Dolphin 내막하 접근 카테터

What is Dolphin 내막하 접근 카테터?

CTO 또는 심하게 폐쇄된 부분의 내막하 교차 후 실제 내강으로의 재진입을 지원하는 하내막 진입 시스템으로 해부 확장을 최소화합니다.

How does Dolphin 내막하 접근 카테터 work?

최소 침습 중재를 위해 설계된 첨단 의료기기. 신뢰할 수 있는 성능과 최적의 임상 결과 제공.

What are the technical specifications?

Dolphin Sub-Intimal Entry Catheter - 1: Product Name: Dolphin Sub-Intimal Entry Catheter. Intended Use: Facilitates subintimal dissection and re-entry in chronic total occlusion (CTO) or heavily diseased vessels (peripheral or coronary). Catheter Design: Specially shaped distal tip or “re-entry” needle to access the true lumen from a subintimal plane. Material: Pebax/Polyamide shaft with braided reinforcement, possible radiopaque or tungsten tip. Outer Diameter (Fr): ~2.0–3.5 Fr for coronary or ~3.5–4.5 Fr for peripheral usage (adjust as appropriate).

Who manufactures Dolphin 내막하 접근 카테터?

Dolphin 내막하 접근 카테터 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 Dolphin 내막하 접근 카테터 belong to?

Dolphin 내막하 접근 카테터 is part of the Comprehensive Catheter & Guidewire Systems product portfolio by INVAMED. This category includes advanced medical devices designed for interventional procedures performed by healthcare professionals worldwide.

Which medical specialties use Dolphin 내막하 접근 카테터?

Dolphin 내막하 접근 카테터 is used by specialists in Arterial, Peripheral. These physicians rely on INVAMED devices for minimally invasive diagnostic and therapeutic procedures.

Is Dolphin 내막하 접근 카테터 CE marked and FDA registered?

Yes. Dolphin 내막하 접근 카테터 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.