The Healthcare Supply Chain Association has announced it submitted its final comments to FDA regarding the proposed rule to establish a Unique Device Identification System for medical devices, ...

FDA has announced it has proposed that most medical devices distributed in the United States carry a unique device identifier, according to a news release. The announcement comes in response to ...

The US Food and Drug Administration (FDA) announced Tuesday, 3 July its intent to implement a long-delayed Unique Device Identifier (UDI) rule, which would mandate most medical devices carry an ...

The American Hospital Association has expressed its support of the FDA, which has proposed a final rule for a unique device identification system, according to an AHA News Now report. A UDI is a ...

In a highly anticipated move, the US Food and Drug Administration (FDA) has announced the final release of the Unique Device Identification (UDI) rule, reflecting a number of changes called for by ...

Dublin, April 07, 2026 (GLOBE NEWSWIRE)-- The "Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Training Course (June 8, 2026)" training has been added to ...

Channeling Johnny Nash and the 1972 classic song, “I Can See Clearly Now,” on July 7, 2021, the Food and Drug Administration issued its final guidance titled, “Unique Device Identification System: ...

CMS is supporting the incorporation of FDA's unique device identifiers in insurance claims forms, a boon to medical researchers who would receive a bounty of data about medical device safety and ...

The global market for digital label printing is projected to reach $20.6 billion by 2035, spurred by stringent regulations in ...

A new system that provides unique labels to identify medical devices is being instituted by the U.S. Food and Drug Administration. Called the unique device identification system (UDI), it will ...

Device makers have argued for years that not all medical device recalls are the same, and thus the FDA should be more forthcoming with the public about the difference between a recall that is ...