BEUDAMED
    378 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    AFX

    FDA Adverse Event
    Injury ·ENDOLOGIX INC.·Product code MIH·April 19, 2018

    AFX

    FDA Adverse Event
    Injury ·ENDOLOGIX INC.·Product code MIH·April 4, 2018

    AFX

    FDA Adverse Event
    Injury ·ENDOLOGIX·Product code MIH·March 31, 2020

    2031527-2012-00115

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·November 21, 2012

    2031527-2012-00119

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·October 30, 2012

    2031527-2012-00118

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·December 14, 2012

    2031527-2012-00122

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·November 8, 2012

    2031527-2012-00120

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·November 21, 2012

    2031527-2012-00112

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·December 14, 2012

    2031527-2012-00094

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·August 15, 2012

    2031527-2012-00091

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·August 15, 2012

    2031527-2012-00095

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·September 11, 2012

    2031527-2012-00109

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·September 26, 2012

    2031527-2016-00231

    FDA Adverse Event
    Injury ·May 19, 2017

    AFX

    FDA Adverse Event
    Injury ·ENDOLOGIX·Product code MIH·July 30, 2018

    AFX

    FDA Adverse Event
    Injury ·ENDOLOGIX·Product code MIH·December 27, 2018

    POWERLINK SYSTEM

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·Product code MIH·November 23, 2011

    POWERLINK SYSTEM

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·Product code MIH·November 23, 2011

    POWERLINK SYSTEM

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·Product code MIH·November 23, 2011

    POWERLINK SYSTEM

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·Product code MIH·November 23, 2011