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ADA TR 1081-2023
FDA's Unique Device Identification (UDI) Program for Dental Devices and Biologics Regulated as Medical Devices
The FDA has issued a rule to establish a system to adequately identify devices through distribution. This rule requires the label of medical devices to include a unique device identifier (UDI), except where the rule provides for an exception or alternative placement.
CONTENT PROVIDER
American Dental Association [ada]
American Dental Association [ada]