The State Drug Administration, the National Health and Health Commission, and the National Health Insurance Bureau "on the second batch of the implementation of the unique marking of medical devices notice" states that from June 1, 2022, the production of medical devices (Class III medical devices) should have a unique marking of medical devices.
The third class medical devices produced by medical device manufacturers need to be fully covered by the unique marking of medical devices, and require the marking management of this class of medical devices in the production, operation, and use of the links to achieve full traceability.