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GUDID (全球UDI数据库)

FDA管理的数据库，包含制造商作为唯一器械标识（UDI）系统一部分提交的器械识别信息。GUDID公开可访问。

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

  1. Obtain DI from an issuing agency.
  2. Prepare GUDID data attributes.
  3. Submit and publish device records.
  4. 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

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相关术语

唯一器械标识(UDI)EUDAMED