The FDA’s Global Unique Device Identification Database (GUDID) contains records submitted by medical device labelers in accordance with the UDI Rule. As of Summer 2019, GUDID contains over 2 million records.
The presentation files below summarize patterns and trends in the GUDID data, including types of devices submitted to GUDID. These slides are free for the public to distribute and use for educational purposes.
Note: The information in these files reflects the data available in GUDID as of the date printed on each slide. GUDID data are sent to AccessGUDID, the publicly accessible web portal for GUDID data, following completion of a seven day editing grace period.