BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LAERDAL SUCTION UNIT

    MDR report key: 448061 · Received March 11, 2003

    Report

    Report Number
    MW1027853
    Event Type
    Malfunction
    Date Received
    March 11, 2003
    Report Date
    March 11, 2003
    Manufacturer
    LAERDAL MEDICAL CORP.
    Product Code
    BTA
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    THE BATTERY CHARGER CONNECTOR FOR THIS ITEM -MOLEX- CAN ALSO BE USED TO CONNECT A PHYSIO CONTROL LP300 DEFIBRILLATOR BATTERY CHARGER, AND VICE VERSA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LAERDAL SUCTION UNIT SUCTION APPARATUS. BTA LAERDAL MEDICAL CORP. SUCTION UNIT *

    Patients

    Seq Age Sex Outcome Treatment
    1 *