ATLAS is a peripheral self-expanding stent system consisting of a OTW delivery catheter and a pre-mounted stent made of nitinol.ATLAS is intended for use in the treatment of stenotic or occlusive lesions in iliac or femoro-popliteal arteries to establish and maintain patency. ATLAS self-expanding stent is indicated for use in percutaneous intravascular implantation in patients with atherosclerotic, radiation-induced and posttraumatic lesions causing vessel stenosis, of haemodynamic significance and intractable in other forms of treatment.
They are applied in the following cases:
unsatisfactory result of a PTA procedure (residual stenosis),
inner vessel membrane delamination,
vessel wall elasticity disorders and pressure from the outside,
recurrent st
ATLAS stent easily adapts it’s shape to the arterial wall and does not dislocate itself after deployment. The elasticity of the stent as well as flexibility of the delivery system allows the use of ATLAS even in tortuous vessels.
ATLAS self-expanding peripheral stent system is intended to improve luminal diameter in the treatment of symptamotic de novo or restenotic lesions up to 180 mm in length in the native superficial femoral artery and/or proximal popliteal arteries with reference vessel diameters ranging from 3.5 mm – 7.5 mm.
CHARACTERISTICS
Made of nitinol laser cutting
(NiTi) – material with higher biocompatibility level and corrosion resistance than medical AISI 316L stainless steel
Increased conformability within unique open-cell design technology
Excellent radial force
High flexibility of the ATLAS stent effects in excellent adaptation to vessel curvature