Atlas Peripheral نظام الدعامة

What is Atlas Peripheral نظام الدعامة?

منصة دعامة محيطية قوية مصممة للآفات الفخذية أو الحرقفية أو المأبضية، مما يضمن الدعم الشعاعي المناسب ومعدلات عودة التضيق المنخفضة في تدخل اعتلال الشرايين المحيطية

How does Atlas Peripheral نظام الدعامة work?

منصة دعامة محيطية قوية مصممة للآفات الفخذية أو الحرقفية أو المأبضية، توفر دعمًا شعاعيًا كافيًا.

What are the technical specifications?

Atlas Peripheral Stent System - 1: Product Name: Atlas Peripheral Stent System. Stent Type: Self-Expanding or Balloon-Expandable (confirm actual design), primarily for femoral, popliteal, or iliac usage. Material: Medical-grade Nitinol (if self-expanding) or Cobalt-Chromium/Stainless Steel (if balloon-expandable). Nominal Stent Diameter Range: Typically 4–10 mm (depending on the vessel size—femoral, iliac, etc.). Stent Length Range: 20–200 mm (varies widely for peripheral coverage).

Who manufactures Atlas Peripheral نظام الدعامة?

Atlas Peripheral نظام الدعامة 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 Peripheral نظام الدعامة belong to?

Atlas Peripheral نظام الدعامة 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 Peripheral نظام الدعامة?

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

Is Atlas Peripheral نظام الدعامة CE marked and FDA registered?

Yes. Atlas Peripheral نظام الدعامة 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.