Radiant™ Balloon-Expandable Covered Stent

The only covered stent indicated for ChEVAR, Radiant stent is used in combination with the Endurant™ II/IIs stent graft system to safely and effectively lengthen aortic proximal sealing zones in juxtarenal aortic abdominal aneurysms (jAAA).  

Overview

Product details

Indicated. Tested. Proven. Safe and effective in ChEVAR.

  • The only covered stent tested and approved for ChEVAR indication with the Endurant II/IIs stent graft system.
  • Radiant covered stent shows significantly better performance in ChEVAR compared to other stent grafts, with 94.6% patency at mid-term follow-up.1
  • EnChEVAR with Endurant II/IIs system + Radiant covered stent demonstrates durable clinical outcomes.2

Predictable, accurate delivery and deployment.

  • Radiopaque markers ensure accurate placement of stent graft during deployment.
  • Radiant stent's open-cell stent design provides flexibility in delivery and placement.
  • Designed to track through torturous arteries and flex to accommodate the renal anatomy.
  • Low profile offers versatility and effective delivery in complex endovascular procedures.

Designed for radial strength and versatility.

  • Radial strength of the stent design maintains vessel patency in ChEVAR.
  • Designed to bend to accommodate and fit the renal anatomy during use with Endurant II/IIs system in ChEVAR.
  • Ability to post-dilate allows a customized solution to various anatomy.
  1. Full stent encapsulation with PTFE material offers an effective barrier to neointimal hyperplasia.
  2. Open-cell stent design provides flexibility in delivery and placement.
  3. Gold radiopaque marker.
  4. Radiopaque markers ensure accurate placement of stent during deployment.
  5. Radial strength of stent design maintains vessel patency.
  6. No FEP (fluorinated ethylene propylene) adhesive for uniform deployment without delamination.
Radiant balloon-expandable covered stent with numbers calling out product features

Features and benefits

Proven, safe, and effective way to lengthen aortic sealing zones

Learn how EnChEVAR with Endurant II/IIs system + Radiant stent provides durable outcomes in challenging hostile sealing zones.

EnChEVAR deployment

Step-by-step deployment of the Endurant II/IIs and Radiant stent grafts for ChEVAR.

Model specifications

Radiant stent graft sizing guidelines

Renal native diameter (mm)

Recommended Radiant diameter (mm)

5.4–6.2 6
6.3–7.2 7

Radiant stent graft size configurations

Diameter (mm)

Stent length (mm)

Catheter length (mm)

Catheter outer diameter (Fr)

6 22 120  6
6 32 120  7
6 38 120  7
6 59 120  7
7 22 120  7
7 32 120  7
7 38 120  7
7 59 120  7

Use this tool to see full ordering information and plan case specifics such as sizing and placement.

Aortic catalog

Choose from a complete portfolio of market-leading aortic vascular therapies to treat aneurysm disease.

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References

1

Pitoulias GA, Torsello G, Austermann M, et al. Outcomes of elective use of the chimney endovascular technique in pararenal aortic pathologic processes. J Vasc Surg. February 2021;73(2):433-442.

2

Donas KP, Torsello GB, Piccoli G, et al. The PROTAGORAS study to evaluate the performance of the Endurant stent graft for patients with pararenal pathologic processes treated by the chimney/snorkel endovascular technique. J Vasc Surg. January 2016;63(1):1-7.

Brief statement: See the device manual for detailed information regarding the instructions for use, the implant procedure, indications, contraindications, warnings, precautions, and potential adverse events. For further information, contact your local Medtronic representative and/or consult the Medtronic website at medtronic.eu. For applicable products, consult instructions for use on www.medtronic.com/manuals. Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser.

Important Reminder: This information is intended only for users in markets where Medtronic products and therapies are approved or available for use as indicated within the respective product manuals. Content on specific Medtronic products and therapies is not intended for users in markets that do not have authorization for use.