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Notice of the National Medical Products Administration on Issuing Three Registration Technical Review Guidelines for Disposable Sterile Urinary Catheters and Other Items
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2018年第80号-f2 Registration & Filing 2018-09-04 2018-08-28
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing Three Guiding Principles for Registration Technical Review of Customized Dentures and Other Items
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2018年第80号-f3 Registration & Filing 2018-09-04 2018-08-28
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice on Publicly Soliciting Opinions on Two Guiding Principles, including the "Guidelines for Technical Review of Dental Digital Impressions Registration"
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20180726-1-f2 Registration & Filing 2018-07-26 2018-07-26
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing Three Registration Technical Review Guidelines for Sleep Respiratory Monitoring Products and Other Products
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2018年第30号-f3 Registration & Filing 2018-05-31 2018-05-25
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Three Registration Technologies, including Endoscopic Cleaning and Disinfection Machines
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2018年第30号-f2 Registration & Filing 2018-05-31 2018-05-25
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Three Registration Techniques, including Anesthesiolaryngoscopy
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2018年第30号-f1 Registration & Filing 2018-05-31 2018-05-25
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing Guiding Principles for the Review of Four Registration Technologies, including Pulse Wave Velocity and Ankle Arm Index Testing Products
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2018年第25号-f4 Registration & Filing 2018-05-18 2018-05-10
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Four Registration Technologies, including Surgical Microscopes
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2018年第25号-f1 Registration & Filing 2018-05-18 2018-05-10
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Four Registration Technologies, including Medical Clean Workbenches
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2018年第25号-f2 Registration & Filing 2018-05-18 2018-05-10
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Four Registration Technologies, including Tonometers
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2018年第25号-f3 Registration & Filing 2018-05-18 2018-05-10
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
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