BEUDAMED
    FDA Adverse Event Other Summary report: N

    1 LIGACLIP ERCA

    MDR report key: 307632 · Received August 22, 2000

    Report

    Report Number
    307632
    Event Type
    Other
    Date Received
    August 22, 2000
    Date of Event
    July 19, 2000
    Report Date
    July 21, 2000
    Manufacturer
    ETHICON ENDO-SURGERY, INC.
    Product Code
    GDO
    Report Source
    User Facility report
    Reporter Location
    FL, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    ETHICON ER320 DID NOT FIRE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 1 LIGACLIP ERCA MULTI CLIP APPLIER GDO ETHICON ENDO-SURGERY, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Other