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Latest Regulations

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Guiding Principles for Registration and Review of Intravascular Recovery Devices
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第9号-f2 Registration & Filing 2023-04-13 2023-04-06
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guidelines for registration and review of hernia repair patches
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第9号-f3 Registration & Filing 2023-04-13 2023-04-13
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guidelines for Writing Instructions for Hard Corneal Contact Lenses (Revised in 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第9号-f6 Registration & Filing 2023-04-13 2023-04-13
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration Review of Contact Lens Care Products (Revised in 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第9号-f4 Registration & Filing 2023-04-13 2023-04-13
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guidelines for Writing Instructions for Soft Hydrophilic Contact Lenses (Revised in 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第9号-f5 Registration & Filing 2023-04-13 2023-04-13
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 Radiofrequency Beauty Equipment (No. 8, 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第8号 Registration & Filing 2023-04-12 2023-04-10
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration and Review of Quantitative Shear Wave Ultrasound Liver Measurement Instruments (No. 7, 2023) issued by the Equipment Review Center of the National Medical Products Administration
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230411 Registration & Filing 2023-04-11 2023-04-10
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 Review of Ultrasound Soft Tissue Surgical Equipment (Revised in 2023) (No. 4 of 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第4号 Registration & Filing 2023-03-31 2023-03-17
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 Intraperitoneal Endoscopic Surgery Systems Part 1: Surgical Instruments (No. 5, 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第5号 Registration & Filing 2023-03-23 2023-03-22
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding Principles for Registration Review of Dental Adhesive Products (No. 3 of 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第3号-f1 Registration & Filing 2023-03-09 2023-03-07
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
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