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About CMDRD
Issuance date
2016
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before2008
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Main Enabling Legislation
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Medical Device Inventory
Regulations
Before 2008
Registration
Technical Review Guiding Principles of Registration for Hard-pipe Endoscope of Class II
Before 2008
Registration
Technical Review Guiding Principles of Registration for Fiber Endoscope of Class II
Before 2008
Registration
The guide for medical device biological assessment and review(SFDA notice No.345 2007)
Before 2008
Import-Export
The Management Measures for Imported Medical Device Inspection and Supervision(AQSIQ Order No.95 2007)
Before 2008
Adverse-Event-Monitoring
The Requirements for Medical Device Adverse Event Monitoring and Re-evaluation (SFDA notice No.766 2008)
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