BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    4151094

    MDR report key: 4151094 · Received September 29, 2014

    Report

    Report Number
    4151094
    Event Type
    Malfunction
    Date Received
    September 29, 2014
    Date of Event
    May 12, 2014
    Report Date
    September 29, 2014
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US

    Patients

    Seq Age Sex Outcome Treatment
    1 3 MO