BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LMB

    MDR report key: 210669 · Received February 17, 1999

    Report

    Report Number
    2021791-1999-00001
    Event Type
    Injury
    Date Received
    February 17, 1999
    Date of Event
    January 5, 1999
    Manufacturer
    DEROYAL INDUSTRIES, INC.
    Product Code
    ITW
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LMB ITW DEROYAL INDUSTRIES, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1