The Next Generation Conformable
Thoracic Device

Designed for flexibility and conformability in tortuous anatomy

The Next Generation Conformable GORE® TAG® Device achieves optimal wall apposition in angulated arch anatomy without excessive radial force, barbs or bare springs.
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NO BARBS OR BARE SPRINGS

  • Minimizes risk of damaging or perforating friable aortas

  • The only thoracic endograft to provide a safe, effective seal in angulated arch anatomy without these potentially damaging features

COMPRESSION RESISTANT

  • Maintains patency in small diameter thoracic aortas characteristic of young patients

  • Stent design maintains wall apposition in angulated arch anatomy without compromising tissue integrity

OFF-THE-SHELF TAPERED DESIGNS

  • Help ensure flexibility and conformability in tortuous anatomy

  • Give physicians more options to match endograft to individual patient anatomies

  • Maintain patency in expected aortic flow velocities

BROAD TREATMENT RANGE

Intended Aortic Diameter (mm)

Device Diameters

The only thoracic endograft approved to treat patients with 16 mm thoracic aortas.

ADAPTED FOR WIDE OVERSIZING RANGE

Intended Aortic Diameter (mm)

Aortic Diameter (mm)

GORE® TAG® Device

Conformable GORE® TAG® Device

The only thoracic endograft engineered to perform in 6-33% oversizing conditions.

The Next Generation GORE® TAG® Device Delivery System

Modified to navigate tortuous thoracic anatomy with increased flexibility and simplicity


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SINGLE-SHEATH INSERTION

  • No re-insertion is necessary if additional devices are required

  • Minimizes vessel trauma and the potential for rupture with multiple sheath insertions

SINGLE-STEP DEPLOYMENT


  • Easy, single-step, twist-and-pull deployment

LOW-PROFILE DESIGN

  • Sheathless, low-profile delivery catheter

  • Increased flexibility while navigating tortuous anatomy in the aortic arch

NEW

CURRENT

MODIFIED RADIOPAQUE OLIVE AND DELIVERY CATHETER

  • New flexible soft tip is designed to enhance trackability and delivery to target landing zone

  • Optimized visibility with radiopaque GORE® TAG® Device olives at both ends of the delivery catheter and radio dense marker embedded in the leading end of the catheter to aid in visualization

The Next Generation of a Legacy

The Conformable GORE® TAG® Device: Built upon the innovative
design and clinical success of the original GORE® TAG® Device


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More than 33,500 GORE® TAG® Devices distributed worldwide

For more than a decade, Gore has worked alongside physicians in the evolution of TEVAR and the continued development of the GORE® TAG® Device. This collaboration has resulted in the distribution of more than 33,500 GORE® TAG® Devices for the treatment of more than 20,000 GORE® TAG® Device patients worldwide.

Aneurysm-Related Death Through Five Years

Percent Survival

Time Post Treatment(Months)

99-01 Open Surgical Control

99-01 GORE® TAG® Device

03-03 GORE® TAG® Device

04-02 GORE® TAG® Device

Freedom From Major Adverse Events Through Five Year

% Free from Major Adverse Event

Time Post Treatment(Months)

99-01 Open Surgical Control

99-01 GORE® TAG® Device

03-03 GORE® TAG® Device

04-02 GORE® TAG® Device

proven clinical results

The GORE® TAG® Device is supported by more than ten years of commerical and clinical data, with up to five years follow-up
KEY

Enrollment

Follow-up

(all patients will be
followed through five years)

THE MOST-STUDIED THORACIC ENDOGRAFT AVAILABLE

With the first clinical implant occuring in 1997, the GORE® TAG® Device has been studied in seven FDA-approved clinical studies, one European clinical trial and one European registry.

35 YEARS OF EXPERIENCE WITH EPTFE GRAFT MATERIAL

Having pioneered ePTFE graft technology 35 years ago, Gore continues to collaborate with physicians and scientists to create a robust and reliable design platform based on proven clinical performance

Gore Aortic Accessories

Each product in the Gore aortic accessory portfolio plays a key role in supporting
Gore's best-in-class EVAR and TEVAR devices in promoting positive outcomes.

GORE® Tri-Lobe Balloon Catheter

Featuring compliant polyurethane balloons, rapid inflation and deflation and uniform and simultaneous lobe inflation, this catheter allows for continuous flow around lobes while inflated, decreasing hemodynamic pressure on inflated balloons.

Available in two 18 Fr introducer sheath compatible sizes:


  • Small (BCM1634) for 16 - 34 mm vessel diameters

  • Large (BCL2645) for 26 - 42 mm vessel diameters


GORE® DrySeal Sheath

  • Minimizes blood loss through an innovative pressurized hemostatic valve

  • Accommodates multiple wires and catheters simultaneously through the valve with minimal blood loss

  • Facilitates hemostasis without intraprocedural manipulation of the valve

Products listed may not be available in all markets.
©2012-2010 W. L. Gore & Associates, Inc. AN1124-EN5 February 2012