Balloon catheter

Copernic & Eclipse

Mono-lumen balloon catheters for remodeling, vasospasm therapy or temporary occlusion.

Properties

Unique mono-lumen balloons for stable remodelling in bifurcation geometries as well as sidewall aneurysms. Easy navigation and maximum support due to compatibility with .012"/.014" Hybrid wires.

 

  • SECLIPSE Hydrospeed Set (incl. Hybrid1214 microguidewire)
  • SCOPERNIC Hydrospeed Set (incl. Hybrid1214 microguidewire)
  • Fast inflation and deflation with high contrast mixtures (1/2)
  • DMSO-compatible

 

Website

www.balt-corp.com

Specifications
Relevant products

Hybrid

Guide wire

The microguidewires combine a distal nitinol core and a proximal steel component.
Related products

Eclipse 2L

Double-lumen balloon catheter

Double-lumen balloon catheter for remodeling, vasospasm therapy or temporary occlusion.

Copernic 2L

Double-lumen balloon catheter

For use in cerebral and peripheral vessels for remodeling and temporary occlusion.
Videos
Legal information

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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