BEUDAMED
    10 results · 23ms · 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

    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

    LCS ROT PLAT BRNG STD/10MM

    FDA Adverse Event
    Other ·DEPUY INTERNATIONAL, LTD.·Product code HRY·January 8, 2007

    ARROW

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 25, 2023

    CODMAN 3000

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 28, 2023

    CODMAN 3000

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 20, 2023

    CODMAN

    FDA Adverse Event
    Death ·CODMAN & SHURTLEFF·Product code LKK·July 18, 2023

    32MM MOD HD CERAMIC -5MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·May 23, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 13, 2012

    CAPSUREFIX

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