Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices introduce an EU identification system for medical devices based on a Unique Device Identifier (UDI).
The UDI-DI/Device module of EUDAMED is used for the manufacturers to provide their UDIs/Devices information and to make it available to everyone
EUDAMED user guide UDI Devices
Playground v 3.11.0
2025