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

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    Filters Status: Injury ×

    RELIEVA SPIN SINUPLASTY SYSTEM

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

    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

    RELIEVA VORTEX SINUS IRRIGATION CATHETER

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

    RELIEVA SINUS BALLOON CATHETER SYS

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code LRC·June 11, 2014

    RELIEVA SPIN BALLOON SINUPLASTY SYSTEM

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code LRC·October 16, 2014

    TRUDI SUCTION, 0 - 1PK

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

    UNKNOWN

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code LRC·September 30, 2015

    ACCLARENT AERA EUSTACHIAN TUBE BALLOON DILATION SYSTEM, 5PK

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code PNZ·August 5, 2024

    UNK_REUSABLE INSTRUMENTS

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code PGW·July 30, 2024

    ACCLARENT AERA EUSTACHIAN TUBE BALLOON DILATION SYSTEM, 1PK

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code PNZ·July 9, 2024

    TRUDI CURETTE, 0, 5IN

    FDA Adverse Event
    Injury ·ACCLARENT, INC.·Product code PGW·July 30, 2024