Manufacturers Face FDA Rule on Unique Device Identifiers

摘要

If they're not already doing it, manufacturers should prepare for the implementation of unique device identifiers (UDI) on their products to abide by an upcoming regulation from the U.S. Food and Drug Administration (FDA), according to an agency expert.rnFDA wants to have the proposed rule-intended to promote better identification of medical devices-published by the end of the year, and there are some tasks that manufacturers can take care of now to get ready.