BEUDAMED
    FDA Adverse Event Injury Summary report: N

    YILIANKANG URIC ACID TEST KIT

    MDR report key: 17058309 · Received June 2, 2023

    Report

    Report Number
    MW5118118
    Event Type
    Injury
    Date Received
    June 2, 2023
    Date of Event
    May 16, 2023
    Report Date
    May 30, 2023
    Manufacturer
    E-LINKCARE MEDITECH CO., LTD
    Product Code
    LFQ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    ITEM WAS CONTAMINATED AND CAUSED INFECTION. HTTPS://WWW.AMAZON.COM/DP/B0B53JY1L2.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    675206 YILIANKANG URIC ACID TEST KIT ACID, URIC, ACID REDUCTION OF FERRIC ION LFQ E-LINKCARE MEDITECH CO., LTD PM900C

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Male Other