Aortic stent grafts
GORE EXCLUDER Iliac Branch Endoprosthesis
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.
GORE EXCLUDER Iliac Branch Endoprosthesis models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| CEB231010A | Catheter Gauge 16 Fr; Lumen/Inner Diameter 10 mm; Lumen/Inner Diameter 23 mm; Length 10 cm | MR Conditional | Available |
| CEB231210A | Length 10 cm; Lumen/Inner Diameter 23 mm; Lumen/Inner Diameter 12 mm; Catheter Gauge 16 Fr | MR Conditional | Available |
| CEB231410A | Catheter Gauge 16 Fr; Lumen/Inner Diameter 14.5 mm; Lumen/Inner Diameter 23 mm; Length 10 cm | MR Conditional | Available |
| HGB161007A | Length 7 cm; Lumen/Inner Diameter 16 mm; Lumen/Inner Diameter 10 mm; Catheter Gauge 12 Fr | MR Conditional | Available |
| HGB161207A | Catheter Gauge 12 Fr; Lumen/Inner Diameter 12 mm; Lumen/Inner Diameter 16 mm; Length 7 cm | MR Conditional | Available |
| HGB161407A | Length 7 cm; Lumen/Inner Diameter 16 mm; Lumen/Inner Diameter 14.5 mm; Catheter Gauge 12 Fr | MR Conditional | Available |
FDA clearances
- PMA P020004 September 2006
Procedures that use aortic stent grafts
Frequently asked questions
What is GORE EXCLUDER Iliac Branch Endoprosthesis 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 Iliac Branch Endoprosthesis?
GORE EXCLUDER Iliac Branch Endoprosthesis 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 Iliac Branch Endoprosthesis come in?
Sizes listed for GORE EXCLUDER Iliac Branch Endoprosthesis: Lumen/Inner Diameter: 10–23 mm; Catheter Gauge: 12–16 Fr; Length: 7–10 cm. Confirm availability with the manufacturer's instructions for use.
Is GORE EXCLUDER Iliac Branch Endoprosthesis MRI safe?
The FDA device database lists GORE EXCLUDER Iliac Branch Endoprosthesis as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is GORE EXCLUDER Iliac Branch Endoprosthesis FDA cleared?
GORE EXCLUDER Iliac Branch Endoprosthesis is covered by FDA submission P020004.
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.