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About CMDRD
Issuance date
2016
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2012
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before2008
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Main Enabling Legislation
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Regulations
2012
Registration
Technical Review Guiding Principles of Registration for Hearing Aid
2012
Registration
Technical Review Guiding Principles of Registration for Medical Vaporizer
2012
Registration
Technical Review Guiding Principles of Registration for Equipment for Preparing Medical Oxygen With Molecular Sieve
2012
Registration
Technical Review Guiding Principles of Registration for Glucometer
2012
Registration
Technical Review Guiding Principles of Registration for Anastomat and Staplers
2012
Registration
Technical Review Guiding Principles of Registration for Power Plant in Surgery
2012
Registration
Technical Review Guiding Principles of Registration for Electrode Products in Surgery
2012
Registration
Technical Review Guiding Principles of Registration for Zirconia All-Ceramic
2012
Registration
Technical Review Guiding Principles of Registration for Coagulation Analyzer
2012
Registration
Technical Review Guiding Principles of Registration for Anaesthesia Machine and Breathing Circuit of Breathing Machine
2012
Registration
Technical Review Guiding Principles of Registration for Ultrasonic Tooth Cleaner
2012
Registration
Technical Review Guiding Principles of Registration for Ultrasonic Doppler Fetal Monitor
2012
Use
Centralized procurement specification for A class large medical equipment(MOH notice No. 96 2012)
2012
Use
Centralized procurement specification for high-value medical consumables(MOH notice No. 86 2012)
2012
Manufacture
Working procedure on unannounced inspection for medical Device Manufacturing Enterprise( SFDA notice No.153 2012)
2012
Administrative-Supervision
The Applicable Rules on Administrative Punishment Discretion for Drug and Medical Device(SFDA notice No.306 2012)
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