BEUDAMED
    FDA Adverse Event Other Summary report: N

    GETINGE VASOVIEW HEMOPRO

    MDR report key: 17011097 · Received May 25, 2023

    Report

    Report Number
    MW5117918
    Event Type
    Other
    Date Received
    May 25, 2023
    Date of Event
    May 23, 2023
    Report Date
    May 23, 2023
    Manufacturer
    MAQUET CARDIOVASCULAR LLC.
    Product Code
    GEI
    Report Source
    Voluntary report
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    VASOVIEW HEMOPRO DEVICE BROKEN WHILE CAUTERIZING IN PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    650217 GETINGE VASOVIEW HEMOPRO ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI MAQUET CARDIOVASCULAR LLC. VASOVIEW HEMOPRO

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Male