BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LAPAROSCOPIC TISSUE MORCLTR

    MDR report key: 3043565 · Received April 9, 2013

    Report

    Report Number
    2210968-2012-06980
    Event Type
    Malfunction
    Date Received
    April 9, 2013
    Date of Event
    September 24, 2012
    Report Date
    June 14, 2024
    Manufacturer
    ETHICON INC.
    Product Code
    HET
    PMA / PMN Number
    K100280
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NL
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    148281 LAPAROSCOPIC TISSUE MORCLTR LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES) HET ETHICON INC. MT216539

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown