Aspirationskatheter

Titan 036 & 070

Indiziert für die Injektion von intravaskulären Flüssigkeiten, die Einführung von interventionellen Devices in das periphere und neurovaskuläre System und/oder die Aspiration von weichen Embolien und Thromben aus dem arteriellen System, einschließlich des peripheren und neurovaskulären Systems.

Merkmale
  • Optimierte Balance zwischen Lumen-Durchmesser, proximaler Support und distaler Navigierbarkeit
  • 12 Übergangszonen zur Maximierung der Flexibilität des distalen Bereiches
  • Hydrophile Beschichtung auf 90 cm

 

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Kompatibel mit

Ballast

Lange Schleuse 6F .088"

Zur Einführung von interventionellen Produkten in das periphere, koronare und neurovaskuläre System.

IVA

(Langes) Arterielles Einführbesteck

Zum Einführen interventioneller und diagnostischer Instrumente in das menschliche Gefäßsystem (z.B. für femorale Zugänge).

DuraSheath

Perkutanes Einführbesteck

Zum Einführen interventioneller und diagnostischer Instrumente in das menschliche Gefäßsystem entwickelt (z.B. für femorale Zugänge).
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Catch View

Stentretriever

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

RYVA / ANRYV

Y-Konnektoren

Verbindungsstück mit hoher Belastungsgrenze.
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Rechtliche Angaben

The TITAN™ 036 Catheter is indicated for general intravascular use, including the neuro and peripheral vasculature. It can be used to facilitate introduction of diagnostic and therapeutic agents. It is not intended for use in coronary arteries. The TITAN 070 Catheter is indicated for injection of intravascular fluids, the introduction of interventional devices into the peripheral and neuro vasculature, and removal/aspiration of soft emboli and thrombi from the arterial system, including the peripheral and neurovasculature. The TITAN™ Catheter System Kit is indicated for injection of intravascular fluids, the introduction of interventional devices into the peripheral and neuro vasculature, and removal/aspiration of soft emboli and thrombi from the arterial system, including the peripheral and neuro vasculature. 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. Not reimbursed. First CE marking:2019. The ballast 088 Long Sheath is indicated for the introduction of interventional devices into the peripheral, coronary and neuro vasculature. 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. Not reimbursed. First CE marking:2018. 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. Carefully read the instructions for use before use. Not reimbursed. First CE marking: 2004. 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 Ballast 088 Long Sheath is indicated for the introduction of interventional devices into the peripheral, coronary, and neuro vasculature. 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. Not reimbursed. First CE marking: 2018.

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