BEUDAMED
    13 results · 54ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PRIMUS (THE BTE WS30)

    FDA Adverse Event
    Other ·BTE TECHNOLOGIES, INC.·Product code ISD·June 18, 2012

    PRIMUSRS

    FDA Adverse Event
    Malfunction ·BTE TECHNOLOGIES, INC.·Product code BXB·February 26, 2013

    ECCENTRON

    FDA Adverse Event
    Other ·BTE TECHNOLOGIES, INC.·Product code IKK·February 27, 2014

    PRIMUS, BTE WS30

    FDA Adverse Event
    Malfunction ·BTE TECHNOLOGIES, INC.·Product code ISD·April 19, 2013

    ER

    FDA Adverse Event
    Other ·BTE TECHNOLOGIES, INC.·Product code IKK·April 19, 2013

    SIMULATOR

    FDA Adverse Event
    Malfunction ·BTE TECHNOLOGIES, INC.·Product code BXB·June 2, 2017

    PRIMUS (THE BTE WS30)

    FDA Adverse Event
    Malfunction ·BTE TECHNOLOGIES, INC.·Product code ISD·February 18, 2015

    ER

    FDA Adverse Event
    Injury ·BTE TECHNOLOGIES, INC.·Product code IKK·December 31, 2013

    EVALTECH

    FDA Adverse Event
    Injury ·BTE TECHNOLOGIES, INC.·Product code IKK·April 4, 2016

    PRIMUSRS

    FDA Adverse Event
    Injury ·BTE TECHNOLOGIES, INC.·Product code ISD·April 6, 2018

    MCU

    FDA Adverse Event
    BTE TECHNOLOGIES, INC.·Product code IKK·April 8, 2016

    PRIMUSRS

    FDA Adverse Event
    Malfunction ·BTE TECHNOLOGIES, INC.·Product code ISD·June 27, 2018

    PRIMUS

    FDA Adverse Event
    Injury ·BTE TECHNOLOGIES, INC.·Product code ISD·August 17, 2017