BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 415061 · Received August 29, 2002

    Report

    Report Number
    2183911-2002-00004
    Event Type
    Malfunction
    Date Received
    August 29, 2002
    Date of Event
    August 15, 2002
    Manufacturer
    CLARUS MEDICAL, LLC.
    Product Code
    GEX
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * GEX CLARUS MEDICAL, LLC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *