Additional 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 (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
.