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 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: Alleviating Compliance Pain ...

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 ...

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 manufacturer of a device sets a unique ID for it. This ID is a string that your Operating System uses to match the device to its package. So, if a device package declares that it can work with ...

Apple has informed app developers that it will no longer allow apps to use the unique device identifier or UDID after May 1, according to a post on Apple's developer website. Instead, Apple requests ...

As the cookie weakens, brands and agencies are looking for an alternative. Cross-device seems to be the answer – but questions remain. AdExchanger examines the state-of-play around cross-device IDs.

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 ...