BEUDAMED
    FDA Adverse Event Injury Summary report: N

    WATER IONIZER

    MDR report key: 589071 · Received April 5, 2005

    Report

    Report Number
    MW1035113
    Event Type
    Injury
    Date Received
    April 5, 2005
    Report Date
    April 5, 2005
    Manufacturer
    ALP CHITO
    Product Code
    JRS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NJ, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    NEWSPAPER AD SAYS PRODUCT WAS FDA APPROVED. CUSTOMER CHECKED WITH FDA AND ALL IS FALSE. CO IS NOT EVEN REGISTERED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 WATER IONIZER * JRS ALP CHITO UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR Required Intervention