BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2520274-2013-062125

    MDR report key: 3329132 · Received September 6, 2013

    Report

    Report Number
    2520274-2013-062125
    Event Type
    Injury
    Date Received
    September 6, 2013
    Date of Event
    September 5, 2012
    Report Date
    August 8, 2013
    Manufacturer
    SYNTHES (USA)
    Product Code
    HRS
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA
    Reporter Occupation
    HEALTH PROFESSIONAL

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    443011 HRS SYNTHES (USA)

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention