VIDA™ PTV Dilatation Catheter, 26mm x 4cm, 100cm catheter


Product Overview

VIDA™ PTV Dilatation Catheter, 26mm x 4cm, 100cm catheter
VIDA - VDA100264


Device Description

A sterile flexible tube with an inflatable balloon designed to perform plastic or restorative surgery on a cardiac valve, i.e., for the dilatation of atrioventricular, aortic, and pulmonary trunk valves. It is typically used for the percutaneous dilatation of commissural fusion in stenotic mitral valves and for annular, cuspal, and calcific nodular fractures, to improve cuspal mobility in adult calcific aortic stenosis, and for leaflet tearing in pulmonic valve stenosis. It may also be used for percutaneous balloon pericardiotomy. This is a single-use device.


Environmental Conditions

No Data Available


Device Sizes

  • Balloon Length, 4 Centimeters
  • Balloon Diameter, 26 Millimeters
  • Shaft Length, 100 Centimeters
    • Balloon Length, 4 Centimeters
    • Balloon Diameter, 26 Millimeters
    • Shaft Length, 100 Centimeters


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: OMZ

    Device Name: Pulmonary (Pulmonic) Valvuloplasty Catheters/Percutaneous Valvuloplasty Catheter

    Device Class: 2

    Physical State: The device is a catheter with a balloon tip.

    Definition: Catheter is used for Percutaneous Transluminal or balloon Valvuloplasty (PTV) of the pulmonary (pulmonic) valve. Used on patients with isolated pulmonary stenosis and also on patients with valvular pulmonary stenosis with other minor congenital heart disease that does not require surgical intervention.

    Submission Type ID: 1

    Review Panel: CV

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: Catheter contains a ballon at the distal end of the shaft. The catheter is inserted into the body and directed towards the pulmonary valve. Once the catheter is placed in the valve, the balloon is expanded which compresses and/or breaks the material causing stenosis.

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: The target area is the pulmonary valve of the heart.

    Regulation Number: 870.1250

    Third Party Flag: N

    Medical Specialty: CV


    Device Identifiers

    Device Id: 00801741090981

    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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