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Latest Regulations
1882 Results
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Guidelines for registration and review of medical diagnostic X-ray equipment containing pediatric applications
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
国药监局通告2021年第104号-f3
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 ultrasound transcranial Doppler blood flow analyzers
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
国药监局通告2021年第104号-f4
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 anti Mullerian hormone assay reagents
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
国药监局通告2021年第104号-f14
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 Review of Hydrogen Peroxide Sterilizers
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
国药监局通告2021年第104号-f5
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 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
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