ALTO Deployment Animation MM 2200 Rev 02

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  • čas přidán 23. 07. 2024
  • Animation featuring ALTO deployment steps.
    ALTO Abdominal Stent Graft System for AAA
    Endovascular Aneurysm Repair (EVAR)
    endologix.com/
    INDICATIONS FOR USE: The ALTO® Abdominal Stent Graft System is indicated for treatment of patients with infrarenal abdominal aortic aneurysms having the vascular morphology suitable for endovascular repair with the device, which includes the following:
    ∙ Adequate iliac/femoral access compatible with vascular access techniques (femoral cutdown or percutaneous), devices, and/or accessories,
    ∙ A proximal aortic landing zone for the sealing ring 7 mm below the inferior renal artery.
    ∙ An aortic sealing zone comprised of healthy aorta defined as:
    - Lack of significant thrombus greater than 8 mm in thickness; at any point along the aortic circumference at the level of 7mm below the inferior renal artery,
    - Lack of significant calcification at the level of 7 mm below the inferior renal artery,
    - Conicity less than 10% as measured from the inferior renal artery to the aorta 7 mm below the inferior renal artery,
    - An inner wall diameter of no less than 16 mm and no greater than 30 mm at 7 mm below the inferior renal artery, and
    - An aortic angle of less than or equal to 60 degrees
    ∙ A distal iliac landing zone:
    - With a length of at least 10 mm, and
    - With an inner wall diameter of no less than 8 mm and no greater than 25 mm.
    CONTRAINDICATIONS: The system is contraindicated for use in patients who have a condition that threatens to infect the graft and in patients with known sensitivities or allergies to the device materials including polytetrafluoroethylene [PTFE], polyethylene glycol [PEG]-based polymers, contrast agents, fluorinated ethylene propylene [FEP], titanium, nickel, platinum, or iridium.
    Refer to Instructions for Use for more information concerning Indications, Contraindications, Specific Anatomic Considerations, Warnings, Precautions, and Adverse Events.
    CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.
    NOTE: Not all product components are available in every country. Please consult with your Endologix representative to confirm product availability.
    ©2020 Endologix LLC. All rights reserved. MM2200 Rev 02

Komentáře • 3

  • @lamp5476
    @lamp5476 Před 5 měsíci

    sick vid

  • @phatman23
    @phatman23 Před 3 lety

    Do you not routinely balloon the limbs? There was no mention during the video so I wanted to ask.

    • @badbwoytrini
      @badbwoytrini Před 2 lety

      Yes we use alto alot and balloon 1:1 w/ compliant balloons just to "iron out" the fabric