BEUDAMED
    758 results · 67ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    COLLECT.NO.QAS KNEE IMPLANTS COLUMBUS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·January 29, 2025

    AS TIBIA EXTENSION STEM 10X52MM CEMENTED

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·April 30, 2026

    VEGA PS+ GLIDING SURFACE T2/2+ 14MM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·April 30, 2026

    AS VEGA PS TIBIAL PLATEAU CEMENTED T2+

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·April 30, 2026

    AE-QAS-K521-53

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·December 19, 2024

    ENDURO

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·November 14, 2024

    UNKNOWN COMPONENT AESCULAP AG VEGA KNEE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 10, 2026

    EXCIA PLASMAPORE-UCAP 8/10 SIZE 13MM

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, INC.·Product code JDI·June 1, 2007

    UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 30, 2026

    UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 30, 2026

    UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 30, 2026

    UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 30, 2026

    COMPONENT OF AN UNKNOWN AESCULAP AG KNEE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·February 26, 2026

    COLLECT.NO.QAS KNEE IMPLANTS VEGA

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·October 6, 2023

    UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·April 18, 2026

    AS TIBIA EXTENSION STEM 10X52MM CEMENTED

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·February 26, 2026