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

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    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·February 5, 2014

    SEQUENT MENISCAL REPAIR DEVICE, CURVED NEEDLE, 3 IMPALNTS

    FDA Adverse Event
    Injury ·CONMED LINVATEC·Product code MBI·November 7, 2012

    ENDO GIA ROTICULATOR 60-3.5 SULU

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GDW·August 30, 2010