The draft of this document was issued on september 24 2013.
Fda global unique device identification database gudid.
Fda gudid user manual v1 1 i.
The us fda udi regulatory database.
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.
Regulated product data must be submitted to the global unique device identification database gudid i e.
The gudid is a database that aims to improve medical device safety and serve as the.
The gudid contains only the device identifier di which serves as the primary key to obtain information in the database.
The global unique device identification database gudid is a database administered by the fda that will serve as a reference catalog for every device with a unique device identifier udi.
Global unique device identification database gudid guidance for industry.
The global unique device identification database gudid pronounced good id is a database administered by the fda as part of the udi system.
The gudid contains device identification information submitted by device companies to the fda.
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.
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.
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