EUDAMED is the IT system developed by the European Commission to implement Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnosis medical devices.
EUDAMED will contain a living picture of the lifecycle of all products being available on the EU market. A large part of the information will be made publicly available.
For further information on EUDAMED, please visit the EUDAMED section of the European Commission website.
