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VenusP-Valve granted IDE approval for clinical trial, unveiling a new chapter for Chinese valve solutions globally

Recently, Venus Medtech (Hangzhou) Inc. ("Venus Medtech"), a leading provider of integrated solutions for transcatheter structural heart valvular therapies in China, announced the Investigational Device Exemption (IDE) full approval for its in-house developed VenusP-Valve from the U.S. Food and Drug Administration (FDA). VenusP-Valve, thus, has become the first China-developed heart valvular system to be approved by the FDA for clinical trial, setting a new milestone in the global footprint of C

Venus Medtech (Hangzhou) Inc : VenusP-Valve granted IDE approval for clinical trial, unveiling a new chapter for Chinese valve solutions globally

Venus Medtech (Hangzhou) Inc : VenusP-Valve granted IDE approval for clinical trial, unveiling a new chapter for Chinese valve solutions globally
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Confirmatory clinical trial of Liwen RF™ ablation system in China concluded

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