MINNEAPOLIS, July 26, 2012 /PRNewswire/ -- On July 10, 2012, the Food and Drug Administration released its proposed rule for Unique Device Identification (UDI) of medical devices in the United States.

Back in 2014, the Department of Health started to take tentative steps towards setting a standard for tracking medical implants, supplies, and instruments. Its Scan4Safety program mandated that all ...

Members of the medical device industry are responding to the U.S. Food and Drug Administration‘s (FDA) proposed rules, published today, regarding the agency’s much anticipated Unique Device ...

Dublin, April 14, 2026 (GLOBE NEWSWIRE)-- The "Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers (June 8, 2026)" training has been added to ResearchAndMarkets.com's ...

IRVING, Texas, Nov. 8, 2012 /PRNewswire/ -- On November 6, Novation submitted comments to the Food and Drug Administration regarding the implementation of a Unique Device Identification (UDI) system ...

In case you didn’t think number crunchers are taking over the world in the age of Big Data, artificial intelligence and “deep learning,” the feds just handed them another victory, this time in the ...

The agency's rule will require most Class III devices, such as automated external defibrillators, to have unique device identifiers on their label and packaging within a year. Sep 23, 2013 A Sept. 20 ...

On May 4, 2015, the FDA launched the most recent component of its “Unique Device Identification System,” or “UDI System,” first created in September of 2013 and required by the Food and Drug ...

The FDA is in the process of implementing the Unique Device Identification (UDI) System in a series of phases. Currently, all Class III and implantable, life-supporting and life-sustaining medical ...

Under the FDA's newly enacted UDI rule, devices must be shipped with a unique identification label. (Click to expand.)--Courtesy of the FDA Stakeholders including the Mayo Clinic, American Association ...

On June 2, 2017, the US Food and Drug Administration (FDA) announced that it plans to delay the dates by which certain Class I devices and unclassified devices must comply with the agency’s unique ...