Additional Windchill Capabilities > Windchill Quality Solutions > Unique Device Identification
Unique Device Identification
The Food and Drug Administration (FDA) requires most medical devices distributed in the United States to carry a unique device identifier. The Unique Device Identification (UDI) module allows users to comply with this rule.
To install the UDI module, see Installing Unique Device Identification.
To create unique device identifiers and submit them to the FDA, see Working with Unique Device Identification.