Vascular Therapies

Pioneering Technology

We are proud of our track record and our continued innovation in the implementation of next-generation medical technologies, that make a difference to patients’ lives around the world. Together with our partner manufacturers, we offer interventional devices and solutions for patients living with Coronary Artery Disease.

Complementing our established cardiovascular portfolio, our endovascular devices offer more solutions for patients whose lives we touch.

Cardiovascular Products

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In the cardiovascular arena, we are focused on the development, manufacture, and commercialization of drug-eluting stents, drug-coated stents, and bare metal stents as well as angioplasty catheters for the treatment of coronary artery disease.

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BioFreedom

BioFreedom is a polymer- and carrier-free Drug Coated Stent with BA9™ (DCS). The combination of a selectively micro-structured abluminal surface (SMS) and Biolimus A9™ make BioFreedom a unique stent. At least 20% of PCI patients are High Bleeding Risk (HBR) requiring an individualized approach, BioFreedom provides a more appropriate treatment strategy.

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Biomatrix Alpha

BioMatrix Alpha™ presents the best in class stent platform design with unique pro-healing coating from the pioneer in abluminal biodegradable technology. It combines the proven safety of a DES with an abluminal biodegradable polymer, the proven efficacy of BA9™ and an innovative cobalt-chromium stent platform design.

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Biomatrix Neoflex

When it comes to biodegradable polymer technology, Biosensors has developed the highest level of expertise and delivered the best results in terms of safety and efficacy. BioMatrix NeoFlex is a stainless steel DES with an enhanced stent delivery system brings exceptional performance in complex lesions and challenging anatomies. It has the highest lipophilicity of the common limus drugs and minimizes systemic exposure and reduces the drug circulating in the bloodstream.

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BioStream

The use of the BioStream™ PTCA catheter is indicated for patients with discrete lesions of the coronary arteries with a reference vessel diameter of 1.50 to 4.00 mm for the purpose of improving the coronary lumen diameter.
The BioStream™ PTCA catheter is indicated for the dilatation of the affected segments of a coronary artery or a coronary bypass in order to enhance myocardial perfusion. The BioStream paclitaxel eluting coronary balloon catheter is especially indicated for the treatment of coronary in-stent restenosis.

Endovascular Products

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BioPath14

BioPath™ 014 is a drug-eluting balloon dilatation catheter designed for percutaneous transluminal angioplasty (PTA) and has been optimized for the treatment of patients with peripheral arterial disease. BioPath™ 014 is intended for infrapopliteal interventions below the knee. This paclitaxel-eluting balloon feature a proprietary shellac coating technology which consistently delivers paclitaxel, an anti-restenotic drug during very brief inflation times, while also minimizing washout of the drug during delivery and placement of the drug-eluting balloon.

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BioPath35

BioPath™ 035 is a drug-eluting balloon dilatation catheter designed for percutaneous transluminal angioplasty (PTA) and has been optimized for the treatment of patients with peripheral arterial disease. BioPath™ 035 is intended for peripheral interventions above the knee. This paclitaxel-eleluting balloon feature a proprietary shellac coating technology which consistently delivers paclitaxel, an anti-restenotic drug during very brief inflation times, while also minimizing washout of the drug during delivery and placement of the drug-eluting balloon.

Peripheral interventions

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Believing in better, simpler treatments

There are common themes across every medical specialty we support: patients want to get better and physicians want simpler, more effective options. That is why we work hard to introduce our minimally invasive medical devices and improve the way they are delivered to hospitals and physicians. We have the freedom to work through a problem for as long as it takes to find the simplest solution.

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Zilver® PTX® Drug-Eluting Peripheral Stents

Indicated for improving luminal diameter for the treatment of de novo or restenotic symptomatic lesions in native vascular disease of the above-the-knee femoropopliteal arteries having reference vessel diameter from 4 mm to 7 mm and total lesion lengths up to 300 mm per patient.

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Zilver Flex® 35 Vascular Stents

The Zilver® vascular stent has been clinically proven to maintain 90% patency in the iliacs at two years. The clinical results prove that patients experienced significant and sustained improvement in ABI and walking scores at two years. Flexibility and radial force are balanced to achieve excellent conformability and fracture resistance.

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Formula® 535 Vascular Balloon-Expandable Stent

Formula® stents are engineered for precision: precise placement, precise treatment, and precise conformability. Balloon lengths are customized to reduce the amount of healthy tissue that is dilatated during treatment.  Formula stents do not shorten, and their ends align with the balloon markers and the stents have additional crowns, which give the stents a more circular shape and improve the scaffolding.
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Flexor® Check-Flo® and Performer® Check-Flo®

The product is used to introduce balloon, closed- and nontapered-end catheters, or other diagnostic and interventional devices.

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Flexor® Ansel

Also used as a device to introduce balloon, closed- and nontapered-end catheters, or other diagnostic and interventional devices.

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Micropuncture®

A product that serves the following clinical divisions: Aortic Intervention, Peripheral Intervention, Critical Care. There are now four Micropucture Access Sets with trays. All of these sets include a palladium-tipped, nitinol wire guide and an EchoTip® needle. The sets, in 4 Fr and 5 Fr and standard and stiffened cannulas, also feature Transitionless-Tip™ coaxial catheter pair technology.

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Amplatz Stiff/Extra-Stiff/Ultra-Stiff Wire Guides

Used for access and catheterization procedures. Provided with an increased inner diameter of wire guide coil provides support with a variety of mandril stiffness options, gradual transition to flexible distal tip helps facilitate atraumatic negotiation of tortuous anatomy and PTFE-coated stainless steel.

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Roadrunner® UniGlide® Hydrophilic Wire Guide

Used to facilitate the placement of devices during diagnostic and interventional procedures. The device enhanced coating provides long-lasting lubricity. Also offers optimum shaft stiffness and tip flexibility, combined with 1:1 torque response and advanced radiopaque materials.

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Roadrunner® PC Hydrophilic Nimble & The Firm Wire Guide

Used for complex diagnostic and interventional procedures where extra support is needed for catheter exchange or manipulation. Equipped with heavy-duty nitinol mandril that provides support and 1:1 torque response to distal platinum spring coil.

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More than 300 different coils

Cook Medical offers the broadest range of embolization products on the market. Embolization products include pushable and detachable coils, PVA particles, microcatheters, and microwire guides. Most coils have a general indication and can be used for both arterial and venous embolization and come in a variety of shapes: Spiral, Tornado (Helical), Straight, Single Loop, J-shape.

Aortic Interventions

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Aortic disease is a progressive condition. Our goal is to provide you with patient and disease-specific devices that help ensure the most durable repair possible for your patients.
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Zenith Alpha™ Thoracic Endovascular Graft Proximal Component

The Zenith Alpha Thoracic Endovascular Graft is indicated for the endovascular treatment of patients with aneurysms or ulcers of the descending thoracic aorta having vascular morphology suitable for endovascular repair, including:

  • Iliac/femoral anatomy that is suitable for access with the required introduction systems
  • Nonaneurysmal aortic segments (fixation sites) proximal and distal to a thoracic aneurysm or ulcer with a length of at least 20 mm, and with a diameter measured outer-wall-to-outer-wall of no greater than 42 mm and no less than 20 mm
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Zenith Alpha™ Thoracic Endovascular Graft Proximal Tapered Component

The Zenith Alpha Thoracic Endovascular Graft is made for the endovascular treatment of patients with aneurysms or ulcers of the descending thoracic aorta having vascular morphology suitable for endovascular repair, including:

  • Iliac/femoral anatomy that is suitable for access with the required introduction systems
  • Nonaneurysmal aortic segments (fixation sites) proximal and distal to a thoracic aneurysm or ulcer with a length of at least 20 mm, and with a diameter measured outer-wall-to-outer-wall of no greater than 42 mm and no less than 20 mm
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Zenith Alpha™ Thoracic Endovascular Graft Distal Component

The Zenith Alpha Thoracic Endovascular Graft is created for the endovascular treatment of patients with aneurysms or ulcers of the descending thoracic aorta having vascular morphology suitable for endovascular repair, including:

  • Iliac/femoral anatomy that is suitable for access with the required introduction systems
  • Nonaneurysmal aortic segments (fixation sites) proximal and distal to a thoracic aneurysm or ulcer with a length of at least 20 mm, and with a diameter measured outer-wall-to-outer-wall of no greater than 42 mm and no less than 20 mm
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Zenith Flex® AAA

The Zenith Flex AAA Endovascular Graft with the Z-Trak® Introduction System and ancillary components are indicated for the endovascular treatment of patients with abdominal aortic or aorto-iliac aneurysms having morphology suitable for endovascular repair.

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Zenith® Spiral-Z® AAA Iliac Leg Graft

The Zenith Spiral-Z AAA Iliac Leg with the Z-Trak® Introduction System is indicated for use with the Zenith AAA Endovascular Graft family of products, including the Zenith Flex® AAA Endovascular Graft, Zenith Renu® Ancillary Graft, Zenith® Fenestrated AAA Endovascular Graft, or Zenith® Branch Iliac Endovascular Graft, during either a primary or a secondary procedure in patients who have adequate iliac/femoral access compatible with the required introduction systems.

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Zenith Flex® AAA Endovascular Graft Main Body Extensions

The Zenith AAA Ancillary Components with the Z-Trak Introduction System are indicated for use with the Zenith AAA graft during either a primary or a secondary procedure in patients who have adequate iliac/femoral access compatible with the required introduction systems. 

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Coda® Balloon Catheter

The Coda and Coda LP Balloon Catheters are intended for temporary occlusion of large vessels, or to expand vascular prostheses.

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Performer™ Introducer and Sets / Extra Large Check-Flo® Introducers

Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices.

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Lunderquist® Extra-Stiff Wire Guide

Used for complex diagnostic and interventional procedures where increased body, flexibility, and low surface friction of the wire guide are needed.

Planning and Sizing

Vega Medical offers comprehensive endovascular aortic repair support—from specialized training, proctored cases, to a global team of  EVAR case planning specialists.

Once you’re ready to plan your case, plan the case yourself or turn to our experienced specialists. No matter how you plan your case, you can count on our support and our trusted, secure case planning application, the Zenith Image Review tool.

For advanced cases, you can count on our planning specialists to determine whether the patient’s anatomy is suitable for a particular endovascular technology. Or benefit from a peer review and consult with a peer who has extensive experience placing Zenith endovascular grafts.

Manufacturers

Availability of product and services may differ by country. Please contact us for more details.

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