Compliance to the UDI regulation includes the FDA public database, GUDID.
The final guidance document of the Global Unique Device Identification Database (GUDID): Guidance for Industry is now available. The complete guidance includes how device labelers interface with GUDID, establishing GUDID accounts and beginning initial submissions, Device Identifier records, HL7 labeling submissions, maintaining and submitting GUDID electronic records.
For more information view the guidance document.