WOUNDEXPRESS IPC PUMP USA


Product Overview

WOUNDEXPRESS IPC PUMP USA
WOUNDEXPRESS - WE100P-USA


Device Description

A system used for the noninvasive treatment and prevention of venous disorders and sequelae such as oedema, deep vein thrombosis (DVT) and pulmonary embolism (PE). It functions by applying sequential pressure to a patient's legs to promote venous blood flow. It consists of a compression pump, control/timing mechanism, tubing and has pneumatic stockings, sleeves, or a suit with several chambers that inflate and deflate sequentially in a pattern beginning at the foot or ankle and continuing to chambers around the calf and thigh. In some systems, each chamber reaches the same pressure but at different times, while others apply greater pressure distally which gradually diminishes higher up.


Environmental Conditions

  • Handling Environment Atmospheric Pressure - millibar
    • 1060.00
    • 700.00
  • Handling Environment Humidity - Percent (%) Relative Humidity
    • 90.00
    • 15.00
  • Handling Environment Temperature - Degrees Celsius
    • 40.00
    • 5.00
  • Storage Environment Atmospheric Pressure - millibar
    • 1060.00
    • 500.00
  • Storage Environment Humidity - Percent (%) Relative Humidity
    • 95.00
    • 20.00
  • Storage Environment Temperature - Degrees Celsius
    • 70.00
    • -25.00

  • Device Sizes

  • Length: 270 Centimeter
  • Height: 150 Centimeter
  • Width: 130 Centimeter
    • Length: 270 Centimeter
    • Height: 150 Centimeter
    • Width: 130 Centimeter


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: JOW

    Device Name: Sleeve, Limb, Compressible

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    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: 870.5800

    Third Party Flag: Y

    Medical Specialty: CV


    Device Identifiers

    Device Id: 05051968042941

    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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