MDCG 2022-7 – Q&A on the Unique Device Identification system under Regulation (EU) 2017/745 and Regulation (EU) 2017/746
This document presents questions and answers on the Unique Device Identification system (UDI system) established under Regulation (EU) 2017/745 on medical devices1 (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices2 (IVDR).
Read the news announcement published by Directorate-General for Health and Food Safety on 20 May 2022.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (20 juillet 2022). MDCG 2022-7 – Q&A on the Unique Device Identification system under Regulation (EU) 2017/745 and Regulation (EU) 2017/746. ELSIBI. Consulté le 18 février 2026 à l’adresse https://doi.org/10.58079/o5zx





