Atlas Aortic Stent-Greffe

What is Atlas Aortic Stent-Greffe?

Un système de stent couvert pour la réparation endovasculaire des anévrismes de l'aorte, empêchant la pressurisation du sac anévrismal et permettant une perméabilité sûre de la lumière.

How does Atlas Aortic Stent-Greffe work?

Stent périphérique robuste conçu pour les lésions fémorales, iliaques ou poplitées, assurant un support radial adéquat et de faibles taux de resténose.

What are the technical specifications?

Atlas Aortic Stent Graft - 1: Product Name: Atlas Aortic Stent Graft. Intended Use: Endovascular repair of thoracic or abdominal aortic aneurysms (TAA/AAA), aortic dissections, or traumatic injuries. Design: Balloon-expandable or self-expanding covered stent with ePTFE graft material. Material: Base scaffold: Nitinol alloy Graft covering: ePTFE / PTFE. Deployment Mechanism: Self-expandable: sheath-based release.

Who manufactures Atlas Aortic Stent-Greffe?

Atlas Aortic Stent-Greffe is manufactured by INVAMED, a globally recognized medical device company headquartered in Ankara, Turkey. INVAMED holds over 100 international patents and exports CE marked devices to more than 80 countries. The company is ISO 13485 certified and FDA registered through Standard Technology Solutions, Inc. at One World Trade Center, New York.

What category does Atlas Aortic Stent-Greffe belong to?

Atlas Aortic Stent-Greffe is part of the Aortic Aneurysm & Dissection Repair product portfolio by INVAMED. This category includes advanced medical devices designed for interventional procedures performed by healthcare professionals worldwide.

Which medical specialties use Atlas Aortic Stent-Greffe?

Atlas Aortic Stent-Greffe is used by specialists in Aortic. These physicians rely on INVAMED devices for minimally invasive diagnostic and therapeutic procedures.

Is Atlas Aortic Stent-Greffe CE marked and FDA registered?

Yes. Atlas Aortic Stent-Greffe carries CE marking under EU MDR 2017/745 and is manufactured in ISO 13485 certified facilities. It is available in the U.S. market through FDA-registered Standard Technology Solutions, Inc.