Glossary · Devices
EUDAMED
European Database on Medical Devices
EUDAMED is the European Commission's database for medical devices and in vitro diagnostics under the MDR and IVDR, with modules for actors, UDI and device registration, notified bodies and certificates, clinical investigations and performance studies, vigilance and market surveillance.
Part of it is public, and four modules (actors, UDI and devices, notified bodies and certificates, market surveillance) became mandatory on 28 May 2026, with the others to follow.
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Definitions written by Anpheros from the official sources linked on each page. General information about standards and regulation, not legal or medical advice. All terms →