BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TARGET DEVICE, HUMERUS T2 HUMERUS

    MDR report key: 3020044 · Received January 25, 2013

    Report

    Report Number
    0009610622-2013-00022
    Event Type
    Malfunction
    Date Received
    January 25, 2013
    Date of Event
    January 5, 2013
    Report Date
    January 10, 2013
    Manufacturer
    STRYKER TRAUMA GMBH
    Product Code
    LXH
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    36799 TARGET DEVICE, HUMERUS T2 HUMERUS INSTRUMENT LXH STRYKER TRAUMA GMBH KP195434

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown Other