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IntraStent LD Family of Unmounted Stents

The Power of Flexible Strength

The IntraStent™ DoubleStrut™ LD, Mega™ LD and Max™ LD Peripheral Stents are unmounted stents made from a stainless steel tube that is cut into an open lattice design. They are designed to be manually crimped onto a non-compliant PTA balloon catheter . After mounting onto a balloon catheter, the stent is expanded and deployed by inflating the balloon.

ev3's original large diameter stent design.

  • Upon its introduction, this device set industry standards for flexibility and profile, leading to superior deliverability and changed the way clinicians viewed large diameter stents. IntraStent™ DoubleStrut™ LD Stent

IntraStent™ DoubleStrut™ LD Stent
  • Unique DoubleStrut design allows unbeatable flexibility
  • 8F sheath compatability
  • No shortening after expansion up to 12 mm
  • Rounded edges minimize potential for lumen trauma

When flexibility is your greatest clinical concern, try the IntraStent DoubleStrut LD Stent

IntraStent™ Mega™ LD Stent

This stent combines the best features of the DoubleStrut LD Stent and the Max LD Stent to create a device that is strong, yet pliant.
  • 5 cell design for increased radial strength over the Doublestrut LD Stent
  • 9F sheath compatibility
  • No shortening when expanding up 12 mm
  • Rounded edges minimize potential for lumen trauma 

When the clinical situation demands strength AND flexibility, look to the IntraStent Mega LD Stent

IntraStent™ Max™ LD Stent

This stent is engineered for strength and coverage, yet is still very deliverable.
  • 6 cell design for maximum strength and coverage
  • 11F sheath compatibility
  • No shortening after expansion to 12 mm
  • Rounded edges minimize potential for lumen trauma

When compressive forces are putting the clinical situation at risk, reach for the IntraStent Max LD Stent
For additional product information please contact your regional sales representative.
The IntraStent peripheral stent is indicated for use in occlusions, lesions at high risk for abrupt closure or threatened closure following percutaneous transluminal angioplasty (PTA) or lesions believed to be at high risk of restenosis following PTA in the common iliac, external iliac, or subclavian arteries. Stenting is intended to improve and maintain artery luminal diameter.
Indications, contraindications, warnings and instructions for use can be found in the product labeling supplied with each device.