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Latest Regulations

1153  Results

Notice of the Equipment Review Center of the National Medical Products Administration on Issuing the Guiding Principles for Registration and Review of Ophthalmic Optical Measurement Equipment (No. 13, 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第13号 Registration & Filing 2023-04-28 2023-04-20
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration Review of Tracheal Intubation Products (Revised in 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230425-f1 Registration & Filing 2023-04-25 2023-04-25
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Guidelines for Registration Review of Disposable Surgical gowns (Revised 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230425-f2 Registration & Filing 2023-04-25 2023-04-25
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration Review of Natural Latex Rubber Condom Products (Revised in 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230425-f3 Registration & Filing 2023-04-25 2023-04-25
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Guidelines for Registration Review of Disposable Vacuum Blood Collection Products (Revised in 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230425-f4 Registration & Filing 2023-04-25 2023-04-25
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration Review of Alloy Products Used in Denture Manufacturing (Revised in 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230425-f5 Registration & Filing 2023-04-25 2023-04-25
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration Review of Negative Pressure Drainage Device Products (Revised in 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230425-f6 Registration & Filing 2023-04-25 2023-04-25
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration Review of Medical Mask Products (Revised in 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230425-f7 Registration & Filing 2023-04-25 2023-04-25
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration Review of Gastric Tube Products (Revised in 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230425-f8 Registration & Filing 2023-04-25 2023-04-25
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Guidelines for Registration Review of Surgical Power Equipment (Revised 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230425-f9 Registration & Filing 2023-04-25 2023-04-25
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
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