BEUDAMED
    5 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    S-ROM M HEAD 36MM +3

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 6, 2013

    PROTECTA XT VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code NIK·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    MENTOR SMOOTH ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·August 21, 2018

    TRULIANT TIB IMP CRC INSERT SZ 4, 12MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·November 29, 2023