BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2242445-2001-00004

    MDR report key: 337407 · Received June 12, 2001

    Report

    Report Number
    2242445-2001-00004
    Event Type
    Injury
    Date Received
    June 12, 2001
    Date of Event
    March 26, 2001
    Product Code
    DYG
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    26894 DYG

    Patients

    Seq Age Sex Outcome Treatment
    1