BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2182596-1997-00375

    MDR report key: 94240 · Received May 27, 1997

    Report

    Report Number
    2182596-1997-00375
    Event Type
    Injury
    Date Received
    May 27, 1997
    Date of Event
    May 16, 1997
    Product Code
    FTR
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1