Additional Windchill Capabilities > Windchill Quality Management 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.