BEUDAMED
    FDA Adverse Event Other Summary report: N

    DORNIER SURGICAL FIBER

    MDR report key: 329520 · Received April 25, 2001

    Report

    Report Number
    9611812-2001-00001
    Event Type
    Other
    Date Received
    April 25, 2001
    Date of Event
    May 2, 2000
    Manufacturer
    DORNIER SURGICAL PRODUCTS, INC
    Product Code
    GEX
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    19333 DORNIER SURGICAL FIBER LASER FIBER GEX DORNIER SURGICAL PRODUCTS, INC HF0600DSSM *

    Patients

    Seq Age Sex Outcome Treatment
    1 *