FDA Issues New FAQ on UDIs for Medical Devices
The Food and Drug Administration issued a new FAQ document on its unique device identifier (UDI) system for medical devices. The guidance contains information on effective dates, label contents, and which products are subject to the new requirements. The UDI…
Sign up for a free preview to unlock the rest of this article
If your job depends on informed compliance, you need International Trade Today. Delivered every business day and available any time online, only International Trade Today helps you stay current on the increasingly complex international trade regulatory environment.
system will begin taking effect Sept. 24 for Class III devices.