Drug Administration Policy Review (12th) : China's 130th innovative medical device approval and listing!
2021-12-25 16:30
On November 9, the State Food and Drug Administration approved the listing of biological hernia repair patches in accordance with the "Special Review Procedure for Innovative Medical Devices". This is the 130th innovative medical device approved for market since the establishment of the "Innovative Medical Device Special Review Channel" in 2014.
Innovative medical device is a medical device with China's invention patent, which belongs to the domestic initiative in technology and the international leader, and has significant clinical application value. The State Food and Drug Administration shall give priority to review and approval on the premise that the standards are not reduced and the procedures are not reduced.
These innovative medical devices are listed, stimulate innovation vitality, release reform dividends, meet the needs of the people, and effectively protect the lives and health of the people!
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