ADA 1081-2019

$11.70

FDA’s Unique Device Identification (UDI) Program for Dental Devices and Biologics Regulated as Medical Devices

Published By	Publication Date	Number of Pages
ADA	2019-02-01	15

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Category: ADA

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Description

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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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