BEUDAMED
    7 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SMR GLENOSPHERE Ø36 MM

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

    SMR SHOULDER

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·October 3, 2024

    UNKNOWN INTELLIJOINT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OLO·May 31, 2022

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 12, 2013

    INFUSOR TWO DAY 2ML/HR 12 PK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 24, 2011

    TRIDENT CERAMIC LINER

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MRA·February 19, 2008

    FEMORAL MODULAR HEAD - M Ø36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·September 8, 2021