• Classification
  • Regulations
  • Standards
  • Support
  • About CMDRD

Issuance date

  • 2016
  • 2015
  • 2014
  • 2013
  • 2012
  • 2011
  • 2010
  • 2009
  • before2008

RegDoc.

  • Main Enabling Legislation
  • Registration
  • Classification
  • Manufacture
  • Distribution
  • Use
  • Import/Export
  • QMS
  • Clinical Verification
  • Labeling/Packaging
  • Adverse Event Monitoring
  • Reevaluation/Recall
  • Administrative Supervision
  • Medical Device Inventory
  • Regulations
  • 2011 Registration
  • Application Materials Guiding Principles of Registration for Antibody Detection Reagent of Influenza virus
  • 2011 Registration
  • Application Materials Guiding Principles of Registration for Nucleic Acid Detection Reagent of Influenza virus
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Injection Pump
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Disposable Vacuum Blood Collection Tube
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Disposable Operating Coat
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Dental Multipurpose Therapy Unit
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Latex Rubber Condom
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Infrared Mammary Gland Examining Equipments
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Customized Denture
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Electronic Sphygmomanometer (Oscillography)
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Motor-Driven Hospital Bed
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Magnetic Therapeutic Product
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Ultrasonic Physiotherapy Equipment
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for 3A semi conductor laser therapeutic machine
  • 2011 Labeling-Packaging
  • Guiding Principles of Instruction of Rigid Gas Permeable Contact Lenses
  • 2011 Registration
  • Application Materials Guiding Principles of Registration for Quantitative Detection of Tumor Markers
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Disposable Infusion and Injection
  • 2011 Registration
  • Technical Review Guiding Principles of Registration for Dental Implant (System)
  • 2011 Registration
  • Application Materials Guiding Principles of Shelf-Life for Passive Implantable Medical Devices
  • 2011 Registration
  • Technical Review Guiding Principles of Virus Inactivating Technology for Allogenic Implantable Medical Device
  • 1
  • 2
  • 2 Page(s)
Copyright © 2015 CIRS Hangzhou Co,.Ltd.