Einsatzbereich Neuroradiologie | plus medica GmbH - plus medica

Intended for use in interventional radiology procedures in the vascular and neurovascular system for: the injection of diagnostic or therapeutic products, the insertion of compatible pushable coils or detachable coils, the insertion of compatible intracranial self-expandable stents, the insertion of compatible thromboembolectomy devices.

Advantages

Ease of trackability through the vasculature

  • Smooth navigation
    provided by the 4 transition zones of suppleness and the hydrophilic coating
  • Gentle access to tortuous anatomy
    allowed by the extra supple tip and enhanced with the soft version

Controlled supportive deliverability

  • Support for stenting
    improved by the coil support and 8 flat nitinol wires
  • Kink resistance
    thanks to a durable sleeve
  • Smooth deliverability
    ensured by the PTFE1 internal coating
  • Visibility
    2 gold radiopaque markers at 3 cm for coiling

    Technical data


    Reference

    Total length (mm)Extra supple part legth (mm)Super flexible part (mm)Flexible part (mm)Rigid part (mm)Proximal outer diameterDistal outer diameterInternal diameterNumber of ORX markersTip shape
    Gama17_D16005020018011702.5F (0.85mm)2.2F (0.74mm).017" (0.43mm)2Straight & shapeable
    Gama17_D_S160010023010011702.5F (0.85mm)2.2F (0.74mm).017" (0.43mm)2Straight & shapeable

    Components

    • a shaping mandrel
    • a pass valve (all references)

    Compatible with

    • Flow diverter: silk vista baby
    • Stent: leo+ baby*
    • Stentriever: catch+ mini & catchview mini*
    • Coils: optima*
    • Compatibility with DMSO4
    • Compatible with DMSO4

    *other devices compatible with a .017’’ microcatheter – check product labels
    4Dymethyl sulfoxide

     

     

    The Gama reinforced microcatheters are intended for use in interventional radiology procedures in the vascular and neurovascular system for: the injection of diagnostic or therapeutic products, the insertion of compatible pushable coils or detachable coils, the insertion of compatible intracranial self-expandable stents, the insertion of compatible thrombo-embolectomy devices. 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-Mark: 2019. 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 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. First CE marking: 2007 (LEO+), 2012 (LEO+ Baby). The self-expandable SILK Vista Baby are designed for the treatment of intracranial aneurysms. 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 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. First CE marking: 2017. 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.