BEUDAMED
    468 results · 49ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    RELIEVA SPIN SINUPLASTY SYSTEM

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·December 12, 2016

    RELIEVA SPIN SINUPLASTY SYSTEM

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·December 12, 2016

    RELIEVA

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·December 23, 2016

    UNKNOWN

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·December 12, 2016

    RELIEVA SPIN SINUPLASTY SYSTEM

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code LRC·September 15, 2015

    RELIEVA SPIN SIUSPLASTY SYSTEM

    FDA Adverse Event
    Malfunction ·ACCLARENT INC·Product code LRC·July 6, 2015

    UNKNOWN

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code KAM·September 25, 2015

    INSPIRA AIR BALLOON CATHETER 5X24

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code KTI·March 29, 2012

    RELIEVA SOLO BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code KAO·March 25, 2009

    RELIEVA ULTIRRA SINUS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·May 14, 2014

    RELIEVA SINUS BALLOON CATHETER SYSTEM

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code KAM·April 11, 2014

    RELIEVA SINUS BALLOON CATHETER SYSTEM

    FDA Adverse Event
    Injury ·ACCLARENT INC.·Product code LRC·June 5, 2014

    RELIEVA ULTIRRA SINUS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·May 9, 2014

    RELIEVA VORTEX 2 SINUS IRRIGATION CATHETER

    FDA Adverse Event
    ACCLARENT, INC.·Product code KAM·April 3, 2014

    INSPIRA AIR BALLOON CATHETER

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code KTI·May 28, 2014

    NONE

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code KAM·March 20, 2010

    NONE

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code KAM·March 3, 2010

    RELIEVA VIGOR GUIDEWIRE

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code KAM·January 9, 2010

    NONE

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code KAM·May 12, 2010

    NONE

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code KAM·May 12, 2010