ADA 1081-2019

ADA 1081-2019

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

41,00 €

Détails

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.

Informations supplémentaires

Auteur American Dental Association
Edité par ADA
Type de document Norme
Nombre de pages 15
Remplace ADA 1081-2015
Mot-clé ADA 1081-2019