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 ...

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 ...

Dublin, Nov. 21, 2024 (GLOBE NEWSWIRE) -- The "Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Training Course" conference has been added to ResearchAndMarkets ...

A Unique Device Identifier (UDI) is an individualized alphanumeric signature associated with a single medical device. Since 2013, the Food and Drug Administration (FDA) has mandated the placement ...

The FDA released its Final Rule for Unique Device Identification requiring all medical devices intended to be used more than once to have a UDI. VeriT.

The FDA is granting an extension for soft contact lens labelers to comply with the requirements of the Unique Device Identification system, which was established Sept. 24, 2013.The UDI Rule ...

Previously, FDA was scheduled to begin enforcement of the UDI system requirements for regulatory labeling, Global Unique Device Identification Database (GUDID) data submission and date formatting ...

A new method of tracking medical device malfunctions, the unique device identification (UDI) number, may lead to a curb in malfunctions of lifesaving devices such as the personal defibrillator ...

The Food and Drug Administration last week released an amendment to its proposed rule for a unique device identification system released in July. The amendment shortens the originally proposed ...

FDA Releases Final Rule for Unique Device Identification Final Rule Represents Significant Industry Shift to Use UDIs DELRAY BEACH, Fla.--(BUSINESS WIRE)-- Digital Angel Corporation ("Digital ...