Welcome to the EUDAMED information centre

EUDAMED is the IT system established by Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnosis medical devices. 

EUDAMED provides a living picture of the lifecycle of medical devices that are made available in the European Union (EU). It integrates different electronic systems to collate and process information about medical devices. EUDAMED aims to enhance overall transparency, including better access to information for public and healthcare professionals, and to enhance coordination between the different Member States in the EU. 

EUDAMED is composed of six modules related to: actor registration, unique device identification (UDI) and device registration, notified bodies and certificates, clinical investigations and performance studies, vigilance and post-market surveillance and market surveillance.