대퇴골, 장골 또는 슬와 병변을 위해 설계된 견고한 주변 스텐트 플랫폼으로 PAD 개입 시 적절한 요골 지지와 낮은 재협착률을 보장합니다.
How does Atlas Peripheral 스텐트 시스템 work?
대퇴동맥, 장골동맥 또는 슬와동맥 병변을 위한 견고한 말초 스텐트 플랫폼. 적절한 방사형 지지력 제공.
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 스텐트 시스템?
Atlas Peripheral 스텐트 시스템 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 스텐트 시스템 belong to?
Atlas Peripheral 스텐트 시스템 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 스텐트 시스템?
Atlas Peripheral 스텐트 시스템 is used by specialists in Arterial, Peripheral. These physicians rely on INVAMED devices for minimally invasive diagnostic and therapeutic procedures.
Is Atlas Peripheral 스텐트 시스템 CE marked and FDA registered?
Yes. Atlas Peripheral 스텐트 시스템 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.
대퇴골, 장골 또는 슬와 병변을 위해 설계된 견고한 주변 스텐트 플랫폼으로 PAD 개입 시 적절한 요골 지지와 낮은 재협착률을 보장합니다.
