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Notice of the Equipment Review Center of the National Medical Products Administration on Issuing the Guiding Principles for Clinical Evaluation, Registration and Review of Electronic Endoscopes of the Same Variety (No. 35 of 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第35号 Registration & Filing 2023-08-30 2023-08-29
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 Clinical Evaluation, Registration and Review of Soft Contact Lenses (No. 33 of 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第33号 Registration & Filing 2023-08-23 2023-08-23
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Announcement of the National Medical Products Administration on the Release of Four Informatization Standards, including the Basic Dataset for Medical Device Registration and Filing Management (No. 103 of 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局公告2023年第103号 Registration & Filing 2023-08-18 2023-08-15
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Normative Documents IVD
Notice on Soliciting Opinions on the Guiding Principles for Classification and Definition of Rehabilitation Digital Therapy Software Products (Draft for Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date NIFDC-20230816 Registration & Filing 2023-08-16 2023-08-16
Status Issued By Level of Legal Effect Product Category Draft Center for … Guidelines Medical Device
Notice on Issuing the Guiding Principles for Clinical Evaluation, Registration and Review of Same Variety Dental Implant Systems by the Equipment Review Center of the National Medical Products Administration (No. 32 of 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第32号 Registration & Filing 2023-08-14 2023-08-14
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 Clinical Evaluation, Registration and Review of Hemodialysis Concentrates (No. 29, 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第29号 Registration & Filing 2023-08-04 2023-08-03
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Notice on Issuing Guiding Principles for Clinical Evaluation, Registration and Review of Medical X-ray Diagnostic Equipment (Class III) of the Same Variety by the Equipment Review Center of the National Medical Products Administration (No. 30, 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第30号 Registration & Filing 2023-08-04 2023-08-03
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 Clinical Evaluation and Registration Review of the Same Product of Positron Emission/X-ray Computed Tomography Systems (No. 31, 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第31号 Registration & Filing 2023-08-04 2023-08-03
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Notice on Soliciting Opinions on the Guiding Principles for Classification and Definition of Medical Dressing Products (Draft for Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date NIFDC-20230804 Registration & Filing 2023-08-04 2023-08-04
Status Issued By Level of Legal Effect Product Category Draft Center for … Guidelines Medical Device
Guidelines for Registration Review of Disposable Membrane Oxygenator (CPB) (Draft for Solicitation of Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20230802-1 Registration & Filing 2023-08-02 2023-08-02
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
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