Intermediate Catheter


Product Overview

Intermediate Catheter
AXS VECTA 71 - INC-11129-125


Device Description

A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device.


Environmental Conditions

  • Special Storage Condition, Specify
    • Store in cool, dry, dark place.

  • Device Sizes

  • Length: 125.0 Centimeter
  • Lumen/Inner Diameter: 0.071 Inch
    • Length: 125.0 Centimeter
    • Lumen/Inner Diameter: 0.071 Inch


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: DQY

    Device Name: Catheter, Percutaneous

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: CV

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: N/A

    Regulation Number: 870.1250

    Third Party Flag: Y

    Medical Specialty: CV


    Code: NRY

    Device Name: Catheter, Thrombus Retriever

    Device Class: 2

    Physical State: N/A

    Definition: The device is intended to restore blood flow by removing thrombus/clots in patients experiencing ischemic stroke. The prior clearances in this category have been limited to simply identifying catheter placed in the peripheral, coronary, and neurovasculature. It is felt that this is a unique claim and should not be combined with previously cleared catheters under a general procode.

    Submission Type ID: 1

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: N/A

    Regulation Number: 870.1250

    Third Party Flag: N

    Medical Specialty: CV


    Code: QJP

    Device Name: Catheter, Percutaneous, Neurovasculature

    Device Class: 2

    Physical State: Percutaneous catheter for neurovasculature

    Definition: To provide vascular access to the neurovasculature for interventional or diagnostic procedures

    Submission Type ID: 1

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: Uses a catheter to provide access to the neurovasculature for interventional or diagnostic procedures

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: Neurovasculature

    Regulation Number: 870.1250

    Third Party Flag: N

    Medical Specialty: CV


    Code: DTL

    Device Name: Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 4

    Review Panel: CV

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: N/A

    Regulation Number: 870.4290

    Third Party Flag: N

    Medical Specialty: CV


    Code: DYB

    Device Name: Introducer, Catheter

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: CV

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: N/A

    Regulation Number: 870.1340

    Third Party Flag: Y

    Medical Specialty: CV


    Device Identifiers

    Device Id: 07613327459227

    Device Type: Primary

    DeviceId Issuing Agency: GS1

    Contains DI Number: N/A

    Package Quantity: N/A

    Package Discontinue Date: N/A

    Package Status: N/A

    Package Type: N/A


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