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CEREBASE™ DA Guide Sheath
Go Distal... More Trackability for More Support1,2*
The Cerebase DA Guide Sheath is indicated for the introduction of interventional devices into the neurovasculature. It is designed for atraumatic vessel interaction with soft, compliant, and rounded distal edges and a highly flexible Dexterous (DEX) tip that can minimize direct vessel wall contact.1
(*) More trackability and more support than NeuronMax™, Infinity™, Shuttle™ and Fubuki™. More support than Ballast™.
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Features & Benefits
Dexterous (DEX) Tip. DEX Tip facilitates tight turns for enhanced tracking through challenging anatomy, gets closer to the target site.1,2,4
Engineered to secure distal access for geometric anchoring resulting in more procedural support1,2,3**. (**) More support than NeuronMax™, Infinity™, Shuttle™, Fubuki™ and Ballast™ when placed in a distal cervical position.
Designed for atraumatic vessel interaction with soft, compliant, and rounded distal edges and a highly flexible Dexterous (DEX) tip that can minimize direct vessel wall contact.1
Large inner diameter ID (.090”).1,4
More proximal shaft stiffness designed for arch support1***. (***) More shaft stiffness than NeuronMax™, Infinity™, Shuttle™, Fubuki™ and Ballast™.
Excellent**** kink resistance in a thin wall design.1 (****) More kink resistance than NeuronMax™, Infinity™, Shuttle™, Fubuki™, Ballast™.
Smooth dilator to catheter tip transition.1
8F short sheath compatible.1 The third-party trademarks used herein are the properties of their respective owners.
Specifications
| Catalog No. | ID | OD (compatible short sheath) | Usable Length |
|---|---|---|---|
| GS9080SD | 0.090" | 8F | 80cm |
| GS9090SD | 0.090" | 8F | 90cm |
| GS9095SD | 0.090" | 8F | 95cm |
References
1. Competitive Test Report 10364599, Rev 1, April 2020.
2. Competitive Test Report 103618595, Rev 2, April 2020.
3. Turk A, Manzoor MU, Nyberg EM, et al. J NeuroIntervent Surg (2012). doi:10.1136/neurintsurg-2011-010256 (1 of 6).
4. Competitive Test Report 103628641, Oct 2019 (EmboVac/LBC).
For product details such as indications, contraindications, warnings, and precautions, please consult the IFU.
150341-200818
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