SURFLASH safety I.V. catheter


Product Overview

SURFLASH safety I.V. catheter
SURFLASH - SR*FNP2032


Device Description

A sterile, thin, flexible tube intended to be inserted into the peripheral vasculature of a patient to enable short-term (< 30 days) intravascular access; it is not intended to be advanced to the central vasculature. It typically includes dedicated accessories to facilitate catheter introduction/placement and function (e.g., connectors, injection ports, stylet and/or wings for fixation). It may be used for blood sampling, monitoring of blood pressure, to administer fluids, medication and/or for the injection of contrast media. This is a single-use device.


Environmental Conditions

  • Special Storage Condition, Specify
    • Stacking limit by 5, Keep away from sunlight, Fragile, handle with care, Keep dry
  • Special Storage Condition, Specify
    • Do not store at extreme temperature and humidity.

  • Device Sizes

  • Catheter Gauge 20 Gauge
  • Length: 1.25 Inch
    • Catheter Gauge 20 Gauge
    • Length: 1.25 Inch


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: FOZ

    Device Name: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: HO

    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: 880.5200

    Third Party Flag: Y

    Medical Specialty: HO


    Device Identifiers

    Device Id: 54987350709863

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 34987350709869

    Package Quantity: 4

    Package Discontinue Date: 8/29/2018 12:00:00 AM

    Package Status: Not in Commercial Distribution

    Package Type: N/A


    Device Id: 34987350709869

    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


    Device Id: 04987350709868

    Device Type: Unit of Use

    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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