Fda Global Unique Device Identification Database Gudid

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Fda global unique device identification database gudid.

The draft of this document was issued on september 24 2013. The global unique device identification database gudid pronounced good id is a database administered by the fda as part of the udi system. Regulated product data must be submitted to the global unique device identification database gudid i e. Fda global udi database gudid as part of the udi system the fda is also created the global unique device identification database gudid which include a set of data attributes for each device marked with a udi.

Global unique device identification database gudid guidance for industry. Fda designed and developed the global unique device identification database gudid to prepare forthe implementation of the udi final rule. The fda is establishing the unique device identification system to adequately identify devices sold in the u s from manufacturing through distribution to patient use. Manufacturers are responsible for submitting and maintaining their own data in the fda s gudid.

Gs1 member organisations across the world will help manufacturers implement with the requirements of the us fda udi regulation to support patient safety and supply chain security. For questions regarding this document contact. Fda gudid user manual v1 1 i. The gudid is a database that aims to improve medical device safety and serve as the.

The us fda udi regulatory database. The global unique device identification database gudid contains key device identification information submitted to the fda about medical devices that have unique device identifiers udi.