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).
The Global Unique Device Identification Database (GUDID) is a database administered by the FDA that serves as a reference catalog for every device with a unique device identifier (UDI).
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).
This section presents an overview of the GUDID account, the user roles, preparatory steps to obtain a GUDID account, how to request a GUDID account and how to manage account changes.
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).
Manufacturers are required by the FDA to submit medical device data to the GUDID1. The database serves as the reference catalog for every device with a Unique Device Identifier (UDI) and contains both required and optional data elements.
GUDID (pronounced “Good ID”) refers to the Global Unique Device Identification Database, a digital catalog created by the FDA to store detailed information on all medical devices with a unique device identifier (UDI).
Device labelers have two options for submitting GUDID data: the GUDID web application and HL7 SPL file submission using the FDA Electronic Submission Gateway.
By using this system, you understand and consent to the following: The Government may monitor, record, and audit your system usage, including usage of personal devices and email systems for...
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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