Description

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.

Product Details

Published:

02/01/2019

Number of Pages:

15

File Size:

1 file , 1.1 MB

Redline File Size:

2 files , 6.3 MB

Note:

This product is unavailable in Ukraine, Russia, Belarus