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Latest Regulations
1153 Results
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Guiding Principles for Registration and Review of Oxygen Supply Systems in Medical Centers
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第35号-f23
Registration & Filing
2022-09-15
2022-09-09
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guiding Principles for Registration and Review of Pre albumin Testing Reagents
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第35号-f8
Registration & Filing
2022-09-15
2022-09-09
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
IVD
Guiding principles for registration and review of fecal calprotectin testing reagents
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第35号-f22
Registration & Filing
2022-09-15
2022-09-09
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
IVD
Guidelines for registration review of glycated hemoglobin analyzers
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第35号-f9
Registration & Filing
2022-09-15
2022-09-09
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guidelines for registration and review of disposable EEG electrodes
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第35号-f10
Registration & Filing
2022-09-15
2022-09-09
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guidelines for registration and review of shortwave therapy equipment
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第35号-f21
Registration & Filing
2022-09-15
2022-09-09
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guiding principles for registration and review of acidic oxidation potential water generators
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第35号-f20
Registration & Filing
2022-09-15
2022-09-09
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guiding principles for registration and review of medical infrared thermometers
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第35号-f19
Registration & Filing
2022-09-15
2022-09-09
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guiding Principles for Registration and Review of High Sensitivity Cardiac Troponin Testing Reagents
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第35号-f11
Registration & Filing
2022-09-15
2022-09-09
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
IVD
Guiding Principles for Registration Review of Medical Air Compressor Units
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第35号-f12
Registration & Filing
2022-09-15
2022-09-09
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
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