|Department of Medical Device Supervision
To track and analyze medical device safety situation and existing problems, and to put forward recommendations on system, mechanism and performance improvement; to supervise the low-level administrative departments in conducting administrative licensing by law, in performing the administrative duty, in detecting and rectifying illegal and improper acts in time; to organize and conduct medical device adverse events monitoring and reevaluation.
There are four divisions:
4 Division of General Affairs
4 Division of Manufacturing Supervision
4 Division of Distribution Supervision
4 Division of Monitoring and Re-evaluation