The Food and Drug Administration (FDA) has announced a final rule for the unique device identification system (UDI)

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#IVTEAM #Intravenous products: Infection Control Today report “The Food and Drug Administration (FDA) has announced a final rule for the unique device identification system (UDI) that, once implemented, will provide a consistent way to identify medical devices.

The UDI system has the potential to improve the quality of information in medical device adverse events reports, which will help the FDA identify product problems more quickly, better target recalls, and improve patient safety. The FDA has worked closely with industry, the clinical community and patient and consumer groups in the development of this rule.”

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