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Relay®Pro

At Terumo Aortic, we follow your lead. That’s why our Relay® family of devices was adapted for excellent performance in every patient’s thoracic aorta.

New Dissection & Transection indications for Relay®Pro in the US. Now indicated to treat all thoracic pathologies.

Low profile without compromise

RelayPro offers a low profile system without compromising performance. The platform utilises the same stent design, materials and foundational Dual Sheath Technology of the proven Relay®Plus.

Sources of Reduction*
  • 38% profile reduction
    Graft material is a tight woven polyester

  • 14% profile reduction
    Optimised radiopaque marker positioning

  • 24% profile reduction
    New thin wall coiled primary introducer outer sheath

  • 21% profile reduction
    Reduction of inner sheath diameter

  • No change
    Identical stents to RelayPlus

  • No change
    Same suture and sewing method as both RelayPlus and TREO®

*Data on file at Terumo Aortic.

Flexible and stable from navigation to deployment

You can feel confident at each key step in the endovascular procedure with the advanced engineering of the Relay® aortic stent graft system.

Low profile delivery

Optimised weave pattern and radiopaque markers to reduce profile while maintaining stent-graft integrity and visualisation.

Wide range of bare stent and non bare stent options

A more personalised approach

The RelayPro system has a wide range of sizes and tapers allowing each patient access to the right solution, every time.

Mechanical advantage for enhanced precision

Forward and backward gear system enhances control and delivery of the stent-graft, in both directions.

Optimal Seal

RelayPro NBS uses an engineered Delivery System to deliver perpendicular landing and optimal stent-graft apposition at the inner curve. Optimised weave pattern and radiopaque markers to reduce profile while maintaining stent-graft integrity and visualisation.

Deployment Animation

Watch the RelayPro deployment animation

Product Disclaimer

Product availability subject to regulatory approval.

An EU Declaration of Conformity may be requested from regulatoryaffairsuk@terumoaortic.com

Instructions for Use

View the eIFU for more information on use, indications, contraindications, warnings/precautions and availability within your market.

Contact a representative 

Discuss your patient’s aortic repair or learn more about our solutions for every segment of the aorta.

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