BEUDAMED
    FDA Adverse Event Other Summary report: N

    LLETZ LOOP

    MDR report key: 281387 · Received June 9, 2000

    Report

    Report Number
    2428235-2000-00002
    Event Type
    Other
    Date Received
    June 9, 2000
    Date of Event
    February 25, 2000
    Report Date
    June 9, 2000
    Manufacturer
    ELLMAN INTERNATIONAL INC.
    Product Code
    JOS
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    PT RECEIVED SHOCK DURING LEEP PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LLETZ LOOP ELECTRODE JOS ELLMAN INTERNATIONAL INC. W3 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 23 YR Other