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 ...

The US Food and Drug Administration (FDA) has finalized a guidance document intended to outline the appropriate use of its Global Unique Device Identification Database (GUDID), an integral part of its ...

The Food and Drug Administration has released guidance to manufacturers for submissions to its Global Unique Device Identification Database (GUDID). It deals with how to set up accounts and begin ...

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 ...

The Food and Drug Administration recently released finalized guidance for medical device labelers for submitting data to the Global Unique Device Identification Database. A draft version of the ...

FDA is building a medical device reference catalog through its Global Unique Device Identification Database, which it is opening to the public. Nancy Crotti FDA has opened the Global Unique Device ...

Hospital groups complain about the delay in rule-setting, the long implementation timetable for the unique device identifier rule, and a new database. Manufacturers of the most potentially dangerous ...

The database will allow consumers, healthcare providers, and product manufacturers to access information tracked on medical devices, with the end goal of improving patient safety, improving device ...

Members of the medical device industry are responding to the U.S. Food and Drug Administration‘s (FDA) proposed rules, published today, regarding the agency’s much anticipated Unique Device ...