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.
1
Three-piece system
with a wide range of sizes, diameters and tapers
to customise to
the needs of each patient
2
Unique leave-behind sheath
detaches after delivery to allow for balloon or other access
3
Built-in flexibility and advanced fixation allows you to treat up to
75° of infrarenal angulation
4
Easy system removal
accomplished through advanced component design that eliminates
need
to recapture a top cap,
allowing for a quicker procedure
5
Proximal clasp for repositioning
during partial deployment
1
Three-piece system
with a wide range of sizes, diameters and tapers
to customise to
the needs of each patient
2
Unique leave-behind sheath
detaches after delivery to allow for balloon or other access
3
Built-in flexibility and advanced fixation allows you to treat up to
75° of infrarenal angulation
4
Easy system removal
accomplished through advanced component design that eliminates
need
to re-capture a top cap,
allowing for a quicker procedure
5
Proximal clasp for repositioning
during partial deployment
RESOURCES
Instructions For Use
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.
