25 Years of TEVAR: GORE® TAG® Conformable Thoracic Stent Graft with ACTIVE CONTROL System
Building on 25 years of TEVAR experience we’ve combined a proven stent graft with controlled, staged deployment, uniquely designed for trusted conformability and anatomical adaptability.
We create solutions engineered to perform as promised
Gore has a long history with TEVAR. We look back on 25 years and think of all the milestones. There's been an enduring benefit to patients over a long period of time."
They were the first ones to come out with a TEVAR device, and a branch arch device, and a dissection indication. They have a whole series of firsts for us and our patients.”
Gore really helped pioneer these devices and advance the technology and make it applicable to everyday treatment of these patients.”
The first time I used the [GORE® TAG® Thoracic Endoprosthesis] I was a resident. Fast forward 20 years, what we are doing now, we couldn't even think about it.”
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* Paid consultant for Gore.
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 EUROPE: The GORE® TAG® Conformable Thoracic Stent Graft is indicated for endovascular repair of all lesions of the descending thoracic aorta, including isolated lesions, such as aneurysm and traumatic transection, and Type B dissections.
CONTRAINDICATIONS: The GORE® TAG® Conformable Thoracic Stent Graft is contraindicated in:
- Patients with known sensitivities or allergies to the device materials
- Patients with a systemic infection who may be at risk of endovascular graft infection