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Terumo Aortic announces US FDA approval for Thoraflex Hybrid

Thoraflex Hybrid is the first of its kind device used in Frozen Elephant Trunk (FET) repair in the United States and was granted Breakthrough Device Designation by the FDA in 2020. Thoraflex Hybrid is a single use medical device combining a Gelweave polyester graft with a Nitinol self-expanding stent graft and is indicated for the […]

Terumo Aortic announces US FDA breakthrough device designation for RelayBranch

The RelayBranch Thoracic Stent-Graft System is implanted in patients with thoracic aortic arch pathologies requiring treatment that includes coverage of the innominate and left common carotid arteries. The purpose of the FDA’s Breakthrough Device Designation program is to fast-track the regulatory review process for certain medical technologies and device-led combination products that satisfy certain criteria; […]

Terumo Aortic announces launch and first commercial use of the Aortic Balloon device

The device assists physicians in the expansion of the aorta when using TREO and RELAY stent-grafts in endovascular aortic repair. Complementing our market leading product range of surgical and endovascular grafts, the Aortic Balloon is a low profile device with 10 F and offers exceptional inflation control and the broadest balloon diameter range, up to […]

Terumo Creates Global Group Music

The composition is based on the concept “Let’s respect the past, dream for the future, and open new doors together.” The track is composed by Mr. Akira Senju, a highly regarded Japanese composer and recipient of numerous awards and honors. Mr. Senju’s 35th anniversary album which was released on October 21 includes ‘TOGETHER’, one of […]

Terumo Aortic announces US FDA Approval for TREO endovascular device

TREO is the only device commercially available for endovascular aneurysm repair (EVAR) with dual proximal fixation and lock stent technology offering physicians the next advancement in endovascular device solutions. It is a three-piece design featuring in situ limb adjustability and provides a wide range of aortic device configurations to specifically address the anatomy of each […]

Terumo Aortic Announces US FDA Breakthrough Device designation for Thoraflex Hybrid device

The purpose of the FDA’s Breakthrough Device Designation program is to fast-track the regulatory review process for certain medical technologies and device-led combination products that satisfy certain criteria; these include providing a more effective treatment or diagnosis of life-threatening or irreversibly debilitating diseases or conditions. The aim of the program is to provide patients and […]

Terumo acquires Aortica Corporation

Terumo Corporation (TSE: 4543) today announced that it has decided to acquire Aortica Corporation, a U.S.-based company dedicated to advancing the science of personalised vascular therapy. Aortica has developed an automated case planning software known as AortaFit™, designed to precisely match fenestrations on an endograft with the unique locations of each individual patient’s branch arteries […]

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Fenestrated TREO Demo - Lukasz Siudmiak

Tuesday 23rd April: 10:30 - 11:30
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TREO Fit Mini-Symposia - Prof Vladimir Makaloski

Tuesday 23rd April: 13:30 - 14:30
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Fenestrated TREO Mini Symposium - Prof Van Herwaarden

Tuesday 23rd April: 15:00 - 16:00
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RelayBranch Demo - Lukasz Siudmiak

Tuesday 23rd April: 16:30 - 17:30
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Fenestrated TREO Demo - Lukasz Siudmiak

Wednesday 24th April: 10:30 - 11:30
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Thoracoflo Mini Symposium - Prof Sabine Wipper

Wednesday 24th April: 13:30 - 14:30
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Fenestrated TREO Demo - Lukasz Siudmiak

Wednesday 24th April: 15:00 - 16:00
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TEVAR Custom Made Demo - Lukasz Siudmiak

Wednesday 24th April: 16:30 - 17:30
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TEVAR Custom Made Demo - Lukasz Siudmiak

Thursday 25th April: 10:30 - 11:30
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