CATEGORY: DOCUMENTATION

GUDID (Global UDI Database)

The FDA-managed database containing device identification information submitted by manufacturers as part of the Unique Device Identification (UDI) system. GUDID is publicly accessible and contains UDI-DI, device descriptions, company information, and contact details.

Last reviewed 2026-08-05 · Reviewed by MedFlux Editorial Board · 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

FDA GUDID ↗

Track regulatory signals related to GUDID (Global UDI Database) across 27 authorities in real time.

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