Mantis PRO Rotational Thrombectomy & Ultra Aspiration

What is Mantis PRO Rotational Thrombectomy & Ultra Aspiration?

機械的な血栓の断片化に加え、深部静脈または動脈閉塞における強力な吸引機能を備えた回転システム。

How does Mantis PRO Rotational Thrombectomy & Ultra Aspiration work?

低侵襲インターベンションのために設計された先進医療機器。信頼性の高い性能と最適な臨床結果を提供。

What are the key features of Mantis PRO Rotational Thrombectomy & Ultra Aspiration?

• Mantis 血栓除去システムは、血栓除去術の分野における飛躍的な進歩を表しており、高度な薬理学的機能と組み合わせた革新的な回転リーフチップ設計を導入しています。
• この最先端のシステムは、血栓の除去において比類のない精度、効率、および安全性を提供するように設計されています。

What are the technical specifications?

カマキリの葉先端回転血栓除去術と超吸引 - 1: 製品名: カマキリの葉の先端回転血栓除去術と超吸引. 使用目的: 末梢系および/または静脈系における血栓または塞栓の機械的破壊および吸引. カテーテルの設計: 葉の形の先端を備えた回転ワイヤー、血栓除去用の吸引ルーメンを内蔵. 材料: ステンレススチールまたはニチノールドライブシャフト、柔軟なポリマー製アウターシース. 回転速度範囲: ~40k ～ 80k rpm (最終仕様を確認してください).

Who manufactures Mantis PRO Rotational Thrombectomy & Ultra Aspiration?

Mantis PRO Rotational Thrombectomy & Ultra Aspiration 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 Mantis PRO Rotational Thrombectomy & Ultra Aspiration belong to?

Mantis PRO Rotational Thrombectomy & Ultra Aspiration is part of the Deep Vein Thrombosis (DVT) product portfolio by INVAMED. This category includes advanced medical devices designed for interventional procedures performed by healthcare professionals worldwide.

Which medical specialties use Mantis PRO Rotational Thrombectomy & Ultra Aspiration?

Mantis PRO Rotational Thrombectomy & Ultra Aspiration is used by specialists in Venous. These physicians rely on INVAMED devices for minimally invasive diagnostic and therapeutic procedures.

Is Mantis PRO Rotational Thrombectomy & Ultra Aspiration CE marked and FDA registered?

Yes. Mantis PRO Rotational Thrombectomy & Ultra Aspiration 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.