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 Food and Drug Administration has released its final rule requiring most medical devices distributed in the United States to include a unique device identifier, according to a report from Premier ...
Sept 20 (Reuters) - The U.S. Food and Drug Administration issued a new rule on Friday requiring medical device makers to include a unique identifier on their products to track devices, monitor them ...
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