BEUDAMED
    FDA Adverse Event Injury Summary report: N

    IMHS

    MDR report key: 1023362 · Received April 2, 2008

    Report

    Report Number
    8010764-2008-00005
    Event Type
    Injury
    Date Received
    April 2, 2008
    Report Date
    March 26, 2008
    Manufacturer
    SMITH & NEPHEW ORTHOPAEDICS, GMBH
    Product Code
    JDS
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NL
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE PT UNDERWENT REVISION DUE TO THE NAIL BREAKING DURING FRACTURE HEALING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IMHS INTERNAL FIXATION - NAIL JDS SMITH & NEPHEW ORTHOPAEDICS, GMBH 05LT93585

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Hospitalization| R