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Medicare Agency Comes On Board With Adding UDIs To Claims Forms

 
• By David Filmore

The acting head of the Center for Medicare and Medicaid Services has signaled his agency's plan to support the effort to get UDIs incorporated as a standard element of insurance claims by signing a letter jointly with the FDA commissioner. Previously, CMS had worried about the move due to the significant system upgrades that hospitals and payers will need to make to support UDIs in claims.

The Center for Medicare and Medicaid Services is finally putting its support behind giving Unique Device Identifiers a place on insurance claims forms. In a letter dated July 13, CMS Acting Administrator Andy Slavitt joined US FDA Commissioner Robert Califf in urging adoption of UDIs for implantable devices on claims forms.

The letter is addressed to the Accredited Standards Committee X12, which has been working to adopt standards that would allow...

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More from United States

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• By Elizabeth Orr

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With LDT Rule DOA, Could FDA Shift Focus To RUOs?

 
• By Brian Bossetta

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• By Derrick Gingery and Sue Sutter

Commissioner Martin Makary told staff that plans are being developed to centralize HR, IT, travel and other functions, which were heavily impacted by the 1 April reduction-in-force.

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• By Brian Bossetta

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More from North America

MDUFA VI Launches With Public Meeting, Call For Comments

 
• By Elizabeth Orr

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Permanent FDA Top Lawyer Expected After HHS Counsel Confirmation

 
• By Sue Sutter

Robert Foster, HHS deputy general counsel and chief counsel for food, research and drugs, is temporarily heading the Office of Chief Counsel, but a permanent appointee is expected after Michael Stuart's confirmation as HHS general counsel.

FDA Drops Package Labeling Guidance For Hernia Mesh Manufacturers

 
• By Brian Bossetta

The US FDA recently published a draft guidance document for manufacturers of mesh products that are used during several types of hernia repair procedures.