BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HAMILTON-C1

    MDR report key: 18022764 · Received October 27, 2023

    Report

    Report Number
    0002937708-2023-00020
    Event Type
    Injury
    Date Received
    October 27, 2023
    Date of Event
    October 18, 2023
    Report Date
    October 27, 2023
    Manufacturer
    HAMILTON MEDCIAL AG
    Product Code
    CBK
    UDI-DI
    07630002800747
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    NV, US
    Reporter Occupation
    003

    Narratives

    Description of Event or Problem · 0

    VENT HAD MESSAGE OF 'LOST ALL OPTIONS' HAD 249011 AND 249013 ERROR CODES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2132512 HAMILTON-C1 HAMILTON-C1 CBK HAMILTON MEDCIAL AG 161001 07630002800747

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown Other