MDCG 2020-16 Rev.3 – Guidance on Classification Rules for in vitro Diagnostic Medical Devices under Regulation (EU) 2017/746 – July 2024
The guidance, relating to the application of Regulation (EU) 2017/746 on in vitro diagnostic medical devices addresses the classification of in vitro diagnostic medical devices and provides clarifications on the classification rules as set out under Annex VIII. This classification guidance also applies to diagnostic or information society services performed on EU patients or devices put in to service through distance sales.
Read the news announcement published by EC Directorate-General for Health and Food Safety on 8 July 2024.
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lsgilbert (12 août 2024). MDCG 2020-16 Rev.3 – Guidance on Classification Rules for in vitro Diagnostic Medical Devices under Regulation (EU) 2017/746 – July 2024. ELSIBI. Consulté le 10 décembre 2024 à l’adresse https://doi.org/10.58079/125v6
