Thromboembolektomiesystem
Zur Wiederherstellung der Durchblutung bei Patienten mit ischämischem Schlaganfall infolge eines intrakraniellen Gefäßverschlusses.
Vorteile
Technische Daten
Artikelnummer | Stentlänge (mm) | Stentriever Ø (mm) | Arbeitslänge (mm) | Pusherlänge (cm) | Anzahl RX Marker distal | Anzahl RX Marker body | Anzahl RX Marker proximal | Kompatibilität Mikrokatheter |
---|---|---|---|---|---|---|---|---|
CATCHVMINI10 | 19 | 4 | 10 | 200 | 3 | 0 | 1 | Vasco+10 |
CATCHVMINI15 | 24 | 4 | 15 | 200 | 3 | 0 | 1 | Vasco+10 |
CATCHVMINI20 | 29 | 4 | 20 | 200 | 3 | 0 | 1 | Vasco+10 |
CATCHV20 | 33 | 5 | 20 | 200 | 3 | 3 | 2 | Vasco+18 |
CATCHV35 | 48 | 5 | 35 | 200 | 3 | 8 | 2 | Vasco+18 |
CATCHVMAXI30 | 45 | 6 | 30 | 200 | 3 | 9 | 2 | Vasco+21 |
CATCHVMAXI40 | 56 | 6 | 40 | 200 | 3 | 15 | 2 | Vasco+21 |
CATCHVMAXI50 | 67 | 6 | 50 | 200 | 3 | 12 | 2 | Vasco+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.