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Latest Regulations

1153  Results

Guiding Principles for Registration Review of Neonatal Blue Light Therapy Equipment
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2021年第104号-f6 Registration & Filing 2021-12-28 2021-12-17
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Guiding Principles for Registration Review of Folic Acid Testing Reagents
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2021年第104号-f13 Registration & Filing 2021-12-28 2021-12-17
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines IVD
Guidelines for Registration Review of Retinol Binding Protein Assay Kit (Immunoturbidimetric Method)
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2021年第104号-f12 Registration & Filing 2021-12-28 2021-12-17
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines IVD
Guiding Principles for Registration and Review of Pepsinogen I/II Detection Reagents
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2021年第104号-f10 Registration & Filing 2021-12-28 2021-12-17
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines IVD
Guidelines for Product Registration Review of Prothrombin Time/Activated Partial Thrombin Time/Thrombin Time/Fibrinogen Detection Reagents
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2021年第104号-f11 Registration & Filing 2021-12-28 2021-12-17
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines IVD
Guiding principles for registration and review of root canal preparation machines
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2021年第104号-f7 Registration & Filing 2021-12-28 2021-12-17
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Guiding principles for registration and review of blood cell analyzers
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2021年第104号-f8 Registration & Filing 2021-12-28 2021-12-17
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Guidelines for registration and review of gait training equipment
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2021年第104号-f9 Registration & Filing 2021-12-28 2021-12-17
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Guiding Principles for Registration Review of Extracorporeal Membrane Oxygenation (ECMO) Circulation Package
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2021年第103号-f1 Registration & Filing 2021-12-20 2021-12-14
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Guidelines for registration and review of disposable abdominal puncture devices
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2021年第103号-f2 Registration & Filing 2021-12-20 2021-12-14
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
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