BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FOLEY CATHETER, 16 FR, 5CC

    MDR report key: 67967 · Received February 12, 1997

    Report

    Report Number
    9611710-1997-00028
    Event Type
    Injury
    Date Received
    February 12, 1997
    Date of Event
    December 30, 1996
    Manufacturer
    SITE-8040297 EUROMEDICAL
    Product Code
    KOD
    Report Source
    Manufacturer report
    Reporter Location
    NY, US

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FOLEY CATHETER, 16 FR, 5CC CATHETER KOD SITE-8040297 EUROMEDICAL PE516 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 *