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 task–force report on transitional provisions (‘legacy devices’ and ‘old’ devices).
Read the news announcement published by the European Commission on 21 October 2021.
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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





