BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SYNTHES

    MDR report key: 1081214 · Received July 15, 2008

    Report

    Report Number
    1081214
    Event Type
    Injury
    Date Received
    July 15, 2008
    Date of Event
    May 23, 2008
    Report Date
    June 20, 2008
    Manufacturer
    SYNTHES
    Product Code
    JDS
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SYNTHES DISTAL FEMORAL NAIL JDS SYNTHES NA 5152-181

    Patients

    Seq Age Sex Outcome Treatment
    1 46 YR Required Intervention
    2 *