Feel Like Running From the FDA?

As you may already know, in 2013, the Food and Drug Administration (FDA) released a final rule regarding a unique device identification (UDI) system for distributors of medical devices.

This requires that all distributors of medical devices must implement a UDI. Manufacturers must submit information to the UDIDID. Here is where you can find the latest updates regarding the UDI:

FDA UDI Rule

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