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Author archives: Lou DeMatteo

A contributing writer at iBASEt. Extensive experience in FDA regulated industries.

01/28

2016

New Acronyms from the FDA: UDI and GUDID

On September 24, 2013, the FDA established a Unique Device Identification (UDI) system to identify all medical devices sold in the U.S. starting from the point of manufacture, through all distribution channels, and to the eventual sale to the consumer.

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