BEUDAMED
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    Filters Status: Malfunction ×

    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 SIUSPLASTY SYSTEM

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

    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 ULTIRRA SINUS BALLOON CATHETER

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

    RELIEVA STRATUS MICROFLOW SPACER

    FDA Adverse Event
    Malfunction ·ACCLARENT INC.·Product code KAM·May 28, 2010

    INSPIRA AIR BALLOON

    FDA Adverse Event
    Malfunction ·ACCLARENT INC.·Product code KNQ·June 25, 2010

    RELIEVA SPIN SINUPLASTY SYSTEM

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·April 15, 2014

    RELIEVA SPIN PLUS KIT, 3 GUIDES, 6MM, 5PK

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·December 19, 2017

    RELIEVA SPIN PLUS KIT, 3 GUIDES, 6MM, 5PK

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·December 7, 2017

    RELIEVA SPINPLUS NAV BALLOON SINUPLASTY SYSTEM, 6X16MM, 3 GUIDE KIT

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·December 1, 2021

    TRUDI SUCTION, 0 - 1PK

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code PGW·June 20, 2022

    RELIEVA SPINPLUS NAV BALLOON SINUPLASTY SYSTEM, 6X16MM, 3 GUIDE KIT

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·June 27, 2022

    TRUDI SUCTION, 70 - 1PK

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code PGW·June 15, 2022

    RELIEVA FLEX SINUS GUIDE CATHETER

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code KAM·August 15, 2015

    INSPIRA AIR BALLOON DILATION SYSTEM, 16X40MM

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code LRC·December 19, 2017

    ACCLARENT AERA

    FDA Adverse Event
    Malfunction ·ACCLARENT, INC.·Product code PNZ·October 10, 2017