2. UDI exists in the entire life cycle of medical device production, circulation, and use, and is the basis for accurate identification of medical device information. Its implementation will reduce the obstacles of insufficient identification of medical devices in the market, quickly and accurately identify key information about the safety and effectiveness of devices, and reduce the resulting medical errors.
3. At the same time, the UDI system can improve the quality of medical device adverse event reporting, identify product problems more effectively, and recall problematic devices more quickly to ensure patient safety.