BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MOGEN CIRCUMCISION CLAMP

    MDR report key: 259871 · Received January 24, 2000

    Report

    Report Number
    6000008-2000-00001
    Event Type
    Malfunction
    Date Received
    January 24, 2000
    Date of Event
    November 2, 1999
    Report Date
    January 24, 2000
    Manufacturer
    E.G. MEDICON
    Product Code
    HFX
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MOGEN CIRCUMCISION CLAMP INSTRUMENT HFX E.G. MEDICON GL7021 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1