BEUDAMED
    FDA Adverse Event Other Summary report: N

    IODOSORB

    MDR report key: 20312312 · Received September 25, 2024

    Report

    Report Number
    MW5160142
    Event Type
    Other
    Date Received
    September 25, 2024
    Date of Event
    September 23, 2024
    Report Date
    September 23, 2024
    Manufacturer
    UNKNOWN
    Product Code
    KOZ
    Report Source
    Voluntary report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    DID NOT WORK FOR THE PATIENT. PAE REPORTED BY HCPO, NO CONSENT TO FOLLOW UP. NO FURTHER INFORMATION/CLARIFICATION AVAILABLE. (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1052914 IODOSORB BEADS, HYDROPHILIC, FOR WOUND EXUDATE ABSORPTION KOZ UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown