Mikrokatheter

Vasco+

Intrazerebraler Mikrokatheter.

Merkmale

Mikrokatheter zur Verwendung mit Mikroführungsdrähten für die Applikation von Platin-Coils, Stents, Thrombektomiesystemen sowie zur Thrombusaspiration.

  • Progressiv gewebeverstärktes, hydrophil beschichtetes Kathetermaterial optimiert die Navigierbarkeit und garantiert Stabilität
  • Verfügbar als .017“ und .021“ Mikrokatheter
  • 2 röntgendichte Marker
  • Geeignet zum Coiling und für den Gebrauch mit dem Stetretriever Catch View
  • Applikation von Leo+ Stents und Silk Flow-Divertern
  • Als VASCO+ Aspi geeignet zur Aspiration von Thromben

 

Webseite

www.balt-corp.com

Spezifikationen
Kompatibel mit

Hybrid

Führungsdraht

Die Mikroführungsdrähte kombinieren einen distalen Nitinolkern und einen proximalen Stahlanteil.

Fargoline

Führungskatheter

Führungskatheter mit Drahtmantel zur optimalen Unterstützung von Mikrokathetern sowie der Aspiration während der Schlaganfalltherapie.
Das könnte Sie auch interessieren

RYVA / ANRYV

Y-Konnektoren

Verbindungsstück mit hoher Belastungsgrenze.

Leo+

Stent

Intrakranieller, selbstexpandierender Stent.

Catch View

Stentretriever

Zur Rekanalisation bei Patienten mit ischämischem Schlaganfall infolge eines intrakraniellen Gefäßverschlusses.
Produktvideo
Rechtliche Angaben

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.

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.

Produktanfrage
Datenschutzbestimmungen*
Was ist die Summe aus 3 und 4?