In this tutorial you will learn how to Overview of Unique Device Identification (UDI). The Unique Device Identification (UDI) module complies with the new Part 830 medical device regulation for the UDI submission process. This module allows users to create unique device identifiers for their medical devices and device packages. Users can then electronically submit the unique device identifiers to the Food and Drug Administration (FDA).... (Show more)(Show less)
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