BEUDAMED
    3 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PREMIUM PLUS CEEA 31 INSTR. W/TILT-TOP

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO·Product code GDW·February 6, 2013

    LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·December 16, 2010

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·July 23, 2014