MED-Guidelines for Technical Review of Registration for Magnetic Resonance Imaging Systems

MED-Brief Introduction to the System for Submitting Periodic Risk Assessment Reports + Notice on the Launch of the Regular Risk Assessment Report Module of the National Medical Device Adverse Event Monitoring Information System

MED-(English Version) Announcement of National Medical Products Administration on Issuing the Guidelines for Technical Review of Clinical Evaluation of Medical Magnetic Resonance Imaging System of the Same Variety(Revision 2020) (No. 12 in 2021)

MED-(Chinese version) Notice by CFDA on the Publication of the List of Category III Medical Devices Exempt from Clinical Trials