BEUDAMED
    FDA Adverse Event Other Summary report: N

    QUIK ABG KIT

    MDR report key: 241957 · Received September 22, 1999

    Report

    Report Number
    1718887-1999-00002
    Event Type
    Other
    Date Received
    September 22, 1999
    Date of Event
    July 1, 1999
    Report Date
    September 16, 1999
    Manufacturer
    MARQUEST MEDICAL PRODUCTS
    Product Code
    CBT
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    RESPIRATORY THERAPIST

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUIK ABG KIT ARTERIAL BLOOD GAS SAMPLING SYRINGE CBT MARQUEST MEDICAL PRODUCTS NA 116325

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other