Smoke Tubing, Canister, Fluid Trap


Product Overview

Smoke Tubing, Canister, Fluid Trap
Neptune - 0703-045-100


Device Description

A screening device installed within the suction tubing line of a suction system, or the suction tubing used with a central vacuum system, to extract particulates from the plume of smoke created typically through the use of various tissue-burning surgical devices (e.g., laser, electrosurgical diathermy device), to prevent clogging of the suction or vacuum system. It will typically have a hydrophobic membrane that retains the particulate/bacterial pathogens through a combination of mechanical, electrostatic, or other means. The device comes in various sizes and designs and can be made of translucent plastic, allowing for inspection when in use. This is a single-use device.


Environmental Conditions

  • Handling Environment Atmospheric Pressure - KiloPascal
    • 106.00
    • 78.00
  • Handling Environment Humidity - Percent (%) Relative Humidity
    • 75.00
    • 30.00
  • Handling Environment Temperature - Degrees Celsius
    • 35.00
    • 10.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: QGI

    Device Name: Air-Handling Apparatus Accessory

    Device Class: 1

    Physical State: The accessory are made from metal or hard plastic that are either located within the parent device or on the peripheral of the parent device.

    Definition: An air-handling apparatus accessory is a supplementary device that is intended to be used with an air-handling apparatus for a surgical operating room. This device provides an interface between the components of the device or can be used to switch electrical power. This generic type of device includes fittings, adapters, couplers, remote switches, and footswitches.

    Submission Type ID: 4

    Review Panel: HO

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: The accessory devices provide an interface between the components of the parent device. These devices are much less complex in nature than the parent device or other components which provide the surgical exhaust mechanism or conduit.

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: NA

    Regulation Number: 878.5080

    Third Party Flag: N

    Medical Specialty: SU


    Device Identifiers

    Device Id: 57613327471514

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 37613327471510

    Package Quantity: 2

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: case


    Device Id: 37613327471510

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 07613327471519

    Package Quantity: 5

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: pack


    Device Id: 07613327471519

    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® is a registered trademark of The GMDN Agency. All rights reserved. The information provided on this site includes data supplied by The GMDN Agency ("GMDN Content"), which is used under licence from The GMDN Agency. Any data/information suppliers who wish to extract GMDN Content from this site in order to use it as a basis for creating and supporting commercial services such as alternative categorisation, alternative GMDN Term assignment, mapping to other categorisations or ontologies, or for AI training purposes, must first obtain an appropriate licence from The GMDN Agency. No such activity is permitted without a licence. For more information on obtaining a licence, please contact The GMDN Agency (https://www.gmdnagency.org/contact-us/). None of the GMDN content constitutes any endorsement, advice, representation or warranty about any specific medical devices that may be described by such content; and no representation or warranty is made in relation to instructions for use, suitability for any application, treatment or condition, regulatory status, or any properties of a particular medical device.

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