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Medical Devices
2023.04.21
Notice on Adjusting the Business Scope of the Electronic Declaration Information System for Medical Device Registration (No. 11, 2023)
2023.04.14
Compliance Analysis | Analysis of Major Differences between GB 9706.1-2020 and GB 9706.1-2007 Standards
2023.04.12
Notice on Issuing the Guiding Principles for Registration and Examination of Radio Frequency Beauty Equipment by the Equipment Review Center of the National Drug Administration (No. 8 of 2023)
2023.04.03
National Drug Administration | 2023 National Medical Device Sampling Product Inspection Plan
2023.03.28
Guangdong Drug Administration | Notice on Optimizing the Inspection, Evaluation and Approval of the New Edition of GB 9706 Series Standards
2023.03.17
Notice on Issuing the Implementation Opinions on Optimizing the Review and Approval of Medical Device Registration by the Zhejiang Provincial Drug Administration
2023.03.08
Warning | Release of typical cases of medical beauty violations (the second batch)
2023.03.03
Warning | Release of typical cases of medical beauty violations (the first batch)
2023.02.28
National Bureau | Announcement on the implementation of the third batch of unique identification of medical devices
2023.02.08
Application Guide | Change of manufacturing address for entrusted production of Class II medical devices in Guangdong Province
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