BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROGAV WITH SHUNTASSISTANT 20

    MDR report key: 7084740 · Received December 5, 2017

    Report

    Report Number
    3004721439-2017-00001
    Event Type
    Malfunction
    Date Received
    December 5, 2017
    Date of Event
    October 26, 2017
    Report Date
    November 30, 2017
    Manufacturer
    CHRISTOPH MIETHKE GMBH & CO. KG
    Product Code
    JXG
    PMA / PMN Number
    K103003
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    AESCULAP INC. (IMPORTER) IS SUBMITTING THIS REPORT ON BEHALF OF CHRISTOPH MIETHKE GMBH & CO. KG (MANUFACTURER). EXEMPTION NUMBER: E2017044. MANUFACTURING SITE EVALUATION: EVALUATION ON-GOING.

    Description of Event or Problem · 0

    COUNTRY OF COMPLAINT: (B)(6). IT WAS REPORTED THAT THE VALVE IS NOT ADJUSTABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    864722 PROGAV WITH SHUNTASSISTANT 20 PRO GAV JXG CHRISTOPH MIETHKE GMBH & CO. KG FV413T 4504861209

    Patients

    Seq Age Sex Outcome Treatment
    1 Other