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 ...

Starting in September, class II medical devices will be required to be equipped with a unique device identifier to be in compliance with UDI regulations. The U.S. Food and Drug Administration passed ...

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 Obama Administration’s Office of Management and Budget has approved and released a long-awaited proposed rule on a unique device identification system for medical devices. The document was ...

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 ...

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.

A U.S. Department of Health and Human Services Office of the Inspector General report released Monday recommends partial adoption of unique device identifiers in the next version of Medicare claims ...

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 ...

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Twelve provider groups -- including Intermountain Healthcare, Geisinger and the American Medical Group Association -- are calling on Centers for Medicare and Medicaid Services Administrator Seema ...

The Food and Drug Administration has released its final rule requiring most medical devices distributed in the United States to include a unique device identifier, according to a report from Premier ...