CATHETER 207F3 FREEZOR3 MED BLUE 7F


Product Overview

CATHETER 207F3 FREEZOR3 MED BLUE 7F
Freezor™ - 207F3


Device Description

A sterile, flexible device intended to be used as part of a cardiac tissue cryosurgical system to cryogenically ablate areas of the endocardium of a beating heart in the treatment of cardiac arrhythmias. It is intended to be introduced into the heart via venous access (e.g., femoral vein) and deliver pressurized liquid refrigerant (e.g., nitrous oxide) to its distal cooling segment to achieve extremely low temperatures through gas expansion; it typically includes sensors (e.g., temperature monitoring). This is a single-use device.


Environmental Conditions

  • Handling Environment Humidity - Percent (%) Relative Humidity
    • 85.00
    • N/A
  • Handling Environment Temperature - Degrees Fahrenheit
    • 136.00
    • -31.00
  • Special Storage Condition, Specify
    • Keep dry
  • Storage Environment Temperature - Degrees Fahrenheit
    • 86.00
    • 59.00

  • Device Sizes

  • Catheter Curve 53mm
  • Catheter Working Length: 108.0 Centimeter
  • Catheter Gauge: 7.0 French
  • Electrode spacing 2.5,5.0,2.5mm
  • Catheter Tip length 4mm
    • Catheter Curve 53mm
    • Catheter Working Length: 108.0 Centimeter
    • Catheter Gauge: 7.0 French
    • Electrode spacing 2.5,5.0,2.5mm
    • Catheter Tip length 4mm


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: LPB

    Device Name: Cardiac Ablation Percutaneous Catheter

    Device Class: 3

    Physical State: N/A

    Definition: This product code pertains to cardiac ablation catheters indicated for general indications, treatment of supraventricular tachycardia (svt) and ventricular tachycardia (vt). This product code excludes ablation catheters indicated for treatment of atrial flutter [product code oad] and atrial fibrillation [product code oae].

    Submission Type ID: 2

    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: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Device Identifiers

    Device Id: 00763000645335

    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


    GMDN ®. © GMDN Agency 2005-2024.
    Educational Resources
    Videos