BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STORZ STEINER ELECTROMECHANICAL MORCILLATOR

    MDR report key: 508019 · Received October 17, 2003

    Report

    Report Number
    508019
    Event Type
    Malfunction
    Date Received
    October 17, 2003
    Date of Event
    August 1, 2003
    Report Date
    September 1, 2003
    Manufacturer
    KARL STORZ ENDOSCOPY AMERICA, INC.
    Product Code
    HFG
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STORZ STEINER ELECTROMECHANICAL MORCILLATOR STORZ STEINER ELECTROMECHANICAL MORCILLATOR HFG KARL STORZ ENDOSCOPY AMERICA, INC. 20712020 *

    Patients

    Seq Age Sex Outcome Treatment
    1 NA