BEUDAMED
    FDA Adverse Event Other Summary report: N

    KARL STORZ

    MDR report key: 3162223 · Received April 29, 2013

    Report

    Report Number
    2027009-2013-00015
    Event Type
    Other
    Date Received
    April 29, 2013
    Manufacturer
    KARL STORZ IMAGING
    Product Code
    FWF
    PMA / PMN Number
    K003325
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UNIT IS CURRENTLY BEING EVALUATED; FINAL ANALYSIS REPORT IS NOT YET AVAILABLE.

    Description of Event or Problem · 1

    PLEASE REFER IMPORTER REPORT # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    184655 KARL STORZ NONE FWF KARL STORZ IMAGING

    Patients

    Seq Age Sex Outcome Treatment
    1