BEUDAMED
    557 results · 20ms · Sources: EU EUDAMED, US FDA

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    DYNATORQUE ATTACHMENT

    FDA Adverse Event
    Other ·PRO-DEX MICRO MOTORS INC.·Product code EFB·October 15, 2013

    PEARL FRACTIONAL ER:YSGG LASER

    FDA Adverse Event
    Other ·Product code GEX·February 16, 2012

    PEARL FRACTIONAL 2790NM ER: YSGG LASER

    FDA Adverse Event
    Other ·CUTERA·Product code GEX·February 17, 2012

    PEARL ER:YSGG LASER

    FDA Adverse Event
    Other ·CUTERA·Product code GEX·March 16, 2012

    PEARL FRACTIONAL

    FDA Adverse Event
    Other ·CUTERA·Product code GEX·January 30, 2012

    FEMTO LDV Z4

    FDA Adverse Event
    Other ·SIE AG, SURGICAL INSTRUMENT ENGINEERING·Product code GEX·May 9, 2014

    FEMTO LDV Z2

    FDA Adverse Event
    Other ·SIE AG SURGICAL INSTRUMENT ENGINEERING·Product code GEX·April 16, 2014

    FEMTO LDV Z6 POWERPLUS

    FDA Adverse Event
    Other ·SIE AG, SURGICAL INSTRUMENT ENGINEERING·Product code GEX·May 9, 2014

    LASE

    FDA Adverse Event
    Other ·CLARUS MEDICAL, LLC.·Product code GEX·March 9, 2004

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    ZERONA

    FDA Adverse Event
    Other ·ERCHONICA MEDICAL·Product code GEX·February 25, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    ENDOSTAT FIBER

    FDA Adverse Event
    Other ·AMERICAN MEDICAL SYSTEMS·Product code GEX·January 28, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    LIGHTSHEER DUET

    FDA Adverse Event
    Other ·RH USA, INC.·Product code GEX·January 8, 2010