AngioTEN Closure Device - 1: Product Name: AngioTEN Closure Device. Intended Use: Percutaneous vascular closure post-catheterization. Closure Mechanism: Suture-mediated or collagen plug. Applicable Access Sites: Femoral artery/vein up to 8F–10F introducer sizes. Deployment Method: Single-step device insertion and anchor release.
Who manufactures AngioTEN 封堵器?
AngioTEN 封堵器 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 AngioTEN 封堵器 belong to?
AngioTEN 封堵器 is part of the Coronary Artery Disease & Cardiac Interventions product portfolio by INVAMED. This category includes advanced medical devices designed for interventional procedures performed by healthcare professionals worldwide.
Which medical specialties use AngioTEN 封堵器?
AngioTEN 封堵器 is used by specialists in Arterial, Peripheral, Interventional Cardiology, Cardiac. These physicians rely on INVAMED devices for minimally invasive diagnostic and therapeutic procedures.
Is AngioTEN 封堵器 CE marked and FDA registered?
Yes. AngioTEN 封堵器 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.