BEUDAMED
    FDA Adverse Event Other Summary report: N

    MYNX GRIP

    MDR report key: 25175592 · Received May 14, 2026

    Report

    Report Number
    MW5188262
    Event Type
    Other
    Date Received
    May 14, 2026
    Date of Event
    May 5, 2026
    Report Date
    May 12, 2026
    Manufacturer
    CORDIS US CORP.
    Product Code
    MGB
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    MYNX CLOSURE DEVICE FAILED. COLLAGEN PORTION DIDN'T FEED PROPERLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    153322 MYNX GRIP DEVICE, HEMOSTASIS, VASCULAR MGB CORDIS US CORP. F2532902

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other