BEUDAMED
    10,000 results · 143ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    LOGIQ E9

    FDA Adverse Event
    Injury ·SEE H10·Product code IYN·October 17, 2018

    SEE # 5

    FDA Adverse Event
    Injury ·SEE # 5·Product code FWM·February 15, 2006

    LOGIQ E9

    FDA Adverse Event
    Injury ·SEE H10·Product code IYN·April 26, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·SEE H10·Product code KWP·September 13, 2012

    EYEBOT

    FDA Adverse Event
    Injury ·123 SEE·Product code QTO·February 17, 2026

    REVIVE SE 4.5MM OUS

    FDA Adverse Event
    Injury ·SEE H10·Product code DXE·March 19, 2018

    COIL-THERMO MECHANICAL

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·December 14, 2018

    COIL-THERMO MECHANICAL

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·December 14, 2018

    UNKMICRUSFRAME

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·December 17, 2018

    COIL-THERMO MECHANICAL

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·December 14, 2018

    GALAXY G3 MINI 1MM X 2.5CM

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·December 11, 2018

    COIL-THERMO MECHANICAL

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·December 14, 2018

    COIL-THERMO MECHANICAL

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·December 13, 2018

    COIL-THERMO MECHANICAL

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·December 14, 2018

    COIL-THERMO MECHANICAL

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·October 18, 2018

    SEE HOSPITAL RECORDS

    FDA Adverse Event
    Injury ·SEE HOSPITAL RECORDS·Product code FTL·September 13, 2011

    UNKMICRUSFRAME

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·December 17, 2018

    MICRUSFRAME10 3.5MM X 6.6CM

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·April 1, 2019

    SEE BLOOD BANK

    FDA Adverse Event
    Injury ·SEE BLOOD BANK·Product code KSO·April 2, 2008

    COIL-THERMO MECHANICAL

    FDA Adverse Event
    Injury ·SEE H.10·Product code KRD·January 23, 2019