BEUDAMED
    12 results · 40ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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
    Malfunction ·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
    Malfunction ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

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

    PRIMARY PLUM SET, 15 MICRON FILTER IN SIGHT CHAMBER, CLAVE SECONDARY PORT, CLAVE

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·March 5, 2020

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 15, 2014

    GOBED+

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 20, 2013

    KDJ

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·July 27, 2011

    FREESTYLE LITE

    FDA Adverse Event
    Injury ·Product code NBW·November 15, 2012