medical devices

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 2024-13
TypeMDCG Guidance
AuthorityMDCG
Publication Date2024-10

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TypeMDCG Guidance
Published ByMDCG
Date2024-10

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