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 ...

DELRAY BEACH, Fla.--(BUSINESS WIRE)-- Digital Angel Corporation ("Digital Angel" or the "Company") (OTC Markets: DIGA), a provider of implantable medical device identification and radiation dose ...

A recent blog post in the reSOURCEs section of the HealthTrust public website discusses how the new UDI system will affect healthcare operations. In 2013, the U.S. Food and Drug Administration (FDA) ...

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 ...

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 ...

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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 ...

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.

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 ...

PITTSBURGH--(BUSINESS WIRE)--Rimsys, a world-leading Regulatory Information Management (RIM) software platform for medical technology companies, announced the release of an innovative and automated ...

QAD ERP Makes it Simpler to Achieve UDI Regulatory Compliance and Ensure Product Integrity from Component to Patient with Backward and Forward Traceability <0> QAD Inc.Ashley DeVan, +1-805-566-6126Sr.

On September 24, 2013, the Food and Drug Administration (FDA) published a Final Rule, which will, over the next several years, require many medical devices distributed in the U.S. to carry a unique ...