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Qiming's Portfolio Company InventisBio Lists on STAR Market - Vimarsana News

Qiming's Portfolio Company InventisBio Lists on STAR Market

/PRNewswire/ -- Qiming Venture Partners' portfolio company InventisBio (SHSE: 688382), a leading company in innovative drug development, today listed on the...

Global Percutaneous Aortic Valve Implantation Market Anticipated to Garner $13,454.6 Million in Revenue, Rising at a CAGR of 13.9% over the Estimated Timeframe, 2021 to 2028 [160-Pages] - Vimarsana News

Global Percutaneous Aortic Valve Implantation Market Anticipated to Garner $13,454.6 Million in Revenue, Rising at a CAGR of 13.9% over the Estimated Timeframe, 2021 to 2028 [160-Pages]

The global percutaneous aortic valve implantation market is expected to see striking growth by 2028, due to the increasing incidences of cardiovascular disorders among people globally. The North

Global Vascular Disease Devices Market Estimated to Surpass $22,610.3 Million and Grow at 6.9% CAGR in the 2021-2028 Timeframe [175-Pages] - Vimarsana News

Global Vascular Disease Devices Market Estimated to Surpass $22,610.3 Million and Grow at 6.9% CAGR in the 2021-2028 Timeframe [175-Pages]

/PRNewswire/ -- Research Dive has added a new report to its offering titled, "Vascular Disease Devices Market by Product (Stents, Balloons, Catheters,...

Filling gap in market: VenusP-Valve™ approved by China's NMPA - Vimarsana News

Filling gap in market: VenusP-Valve™ approved by China's NMPA

/PRNewswire/ -- On July 11, 2022, VenusP-ValveTM, Venus Medtech's in-house developed innovative transcatheter pulmonic valve replacement (TPVR) system, was...

Filling gap in market: VenusP-Valve approved by China's NMPA - Vimarsana News

Filling gap in market: VenusP-Valve approved by China's NMPA

HANGZHOU, China, July 13, 2022 /PRNewswire/ -- On July 11, 2022, VenusP-ValveTM, Venus Medtech's in-house developed innovative transcatheter pulmonic valve replacement (TPVR) system, was approved by China's National Medical Products Administration (NMPA) for the treatment of severe pulmonary regurgitation (3+) in patients after congenital heart defects (CHD) procedure with native right ventricular outflow tract (RVOT). The approval has made VenusP-ValveTM the first TPVR product to be marketed in China, marking another milestone following its CE MDR approval. As the first self-expanding...