MicroPort CardioFlow Medtech Corporation (2160.HK), headquartered in Shanghai, China and founded in 2009, develops, manufactures and commercializes transcatheter and surgical medical devices focused on structural heart diseases including valvular heart conditions and left atrial appendage closure; its core products comprise the VitaFlow series transcatheter aortic valve implantation (TAVI) systems such as VitaFlow Liberty (the world's first electric retrievable TAVI system with EU CE-MDR certification in 2024), VitaFlow Liberty Flex and VitaFlow IV, Alwide balloon catheters including Alwide Plus, procedural accessories like Alpass Introducer Set and Angelguide super stiff guidewire, AnchorMan left atrial appendage closure (LAAC) systems, transcatheter mitral valve (TMV) and tricuspid valve (TTV) products in development, and surgical valves and accessories. The company serves physicians and patients through total solutions for structural heart treatments, with its TAVI products and accessories implanted in over 700 core hospitals across more than 20 countries and regions worldwide, treating over 10,000 patients; it operates primarily in China and internationally. Recent developments include the first commercial implantations of VitaFlow Liberty in Türkiye in 2025 highlighting its retrievability and efficiency, a strategic investment as largest shareholder in partner 4C Medical's US$175 million Series D financing in March 2025 to advance transcatheter mitral valve replacement, and a proposed US$680 million merger with MicroPort Cardiac Rhythm Management (a MicroPort Scientific subsidiary) announced in September 2025 to create a diversified global heart disease platform under Hong Kong Listing Rules Chapter 18A.