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Phoenix atherectomy system Rotational atherectomy system

Phoenix atherectomy system

Rotational atherectomy system

Εύρεση παρόμοιων προϊόντων

The Phoenix atherectomy system combines the benefits of existing atherectomy systems to deliver a unique atherectomy option to help physicians tailor the treatment approach for each patient.¹ It cuts, captures, and clears diseased tissue with one insertion. Phoenix treats a broad range of tissue types, from soft plaque to calcified arteries, and can be used for lesions above and below the knee.²,³

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Features
Front cutter
Front cutter

Front cutter

Front cutter clears tissue in a way that may help reduce potential trauma to the vessel.³
Capture and clearance
Capture and clearance

Capture and clearance

Continuous capture and passive clearance of debulked material into the catheter resulted in a 1% rate of symptomatic distal emboli in the EASE trial.⁴
Ease of use
Ease of use

Ease of use

Phoenix is battery-powered and handle-operated. No capital equipment or additional procedural accessories are required.
Deliverability
Deliverability

Deliverability

Low-profile, front-cutting design allows for direct lesion access without having to first pass a nosecone. The over-the-wire design aids in trackability and pushability of catheter.
Versatility
Versatility

Versatility

Offering of 3 catheter diameters has been shown to effectively treat most peripheral vasculature.⁴ • 1.8 and 2.2mm tracking catheters are suited for treating small vessels or highly stenosed lesions. • 2.2 deflected catheter suited for more lumen gain in above and below the knee lesions.* • 2.4mm (deflecting) catheter is suited for larger vessels or eccentric lesions.³

Προδιαγραφές

1.8mm x 130cm tracking catheter
1.8mm x 130cm tracking catheter
Part Number
  • P18130K
Introducer size
  • 5F (<gt/>1.8 mm)
Working length
  • 130 cm
Guidewire diameter
  • 0.014”
1.8mm x 149cm tracking catheter
1.8mm x 149cm tracking catheter
Part Number
  • P18149K
Introducer size
  • 5F (<gt/>1.8 mm)
Working length
  • 149 cm
Guidewire diameter
  • 0.014”
2.2mm x 130cm tracking catheter
2.2mm x 130cm tracking catheter
Part Number
  • P22130K
Introducer size
  • 6F (<gt/>2.2 mm)
Working length
  • 130 cm
Guidewire diameter
  • 0.014”
2.2mm x 149cm tracking catheter
2.2mm x 149cm tracking catheter
Part Number
  • P22149K
Introducer size
  • 6F (<gt/>2.2 mm)
Working length
  • 149 cm
Guidewire diameter
  • 0.014”
2.4mm x 127cm deflecting catheter
2.4mm x 127cm deflecting catheter
Part Number
  • PD24127K
Introducer size
  • 7F (<gt/>2.4 mm)
Working length
  • 127 cm
Guidewire diameter
  • 0.014”
Phoenix guidewire
Phoenix guidewire
Part Number
  • PD24127K
Product
  • Phoenix guidewire
Length
  • 300 cm
Wire Support Level
  • Light

Documentation

Brochure (4)

Brochure

  • 1. Rotational atherectomy refers to the Phoenix family of products. 2.4mm deflecting catheter and 2.2 mm auto-deflected catheter have directional cutting ability.
  • 2. Monitor flow of excised material into the disposal reservoir during operation of the Catheter. If flow of excised material ceases during the procedure, this is a sign that the Catheter drive system (cutter, torque shaft, or Handle motor drive) may not be operating properly.
  • 3. The Phoenix atherectomy 1.8 mm tracking catheter is indicated for vessels 2.5 mm in diameter or above. The Phoenix atherectomy 2.2 mm tracking, deflected and 2.4 mm deflecting catheters are indicated for vessels 3.0 mm in diameter or above. While the 1.8 mm and 2.2 mm tracking & deflected catheters are indicated for femoral, popliteal, or distal arteries located below the knee, the Phoenix 2.4 mm deflecting catheter is indicated for femoral and popliteal only.
  • 4. Davis T, Ramaiah V, Niazi K, Martin Gissler H, Crabtree T. Safety and effectiveness of the Phoenix Atherectomy System in lower extremity arteries: Early and midterm outcomes from the prospective multicenter EASE study. Vascular. 2017 Dec;25(6):563-575
  • 5. Case study results are not predictive. Results in other cases may vary.
  • 6. Case performed by Dr. Christopher LeSar at the Vascular Institute of Chattanooga.
  • 7. Case performed by Dr. Joseph Griffin at Baton Rouge General Hospital.
  • 8. Center mass cutting device when the guidewire is centered.
  • 9. Case performed by Dr. William Crowder in Jackson, Mississippi.
  • 10. Case performed by Dr. Tom Davis in Detroit, MI.
  • * vs. 2.2 tracking catheter, based on bench tests. Bench test results not indicative of clinical performance. 2.2mm deflected catheter was not included in the EASE trial.

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