BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HAMILTON-C1

    MDR report key: 21011460 · Received December 24, 2024

    Report

    Report Number
    3016723884-2024-00016
    Event Type
    Malfunction
    Date Received
    December 24, 2024
    Date of Event
    November 26, 2024
    Report Date
    December 24, 2024
    Manufacturer
    HAMILTON MEDCIAL AG
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    NV, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    CUSTER CALLED AND SAID THEY HAD 232008, 246005, 285002, 232035 ERROR CODES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2280822 HAMILTON-C1 HAMILTON-C1 CBK HAMILTON MEDCIAL AG 1610010

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other