FDA's Unique Device Identification (UDI) System: <--- follow this link to the FDA's free video
"FDA has issued a proposed rule on the establishment of a Unique Device Identification System. This system would require most medical devices distributed in the U.S. to carry a Unique Device Identifier (UDI). This system, comprised of the UDI code, application of the UDI to device labeling and packaging, and a related database, is designed to provide a standardized way to identify devices across all information sources and systems, including electronic health records and devices registries."
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Tuesday, July 17, 2012
FDA's Unique Device Identification (UDI) System - Free FDA Video
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