Intrakranieller selbstexpandierender Nitinolstent
Das Stentsystem zur Behandlung breitbasiger intrakranieller Aneurysmen und intrakranieller Stenosen.
Vorteile
Technische Daten
Artikelnummer | Gefäßdurchmesser | Länge bei | Unconstrained Stent | Kompatibler Mikroführungskatheter | ||
---|---|---|---|---|---|---|
Leo+ baby 2,0 | LEO.2,0x12 LEO.2,0x18 LEO.2,0x25 | 1,5 - 2,5 | 12 18 25 | 2,7 | 8 12 16 | VASCO+10 |
Leo+ baby 2,5 | LEO.2,5x12 LEO.2,5x18 LEO.2,5x25 LEO.2,5x30 LEO.2,5x35 | 2,0 - 3,1 | 12 18 25 29 35 | 3,2 | 8 12 16 19 23 | VASCO+10 |
Leo+ baby 3,0 | LEO.3,0x12 LEO.3,0x18 LEO.3,0x25 LEO.3,0x35 | 2,5 - 3,6 | 12 18 35 35 | 3,8 | 9 13 16 24 | VASCO+10 |
Leo+ 3,5 | LEO.3,5X12 LEO.3,5X18 LEO.3,5X25 LEO.3,5X30 LEO.3,5X35 LEO.3,5X50
| 3,10 - 4,25 | 12 18 25 30 35 50 | 4,4 | 9 12 17 19 24 35 | VASCO+21 |
Leo+ 4,5 | LEO.4,5X15 LEO.4,5X20 LEO.4,5X25 LEO.4,5X30 LEO.4,5X40 LEO.4,5X50 LEO.4,5X75 | 4,25 – 5,30 | 15 21 26 30 40 51 75 | 5,4 | 12 15 18 21 28 37 55 | VASCO+25 |
Leo+ 5,5 | LEO.5,5X25 LEO.5,5X30 LEO.5,5X35 LEO.5,5X50 LEO.5,5X60 LEO.5,5X75 | 5,30 – 6,50 | 26 31 36 52 60 75 | 6,7 | 18 21 26 35 42 51 | VASCO+28 |
LEO+ and Leo+ Baby are self-expanding intracranial stents indicated for use in the treatment of intracranial aneurysms in association with embolization coils. 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 ©2017 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 and affiliates shall exclusively be used in accordance with the package inserts which have been updated and included in the boxes. LEO+ and LEO+ baby are class III CE marked (LNE/G-Med CE0459) according to the Medical Device Directive 93/42/EEC (Since 2007 for LEO+, since 2012 for LEO+ Baby).