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Réduit potentiellement la quantité de produit de contraste injecté grâce à l’injection très sélective sur site et à la précision de la visualisation.

Ensures precise visualization of the targeted area thanks to the strategic positioning of the radiopaque components (a flexible tip and markers at each end of the balloon and on the proximal side of the contrast distribution orifices).

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The injection system consists of three (3) holes located upstream and near the angioplasty balloon for the delivery of the contrast agent when the balloon is either inflated (vessel occluded) or deflated. A radiopaque marker, located on the proximal side of the holes, makes it possible to visualize the injection site.

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Potentially minimizes the time of exposure to radiation thanks to the use of a unique device reducing intravascular navigation times.

Potentially reduces the quantity of contrast product injected thanks to the very selective injection on site and the precision of the visualization.

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NexStep Medical received the FDA 510(k) approval for the All’InCath 035M balloon dilatation catheter used for percutaneous transluminal angioplasty (PTA). “After all these years of …

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The All’InCath 035M is avalable for sale exclusively in USA.  Federal (United States) law restricts this device to sale by or on the order of a physician.

The balloon mounted at the distal end of the catheter has two radiopaque markers indicating the dilation section of the balloon, and allowing its positioning at the lesion site. The balloon is inflated to a known diameter for a specific pressure.

Minimise potentiellement le temps d’exposition aux radiations grâce à l’emploi d’un dispositif unique réduisant les temps de navigation intravasculaire.

The All’InCath 035M is a balloon catheter for percutaneous transluminal angioplasty (PTA) that allows  injection of contrast agents in the same device.

The All’InCath 035M is a balloon catheter for percutaneous transluminal angioplasty (PTA) that allows injection of contrast agents in the same device.

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This device is appropriate for the treatment of arterial lesions located in the peripheral vascular system, including the iliac, femoral, popliteal and renal arteries, as well as obstructive lesions of native or synthetic arteriovenous dialysis fistulas.

The body of the catheter consists of the independent channels allowing the injection of contrast agent and inflation-deflation of the balloon, while holding the guide wire in place.

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– Treat the vessel by inflating a semi-compliant balloon– Provide an angiographic visualization of the vascular system, before and after dilatation, by injection of radiopaque contrast agent using the same catheter, guidewire in place.

NexStep Medical announces the successful treatment of its patients as part of the First-in-Human experience. All patients were treated by it’s All’InCath 035M product and …

NexStep Medical, a French medical device company, was founded in 2014 by three partners:a vascular and endovascular surgeon and two active investors.

On its first active market in the US (510(k) delivered) NexStep proposes to make PTA procedures simpler, faster and smarter, and thus facilitate/optimize angioplasty in its daily practice.

Reduces the usual procedure from 3 to 1 step, thus limiting intravascular manipulation, navigation and mobilization of the guidewire and catheter.

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NexStep is a privately-held medical device company that has been developing products in the area of percutaneous transluminal angioplasty since 2014.

Assure une visualisation précise de la zone ciblée grâce au positionnementstratégique des composantsradio-opaques (un tip souple et des marqueurs à chaque extrémité du ballonnet et du côté proximal des orifices de distribution du contraste).

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Permet de réduire laprocédure habituelle de3 à 1 étape, limitantainsi les manipulationsintravasculaires, les navigations et les mobilisations du fil guide et du cathéter.