BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Mygen V-1000 RF System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PAGEWRITER CARDIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMMUNOCAP ALLERGEN F20, ALMOND MODEL: 14-4179-01

    FDA 510(k)
    FDA Class 2 ·Immunology

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·June 20, 2013

    COULTER LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·July 1, 2011

    ITREL 3

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code LGW·September 29, 2008

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·November 10, 2021

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·January 15, 2026