Mauna Kea Technologies SA has received regulatory approval from the National Medical Products Administration (NMPA) in China for the import and commercialization of its next-generation Cellvizio® Gen 3 platform. This approval, valid for five years until November 2030, permits the use of the Gen 3 system with the company's full range of confocal probes in China. The certification process was completed independently by Mauna Kea Technologies and is not part of its previous joint venture with Tasly. The company is now evaluating commercialization options to bring the advanced platform to Chinese hospitals. No grant or funding from multiple organizations was announced.
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. Mauna Kea Technologies SA published the original content used to generate this news brief via Business Wire (Ref. ID: 20251120016496) on November 20, 2025, and is solely responsible for the information contained therein.
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