Venus MedTech (Hangzhou) Inc. has announced the formal submission of all application materials for CE MDR marking to a European Notified Body for its Cardiovalve transcatheter tricuspid valve replacement system. This voluntary announcement updates shareholders and potential investors on the latest business development and product research progress. The Cardiovalve System is designed to treat both mitral and tricuspid regurgitation, featuring a transfemoral approach and a large annulus design suitable for approximately 95% of patients. The company cautioned that there is no guarantee of eventual marketing approval for the product. No grant or funding from multiple organizations was mentioned.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Venus MedTech HangZhou Inc. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20251224-11966071), on December 23, 2025, and is solely responsible for the information contained therein.
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