Division of Medical Device Safety Supervision

To undertake the supervision and administration of medical device of whole process of production, circulation and use;to track and analyze medical device safety situation and existing problems,and to put forward recommendations on system, mechanism and performance improvement;to formulate the way of supervision and management of specific measures, and organize their implementation;to supervise the low-level administrative departments in performing the administrative duty, in detecting and rectifying illegal and improper acts in time.To organize the implementation of medical device classification system and operational quality specification; to verify the registered authenticity work;to organize and conduct medical device adverse events monitoring and reevaluation; to undertake medical device risk monitoring; to undertake the supervision and administration of medical device sales network; to implement and supervise problem product recalls and disposal work.