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Guidelines for Registration and Review of Pathogen Specific M-type Immunoglobulin Qualitative Testing Reagents (Revised)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20220623-f5 Registration & Filing 2022-06-23 2022-06-23
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines IVD
Notice on the Release of Clinical Evaluation Recommended Pathways for Related Products in Subcategories 02, 03, 05, 06, 16, 18, and 20 of the Classification Catalogue of Medical Devices (No. 24, 2022)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第24号 Clinical Evaluation 2022-06-16 2022-06-16
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Announcements Medical Device
Notice of the Comprehensive Department of the National Medical Products Administration on Revising and Issuing the Basic Catalogue of Government Information Active Disclosure by the National Medical Products Administration
Regulation No. Product LifeCycle Issued Date Implemented Date 药监综〔2022〕58号 Supervision & Inspection 2022-06-07 2022-06-02
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Normative Documents IVD
Circular of the Center for Organic Examination of the State Food and Drug Administration on Issuing the Guidelines for Registration and Examination of Fundus Image Assisted Diagnosis Software for diabetes Retinopathy (No.23 in 2022)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2022年第23号 Registration & Filing 2022-06-02 2022-06-02
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guidelines for Naming Common Names of Physical Therapy Devices
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2022年第26号-f2 Registration & Filing 2022-06-02 2022-05-26
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Guidelines for Naming Common Names of Active Surgical Instruments
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2022年第26号-f1 Pre-Market 2022-06-02 2022-05-26
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Guidelines for Naming Common Names of Patient Carrying Devices
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2022年第26号-f3 Pre-Market 2022-06-02 2022-05-26
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Guidelines for naming common names of ophthalmic instruments
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2022年第26号-f4 Pre-Market 2022-06-02 2022-05-26
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Guidelines for Naming Common Names of Infusion, Nursing, and Protective Devices
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2022年第26号-f5 Pre-Market 2022-06-02 2022-05-26
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Guidelines for Naming Common Names of Clinical Laboratory Devices
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2022年第26号-f6 Pre-Market 2022-06-02 2022-05-26
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
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