BEUDAMED
    FDA Adverse Event Summary report: N

    GENICON

    MDR report key: 6686560 · Received June 28, 2017

    Report

    Report Number
    MW5070794
    Date Received
    June 28, 2017
    Date of Event
    June 19, 2017
    Report Date
    June 28, 2017
    Manufacturer
    GENICON
    Product Code
    JOK
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    DURING LAPAROSCOPIC SURGERY, THE GENICON DISPOSABLE SCISSOR HANDPIECE FAULTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    454030 GENICON GENICON DISPOSABLE SCISSOR HAND JOK GENICON 17583-F

    Patients

    Seq Age Sex Outcome Treatment
    1