Guidance - MDCG
MDR extension Proposal
MDCG 2023-3 (Questions and Answers on vigilance terms and concepts as outlined in the Regulation (EU) 2017/745 on medical devices)
MDCG 2020-3 Rev.1 (Guidance on significant changes regarding the transitional provision under Article 120 of the MDR with regard to devices covered by certificates according to MDD or AIMDD)
MDCG 2022-7 Questions and Answers on the Unique Device Identification system under Regulation (EU) 2017/745 and Regulation (EU) 2017/746
UDI Devices - user guide (Settembre 2023)
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