ADA 1081 PDF
ADA 1081 PDF
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ADA 1081 PDF

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FDA's Unique Device Identifiction (UDI) Program for Dental Devices and Biologics Regulated as Medical Devices – Technical Report

Published byPublication DateNumber of Pages
ADA02/01/201915
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ADA 1081 – FDA's Unique Device Identifiction (UDI) Program for Dental Devices and Biologics Regulated as Medical Devices– Technical Report

ADA 1081-2019: 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.

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