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Latest Regulations

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Notice on Public Solicitation of Key Points for Animal Trial Evaluation of Extracorporeal Membrane Oxygenation (ECMO) Consumable Products (Draft for Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230710 Registration & Filing 2023-07-10 2023-07-10
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Review Key Points Medical Device
Notice on Issuing Guiding Principles for Clinical Evaluation, Registration and Review of the Same Variety of Respirators by the Equipment Review Center of the National Medical Products Administration (No. 21, 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第21号 Registration & Filing 2023-07-10 2023-07-05
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Key points for technical evaluation of imaging ultrasound artificial intelligence software (process optimization functions)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第23号-f1 Registration & Filing 2023-07-10 2023-07-10
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Review Key Points Medical Device
Key points for performance evaluation and evaluation of artificial intelligence analysis software for pathological images
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第23号-f2 Registration & Filing 2023-07-10 2023-07-10
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Review Key Points Medical Device
Key points for clinical evaluation and evaluation of artificial intelligence analysis software for pathological images
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第23号-f3 Registration & Filing 2023-07-10 2023-07-10
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Review Key Points Medical Device
Key points for performance evaluation and evaluation of flow cytometry artificial intelligence analysis software for blood diseases
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第23号-f4 Registration & Filing 2023-07-10 2023-07-10
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Review Key Points Medical Device
Guiding Principles for Registration and Review of Blood Melting Devices
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第22号-f1 Registration & Filing 2023-07-07 2023-07-06
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding principles for registration and review of medical respiratory humidifiers
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第22号-f2 Registration & Filing 2023-07-07 2023-07-06
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding principles for registration and review of intestinal hydrotherapy machines
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第22号-f3 Registration & Filing 2023-07-07 2023-07-06
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding principles for registration review of medical molecular sieve oxygen concentrators
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第22号-f4 Registration & Filing 2023-07-07 2023-07-06
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
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