Medical Device Catalogue

China medical device

Some content adjustments in the “Medical Device Classification Catalogue”

In order to further deepen the reform of the medical device review and approval system, based on the actual development and supervision of the medical device industry, and in accordance with the relevant requirements of the “Regulations on the Supervision and Administration of Medical Devices” and the “Dynamic Adjustment Work Procedures for the Classification of …

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Explanation for the revision of “Class I Medical Device Product Catalogue”

In order to implement the requirements of the “Regulations on the Supervision and Administration of Medical Devices” (Decree No. 739 of the State Council) regarding the classified management of medical devices, deepen the reform of the medical device review and approval system, further guide the filing of Class I medical devices, and boost the development …

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