BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    36CM PERM CATH KIT X5

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code MSD·February 20, 2014

    ZEPHYR XL DR

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWP·November 21, 2012

    4.0MM CANC LOCK SCRW 44MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HRS·September 17, 2010

    UNK HIP FEMORAL HEAD METAL ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023

    UNK HIP FEMORAL SLEEVE ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 7, 2023

    UNK HIP FEMORAL SLEEVE ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023

    UNK HIP FEMORAL HEAD METAL ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023

    UNK HIP ACETABULAR CUP ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 7, 2023

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 7, 2023

    UNK HIP ACETABULAR CUP ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023