WavelinQ™ 4F EndoAVF System


Product Overview

WavelinQ™ 4F EndoAVF System
WavelinQ - W04200


Device Description

A flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes (e.g., straight, hockey stick). It is not intended solely for infusion, is not intended to access superselective small vessels, and does not include a transseptal needle. It may include a disposable percutaneous introduction set or shaft visualization electrodes. This is a single-use device.


Environmental Conditions

No Data Available


Device Sizes

  • Arterial Catheter Length, 50 Centimeters
  • Catheter Gauge: 4 French
  • Venous Catheter Length, 43 Centimeters
    • Arterial Catheter Length, 50 Centimeters
    • Catheter Gauge: 4 French
    • Venous Catheter Length, 43 Centimeters


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: PQK

    Device Name: Percutaneous Catheter For Creation Of An Arteriovenous Fistula For Hemodialysis Access

    Device Class: 2

    Physical State: The percutaneous catheter is generally constructed of synthetic materials such as plastic and introduced into the body using a guidewire. The catheter may be manufactured in multiple sizes to allow for the creation of a fistula in vessels of different sizes. The catheter may or may not be connected to a power source to deliver energy to the site of fistula creation. The catheter may incorporate additional technology to facilitate the alignment and connection between the artery and the vein.

    Definition: Percutaneous catheter for creation of an arteriovenous fistula for hemodialysis access. This device is a single use percutaneous catheter system that creates an arteriovenous fistula in the arm of patients with chronic kidney disease who need hemodialysis.

    Submission Type ID: 1

    Review Panel: CV

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: The catheter creates an arteriovenous fistula (AVF), which is a physical connection between an artery and an adjacent vein, by mechanical means or by delivering energy such as heat or radiofrequency (RF) energy. The fistula allows high-pressure blood from the artery to flow into the vein, which increases the size of the vein and allows needle access for hemodialysis.

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: Arteriovenous fistulas created in the blood vessels of the arm. These may include radiocephalic, brachiocephalic, brachiobasilic, and ulnar artery-ulnar vein fistulas.

    Regulation Number: 870.1252

    Third Party Flag: N

    Medical Specialty: CV


    Device Identifiers

    Device Id: 00801741182754

    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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