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　　心通医疗-B（02160）发布公告，于2024年12月16日，集团自主研发的第三代经导管主动脉瓣植入术（TAVI）产品VitaFlow Liberty® Flex经导管主动脉瓣可回收可控弯输送系统（‘VitaFlow Liberty® Flex’）获得中国国家药品监督管理局颁发的注册批准。

　　VitaFlow Liberty® Flex为VitaFlow Liberty®输送系统的升级款产品，可与集团已获批的主动脉瓣膜配合使用，其传承了VitaFlow Liberty®输送系统的所有优势，并创新性地增加了3D空间调弯功能。其独有的内管调弯技术可使瓣膜在释放过程中保持同轴，植入更稳定精准，过弓以及跨瓣也更顺畅安全。

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