BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR26000096-000

    MDR report key: 24945619 · Received April 21, 2026

    Report

    Report Number
    COR26000096-000
    Event Type
    No answer provided
    Date Received
    April 21, 2026
    Report Date
    April 6, 2026
    Product Code
    REU
    Report Source
    Manufacturer report
    Reporter Location
    NH, US
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    995021 REU

    Patients

    Seq Age Sex Outcome Treatment
    1 NA