BEUDAMED
    FDA Adverse Event Injury Summary report: N

    6000027-1999-00002

    MDR report key: 234924 · Received August 4, 1999

    Report

    Report Number
    6000027-1999-00002
    Event Type
    Injury
    Date Received
    August 4, 1999
    Date of Event
    June 20, 1999
    Product Code
    LDF
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 Implant LDF

    Patients

    Seq Age Sex Outcome Treatment
    1