BEUDAMED
    FDA Adverse Event Other Summary report: N

    KARL STORZ

    MDR report key: 3162249 · Received April 26, 2013

    Report

    Report Number
    9610617-2013-00019
    Event Type
    Other
    Date Received
    April 26, 2013
    Manufacturer
    KARL STORZ GMBH & CO. KG
    Product Code
    FCL
    PMA / PMN Number
    K052680
    Report Source
    Manufacturer report

    Narratives

    Description of Event or Problem · 1

    (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    181693 KARL STORZ CALCULASE FCL KARL STORZ GMBH & CO. KG

    Patients

    Seq Age Sex Outcome Treatment
    1