We can handle your UDI Coding Needs. We operate strictly under the guides of the FDA The FDA has established and continues to implement a unique device identification system to adequately identify medical devices through their distribution and use.
When fully implemented, the label of most devices will include a unique device identifier (UDI) in human- and machine-readable form.
Device labelers must also submit certain information about each device to the FDA’s Global Unique Device Identification Database (GUDID)