BEUDAMED
    FDA Adverse Event Other Summary report: N

    KARL STORZ

    MDR report key: 503622 · Received December 4, 2003

    Report

    Report Number
    2020550-2003-00029
    Event Type
    Other
    Date Received
    December 4, 2003
    Date of Event
    November 17, 2003
    Manufacturer
    KARL STORZ GMBH & CO. KG
    Product Code
    FFK
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    NJ, US
    Reporter Occupation
    NURSE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KARL STORZ EHL PROBE FFK KARL STORZ GMBH & CO. KG 27080EA 24513

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other