Sonic
Intrazerebraler Mikroinfusionskatheter
DMSO-kompatibler gewebeverstärkter Mikrokatheter mit FuseCath ablösbarer Katheterspitze.
[Bildquelle: © peter neu | neuezeiten-werbeagentur.de]
Vorteile
- Gewebeverstärkt für die Verwendung mit DMSO-basierenden Embolisaten.
- Kompatibel mit .007" Mikroführungsdraht HYBRID007.
- Patentierte FuseCath Katheterspitze ablösbar nach Blockierung durch Embolisatreflux.
- Verfügbar in Längen von 165 cm bis 190 cm als 1,2F bis 1,5F-Mikrokatheter.
Technische Daten
| Artikelnummer | Totale Länge (cm) | Distale Spitze O.D. | Distale Spitze I.D. (mm) | Fusecath Länge (cm) | Füllvolumen mit Adapter | Füllvolumen ohne Adapter | Max. Reflux Squid / Onyx (cm) | Enthaltener Führungsdraht |
|---|---|---|---|---|---|---|---|---|
| SONIC1.2F15 | 167 | 1,2F | 0,23 | 1,5 | 0,24 | 0,28 | 2 | .007" |
| SONIC1.2F25 | 167 | 1,2F | 0,23 | 2,5 | 0,25 | 0,29 | 3 | .007" |
| SONIC1.2F35 | 167 | 1,2F | 0,23 | 3,5 | 0,25 | 0,29 | 4 | .007" |
| SONIC1.2F25.190 | 190 | 1,2F | 0,23 | 2,5 | 0,28 | 0,32 | 3 | .007" |
| SONIC1.5F15 | 167 | 1,5F | 0,30 | 1,5 | 0,26 | 0,30 | 2 | .008" |
| SONIC1.5F25 | 167 | 1,5F | 0,30 | 2,5 | 0,26 | 0,30 | 3 | .008" |
| SONIC1.5F35 | 167 | 1,5F | 0,30 | 3,5 | 0,25 | 0,29 | 4 | .008" |
SONIC is a reinforced microcatheter intended for selective and hyper selective vascular catheterization for diagnostic or therapeutic purposes. 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 instruction of use before use. First CE marking: 2012.SQUID/SQUIDPeri is a non-adhesive liquid embolic agent indicated in the embolization of lesions in the peripheral and neurovasculature. Class III CE0297 in compliance with Medical Device Directive (MDD 93/42/EEC amended by 2007/47/EC) Manufactured by EMBO-FLUSSIGKEITEN AG. Route des Avouillons, CH 1196 GLAND, Switzerland. First CE marking: 2012.SPIF, flow coils intended for the embolization of vascular malformations of the vasculature. 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: 2008.The content of this document, in particular data, information, trademarks and logos is BALT SAS’s and affiliates sole property. © 2018 BALT and its affiliates, all rights reserved. Consequently, all representation and/or reproduction, whether in part or in full, is forbidden and would be considered a violation of BALT SAS and its affiliates’ copyrights and other intellectual proprietary rights. This document with associated pictures is non-contractual and is solely dedicated to healthcare professionals and BALT’s distributors (BALT’s supplier’s distributors). The products commercialized by BALT shall exclusively be used in accordance with the instructions for use included in the boxes.