BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2214133-2012-00181

    MDR report key: 2843286 · Received November 22, 2012

    Report

    Report Number
    2214133-2012-00181
    Event Type
    Malfunction
    Date Received
    November 22, 2012
    Report Date
    February 29, 2012
    PMA / PMN Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    NOT APPLICABLE
    Health Professional
    N

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown