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 ...

Opportunities exist for enhancing medical device safety and compliance through improved labeling that meets regulatory standards. These include employing clear information, symbols to bridge language ...

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, ...

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 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 ...

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 ...

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 ...

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