BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRO-VENT PLUS ARTERIAL BLOOD GAS KIT

    MDR report key: 226813 · Received June 11, 1999

    Report

    Report Number
    1217052-1999-00017
    Event Type
    Injury
    Date Received
    June 11, 1999
    Date of Event
    May 1, 1999
    Manufacturer
    SIMS PORTEX INC.
    Product Code
    GJE
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRO-VENT PLUS ARTERIAL BLOOD GAS KIT TRAY, BLOOD COLLECTION GJE SIMS PORTEX INC. NA

    Patients

    Seq Age Sex Outcome Treatment
    1