Shanghai, China, 1 September 2021 — On 30th August 2021, MicroPort CardioFlow Medtech Corporation (MicroPort CardioFlow), a subsidiary of MicroPort Scientific Corporation, announced that its transcatheter aortic valve system – the VitaFlow Liberty™ Transcatheter Aortic Valve and Retrievable Delivery System (VitaFlow Liberty™) – has received approval for marketing by China’s National Medical Products Administration (NMPA). As the first motorized retrievable transcatheter aortic valve system approved for marketing, VitaFlow Liberty™ leads as the first motorized retrievable system in the Transcatheter Aortic Valve Implantation (TAVI) market.
The VitaFlow Liberty™ is the next-generation product of the VitaFlow® Transcatheter Aortic Valve and Delivery System (“VitaFlow®”), approved for marketing in 2019. Inheriting the unique design from VitaFlow®, VitaFlow Liberty™ features a hybrid density stent with double-layer skirts and a bovine pericardial leaflet. The retrievable delivery system of VitaFlow Liberty™ comes with an innovative motorized handle, allowing for fast, stable and accurate release and retrieval. In addition, VitaFlow Liberty™ is currently the only delivery system in the Chinese market whose distal end can be bent 360 degrees, providing superior flexibility to help minimize blood vessel damage and reduce the risk of complications. The motorized handle also provides surgeons with better control over the retrieval and repositioning of the valve.
Guoming Chen, Executive Director and President of MicroPort CardioFlow, said, “MicroPort CardioFlow has an extensive product portfolio in the field of transcatheter aortic therapy, providing clinicians with comprehensive transcatheter aortic therapy solutions. The upgrade of VitaFlow Liberty™ lies in the unique features provided by the innovative delivery system, which further improve the surgical experience. We believe that our ability to continuously innovate will ensure the core competitiveness of our future products for the benefit of more patients.”
In addition to VitaFlow Liberty™,MicroPort CardioFlow's first-generation Angelguide® preshaped super stiff guidewire (Angelguide®) was also approved for marketing. The guidewire features high support and smooth transition for guidewire and guide trail, thus reducing blood vessel damage and improving release precision.
Dr. Qiyi Luo, Chief Technology Officer of MicroPort® and Chairman of the Board of Directors o fMicroPort CardioFlow, commentged, “Within years of the launch of VitaFlow®, the product is already used in more than 220 heart centers across China, allowing MicroPort® to become a key player in the Chinese heart valve market. We are now more confident and motivated to accelerate our development of medical devices for valvular heart disease. With the market launch of the VitaFlow Liberty™ System, MicroPort CardioFlow will be able to better meet clinical needs, and provide better clinical outcomes.”