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CATÉGORIE: DOCUMENTATION
GUDID (Base de données UDI mondiale)
La base de données gérée par la FDA contenant les informations d'identification des dispositifs soumises dans le cadre du système IUD.
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
GUDID is FDA’s Global Unique Device Identification Database where labelers submit device identifier data for UDI-regulated devices.
PROCESS / STEPS
- Obtain DI from an issuing agency.
- Prepare GUDID data attributes.
- Submit and publish device records.
- Update records when packaging or device versions change DIs.
EXAMPLES
- Hospital systems and supply chains rely on GUDID for device identification interoperability.
RELATED GUIDES & TOOLS
SOURCES
Track regulatory signals related to GUDID (Base de données UDI mondiale) across 27 authorities in real time.
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