Cirtec Services GmbH was founded in 2020 as a subsidiary of Cirtec Medial Inc. It is located in Birkenfeld, Germany at the foot of the Black Forest, and is close to Stuttgart, one of the leading economic areas of the world.
Cirtec Medical’s Corporate Headquarters are based in Brooklyn Park, Minnesota, USA. Brian Highley, CEO of Cirtec Medical Inc. is pleased to invest in our location in Germany and further expand our business in Europe by providing custom solutions to our customers worldwide. We will be able to provide a much broader portfolio out of Germany to all our customers and different industries. Risk mitigation also plays a huge role in having redundant capabilities in two continents.
Cirtec Services GmbH will expand the capabilities we have in Cirtec USA and at Vascotube in Germany. In addition to our current capabilities, we have established new process lines for seamless tubing manufacturing focusing on AAA and other venous indications. In addition to tubing, we are able to provide Laser cutting services (Fiber-laser and Femto-laser) for stents and heart valves as well as all required downstream processes like heat treatment and electro-polishing services.
With this new investment in Germany, we now have the ability to support your R&D projects from tube manufacturing, to laser cutting and electropolishing, to all required lab services and test methods allowing solid and validated processing and testing capabilities.
We are focused on being your R&D partner for rapid prototype parts and R&D project work. We are the right partner for projects including self-expanding stents, heart valves as well as self-expanding or balloon-expandable devices.
While we usually work with Nitinol, we also have experience working with CoCr, MP35, L605 material.
Our team has more than 120 years of tube drawing and Medical Device experience. We are here to support your busines through the entire manufacturing process. Our processes conform to ISO 13485 standards and we understand your challenges related to FDA registered products and the Quality and Regulatory aspects of your business.
After completing the R&D phase of your project, we are able to perform full manufacturing at our other facilities.
DIN EN ISO 13485
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