Federal Register Notice: FDA is making available a guidance entitled Global Unique Device Identification Database (GUDID): Guidance for Industry. FDA has updated sections of the draft guidance of the same name. The guidance includes information about how device labelers (in most instances, the device manufacturer) will interface with the GUDID by establishing GUDID accounts and beginning their initial submissions. Draft guidance sections on the device identifier (DI) module have not been finalized in this document and will be addressed in a future document. To download this guidance, click here. To view this notice, click here.