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ADA 1081-2019

M00003577

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ADA 1081-2019 FDA's Unique Device Identifiction (UDI) Program for Dental Devices and Biologics Regulated as Medical Devices - Technical Report

standard by American Dental Association, 02/01/2019

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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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Published: 02/01/2019 Number of Pages: 15 File Size: 1 file , 1.1 MB Redline File Size: 2 files , 6.3 MB