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Latest Regulations

1061  Results

Guiding Principles for Registration Review of Medical Air Compressor Units
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第35号-f12 Registration & Filing 2022-09-15 2022-09-09
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guidelines for registration and review of disposable surgical caps
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第35号-f18 Registration & Filing 2022-09-15 2022-09-09
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding principles for registration and review of medical sterile ultrasound coupling agents
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第35号-f13 Registration & Filing 2022-09-15 2022-09-09
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration Review of Medical Protective Clothing Products
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第35号-f14 Registration & Filing 2022-09-15 2022-09-09
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding principles for registration and review of heart type fatty acid binding protein assay reagents
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第35号-f16 Registration & Filing 2022-09-15 2022-09-09
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration Review of Cyclosporine and Tacrolimus Testing Reagents
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第35号-f15 Registration & Filing 2022-09-15 2022-09-09
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines IVD
Guiding principles for registration and review of non chronic wound patches
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第35号-f17 Registration & Filing 2022-09-15 2022-09-09
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Notice of the Equipment Review Center of the National Medical Products Administration on Issuing the Guiding Principles for Registration and Review of Quantitative Testing in Vitro Diagnostic Reagent Analysis Performance Evaluation (No. 32 of 2022)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第32号 Registration & Filing 2022-08-26 2022-08-26
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines IVD
Circular of the Center for Organic Examination of the State Food and Drug Administration on Issuing the Key Points for Technical Review of the novel coronavirus Nucleic Acid Sampling Equipment in the Oropharynx (Trial) (No. 33 in 2022)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第33号 Registration & Filing 2022-08-26 2022-08-26
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Review Key Points Medical Device
Notice on Public Solicitation of Opinions on the Guiding Principles for Registration and Review of Remote Monitoring Systems (Draft for Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20220822 Registration & Filing 2022-08-22 2022-08-22
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
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