BEUDAMED
    5 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MODULUS-STRUM. - ESTRATTORE

    FDA Adverse Event
    Malfunction ·LIMACORPORATE S.P.A.·Product code KWY·August 26, 2021

    UNKNOWN HIP STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·January 10, 2013

    ITREL 3

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code LGW·November 5, 2010

    LIGAMAX CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 7, 2014

    FEMORAL MODULAR HEAD - M Ø32MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·August 26, 2021