Global Unique Device Identification Market Is Expected to Grow with a Healthy CAGR During Forecast Period of 2017 to 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. It should be able to identify the device through...
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