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Si, sono un operatore sanitario
Note: Ai sensi e per gli effetti dell’Art. 76 D.P.R. 445/2000 consapevole della responsabilità e delle conseguenze civili e penali previste in caso di dichiarazioni mendaci e/o formazione od uso di atti falsi, nonché in caso di esibizione atti contenenti dati non più corrispondenti a verità e consapevole altresì che qualora emerga la non veridicità del contenuto della presente decadranno i benefici per i quali la stessa è rilasciata confermo di essere un OPERATORE SANITARIO.
I contenuti presenti in questo sito contengono informazioni rivolte agli operatori sanitari, in quanto si riferiscono a prodotti rientranti nella categoria dei dispositivi medici che richiedono l’impiego o l’intervento da parte di professionisti del settore medico-sanitario.
Choose the AAA proven solution as varied as your patients. The Endurant™ II system family of products provides the standard of care with a legacy of clinical success for the treatment of abdominal aortic aneurysm (AAA). For the past 5 years, the Endurant II stent graft system has been used in 1 out of 2 EVAR cases.* Only the Endurant II stent graft has the deep clinical experience and favorable clinical outcomes designed to treat both straightforward and challenging anatomy.
Select the low-profile, next-generation thoracic endovascular aortic repair (TEVAR) device, the Valiant Navion™ thoracic stent graft system. Leveraging more than 20 years of endovascular experience and the proven platforms of Endurant™ and Valiant™ stent graft systems, the Valiant Navion system brings enhanced control, improved vascular access and greater customization, and continues to deliver the conformability and accuracy you have come to expect. With its reimagined design, the Valiant Navion graft allows you the freedom to do more with a single TEVAR device and treat more patients with lesions of the descending thoracic aorta.†
Select the Valiant™ thoracic stent graft with the Captivia™ delivery system for your thoracic endovascular aortic repair (TEVAR) procedures. Designed to provide conformability, control, and accuracy, the stent graft system offers a broad set of options to treat a wide range of patient anatomies. With more than 100,000 patients treated worldwide,* the Valiant stent graft has a proven track record of success in treating all lesions of the descending thoracic aorta.
Provide transmural fixation of the endograft to the aorta with the Heli-FX™ EndoAnchor™ system. The Heli-FX EndoAnchor system enhances durability to the level of a surgical anastomosis and addresses concerns for future complications. One year data shows decreased neck dilatation, decreased Type Ia endoleak rates, and a significant increase in sac regression.1
Expand possibilities with the Reliant™ stent graft balloon catheter: the versatile, reliable, and conformable solution you need for stent graft procedures and temporary occlusion of the aorta and large vessels.
Precisely guide your next intervention with the TourGuide™ steerable sheath. The sheath can deflect up to 180° to facilitate the delivery of diagnostic and therapeutic devices to a wide variety of vessel takeoffs and challenging anatomical areas.†
The TourGuide steerable sheath is available for sale in the United States and Europe.
Achieve superior seal and tracking in straightforward and complex anatomies with the Sentrant™ introducer sheath.‡
Data on file at Medtronic.
Bench test data on file at Medtronic. Test data not indicative of clinical performance.
Bench test data on file at Medtronic. Data only valid on Sentrant™ Introducer Sheath sterilized via irradiation. Test data not indicative of clinical performance. Bench Test compared Cook Check-Flo™* Performer™* Introducer Sheath and Gore DrySeal™* Introducer Sheath 12F and 18F to Sentrant Introducer Sheath 12F and 18F sterilized via irradiation.
™* Third party brands are trademarks of their respective owners.
One Year Propensity Matched Comparison of EVAR in Hostile Neck Patients with and without EndoAnchors, presentation by Bart Muhs, MD, Veith 2016. Corelab was used to measure aneurysm diameters: dilatation was defined as the difference between 1-month and 12-month aortic neck diameters post-procedure.
Medtronic Italia S.p.A. Società soggetta ad attività di direzione e coordinamento da parte di Medtronic PLC.
Cap. soc. € 1.200.487,00 - Registro Imprese N. 281327 Tribunale Milano - R.E.A. N. 1275682 - Cod. Fisc./P.IVA 09238800156.
Sede Legale e Uffici Via Varesina, 162 Edificio Raimondi - 20156 Milano.