MDCG 2022-4 rev.1 – Guidance on appropriate surveillance regarding MDR Art.120 transitional provisions – devices covered by MDD or AIMDD certificates – December 2022
The guidance document outlines the activities to be performed by notified bodies as part of the appropriate surveillance defined in Article 120(3) second subparagraph of the Medical Device Regulation.
Read the news announcement published by EC Directorate-General for Health and Food Safety on 16 December 2022.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (24 janvier 2023). MDCG 2022-4 rev.1 – Guidance on appropriate surveillance regarding MDR Art.120 transitional provisions – devices covered by MDD or AIMDD certificates – December 2022. ELSIBI. Consulté le 16 janvier 2025 à l’adresse https://doi.org/10.58079/o669
