BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    KARL STORZ

    MDR report key: 3193621 · Received June 21, 2013

    Report

    Report Number
    9610617-2013-00026
    Event Type
    Malfunction
    Date Received
    June 21, 2013
    Manufacturer
    KARL STORZ GMBH & CO. KG
    Product Code
    HIH
    PMA / PMN Number
    K882270
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    INSTRUMENT HAS NOT BEEN RETURNED FOR EVALUATION.

    Description of Event or Problem · 1

    (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    282554 KARL STORZ WORKING ELEMENT HIH KARL STORZ GMBH & CO. KG

    Patients

    Seq Age Sex Outcome Treatment
    1