Federal Agency Supports UDI Inclusion in Medicare Claims Forms
The lack of medical device-specific information in Medicare claims forms wastes time and money when it comes to replacing recalled or defective devices, according to an early alert issued by the Office of the Inspector General for the US Department of Health & Human Services. The unique device identifier system, established by FDA and currently being phased in, calls for medical devices to display a barcode label of sorts that includes product information.
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