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 ステントシステム?
Atlas Peripheral ステントシステム 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 ステントシステム belong to?
Atlas Peripheral ステントシステム 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 ステントシステム?
Atlas Peripheral ステントシステム is used by specialists in Arterial, Peripheral. These physicians rely on INVAMED devices for minimally invasive diagnostic and therapeutic procedures.
Is Atlas Peripheral ステントシステム CE marked and FDA registered?
Yes. Atlas Peripheral ステントシステム 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.
