RELAY - Endovascular Device
From Endovascular
RELAY® endovascular devices are designed to help you achieve maximum precision and control in the thoracic aorta.
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Product Details
UNIQUELY INSPIRED FOR IDEAL PLACEMENT
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.
- Designed to respect the thoracic anatomy
- Dual sheath technology for accuracy and control
- Partial expansion allows for predictable and precise deployment
FLEXIBLE AND STABLE FROM NAVIGATION TO DEPLOYMENT
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.
1 DUAL SHEATH SYSTEM
allows for staged graft expansion and precise deployment
2 WIDE RANGE OF SIZES AND TAPERS
to provide the best solution for your patients
3 Designed to help you
MINIMISE ACCESS VESSEL TRAUMA
4 Optimal navigation to target landing site due to
PRE-CURVED INNER CATHETER
5 Performance zones offer you
PRECISE RADIAL LOAD FOR SEALING AND FIXATION
6 REINFORCED OUTER SHEATH
with hydrophilic coating
Product Disclaimer
RELAY®
Available in: Asia (China only)
RELAY®PLUS
Available in: United States, Latin America, Europe, Rest of World
Certified by SGS (0120) according to MDD93/42/EEC as amended 2007/47/EC. Caution: Federal Law (US) restricts this device to sale by or on the order of a physician.
RELAY®PLUS NBS
Available in: Latin America, Europe, Asia (except for Japan), Rest of World
Certified by SGS (0120) according to Council Directive 93/42/EEC as amended 2007/47/EC. Relay®NBS Plus is not approved in the US.
RELAY®PRO
Available in: Europe
Certified by SGS (0120) according to MDD 93/42/EEC as amended 2007/47/EC. Caution: Federal Law (US) restricts this device to investigational use only. RELAY®PRO is not approved in the United States or Japan.
CUSTOM MADE
Available in: Europe, South America, Asia Pacific, Non-EU Africa
Custom-made devices do not bear CE Mark. According to the medical device law, physician prescription is required. Custom-made option is not available in the United States. Delivery time: 3 weeks from physician design approval to operating room delivery.
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