Atlas Peripheral Stent System

What is Atlas Peripheral Stent System?

A robust peripheral stent platform designed for femoral, iliac, or popliteal lesions, ensuring adequate radial support and low restenosis rates in PAD intervent

How does Atlas Peripheral Stent System work?

A robust peripheral stent platform designed for femoral, iliac, or popliteal lesions, ensuring adequate radial support and low restenosis rates in PAD interventions.

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 Stent System?

Atlas Peripheral Stent System 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 Stent System belong to?

Atlas Peripheral Stent System 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 Stent System?

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

Is Atlas Peripheral Stent System CE marked and FDA registered?

Yes. Atlas Peripheral Stent System 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.