Ballonkatheter

Copernic & Eclipse

Mono-Lumen-Ballonkatheter zum Remodeling, zur Vasospasmustherapie oder zur temporären Okklusion.

Merkmale

Einzigartige Mono-Lumen-Ballone zum stabilen Remodelling in Bifurkationsgeometrien sowie bei Seitwandaneurysmen. Einfache Navigation und maximaler Support durch die Kompatibilität mit den .012“/.014“ Hybrid-Drähten.

 

  • SECLIPSE Hydrospeed Set (inkl. Mikroführungsdraht Hybrid1214)
  • SCOPERNIC Hydrospeed Set (inkl. Mikroführungsdraht Hybrid1214)
  • Schnelle Inflation und Deflation bei hohen Kontrastmittel-Mischungen (1/2)
  • DMSO-kompatibel

 

Webseite

www.balt-corp.com

Spezifikationen
Kompatibel mit

Hybrid

Führungsdraht

Die Mikroführungsdrähte kombinieren einen distalen Nitinolkern und einen proximalen Stahlanteil.
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Eclipse 2L

Ballonkatheter

Doppel-Lumen-Ballonkatheter zum Remodeling, zur Vasospasmustherapie oder zur temporären Okklusion.

Copernic 2L

Doppel-Lumen-Ballonkatheter

Zur Anwendung beim Remodeling und temporärer Okklusion in zerebralen und peripheren Gefäßen.
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Rechtliche Angaben

COPERNIC and ECLIPSE are occlusion catheters indicated for use in the neurovasculature and peripheral system to temporarily stop or control blood flow, to treat vasospasms 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, 10 rue de la Croix Vigneron, 96160 Montmorency, France. Carefully read the instructions for use before use. First CE marking: 2001 (COPERNIC), 2006 (ECLIPSE). HYBRID guidewires are 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. First CE marking: 2010. The guiding catheter FARGO is intended to facilitate the introduction of micro-catheters for therapeutic and diagnostic 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. First CE marking: 2009.

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