BEUDAMED
    7 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 3, 2013

    FEMOSTOP

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS, INC.·Product code MGB·November 21, 2003

    LOW PROFILE CROSSLINK SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 30, 2015

    PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·April 3, 2013

    3003496686-2011-16856

    FDA Adverse Event
    Injury ·March 24, 2011

    CUSTOM KIT

    FDA Adverse Event
    Other ·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·April 24, 2008

    FEMOSTOP

    FDA Adverse Event
    Injury ·RADI MEDICAL SYSTEMS·Product code DXC·August 20, 2003