BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2183541-1997-00060

    MDR report key: 97825 · Received June 13, 1997

    Report

    Report Number
    2183541-1997-00060
    Event Type
    Injury
    Date Received
    June 13, 1997
    Date of Event
    May 13, 1997
    Product Code
    ESW
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1