BEUDAMED
    FDA Adverse Event Injury Summary report: N

    6000027-1997-00001

    MDR report key: 63602 · Received January 17, 1997

    Report

    Report Number
    6000027-1997-00001
    Event Type
    Injury
    Date Received
    January 17, 1997
    Date of Event
    November 24, 1996
    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