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Unique Device Identification Module for Quality
PTC Windchill 10.2 contains a new module to comply with the new Part 830 medical device regulation for the Unique Device Identification (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) Global Unique Device Identification Database (GUDID).