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Latest Regulations
1789 Results
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Guiding Principles for Registration Review of Small Needle Knife Products
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第43号-f1
Registration & Filing
2022-11-25
2022-11-10
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guiding Principles for Registration and Examination of acupuncture and moxibustion Needle Products
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第43号-f2
Registration & Filing
2022-11-25
2022-11-10
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guiding principles for registration and review of disposable sterile triangular needle products
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第43号-f3
Registration & Filing
2022-11-25
2022-11-10
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guiding Principles for Registration and Review of Traditional Chinese Medicine Fumigation Treatment Equipment
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第43号-f4
Registration & Filing
2022-11-25
2022-11-10
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guiding principles for registration and review of electric cupping machines
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第43号-f5
Registration & Filing
2022-11-25
2022-11-10
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guiding Principles for Registration Review of Disinfection Cotton Tablets (Sticks, Balls)
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第43号-f6
Registration & Filing
2022-11-25
2022-11-10
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guidelines for registration review of liquid chromatography tandem mass spectrometry systems
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第43号-f7
Registration & Filing
2022-11-25
2022-11-10
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guidelines for Clinical Evaluation, Registration and Review of Gene Sequencers
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第40号-f1
Registration & Filing
2022-11-24
2022-11-24
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
Medical Device
Guiding principles for clinical trials of in vitro diagnostic reagents using samples from human biological sample banks
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第40号-f2
Registration & Filing
2022-11-24
2022-11-24
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
IVD
Guidelines for Clinical Evaluation, Registration and Review of Microsatellite Instability (MSI) Detection Reagents
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE通告2022年第40号-f3
Registration & Filing
2022-11-24
2022-11-24
Status
Issued By
Level of Legal Effect
Product Category
Valid
CMDE/Center for …
Guidelines
IVD
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