A long-awaited U.S. Food and Drug Administration proposed rule requiring unique identifiers on medical devices was published July 10 in the Federal Register. See Also: Reduce Cloud Risk in Healthcare ...

In an "early alert," the Office of Inspector General for Health and Human Services (HHS OIG) has asked CMS to work to add device identifier information to health insurance claim forms. The urging came ...

Lack of medical device-specific information in patient claims forms impedes the government’s ability to track Medicare costs related to the replacement of defective or recalled devices, according to a ...

The U.S. Food and Drug Administration submitted a proposed final rule on unique medical device identifiers to the Office of Management and Budget for review, Health Data Management has reported. The ...

Every medical device has its own unique code, allowing manufacturers to keep track of their products once they enter the market. But while these codes are critical for recalling faulty devices or ...

A range of patient advocacy groups is urging the Office of Management and Budget to release a final Unique Device Identification (UDI) rule as soon as possible. In a letter to OMB Director Sylvia ...

The Food and Drug Administration has announced its proposal to create a unique device identification (UDI) system, which will impact both suppliers and providers. The rule itself has its genesis in a ...

Sen. Elizabeth Warren, D-Massachusetts, took the Centers for Medicare and Medicaid Service to task on Tuesday for waffling on the policy to add unique device identifier information to Medicare claims ...

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