Today, the U.S. Food and Drug Administration (FDA), in partnership with the National Institutes of Health National Library of Medicine (NLM), is making data on devices with unique device identifiers ...

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 ...

The healthcare supply chain has seen its share of ups and downs this year. In the early months of the COVID-19 pandemic crisis, product shortages were exacerbated by a lack of supply-chain visibility.

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 ...

A week after federal legislators and hospitals pressed the Office of Management and Budget about the release of a final unique device identification rule, the U.S. Food and Drug Administration ...

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, ...

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 ...

There are a few key drivers for the Unique Device Identification market one of which is the desire to adopt a single global standard. If all medical devices manufacturers conform to it, it makes life ...

Novation has called the FDA’s proposed rule implementing a Unique Device Identification system for medical devices a “significant milestone for patient safety,”according to a news release. “A robust ...

Arkose Labs today announced the launch of Arkose Device ID, a device identification solution that combines precise device tracking with session-based risk signals and anti-spoofing technology. Arkose ...