Microcatheter

Vasco+

Intracerebral microcatheter.

Properties

Microcatheter for the application of platinum coils, stents, thrombectomy systems as well as for thrombus aspiration.

  • Progressive braiding along the catheter and hydrophilic coating optimizes navigability and guarantees stability
  • Available in .017" and .021"
  • 2 radiopaque markers
  • Suitable for coiling and for use with the Catch View stent retriever
  • Application of Leo+ stents and Silk Flow diverters
  • Suitable as VASCO+ Aspi for aspiration of thrombi

 

Website

www.balt-corp.com

Specifications
Relevant products

Hybrid

Guide wire

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

Fargoline

Guiding catheter

Guiding catheter with hydrophilic coating for optimal support of microcatheters as well as aspiration during stroke therapy.
Related products

RYVA / ANRYV

Y-Connectors

Y-Connector resistant to high pressure.

Leo+

Stent

Intracranial self-expanding stent.

Catch View

Stentretriever

For recanalization in patients with ischaemic stroke due to intracranial vessel occlusion.
Videos
Legal information

Vasco+ is a reinforced micro-catheter 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. The self-expandable SILK+ stents and SILK Vista Baby are designed for the treatment of intracranial aneurysms and should be used only by clinicians trained in the placement of intracranial stents. 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:2012. The self-expandable LEO+/LEO+ Baby stent is designed for the treatment of intracranial aneurysms in association with embolization coils. 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. French reimbursement codes 3101316 and 3171593.First CE marking:2007 (LEO+),2012 (LEO+Baby) CATCH+ and CATCHView are designed for use in the flow restoration of patients with ischemic stroke due to large intracranial vessel occlusion. They are indicated to restore blood flow in the neurovasculature of patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA), who fail IV t-PA therapy or as a supplement treatment of initiated IV t-PA therapy. The CATCH+ and CATCHView thromboembolectomy devices should only be used by physicians trained in interventional neuroradiology and treatment of ischemic stroke. 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:2012 (CATCH+), 2018 (CATCHView). The Optima Coil System is intended for use in the peripheral and neurovasculature to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels. Class III CE0297 in compliance with Medical Device Directive (MDD 93/42/EEC amended by 2007/47/EC).Manufactured by BALT USA LLC. Carefully read the instructions for use before use. French reimbursement code 3162217.First CE marking:2017. The Barricade Coil System (BCS) is intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae. The BCS is also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature. The device should only be used by physicians who have undergone pre-clinical training in all aspects of BCS procedures as prescribed by Balt. Class III CE0297 in compliance with Medical Device Directive (MDD 93/42/EEC amended by 2007/47/EC). Manufactured by BALT USA, LLC. Carefully read the instructions for use before use. First CE-Mark: 2012.

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