BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1518293-1997-00002

    MDR report key: 98191 · Received June 11, 1997

    Report

    Report Number
    1518293-1997-00002
    Event Type
    Injury
    Date Received
    June 11, 1997
    Date of Event
    May 2, 1997
    Product Code
    DXT
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1