top of page
Writer's pictureteam IntMeDA

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.


source regulatory affairs professionals society

9 views0 comments

Recent Posts

See All

Medtech industry outlook 2021

Dear all, here are the great sources that caught our eye in the last weeks regarding the medical device industry outlook as of 2021....

Comments


bottom of page