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 €

Detalles

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.

Información adicional

Autor American Dental Association
Publicado por ADA
Tipo de Documento Norma
Número de páginas 15
Reemplaza ADA 1081-2015
Palabra clave ADA 1081-2019