Editor's Note
The Food and Drug Administration announced that new data elements will be available on AccessGUDID, in the download files and in the APIs, as of April 2.
Data for FDA Premarket Submission Number and FDA Premarket Supplement Number will not be provided until this summer.
The FDA is asking participants to review the information and to make sure their systems are able to download and process the updated files.
The Global Unique Device Identification Database (GUDID) includes key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers.
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