BEUDAMED
    FDA Adverse Event Other Summary report: N

    FEMTO LDV

    MDR report key: 3843790 · Received May 24, 2014

    Report

    Report Number
    3005643720-2014-00022
    Event Type
    Other
    Date Received
    May 24, 2014
    Date of Event
    May 15, 2014
    Report Date
    May 23, 2014
    Manufacturer
    SIG AG, SURGICAL INSTRUMENT ENGINEERING
    Product Code
    HQF
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    VACUUM LOSS, INCOMPLETE FLAP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    309671 FEMTO LDV FEMTO LDV Z6 POWERPLUS HQF SIG AG, SURGICAL INSTRUMENT ENGINEERING

    Patients

    Seq Age Sex Outcome Treatment
    1