Atlas Endovasküler Stent Greft

What is Atlas Endovasküler Stent Greft?

İliak veya femoral segmentlerdeki anevrizmaların veya tıkayıcı lezyonların güvenli bir şekilde tıkanmasını sağlayan, yırtılma veya yeniden tıkanma riskini azaltan kapalı bir periferik stent greft

How does Atlas Endovasküler Stent Greft work?

İliak veya femoral segmentlerdeki anevrizma veya oklüzif lezyonların güvenli oklüzyonunu sağlayan, rüptür veya yeniden tıkanma riskini azaltan kaplı periferik stent greft.

What are the technical specifications?

Atlas Endovascular Stent Graft - 1: Product Name: Atlas Endovascular Stent Graft. Intended Use: Endovascular repair of peripheral aneurysms, arterial occlusive disease, or traumatic injuries (iliac, femoral, popliteal). Graft Material: ePTFE covering over metal scaffold. Scaffold Material: Nitinol (self-expanding depending on design). Deployment Method: Over-the-wire with introducer sheath (commonly 14F–18F, depending on stent diameter).

Who manufactures Atlas Endovasküler Stent Greft?

Atlas Endovasküler Stent Greft 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 Endovasküler Stent Greft belong to?

Atlas Endovasküler Stent Greft is part of the Peripheral Arterial Disease (PAD) product portfolio by INVAMED. This category includes advanced medical devices designed for interventional procedures performed by healthcare professionals worldwide.

Which medical specialties use Atlas Endovasküler Stent Greft?

Atlas Endovasküler Stent Greft is used by specialists in Arterial, Peripheral. These physicians rely on INVAMED devices for minimally invasive diagnostic and therapeutic procedures.

Is Atlas Endovasküler Stent Greft CE marked and FDA registered?

Yes. Atlas Endovasküler Stent Greft 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.