Führungsdraht

Hybrid

Die Mikroführungsdrähte kombinieren einen distalen Nitinolkern und einen proximalen Stahlanteil.

Merkmale

Hybrid-Drähte sind die optimale Kombination aus Flexibilität sowie Dreh- und Schubeigenschaften. Mit dem .007“ Hybrid ist BALT der Hersteller des feinsten Führungsdrahtes der Welt. Proximal optimierter Edelstahl unterstützt die Drehstabilität und den Vorschub.

 

  • Distaler Nitinolkern ermöglicht eine sehr hohe Flexibilität für optimale Navigierbarkeit bei bester Formbeständigkeit der vorkonfigurierten Drahtspitzen (DA/J)
  • Einzigartige DA-Konfiguration (double angle) der Mikrodrahtspitze verfügbar
  • Erhältlich in den distalen Kalibern von .007″, .008“, .012“ und .014“
  • 300 cm-Wechseldrähte in .010“ und .012“ lieferbar

 

Webseite

www.balt-corp.com

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Rechtliche Angaben

HYBRID are guidewires designed to facilitate the insertion of catheters into intracranial vascular branches for diagnostic or therapeutic use. Class III CE0297 in compliance with Medical Device Directive (MDD 93/42/EEC amended by 2007/47/EC). Manufactured by BALT Extrusion SAS. Carefully read the instructions for use before use. Not reimbursed. First CE marking:2010. SONIC are braided micro-catheters 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 SAS. Carefully read the instructions for use before use. Not reimbursed. First CE marking: 2005. BALTACCI are micro-catheters intended for selective and hyperselective vascular catheterization for diagnostic and therapeutic purposes. Class III CE0297 in compliance with Medical Device Directive (MDD 93/42/EEC amended by 2007/47/EC). Manufactured by BALT EXTRUSION SAS. Carefully read the instructions for use before use. Not reimbursed. First CE marking: 1998. MAGIC are micro-catheters intended for selective and hyperselective vascular catheterization for diagnostic and therapeutic purposes. Class III CE0297 in compliance with Medical Device Directive (MDD 93/42/EEC amended by 2007/47/EC). Manufactured by BALT EXTRUSION SAS. Carefully read the instructions for use before use. Not reimbursed. First CE marking: 1998. VASCO+ are reinforced micro-catheters 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 self-expanding 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 SAS. Carefully read the instructions for use before use. Not reimbursed. First CE marking: 2004. COPERNIC are occlusion catheters indicated for use in the neurovasculature and peripheral system to temporarily stop or control blood flow, to treat vasospasmes and embolization of aneurysms with balloons. Class III CE0297 in compliance with Medical Device Directive (MDD 93/42/EEC amended by 2007/47/EC). Manufactured by BALT EXTRUSION SAS. Carefully read the instructions for use before use. Not reimbursed. First CE marking: 1998. The content of this document, in particular data, information, trademarks and logos is BALT SAS and affiliate’s sole property. © 2019 BALT SAS and affiliates, all rights reserved. All representation and/or reproduction, whether in part or in full, is forbidden and would be considered a violation of BALT SAS and 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.

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