To effectively respond to particularly significant unexpected public health emergencies and other serious threats to public health and to provide guidance on the emergency use of medical devices, the National Medical Products Administration (NMPA) has, in conjunction with the National Health Commission and the National Disease Control and Prevention Administration, formulated the "Management Regulations for the Emergency Use of Medical Devices (Trial)." This regulation is hereby released and will be implemented from the date of its publication in accordance with the "Medical Device Supervision and Management Regulations" (State Council Decree No. 739).

 

 

Reference:

Announcement of the National Medical Products Administration, National Health Commission, and National Disease Control and Prevention Administration on the Issuance of Regulations on the Management of Emergency Use of Medical Devices (Trial)