AccessGUDID (http://accessgudid.nlm.nih.gov/) is now publicly available so anyone can search and download information that device labelers have submitted to the FDA’s GUDID about their medical devices. Because the UDI system is being phased in over the next several years, labelers are currently submitting data on only the highest risk medical devices, a small subset of marketed devices. But as the system is implemented according to the UDI compliance timeline, the records of all medical devices required to have a UDI will be included.
Identification Labs maintains a highly experienced team which can assist companies with FDA UDI barcode and packaging certification, data validation, and data migration. Contact us today to see what our experience can do for your company.
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