Dispositivo de Revascularização Intracraniana KinG
A retentor de stent ou restabelecimento do caudal dispositivo para tratamento de doenças agudas acidente vascular cerebral isquémicoO sistema de tratamento de coágulos de sangue é um sistema de tratamento de coágulos de sangue, que captura e remove grandes coágulos das artérias intracranianas, restaurando rapidamente a perfusão.
O King Vascular Revascularization Device é um stent-based retrieval system designed to restore cerebral blood flow in patients presenting with acute ischemic stroke due to large intracranial vascular occlusion. Incorporating overlapping stent technology, King Vascular effectively captures e removes thrombus while reinvigorating cerebral perfusion—making it a rapid e inovador approach for neurovascular revascularization.
Overlapping Stent Construction
- Enhanced Clot Capture: The device’s multi-layer stent struts increase contact with thrombus, improving retrieval efficacy in large or tough clots.
- Optimized Vessel Conformability: Overlapping cells allow the stent to adapt closely to the tortuous geometry of intracranial arteries, ensuring stable engagement throughout the retrieval process.
Neurovasculature Compatibility
- Broad Anatomical Coverage: Suitable for the internal carotid artery (ICA), M1/M2 segments of the middle cerebral artery, basilare vertebral arteries.
- Dedicated Neurovascular Materials: Constructed to retain flexibility in smaller-caliber and curved intracranial vessels, reducing the risk of vessel trauma during navigation and retrieval.
Rapid & Innovative Clot Retrieval
- Seamless Deployment: Designed for rapid insertion and retrieval under fluoroscopic guidance, decreasing overall device manipulation.
- High Visibility Markers: Radiopaque markers along the stent struts ensure precise positioning and real-time feedback under angiography.
Flow Restoration
- Improved Patency: The stent lattice temporarily expands the occluded segment, promoting partial or complete flow restoration even before full clot retrieval.
- Multiphase Extraction: Operators can perform multiple passes if needed, targeting residual thrombus while maintaining cerebral perfusion.
- Enhanced Clot Capture: The device’s multi-layer stent struts increase contact with thrombus, improving retrieval efficacy in large or tough clots.
- Optimized Vessel Conformability: Overlapping cells allow the stent to adapt closely to the tortuous geometry of intracranial arteries, ensuring stable engagement throughout the retrieval process.
- Broad Anatomical Coverage: Suitable for the internal carotid artery (ICA), M1/M2 segments of the middle cerebral artery, basilare vertebral arteries.
- Dedicated Neurovascular Materials: Constructed to retain flexibility in smaller-caliber and curved intracranial vessels, reducing the risk of vessel trauma during navigation and retrieval.
- Seamless Deployment: Designed for rapid insertion and retrieval under fluoroscopic guidance, decreasing overall device manipulation.
- High Visibility Markers: Radiopaque markers along the stent struts ensure precise positioning and real-time feedback under angiography.
- Improved Patency: The stent lattice temporarily expands the occluded segment, promoting partial or complete flow restoration even before full clot retrieval.
- Multiphase Extraction: Operators can perform multiple passes if needed, targeting residual thrombus while maintaining cerebral perfusion.
Especificações do produto
Especificação | Detalhe / Valor |
Nome do produto | Dispositivo de Revascularização Intracraniana KinG |
Utilização prevista | Acute ischemic stroke treatment in large vessel occlusion (LVO), mechanical thrombectomy within intracranial arteries |
Device Type | Stent retriever or revascularization device with self-expanding design |
Material | Medical-grade nitinol (Nickel-Titanium) or cobalt-chromium alloy |
Mecanismo de implantação | Microcatheter-based insertion, typically 0.021”–0.027” ID |
Marcadores radiopacos | Distal and proximal markers for fluoroscopic visualization |
Length & Diameter Range | ~15–40 mm length, 3–6 mm diameter (depending on specific code) |
Compatibilidade | Guide catheter or sheath (≥ 5F–6F) for intracranial access, 0.014” wire guidance |
Esterilidade | Estéril, de utilização única |
Prazo de validade | ~3–5 years at 15–25 °C in sealed packaging |
Indicações clínicas | Large vessel occlusion in the anterior or posterior circulation, e.g., M1, M2, ICA terminus, basilar artery |
Contra-indicações | Extreme vessel tortuosity, advanced intracranial stenosis, known nickel allergy |
Matriz de tamanhos e encomendas
Device Diameter (mm) | Device Length (mm) | Microcatheter ID (inch) | Código do produto | Notas |
3.0 | 20 | 0.021" | KNG-3.0x20-021 | Smaller stent retriever for distal M2 or narrower vessels |
3.0 | 28 | 0.021" | KNG-3.0x28-021 | Extended length, same diameter |
4.0 | 20 | 0.021" | KNG-4.0x20-021 | Mid-range diameter, short retriever for M1 |
4.0 | 28 | 0.027" | KNG-4.0x28-027 | Longer device, larger microcatheter needed |
4.5 | 28 | 0.027" | KNG-4.5x28-027 | Wider diameter for proximal ICA or large M1 |
4.5 | 35 | 0.027" | KNG-4.5x35-027 | Extended coverage in wide vessel occlusions |
6.0 | 40 | 0.027" | KNG-6.0x40-027 | Largest diameter for basilar tip or wide ICA |