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Business · 26/04/2019

FDA Announces Availability of Guidance on Unique Device Identification for Convenience Kits

The Food and Drug Administration (FDA) has released a final guidance document outlining its interpretation of the definition of a convenience kit, which provides an exception to the unique device identification system regulations for devices packaged within convenience kits bearing a UDI

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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