Aspiration Catheter

Titan 036 & 070

Indicated for the injection of intravascular liquids, the introduction of interventional devices into the peripheral and neurovascular system and/or the aspiration of soft emboli and thrombi from the arterial system, including the peripheral and neurovascular system.

Properties
  • Optimized balance between lumen diameter, proximal support and distal navigability
  • 12 transition zones to maximize distal flexibility
  • Hydrophilic coating on 90 cm

 

Website

www.balt-corp.com

Downloads
Specifications
Relevant products

Ballast

Long Sheath 6F .088”

To introduce interventional products into the peripheral, coronary, and neurovascular system.

IVA

(Long) Arterial introducer

Indicated for insertion of interventional and diagnostic instruments into the human vasculature (e.g. for femoral access).

DuraSheath

Percutaneous introducer sheath

Designed for insertion of interventional and diagnostic instruments into the human vasculature (e.g. for femoral access).
Related products

Catch View

Stentretriever

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

RYVA / ANRYV

Y-Connectors

Y-Connector resistant to high pressure.
Videos
Legal information

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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