The UDI domain provides access to the UDI module of Windchill. The UDI module allows users to comply with the Part 830 medical device regulation for the UDI submission process. Users can electronically submit unique device identifiers for their medical devices and device packages to the Food and Drug Administration (FDA) Global Unique Device Identification Database (GUDID). Use the services provided by this domain to read the UDI super set data, and to create and modify the UDI super set objects. Users can add, remove, or modify the details present in the “table data” step of the UDI super set object. Users can update the UDI super set object based on the permission present in policy administration.

The following table lists the significant OData entities available in the UDI domain. To see all the OData entities available in the UDI domain, refer to the EDM of the domain. The domain EDM is available at the metadata URL.