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

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    Filters FDA Adverse Event ×

    AESTIVEA 7900

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA·Product code CBK·March 11, 2014

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·November 13, 2012

    CAPSURE

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2015

    Y-KNOT FLEX 1.3MM ALL-SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code MBI·September 19, 2017