- Regulatory House
Module UDI/Devices registration and Notified Bodies and Certificates were launched
The European Commission has launched two more modules of the EUDAMED database for voluntary use.
One of them is device identification system based on a unique device identifier (UDI) allowing easier traceability of medical devices, the second modul should inform about any information regarding certificates - issued, suspended, reinstated, withdrawn or refused and other restrictions imposed on these certificates. Such information is accessible to the public.
More information, including user manuals, can be found on the European Commission's website.