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CATÉGORIE: REGULATORY PATHWAYS
EUDAMED
La base de données européenne sur les dispositifs médicaux — une plateforme informatique centralisée sous l'EU MDR avec 6 modules couvrant l'enregistrement des acteurs, l'IUD, les certificats, les investigations cliniques, la vigilance et la surveillance du marché.
Last reviewed 2026-08-05 · Reviewed by MedFlux Editorial Board · Editorial policy
Expanded process notes below are currently maintained in English; the short definition above is localized. See our editorial policy.
WHEN IT APPLIES
EUDAMED is the EU database platform under MDR/IVDR for actors, UDI/devices, certificates, clinical investigations, vigilance, and market surveillance modules as they become mandatory.
PROCESS / STEPS
- Register economic operators and obtain SRNs when required.
- Prepare UDI-DI data and device registration packages.
- Align certificate and vigilance submissions with NB and competent authorities.
- Keep records synchronized when device versions or actors change.
EXAMPLES
- Manufacturers register as actors before placing devices under MDR obligations.
RELATED GUIDES & TOOLS
SOURCES
Track regulatory signals related to EUDAMED across 27 authorities in real time.
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