BEUDAMED
    19 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/10 MM R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 12, 2021

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/12 MM R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 11, 2022

    UNKNOWN CERAMIC HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·August 9, 2017

    UNKNOWN CERAMIC HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·August 9, 2017

    UNKNOWN BI METRIC INTERLOC STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDL·August 8, 2017

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORP.·Product code LGW·February 21, 2008

    UNKNOWN BI METRIC INTERLOC STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDG·August 9, 2017

    UNKNOWN UNIVERSAL RINGLOC SHELL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDG·August 9, 2017

    UNKNOWN M2A RINGLOC LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 8, 2017

    UNKNOWN RINGLOC ARCOM LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 8, 2017

    UNKNOWN UNIVERSAL RINLOC SHELL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 8, 2017

    UNKNOWN CO CR HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 8, 2017

    UNKNOWN UNIVERSAL RINGLOC CUP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 9, 2017

    UNKNOWN UNIVERSAL RINGLOC SHELL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWZ·August 8, 2017

    UNKNOWN M2A RINGLOC LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 9, 2017

    UNKNOWN BI METRIC INTERLOC STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 8, 2017

    UNKNOWN BI METRIC INTERLOC STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·August 9, 2017

    UNKNOWN CO CR HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 9, 2017

    SINGLE USE 3-LUMEN EXTRACTION BALLOON V

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FGE·October 1, 2024