Premier strongly supports the implementation of a unique device identifier system and commends the FDA for issuing the proposed rule. UDI is the missing link to protect patient safety. Enabling ...

A coalition in late March sent a letter to FDA commissioner Andrew von Eschenbach supporting a mandatory unique device identification (UDI) system and asking him to set a timeline to implement one.

In a highly anticipated move, the US Food and Drug Administration (FDA) has announced the final release of the Unique Device Identification (UDI) rule, reflecting a number of changes called for by ...

In today’s world – whether at work or at home – I’d be lost without the smartphone that helps me do so much more than just communicate. It knows where I am now and how to get where I want to be next.

Arkose Labs today announced the launch of Arkose Device ID, a device identification solution that combines precise device tracking with session-based risk signals and anti-spoofing technology. Arkose ...

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 ...

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 ...

SAN MATEO, Calif.--(BUSINESS WIRE)--Arkose Labs, the leader in digital risk intelligence, enabling genuine users, mitigating bots and advancing fraud detection modules, today announced the launch of ...