BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LONG 45 ENDOCUTTER

    MDR report key: 1040260 · Received April 28, 2008

    Report

    Report Number
    1527736-2008-02489
    Event Type
    Injury
    Date Received
    April 28, 2008
    Product Code
    GDW
    PMA / PMN Number
    K020779
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LONG 45 ENDOCUTTER GDW UNK

    Patients

    Seq Age Sex Outcome Treatment
    1