Interpretation of the "Classification Catalogue of In Vitro Diagnostic Reagents" and the "Notice on Matters Related to the Implementation of the Classification Catalogue of In Vitro Diagnostic Reagent

Interpretation of the "Announcement on Standardizing the Classification and Definition of Medical Device Products"

Interpretation of the "Announcement on Further Clarifying the Relevant Requirements for Radiofrequency Therapy Instrument Products"

Notice of the General Office of the State Food and Drug Administration on the issuance of the "Appendix to the Medical Device Business Quality Management Standards"

Notice of the General Office of the State Food and Drug Administration on the classification and definition of "degradable expandable hemostatic sponge" products

Notice of the General Office of the National Medical Products Administration on Issuing the 2024 National Medical Device Sampling Inspection Product Inspection Plan

Notice of the State Food and Drug Administration on Issuing the Guiding Principles for On-site Inspection of Medical Device Business Quality Management Specifications

[China Medical Products Administration] Publicly soliciting opinions on the "Medical Device Management Law of the People's Republic of China (Draft for Soliciting Comments)"