Aortic stent grafts

GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral

by W. L. Gore & Associates, Inc.

A non-bioabsorbable tubular device typically implanted at the junction of the abdominal aorta and the common iliac arteries to reduce pressure on an abdominal aortic aneurysm (AAA) [includes aortoiliac aneurysm]; it does not contain anticoagulants or pharmaceuticals. It is percutaneously inserted via the femoral artery to the site of implantation where it self-expands. It is made of a metallic mesh structure with a polymer tube (endovascular graft) and is typically available as a: 1) single tube for insertion into the aorta and/or one iliac artery; or 2) two-part bifurcation design (e.g., Y-shaped tube) for insertion through both iliac arteries.

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GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
CXT201212Lumen/Inner Diameter 20 mm; Length 12 cm; Catheter Gauge 15 Fr; Outer Diameter 12 mm MR ConditionalAvailable
CXT201412Lumen/Inner Diameter 20 mm; Length 12 cm; Catheter Gauge 15 Fr; Outer Diameter 14.5 mm MR ConditionalAvailable
CXT231212Lumen/Inner Diameter 23 mm; Length 12 cm; Catheter Gauge 15 Fr; Outer Diameter 12 mm MR ConditionalAvailable
CXT231412Lumen/Inner Diameter 23 mm; Length 12 cm; Catheter Gauge 15 Fr; Outer Diameter 14.5 mm MR ConditionalAvailable
CXT261212Lumen/Inner Diameter 26 mm; Length 12 cm; Catheter Gauge 16 Fr; Outer Diameter 12 mm MR ConditionalAvailable
CXT261412Lumen/Inner Diameter 26 mm; Length 12 cm; Catheter Gauge 16 Fr; Outer Diameter 14.5 mm MR ConditionalAvailable
CXT281212Lumen/Inner Diameter 28.5 mm; Length 12 cm; Catheter Gauge 16 Fr; Outer Diameter 12 mm MR ConditionalAvailable
CXT281412Lumen/Inner Diameter 28.5 mm; Length 12 cm; Catheter Gauge 16 Fr; Outer Diameter 14.5 mm MR ConditionalAvailable
CXT321414Lumen/Inner Diameter 32 mm; Length 14 cm; Catheter Gauge 18 Fr; Outer Diameter 14.5 mm MR ConditionalAvailable
CXT361414Lumen/Inner Diameter 36 mm; Length 14 cm; Catheter Gauge 18 Fr; Outer Diameter 14.5 mm MR ConditionalAvailable

FDA clearances

Procedures that use aortic stent grafts

Frequently asked questions

What is GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral used for?

A non-bioabsorbable tubular device typically implanted at the junction of the abdominal aorta and the common iliac arteries to reduce pressure on an abdominal aortic aneurysm (AAA) [includes aortoiliac aneurysm]; it does not contain anticoagulants or pharmaceuticals. It is percutaneously inserted via the femoral artery to the site of implantation where it self-expands. It is made of a metallic mesh structure with a polymer tube (endovascular graft) and is typically available as a: 1) single tube for insertion into the aorta and/or one iliac artery; or 2) two-part bifurcation design (e.g., Y-shaped tube) for insertion through both iliac arteries.

Who makes GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral?

GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral is made by W. L. Gore & Associates, Inc.. It is listed under aortic stent grafts (evar/tevar) in our device library.

What sizes does GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral come in?

Sizes listed for GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral: Lumen/Inner Diameter: 20–36 mm; Length: 12–14 cm; Catheter Gauge: 15–18 Fr. Confirm availability with the manufacturer's instructions for use.

Is GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral MRI safe?

The FDA device database lists GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral as MR Conditional. Always follow the specific MRI conditions in the labeling.

Is GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral FDA cleared?

GORE EXCLUDER Conf AAA Endo - Trunk-Ipsilateral is covered by FDA submission P200030.

How do I contact a W. L. Gore & Associates, Inc. sales representative?

W. L. Gore & Associates, Inc. has not listed representatives on LA Vascular yet. Visit the W. L. Gore & Associates, Inc. company page for contact details.

Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.

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