BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TEMPUS PRO

    MDR report key: 19895155 · Received August 2, 2024

    Report

    Report Number
    3003832357-2024-00590
    Event Type
    Malfunction
    Date Received
    August 2, 2024
    Date of Event
    July 25, 2024
    Report Date
    October 29, 2024
    Manufacturer
    REMOTE DIAGNOSTIC TECHNOLOGIES LTD.
    Product Code
    MHX
    UDI-DI
    05060472441058
    PMA / PMN Number
    K201746
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    UPDATED THE FOLLOWING REPORTED PROBLEM CODE, CONCLUSION CODE GRID, EVALUATION RESULTS CODE GRID, COMPONENT CODE GRID ORIGINALLY PROVIDED ON MFR REPORT NUMBER 3003832357-2024-00590.

    Description of Event or Problem · 0

    IT HAS BEEN REPORTED THAT THE DEVICE SCREEN GOES BLANK AND DOES NOT TURN ON.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    384141 TEMPUS PRO MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) MHX REMOTE DIAGNOSTIC TECHNOLOGIES LTD. 00-1026-R 05060472441058

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown