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

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    Filters FDA Adverse Event ×

    8.0M PINNACLE3

    FDA Adverse Event
    Injury ·PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.·Product code MUJ·March 1, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWP·August 8, 2014