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 ...

We believe that a CMS requirement to include Unique Device Identifier (UDI) information in billing data is the key to realizing the benefits of a UDI. A Unique Device Identifier (UDI) is an ...

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 ...

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 ...

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.

The Food and Drug Administration last week released an amendment to its proposed rule for a unique device identification system released in July. The amendment shortens the originally proposed ...

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 ...

SAN MATEO, Calif.--(BUSINESS WIRE)--Arkose Labs, the leading proactive fraud deterrence provider, today announced the latest release of Arkose Device ID, a solution within the new Arkose Titan™ ...

The Association for Professionals in Infection Control and Epidemiology, joining with other members of the Advancing Patient Safety Coalition, has sent a letter to the FDA urging for the immediate ...

A few short months from now, manufacturers of Class III medical devices must comply with FDA’s unique device identification (UDI) rule. Part 1 of this series focused on the need for companies to start ...