BEUDAMED
    FDA Adverse Event Other Summary report: N

    FEMTO LDV Z6 POWERPLUS

    MDR report key: 3817520 · Received May 9, 2014

    Report

    Report Number
    3005643720-2014-00021
    Event Type
    Other
    Date Received
    May 9, 2014
    Date of Event
    April 10, 2014
    Report Date
    May 6, 2014
    Manufacturer
    SIE AG, SURGICAL INSTRUMENT ENGINEERING
    Product Code
    GEX
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    INCOMPLETE FLAP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    282054 FEMTO LDV Z6 POWERPLUS Z6 GEX SIE AG, SURGICAL INSTRUMENT ENGINEERING 510.003.006

    Patients

    Seq Age Sex Outcome Treatment
    1