Zur Wiederherstellung der Durchblutung bei Patienten mit ischämischem Schlaganfall infolge eines intrakraniellen Gefäßverschlusses.

    [Bildquelle: © peter neu | neuezeiten-werbeagentur.de]

    Vorteile

    • Expansion bis zu 6 mm im Durchmesser.
    • Pusher mit neuem Design für eine verbesserte Navigation dank größerer Flexibilität.
    • Nitinol Laser-cut mit geschlossenem Zell-Design für optimale Behandlung.
    • Kontrollierte Verkürzung.
    • Der Längsschlitz ermöglicht die Expansion bis zu 6 mm im Durchmesser (bei der MAXI Ausführung uneingeschränkter Durchmesser) und die Kompression des Stent-Retrievers in kleinen Gefäßen.
    • Zusätzliche Marker. Verbesserte Sichtbarkeit & einfachere Lagebeurteilung.
    • Sichere Bestimmung der Gesamtlänge und der Arbeitslänge des Stent-Retrievers.
    • Das Verhalten des Stent-Retrievers im Körper ist einfach zu beobachten.
    • Zuverlässige Navigation.
    • Distaler und proximaler Zugang dank der Vasco+ Produktpalette.
    • Schlaganfallbehandlung 10 mm bis 50 mm.

    Technische Daten


    ArtikelnummerStentlänge (mm)Stentriever Ø (mm)Arbeitslänge (mm)Pusherlänge (cm)Anzahl RX Marker distalAnzahl RX Marker bodyAnzahl RX
    Marker proximal
    Kompatibilität Mikrokatheter
    CATCHVMINI1019410200301Vasco+10
    CATCHVMINI1524415200301Vasco+10
    CATCHVMINI2029420200301Vasco+10
    CATCHV2033520200332Vasco+18
    CATCHV3548535200382Vasco+18
    CATCHVMAXI3045630200392Vasco+21
    CATCHVMAXI40566402003152Vasco+21
    CATCHVMAXI50676502003122Vasco+21

     

    CATCHView is designed for use in the flow restoration of patients with ischemic stroke due to large intracranial vessel occlusion. It is indicated to restore blood flow in the neurovasculature of patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA), who fail IV t-PA therapy or as a supplement treatment of initiated IV t-PA therapy. The CATCHView thromboembolectomy device should only be used by physicians trained in interventional neuroradiology and treatment of ischemic stroke. Class III CE0297 in compliance with Medical Device Directive (MDD 93/42/EEC amended by 2007/47/ EC). Manufactured by BALT Extrusion. Carefully read the instructions for use before use. First CE marking:2018. VASCO+ Reinforced micro-catheters are intended: for injection of diagnostic or therapeutic products; to position pushable
    coils “SPIRALES” or detachable coils especially the ones of MDS « mechanical detachment system »; for the use of the selfexpanding stent LEO+ or SILK+. Class III CE0297 in compliance with Medical Device Directive (MDD 93/42/EEC amended by 2007/47/EC). Manufactured by BALT Extrusion. Carefully read the instructions for use before use. First CE marking:2004. The content of this document, in particular data, information, trademarks and logos are BALT S.A.S and affiliates’ sole property.
    Consequently, all representation and/ or reproduction, whether in part or in full, is forbidden and would be considered a violation of BALT S.A.S and affiliates’ copyrights and other intellectual proprietary rights ©2018 BALT S.A.S and affiliates all rights reserved. This document with associated pictures are non-contractual and are solely dedicated to healthcare professionals and BALT S.A.S and affiliates’ distributors. The products commercialized by BALT S.A.S or affiliates shall exclusively be used in accordance with the instructions for use included in the boxes.