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GUDID (Globale UDI-Datenbank)
Die von der FDA verwaltete Datenbank mit Geräteidentifikationsinformationen als Teil des UDI-Systems.
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 (Globale UDI-Datenbank) across 27 authorities in real time.
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