Vitestro Netherlands Europe United Kingdom

07.08.2025 - 18:08:45

Vitestro Achieves CE Marking for Autonomous Blood Drawing Device

by leading European hospitals and clinical laboratories. With the CE marking secured, Vitestro plans a limited market release at these selected hospitals in the next 12 months. Production will be scaled up afterwards, adhering to Vitestro's demonstrated Quality Assurance processes.

Maxine Moor, VP of Commercial Europe "Vitestro has been interacting with clinical labs throughout Europe for the past years. They confirmed the huge need for phlebotomy automation and couldn't wait for this innovation! We are eager to start the implementation of our devices in hospitals and laboratories in the coming 12 months. While we will start within the Netherlands and Denmark, we have huge, broader international ambitions. With the CE mark, we are also meeting regulatory demands for the UK market."

About Vitestro

Founded in 2017, Vitestro is committed to improving the blood draw experience for patients and clinicians. With its revolutionary autonomous blood draw technology and a team of more than 80 highly skilled specialists in medical robotics, artificial intelligence, imaging software, and healthcare commercialization, Vitestro is transforming the blood draw industry globally. Vitestro is based in Utrecht, The Netherlands.

For more information, visit https://vitestro.com.

Regulatory status

The Vitestro blood draw device received a CE mark in July 2024. It does not have FDA approval and is therefore not available for sale in the US.

Photo - https://mma.prnewswire.com/media/2490674/Vitestro.jpg
Logo - https://mma.prnewswire.com/media/2490675/Vitestro_Logo.jpg