AORTIC INTERVENTION

Semi compliant balloon is made of polyurethane, offering an alternative to latex balloons.

Radiopaque markers placed at both the proximal and distal segments of the balloon.

Long tapered tip minimizes vessel trauma.

Flexible enough for tortuous anatomy or crossover procedures, yet provides extra support when needed.

Three-step construction enables flexibility for tight anatomy.

Stiffer shaft provides pushability.

Softer dilator improves trackability.

For procedures that involve the largest endovascular devices, this wire guide provides maximum support as well as precise tip visualisation.

• The stainless steel micro coil tip enhances visibility under fluoroscopy
• The thick stainless steel mandril provides maximum support
• The PTFE-coated stainless steel outer coil ensures smooth manipulation and eases passage
• The flexible tip helps facilitate atraumatic vessel selection

Nester Embolization Coils and Micro coils are made of platinum with spaced synthetic fibers and are supplied preloaded in a loading cartridge.
They are designed to be delivered to the target vessel using a soft, straight wire guide through a standard angiographic catheter.
Our range of diameters and lengths in the COOK Embolization Coil portfolio are:

• Designed to form a tight occluding mass.
• Made of soft platinum for tight packing.
• Fully fibered for thrombogenicity.
• Easily visible under fluoroscopy.
• MR conditionally safe at 3 T and 1.5 T.
• Useable alone or in combination with other pushable and detachable embolization coils.

Vascular access needle.

Adequate iliac/femoral access compatible with a 20 French (7.7 mm O.D.) introduction system.
Non-aneurysmal external iliac artery fixation segment distal to the aneurysm; with a length of at least 20 mm and with a diameter measured outer wall to outer wall of no greater than 11 mm and no less than 8 mm.
Non-aneurysmal internal iliac artery segment distal to the aneurysm: with a length of at least 10 mm (with 20-30 mm being preferred) and with a diameter acceptable for proper sealing.

The patient must have aneurysmal morphology suitable for endovascular repair, including:

• adequate femoral/iliac access compatible with the required delivery systems;
• a non-aneurysmal infrarenal aortic segment (neck) proximal to the aneurysm with a length of at least 4 mm, i.e. at least 4 mm circumferential wall contact around fenestrations and/or limits of scallop;
• a diameter measured outer wall to outer wall of no greater than 31 mm and no less than 19 mm;
• an angle less than 45 degrees relative to the long axis of the aneurysm;
• an angle less than 45 degrees relative to the axis of the suprarenal aorta;
• an ipsilateral iliac artery distal fixation site greater than 10 mm in length and 9-21 mm in diameter (measured outer wall to outer wall);
• and, a contralateral iliac artery distal fixation site greater than 10 mm in length and 7-21 mm in diameter.

Cook offers disease-specific treatment options that are designed to help you provide a durable repair in the thoracic aorta. View product indications for use, component ordering information, introduction system, and graft specifications.

Expect control of your endovascular procedures for better outcomes.
Zenith TX2 with Pro-Form was specifically designed to give you more control over clinical performance, which can help you achieve a higher standard of patient care through better outcomes and by saving clinical resources. TX2 with Pro-Form allows you to offer your patients targeted treatment options for aneurysms or ulcers of the descending thoracic aorta.

The Zenith Alpha Abdominal Endovascular Graft is indicated for the endovascular treatment of patients with abdominal aortic or aortoiliac aneurysms having morphology suitable for endovascular repair.

The Zenith Flex AAA Endovascular Graft with the Z-Trak® Introduction System and ancillary components are indicated for the endovascular treatment of patients with abdominal aortic or aorto-iliac aneurysms having morphology suitable for endovascular repair.

Adequate iliac/femoral access compatible with a 20 French (7.7 mm O.D.) introduction system.
Non-aneurysmal external iliac artery fixation segment distal to the aneurysm; with a length of at least 20 mm and with a diameter measured outer wall to outer wall of no greater than 11 mm and no less than 8 mm.
Non-aneurysmal internal iliac artery segment distal to the aneurysm: with a length of at least 10 mm (with 20-30 mm being preferred) and with a diameter acceptable for proper sealing.