top of page

EC Explains What UDI Information to Provide for Eudamed



The European Commission on Friday released three documents, including two on the Medical Device Regulation (MDR) and the In Vitro Diagnotic Regulation (IVDR) and what data from the unique device identifier (UDI) needs to be included in the Eudamed database of devices and IVDs, and another document on the Eudamed device data dictionary.

Read more


source regulatory affairs professionals society

7 views0 comments

Recent Posts

See All

Dear all, here are the great sources that caught our eye in the last weeks regarding the medical device industry outlook as of 2021. Including: - EY report, 2021 - McKinsey report, 2021 - MedTech Dive

bottom of page