BEUDAMED
    4 results · 62ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SKINPEN

    FDA Adverse Event
    Injury ·CROWN LABORATORIES, INC.·Product code QAI·August 24, 2022

    DIAMOND CROWN

    FDA Adverse Event
    Injury ·DRM RESEARCH LABORATORIES, INC.·Product code DZE·February 21, 2011

    ARTGLASS

    FDA Adverse Event
    Malfunction ·HERAEUS KULZER INC.·Product code DZN·December 10, 2002

    EVOLUT FX VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·May 29, 2024