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MDCG 2019-6 rev.5 – Questions and answers: Requirements relating to notified bodies (February 2025)

This document presents questions and answers on requirements relating to notified bodies under Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices. The issues covered by this document have been identified in the context of joint assessments,and the document may be updated from time to time as new issues are identified.

Read the news announcement published by Directorate-General for Health and Food Safety on 7 February 2025.


OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (18 mars 2025). MDCG 2019-6 rev.5 – Questions and answers: Requirements relating to notified bodies (February 2025). ELSIBI. Consulté le 19 janvier 2026 à l’adresse https://doi.org/10.58079/13icy


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