Weber explains how medical device manufacturers can keep on track with UDI requirements
The FDA’s ruling requiring UDI’s (Unique Device Identifiers) to be assigned to medical devices and their related packaging will undoubtedly bring many benefits. Patient safety will be greatly enhanced through increased protection from counterfeit devices and the ability to identify a device, even when it has been separated from its packaging will make it much easier to link the product to its original manufacturer in the event of problems.