BEUDAMED
    225 results · 39ms · Sources: EU EUDAMED, US FDA

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    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·Product code CAZ·February 26, 2020

    EPIDURAL CATHETERIZATION KIT NRFIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code BSO·September 10, 2024

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·January 9, 2020

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code BSO·October 24, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·October 24, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code BSO·December 13, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code BSO·December 27, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·December 2, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·November 26, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code BSO·December 27, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·October 24, 2019

    EPIDURAL CATHETERIZATION KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code OGE·December 11, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·December 17, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code BSO·November 13, 2019

    ANESTHESIA CONDUCTION KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·November 26, 2019

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 9, 2013

    CORAIL2 STD SIZE 10

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A·Product code KWA·November 19, 2010

    M2A-MAGNUM MOD HD SZ 54MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 1, 2014

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL INC.·Product code CAZ·January 2, 2020

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·Product code CAZ·February 11, 2020