FDA Pushes Back Enforcement of UDI Requirements for Class I, Unclassified Devices
By Zachary Brennan -
Published 12 January 2018
The US Food and Drug Administration (FDA) said Friday that it will delay its enforcement of certain unique device identification (UDI) system requirements for class I and unclassified devices by two years.
Categories: News, US, CDRH, Compliance, Due Diligence, Government affairs, Medical Devices
Tags: unique device identification, Class I, unclassified devices, UDI enforcement