BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2182596-1997-00296

    MDR report key: 87897 · Received April 30, 1997

    Report

    Report Number
    2182596-1997-00296
    Event Type
    Injury
    Date Received
    April 30, 1997
    Date of Event
    April 10, 1995
    Product Code
    FTR
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FTR 1569000 3162-84-B, 3150-84-B

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN