BEUDAMED
    4 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CA-1000

    FDA Adverse Event
    Injury ·TOA MEDICAL ELECTRONICS·Product code GKP·January 6, 1997

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 15, 2013

    M2A-MAGNUM PF CUP 52ODX46ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 29, 2014

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011