Aortic accessories

The next generation in aortic accessories

Each accessory plays a key role in supporting our best-in-class EVAR and TEVAR devices, promoting positive outcomes.

GORE® DrySeal Flex Introducer Sheath

GORE® DRYSEAL Flex Introducer Sheath

  • Deliver with ease: Hydrophilic coating and enhanced flexibility provide exceptional access to challenging anatomies and branch vessels.
  • Minimize blood loss: Exclusive GORE® DRYSEAL Valve enables introduction of multiple devices with proven hemostasis control. 
  • Care for more patients: Optimized profile and configurations provide tailored delivery options for a broad range of patient anatomy. 
  • Complete confidence: Engineered for use with our endovascular portfolio.
Tri-lobe balloon catheter

GORE® Tri-Lobe Balloon Catheter

  • Continuous blood flow: Unique design allows flow around the lobes while inflated.
  • Decreased hemodynamic pressure on the inflated balloons with approximately 80% of flow for distal perfusion.1
  • Minimizes potential for endoprosthesis movement and blood pressure spikes post deployment due to significantly reduced hemodynamic pressures.2
  • Rapid, uniform and simultaneous inflation and deflation.
gore molding occlusion balloon

The GORE® Molding & Occlusion Balloon

  • Optimize seal: Proven radial expansion force across the range of EVAR device sizes (10–37 mm). 
  • Minimize risk: Engineered with a 10 Fr low profile to reduce access-related complications. 
  • Enhance control: Designed for excellent pushability and trackability with uncompromised inflation/deflation time.
  1. Bloss R, Krall B. Balloon Testing on Pulse Duplicator. Flagstaff, AZ: W. L. Gore & Associates, Inc.; 2009. [Technology notebook]. 1088.  
  2. Gendron M. Simulated Use Testing of Aortic Balloon Catheter for Design Verification – Final Amendment. Flagstaff, AZ: W. L. Gore & Associates, Inc; 2008. [Work plan]. MD39672.

eIFU Symbol

INDICATIONS FOR USE IN THE U.S.: The GORE® DRYSEAL Flex Introducer Sheath is intended to be inserted in the vasculature to provide a conduit for the insertion of endovascular devices while minimizing blood loss associated with such insertions. CONTRAINDICATIONS: There are no known contraindications for this device. Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly

INDICATIONS FOR USE IN THE U.S.: The GORE® Tri-Lobe Balloon Catheter is indicated to facilitate in the endovascular repair of the thoracic or abdominal aorta due to lesions including aneurysms, dissections, trauma, and penetrating aortic ulcers. CONTRAINDICATIONS: There are no known contraindications. Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly

INDICATIONS FOR USE IN THE U.S.: The GORE® Molding and Occlusion Balloon Catheter is intended for temporary occlusion of large diameter vessels or to assist the expansion of self-expanding endovascular prostheses (stent grafts). CONTRAINDICATIONS: The GORE® Molding and Occlusion Balloon Catheter is contraindicated in patients who: are contraindicated to contrast media or anticoagulants; have an arterial entry site that cannot accommodate a 10 Fr introducer sheath; are minors; are pregnant. Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly

Sizing, availability, and pricing varies by country. Please check with your Gore representative for availability. 

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