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ADA 1081-2019
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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
Full Description
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.
M00000912
2021-05-12
New product
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