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.

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 ...

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 ...