The US Food and Drug Administration (FDA) issued an updated final guidance on Tuesday addressing the submission of unique device identifiers (UDIs) to the Global Medical Device Nomenclature Database ...
After discovering a security flaw in the Global Unique Device Identification Database (GUDID), the US Food and Drug Administration (FDA) is giving device makers an additional month to comply with new ...
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 ...
AURORA, ONTARIO--(Marketwired - Apr 8, 2015) - Commport Communications International, Inc. (Commport), a leader in the healthcare solutions marketplace, announced today that it has entered into a ...
The perceived ambiguity of the US Food and Drug Administration’s (FDA) guidance on Unique Device Identifier (UDI) requirements for combination medical devices could lead to inconsistent implementation ...
One day before the U.S. Food and Drug Administration’s (FDA) deadline for medical device companies to submit Class III product data to the FDA’s Production Global UDI Database (GUDID), GHX announced ...
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