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 Endovascular 覆膜支架?
Atlas Endovascular 覆膜支架 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 Endovascular 覆膜支架 belong to?
Atlas Endovascular 覆膜支架 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 Endovascular 覆膜支架?
Atlas Endovascular 覆膜支架 is used by specialists in Arterial, Peripheral. These physicians rely on INVAMED devices for minimally invasive diagnostic and therapeutic procedures.
Is Atlas Endovascular 覆膜支架 CE marked and FDA registered?
Yes. Atlas Endovascular 覆膜支架 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.
