BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BABY-VAC

    MDR report key: 310702 · Received November 22, 2000

    Report

    Report Number
    MW4002918
    Event Type
    Malfunction
    Date Received
    November 22, 2000
    Date of Event
    November 1, 2000
    Report Date
    November 21, 2000
    Manufacturer
    CAG INT'L
    Product Code
    GCX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NJ, US
    Reporter Occupation
    NURSE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BABY-VAC HARD PLASTIC INFANT NASAL SUNCTIONING DEVICE AC GCX CAG INT'L NI NI

    Patients

    Seq Age Sex Outcome Treatment
    1 NA