Stena 다층 유량 조절기 for Aortic Applications

What is Stena 다층 유량 조절기 for Aortic Applications?

대동맥류를 위한 다층 흐름 전환 스텐트로서 안정적인 층류 흐름을 촉진하여 측분지 관류를 유지하면서 동맥류 낭 압력을 감소시킵니다.

How does Stena 다층 유량 조절기 for Aortic Applications work?

대퇴동맥, 장골동맥 또는 슬와동맥 병변을 위한 견고한 말초 스텐트 플랫폼. 적절한 방사형 지지력 제공.

What are the technical specifications?

Stena Multi-Layer Flow Modulator (Aortic Applications) - 1: Product Name: Stena Multi-Layer Flow Modulator (Aortic). Intended Use: Endovascular management of thoracic or abdominal aortic aneurysms (TAA/AAA), certain aortic dissection flow diversion. Design: Multi-layer braided self-expanding stent, engineered to modulate arterial flow while preserving branch perfusion. Material: Medical-grade Nitinol (Nickel-Titanium), layered mesh construction. Deployment Mechanism: Self-expanding via sheath retraction, no balloon inflation needed.

Who manufactures Stena 다층 유량 조절기 for Aortic Applications?

Stena 다층 유량 조절기 for Aortic Applications 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 Stena 다층 유량 조절기 for Aortic Applications belong to?

Stena 다층 유량 조절기 for Aortic Applications is part of the Aortic Aneurysm & Dissection Repair product portfolio by INVAMED. This category includes advanced medical devices designed for interventional procedures performed by healthcare professionals worldwide.

Which medical specialties use Stena 다층 유량 조절기 for Aortic Applications?

Stena 다층 유량 조절기 for Aortic Applications is used by specialists in Aortic. These physicians rely on INVAMED devices for minimally invasive diagnostic and therapeutic procedures.

Is Stena 다층 유량 조절기 for Aortic Applications CE marked and FDA registered?

Yes. Stena 다층 유량 조절기 for Aortic Applications 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.