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US FDA Proposes More Stringent UDI Requirements For Some Device 'Convenience Kits'

This article was originally published in SRA

Executive Summary

The US Food and Drug Administration is inviting stakeholder feedback on its proposal to impose more stringent unique device identification (UDI) labeling requirements to make it easier to track individual components of "convenience kits" if they are reused or used in different procedures1,2.

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