FDA releases final rule on unique device identifiers
FDA releases final rule on unique device identifiers — Rule emphasizes improving quality of information for adverse event reporting
They say that good things come to those who wait, and professionals in just about every sector of healthcare have been patiently waiting-nearly six years, in fact-for the FDA’s final ruling on unique device identifiers (UDI) for medical devices, with the expectation that the new system will provide needed changes regarding medical device safety.