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

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    Filters Status: Injury ×

    PRESSUREWIRE¿ X GUIDEWIRE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code DXO·May 12, 2022

    PRESSUREWIRE¿ X GUIDEWIRE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code DXO·January 23, 2023

    PRESSUREWIRE¿ X GUIDEWIRE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code DXO·October 26, 2023

    PRESSUREWIRE¿

    FDA Adverse Event
    Injury ·LIGHTLAB IMAGING, INC.·Product code DXO·October 28, 2025

    PRESSUREWIRE¿ X GUIDEWIRE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code DXO·May 6, 2024

    PRESSUREWIRE¿

    FDA Adverse Event
    Injury ·LIGHTLAB IMAGING, INC.·Product code DXO·May 7, 2024

    PRESSUREWIRE¿

    FDA Adverse Event
    Injury ·LIGHTLAB IMAGING, INC.·Product code DXO·February 21, 2025

    PRESSUREWIRE¿

    FDA Adverse Event
    Injury ·LIGHTLAB IMAGING, INC.·Product code DXO·December 29, 2025

    PRESSUREWIRE¿

    FDA Adverse Event
    Injury ·LIGHTLAB IMAGING, INC.·Product code DXO·July 10, 2025

    PRESSUREWIRE¿ X GUIDEWIRE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code DXO·April 10, 2023

    PRESSUREWIRE¿ X GUIDEWIRE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code DXO·October 25, 2022

    PRESSUREWIRE¿ X GUIDEWIRE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code DXO·July 14, 2023

    PRESSUREWIRE¿ X GUIDEWIRE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code DXO·October 4, 2022

    NITINOL COMPRESSION STAPLE, 9W X 7L

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code JDR·November 12, 2025

    NITINOL COMPRESSION STAPLE, 9W X 10L

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code JDR·April 18, 2024

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·November 5, 2019

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·November 5, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·November 5, 2019

    CONCORDE BUL LOR 9X8X23, 5 DG

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL CH·Product code MAX·October 8, 2020

    AMIS LEG POSITIONER

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code FWX·December 16, 2016