Comprehensive list of links to the UDI rule and guidances, training for industry, UDI and GUDID technical resources, and dockets.| U.S. Food and Drug Administration
This requires UDI data submitted to GUDID to be of a high quality such that all stakeholders in the healthcare community have sufficient confidence in the accuracy and completeness of that data. This will enable the GUDID to be a reference source of data used in downstream systems.| U.S. Food and Drug Administration
Device labelers have two options for submitting GUDID data: the GUDID web application and HL7 SPL file submission using the FDA Electronic Submission Gateway.| U.S. Food and Drug Administration