Caution: Custom made devices are not available in the USA.
Fenestrated® TREO
Advancing Fenestrated Horizons
The Fenestrated TREO platform, based on the TREO® Abdominal Stent-Graft System, is a simple trimodular system.
The All-Encompassing Next Generation Fenestrated Endograft.
The Fenestrated TREO platform, based on the TREO Abdominal Stent-Graft System, is a simple trimodular system.
Reliable staged expansion for a controlled deployment
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Circumferential suture wraps
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Modified distal clasping to improve torque control
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Ability to cannulate from above and below
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Ability to reposition graft while partially deployed
Freedom to position fenestrations
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Up to 5 fenestrations
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Freedom to position stents and fenestrations as required
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Circumferential radiopaque marker for improved visualisation and alignment accuracy
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Ability to reposition graft while partially deployed
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Main body can allow up to 40mm of free space between springs for fenestration placement
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Fenestration sizes up to 12mm
Optimised stent configuration
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Fully configurable support positioning for optimal fenestration placement
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Additional sealing stents can be added to provide a longer proximal sealing zone
Ability to cannulate from above
Circumferential radiopaque marker for improved visualisation and alignment accuracy
Trusted low profile device
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Reducing ties mechanism allows graft repositioning until completely opened
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60cm low profile sheath with hydrophilic coating and flexible tip for easier navigation
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The clasp mechanism keeps control of deployment and allows precise placement with cranial and caudal adjustment before the bare stent is released
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The mechanical deployment provides controlled and stable stent-graft deployment
We are committed to delivering the best solution to meet the needs of your patient and your practice.
Tailored Design
The Custom Solutions programme provides you with options for patients that may require a custom approach.
Collaborative Service
Our team works hand in hand with you to deliver a customised solution for your patient.
Delivery: 6 weeks from design approval.
Caution: Custom Solutions are not available in the USA.
References
Data on File
Product Disclaimer
Custom made devices are specifically made in accordance with a written prescription of any person authorised by national law by virtue of that person’s professional qualifications; which gives (1) specific design characteristics provided under that person’s responsibility and (2) is intended for the sole use of a particular patient exclusively to meet their individual conditions and needs.
Custom made devices are not available in the US and availability is subject to local regulatory approval.
Instructions for Use
An IFU is provided with each custom device.
View the eIFU for more information on use, indications, contraindications, warnings/precautions and availability within your market.
Contact us
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