TREO® PRODUCT FAMILY

TREO® provides a wide range of endovascular device configurations to
address the abdominal anatomy of each individual patient.

CERTAINTY SIMPLIFIED. AND DELIVERED.

Experience steady reassurance from the moment you deliver TREO®.
It’s optimised to treat your patient’s unique aorta.


Two levels of confident fixation that enable treatment of up to 75° of neck angulation


Lock stent technology works to prevent modular disconnection


Unique leave-behind sheath to simplify the procedure


Optimised for performance


Thousands of configurations to accommodate breadth of patients


ENGINEERED FOR A PERSONAL APPROACH

Every feature of TREO® contributes to ideal performance in your endovascular procedure — and your patient’s abdominal aorta.

RESOURCES

Instructions For Use

TREO® IFU

Product Disclaimer

TREO®
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. TREO® is not approved in the United States.

TREOVANCE®
Available in: Europe, Asia Pacific, Latin America, Rest of World
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. TREOVANCE® is not approved in the United States.

TREO® AUI & Occluder
Available in: Europe, South America, Asia Pacific, Non-EU Africa
Certified by SGS (0120) according to MDD 93/42/EEC as amended 2007/47/EC. TREO® AUI & Occluder are not approved in the US.

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.