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MDCG 21-25 – Regulation (EU) 2017/745 – application of MDR requirements to ‘legacy devices’ and to devices placed on the market prior to 26 May 2021 in accordance with Directives 90/385/EEC or 93/42/EEC

The Medical Device Coordination Group (MDCG) published on 19 October 2021 a taskforce report on transitional provisions (‘legacy devices’ and ‘old’ devices).

Read the news announcement published by the European Commission on 21 October 2021.


OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (14 mars 2022). MDCG 21-25 – Regulation (EU) 2017/745 – application of MDR requirements to ‘legacy devices’ and to devices placed on the market prior to 26 May 2021 in accordance with Directives 90/385/EEC or 93/42/EEC. ELSIBI. Consulté le 13 janvier 2026 à l’adresse https://doi.org/10.58079/o5vk


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