AFX2 Deployment Animation
INDICATIONS FOR USE: The Endologix AFX®2 Endovascular AAA Systems are indicated for treatment of patients with abdominal aortic aneurysms having the vascular morphology suitable for endovascular repair using a surgical vascular access technique or a bilateral percutaneous technique; a non-aneurysmal aortic neck between the renal arteries and the aneurysm: with length of greater than or equal to 15mm, diameter greater than or equal to 18 to less than or equal to 32mm and neck angle of less than or equal to 60° to the body of the aneurysm; aortic length greater than or equal to 1.0cm longer than the body portion of the chosen bifurcated model; common iliac artery distal fixation site with length greater than or equal to 15mm, diameter of greater than or equal to 10 to less than or equal to 23mm, and with ability to preserve at least one hypogastric artery; and with an iliac angle of greater than or equal to 90° to the aortic bifurcation. Extension stent grafts must have the ability to overlap the bifurcated stent graft by at least 30 to 40mm proximally and at least 15 to 20mm distally.
CONTRAINDICATIONS: The Endologix AFX/AFX2 Endovascular AAA Systems are contraindicated for use in patents who have a condition that threatens to infect the graft and in patients with sensitivities or allergies to the device materials. Refer to the Instructions for Use for more information concerning Indications, Contraindications, Warnings and Precautions, and Adverse Events.
CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician. Rx only.
Note: Endologix products and associated components are not available in all countries or regions. Please consult with your Endologix representative for details regarding product availability.
CE marked. Please refer to current product instructions for use.
Endologix is a registered trademark of Endologix, Inc. in United States, Europe and Japan, AFX is a registered trademark of Endologix, Inc. in United States, Argentina, Europe, and Japan and DuraPly, VELA, and ActiveSeal are trademarks of Endologix, Inc. All other trademarks are the property of their respective owners.
©2016 Endologix Inc. All rights reserved.
Видео AFX2 Deployment Animation канала Endologix
CONTRAINDICATIONS: The Endologix AFX/AFX2 Endovascular AAA Systems are contraindicated for use in patents who have a condition that threatens to infect the graft and in patients with sensitivities or allergies to the device materials. Refer to the Instructions for Use for more information concerning Indications, Contraindications, Warnings and Precautions, and Adverse Events.
CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician. Rx only.
Note: Endologix products and associated components are not available in all countries or regions. Please consult with your Endologix representative for details regarding product availability.
CE marked. Please refer to current product instructions for use.
Endologix is a registered trademark of Endologix, Inc. in United States, Europe and Japan, AFX is a registered trademark of Endologix, Inc. in United States, Argentina, Europe, and Japan and DuraPly, VELA, and ActiveSeal are trademarks of Endologix, Inc. All other trademarks are the property of their respective owners.
©2016 Endologix Inc. All rights reserved.
Видео AFX2 Deployment Animation канала Endologix
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