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Contego Medical, LLC recently announced that it has received CE Marking of its Vanguard IEP™ Peripheral Balloon Angioplasty System with Integrated Embolic Protection. The Company intends to launch the Vanguard IEP System in Europe to endovascular specialists performing lower limb angioplasty procedures.

The Vanguard IEP System represents the latest innovation of Contego’s Integrated Embolic Protection (IEP™) technology, incorporating a peripheral angioplasty balloon and distal embolic filter on the same catheter. The system protects the lower limbs during angioplasty without the need for additional devices or exchanges. The Vanguard IEP System has an over-the-wire design with a sheathless integrated 150-micron pore filter distal to the angioplasty balloon. The Vanguard IEP System is the first filter to feature in-vivo adjustability to suit varying vessel sizes and maximize capture efficiency.

“The CE Mark for the Vanguard IEP System expands our product portfolio of novel devices designed to provide enhanced safety during peripheral vascular procedures,” said Ravish Sachar, M.D., CEO and Founder of Contego Medical. “We are eager to positively impact this growing patient population, with an estimated 200 million people affected by peripheral arterial disease worldwide.”

“The Vanguard IEP System is an important step toward enhancing safety for patients undergoing peripheral angioplasty for occlusive disease,” said Professor Thomas Zeller, Director of the Department of Angiology at Universitaets-Herzzentrum Freiburg in Bad Krozingen, Germany and Principal Investigator of the upcoming Vanguard clinical study. “This device will be of particular importance to patients at high risk for distal embolization, such as those with acute limb ischemia or chronic total occlusions, as well as those at higher risk should embolization occur, such as patients with critical limb ischemia and diabetes mellitus.”

Contego has established a premier distribution network throughout Europe to sell the Vanguard IEP System. Their first IEP device, the Paladin® Carotid Post-Dilation Balloon System was launched in Europe in 2016.

About Contego Medical
Contego Medical, LLC is a medical device company dedicated to the development of novel medical devices for cardiovascular and peripheral vascular procedures. The company’s Integrated Embolic Protection (IEP) platform, which combines embolic protection and treatment into one device, is designed to simplify catheter-based procedures and improve patient outcomes. Contego Medical is based in Raleigh, North Carolina, USA.

The Vanguard IEP System is CE marked and available for sale in select European countries.

Vanguard IEP, Paladin and IEP are all trademarks of Contego Medical, LLC.

For Further Information
More on the peripheral vascular device market in Europe can be found in a series of reports published by iData Research entitled the European Market Report Suite for Peripheral Vascular Devices. The suite covers reports on the following markets: Peripheral Vascular Stents, Percutaneous Transluminal Angioplasty Balloon Catheters, Atherectomy Devices, Chronic Total Occlusion Devices, Embolic Protection Devices, Stent-Grafts, Surgical Grafts, Arteriovenous Access Thrombectomy Devices, Inferior Vena Cava Filters, Diagnostic and Interventional Catheters, Standard and Hydrophilic Guidewires, Introducer Sheaths, Vascular Closure Devices and Transcatheter Embolization Devices.

The iData report series on peripheral vascular devices covers the U.S. and 15 countries in Europe including Austria, Belgium, Denmark, Finland, France, Germany, Italy, Luxembourg, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland, and the United Kingdom. Reports provide a comprehensive analysis including units sold, procedure numbers, market value, forecasts, as well as detailed competitive market shares and analysis of major players’ success strategies in each market and segment. To find out more about peripheral vascular market data or procedure data, register online or email us at [email protected] for a European Market Report Suite for Peripheral Vascular Devices brochure and synopsis.

About iData Research
iData Research is an international market research and consulting firm, dedicated to providing the best in business intelligence for the medical device industry. Our research empowers our clients by providing them with the necessary tools to achieve their goals and do it right the first time. iData covers research in: Spinal Implants and VCF, Spinal MIS, Orthopedic Soft Tissue Repair and Regeneration, Orthopedic Trauma, Large & Small Joints, Dental Operatory Equipment, Dental Material, Dental Lasers, Dental Prosthetics, Dental CAD/CAM, Dental Bone Graft Substitutes, Ophthalmics, Ultrasound, X-Ray Imaging, Diagnostic Imaging, Oncology, Vascular Access, Interventional Cardiology, Cardiac Surgery, Cardiac Rhythm Management, Electrophysiology, Operating Room Equipment, Surgical Microscopes, Robotics and Surgical Navigation, Laparoscopy, Urology, Gynecology, Endoscopy, Anesthesiology, Wound Management, Orthopedics and more.

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About Procedure Tracker
Procedure number data is available from iData’s Procedure Tracker service, which allows subscribers to define and analyze procedure data segmented by state, region, hospital, surgery centre, and physician. A customizable dashboard sorts procedure data for further analysis and research.

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iData Research’s Reimbursement Policy Tracker enables medical device, dental, pharmaceutical and healthcare professionals to receive real-time policy updates from hundreds of insurance companies and 60,000+ policies across all therapeutic areas in the United States.

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