Unique Device Identification Market Trends Estimates High Demand by 2025
Unique Device Identification intends to assign a unique identification to medical devices sold within the United States. It was signed into law on 27th September 2007 as a part of the Food And Drug Administration Amendments Act of 2007. It requires the label of each device to bear a unique identification unless another location is specified by the F.D.A or an exception is made for that particular device or its grouping.
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