BEUDAMED
    6 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DEPUY/CMW 2G

    FDA Adverse Event
    Injury ·DEPUY CMW - 9610921·Product code LOD·December 27, 2019

    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

    PFC SIG RPF CEM FEM SZ 4 RT

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS1219655·Product code NJL·September 16, 2014

    Y-KNOT FLEX 1.3MM ALL-SUTURE ANCHOR

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