BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PORTEX CUFF INFLATOR PRESSURE GAUGE

    MDR report key: 14014018 · Received April 5, 2022

    Report

    Report Number
    3012307300-2022-05828
    Event Type
    Malfunction
    Date Received
    April 5, 2022
    Date of Event
    January 1, 2022
    Report Date
    April 5, 2022
    Manufacturer
    NULL
    Product Code
    LNZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SW
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PRODUCT SMELLS BAD UPON OPENING. NO ADDITIONAL INFORMATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    906936 PORTEX CUFF INFLATOR PRESSURE GAUGE CHANGER, TUBE, ENDOTRACHEAL LNZ 4172506

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown