BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TRIGEN

    MDR report key: 1180102 · Received September 29, 2008

    Report

    Report Number
    1020279-2008-00261
    Event Type
    Injury
    Date Received
    September 29, 2008
    Date of Event
    August 26, 2008
    Report Date
    September 18, 2008
    Manufacturer
    SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.
    Product Code
    JDS
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE PATIENT UNDERWENT SURGICAL INTERVENTION DUE TO THE DRILL BIT BREAKING OFF IN THE NAIL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRIGEN INSTRUMENT JDS SMITH & NEPHEW, INC., ORTHOPAEDIC DIV. 02FM07122

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Hospitalization| R