BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9612164-2011-00053

    MDR report key: 2061476 · Received March 16, 2011

    Report

    Report Number
    9612164-2011-00053
    Event Type
    Malfunction
    Date Received
    March 16, 2011
    Date of Event
    February 10, 2011
    Report Date
    February 16, 2011
    Manufacturer
    MEDTRONIC IRELAND
    PMA / PMN Number
    P060033
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown UNK.