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Catalogue numbers for GORE® EXCLUDER® AAA Endoprosthesis

Trunk - Ipsilateral Leg Endoprosthesis
GORE® C3® Delivery System Catalogue Number Aortic Endoprosthesis Diameter (mm) Iliac Endoprosthesis Diameter (mm) Endoprosthesis Length (cm)
RLT231212 23 12 12
RLT231214 23 12 14
RLT231216 23 12 16
RLT231218 23 12 18
RLT231412 23 14.5 12
RLT231414 23 14.5 14
RLT231416 23 14.5 16
RLT231418 23 14.5 18
RLT261212 26 12 12
RLT261214 26 12 14
RLT261216 26 12 16
RLT261218 26 12 18
RLT261412 26 14.5 12
RLT261414 26 14.5 14
RLT261416 26 14.5 16
RLT261418 26 14.5 18
RLT281212 28.5 12 12
RLT281214 28.5 12 14
RLT281216 28.5 12 16
RLT281218 28.5 12 18
RLT281412 28.5 14.5 12
RLT281414 28.5 14.5 14
RLT281416 28.5 14.5 16
RLT281418 28.5 14.5 18
RLT311413 31 14.5 13
RLT311415 31 14.5 15
RLT311417 31 14.5 17
RLT351414 35 14.5 14
RLT351416 35 14.5 16
RLT351418 35 14.5 18
Contralateral Leg Endoprosthesis*
Catalogue Number Distal Diameter (mm) Endoprosthesis Length (cm)
PLC121000 12 10
PLC121200 12 12
PLC121400 12 14
PLC141000 14.5 10
PLC141200 14.5 12
PLC141400 14.5 14
PLC161000* 16 9.5
PLC161200* 16 11.5
PLC161400* 16 13.5
PLC181000* 18 9.5
PLC181200* 18 11.5
PLC181400* 18 13.5
PLC201000* 20 9.5
PLC201200* 20 11.5
PLC201400* 20 13.5
PLC231000* 23 10
PLC231200* 23 12
PLC231400* 23 14
PLC271000* 27 10
PLC271200* 27 12
PLC271400* 27 14

* PLEASE NOTE: All large diameter Contralateral Leg Endoprostheses (16, 18, 20, 23, 27 mm) can be used as Iliac Extenders.

Aortic Extender Endoprosthesis
Catalogue Number Endoprosthesis Diameter (mm) Endoprosthesis Length (cm)
PLA230300 23 3.3
PLA260300 26 3.3
PLA280300 28.5 3.3
PLA320400 32 4.5
PLA360400 36 4.5
Iliac Extender Endoprosthesis
Catalogue Number Distal Diameter (mm) Endoprosthesis Length (cm)
PLL161007 10 7
PLL161207 12 7
PLL161407 14.5 7

 

GORE® EXCLUDER® Iliac Branch Endoprosthesis Iliac Branch Component
Catalogue Number Diameter Iliac End (mm) Iliac Branch Component Length (cm)
CEB231010A 10 10
CEB231210A 12 10
CEB231410A 14.5 10

 

Internal Iliac Component
Catalogue Number Diameter Iliac End (mm) Iliac Branch Component Length (cm)
HGB161007A 10 7
HGB161207A 12 7
HGB161407A 14.5 7

 

GORE® DRYSEAL Flex Introducer Sheath
Catalogue NumberSheath Size (Fr)Minimum Sheath ID (mm)Nominal Sheath OD (mm)Working Length (cm)
DSF1233124.04.733
DSF1245124.04.745
DSF1433144.75.333
DSF1533155.05.633
DSF1633165.36.133
DSF1833186.06.733
DSF2033206.77.533
DSF2065206.77.565
DSF2233227.38.233
DSF2265227.38.265
DSF2433248.08.833
DSF2465248.08.865
DSF2633268.79.533
DSF2665268.79.565

 

GORE® Tri-Lobe Balloon Catheter
Catalogue Number Vessel Diameter (mm)
BCM1634 16–34

 

GORE® Molding & Occlusion Balloon
Catalogue Number Balloon inflation range (mm) Balloon length (cm) Catheter length (cm) Wire compatibility
MOB37 10-37 4 90 0.035

 

INDICATIONS FOR USE IN THE U.S.: Trunk-Ipsilateral Leg and Contralateral Leg Endoprosthesis. The GORE® EXCLUDER® AAA Endoprosthesis is intended to exclude the aneurysm from the blood circulation in patients diagnosed with infrarenal abdominal aortic aneurysm (AAA) disease and who have appropriate anatomy as described below: Adequate iliac/femoral access; Infrarenal aortic neck treatment diameter range of 19–32 mm and a minimum aortic neck length of 15 mm; Proximal aortic neck angulation ≤ 60°; Iliac artery treatment diameter range of 8–25 mm and iliac distal vessel seal zone length of at least 10 mm. Aortic Extender and Iliac Extender Endoprosthesis. The Aortic and Iliac Extender Endoprostheses are intended to be used after deployment of the GORE® EXCLUDER® AAA Endoprosthesis. These extensions are intended to be used when additional length and/or sealing for aneurysmal exclusion is desired. CONTRAINDICATIONS: The GORE® EXCLUDER® AAA Endoprosthesis is contraindicated in: patients with known sensitivities or allergies to the device materials; patients with a systemic infection who may be at increased risk of endovascular graft infection. 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.: Iliac Branch and Internal Iliac Components. The GORE® EXCLUDER® Iliac Branch Endoprosthesis (IBE) is intended to be used with the GORE® EXCLUDER® AAA Endoprosthesis or the GORE® EXCLUDER® Conformable Endoprosthesis to isolate the common iliac artery from systemic blood flow and preserve blood flow in the external iliac and internal iliac arteries in patients with a common iliac or aortoiliac aneurysm, who have appropriate anatomy, including: Adequate iliac/femoral access; Minimum common iliac diameter of 17 mm at the proximal implantation zone of the IBE; External Iliac artery treatment diameter range of 6.5–25 mm and seal zone length of at least 10 mm; Internal iliac artery treatment diameter range of 6.5–13.5 mm and seal zone length of at least 10 mm; Adequate length from the lowest major renal artery to the internal iliac artery to accommodate the total endoprosthesis length, calculated by adding the minimum lengths of required components, taking into account appropriate overlaps between components. GORE® EXCLUDER® Components used in conjunction with GORE® EXCLUDER® Iliac Branch Endoprosthesis: Trunk-Ipsilateral Leg Component. The Trunk-Ipsilateral Leg is intended to provide proximal seal and fixation for the endovascular repair of the aneurysm. For more information on the Trunk-Ipsilateral Leg Component indications for use and deployment, see the GORE® EXCLUDER® AAA Endoprosthesis or the GORE® EXCLUDER® Conformable Endoprosthesis Instructions for Use. Contralateral Leg Endoprosthesis Component. The Contralateral Leg Endoprosthesis is intended to bridge the GORE® EXCLUDER® Device Trunk-Ipsilateral Component to the GORE® EXCLUDER® Iliac Branch Endoprosthesis following deployment of the GORE® EXCLUDER® Iliac Branch Endoprosthesis. Additionally, the Contralateral Leg Endoprosthesis is intended to be used for distal extension of the Iliac Branch Component in the external iliac artery. The Iliac Branch Component can treat external iliac artery diameters up to 13.5 mm. This ability to extend the Iliac Branch Component distally with any Contralateral Leg Endoprosthesis expands the external iliac artery treatment range up to 25 mm. For more information on the Trunk-Ipsilateral Leg and Contralateral Leg Endoprosthesis Component indications for use and deployment, see the GORE® EXCLUDER® AAA Endoprosthesis Instructions for Use. Aortic Extender and Iliac Extender Components. The Aortic and Iliac Extender Components can be used after deployment of the GORE® EXCLUDER® Iliac Branch and GORE® EXCLUDER® AAA Endoprostheses or the GORE® EXCLUDER® Conformable Endoprosthesis. These extensions are used when additional length and/or sealing for aneurysmal exclusion is desired. For more information on Aortic Extender and Iliac Extender indications for use and deployment, see the GORE® EXCLUDER® AAA Endoprosthesis or the GORE® EXCLUDER® Conformable Endoprosthesis Instructions for Use. CONTRAINDICATIONS: The GORE® EXCLUDER® Iliac Branch Endoprosthesis is contraindicated in: patients with known sensitivities or allergies to the device materials. All components of the GORE® EXCLUDER® Iliac Branch Endoprosthesis, the GORE® EXCLUDER® AAA Endoprosthesis and GORE® EXCLUDER Conformable Endoprosthesis contain ePTFE, FEP, nitinol (nickel-titanium alloy) and gold. Patients with a systemic infection who may be at increased risk of endovascular graft infection. 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® 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.

231315160-EN