Excellent Read Here! FDA Commissioner Scott Gottlieb, M.D., commits to improving the FDA regulated recall process. The current push and ongoing focus of improving this process only further supports our mission of engaging and educating patients to better manage their health!
UDI stands for Unique Device Identifier. Barcodes aren’t just for the department stores anymore. UDI is becoming a standard topic among healthcare providers. Check out this article by Karen Conway, Executive Director, Industry Relations, GHX
Compliance Dates for UDI Requirements The table below outlines key compliance dates in the UDI final rule. Compliance Date Requirement 1 year after publication of the final rule (September 24, 2014) The labels and packages of class III medical devices and devices licensed under the Public Health Service Act (PHS Act) must bear a UDI….