BEUDAMED
    114 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event × Regulation: Us FDA × Clear all

    ROTAFLOW CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KFM·December 1, 2014

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON PAH·Product code PAH·February 27, 2013

    LZH PUMP, INFUSION, ENTERAL

    FDA Adverse Event
    Malfunction ·ABBOTT NUTRITION·Product code LZH·October 16, 2008

    LZH PUMP, INFUSION, ENTERAL

    FDA Adverse Event
    Malfunction ·ABBOTT NUTRITION·Product code LZH·October 9, 2008

    ETEST® METRONIDAZOLE MZH

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code JWY·April 28, 2016

    ETEST® METRONIDAZOLE MZH

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code JWY·May 3, 2016

    ETEST® METRONIDAZOLE MZH

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code JWY·April 28, 2016

    ETEST® METRONIDAZOLE MZH

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code JWY·April 28, 2016

    FORCE FX P9H 1064EA

    FDA Adverse Event
    VALLEYLAB·Product code DRX·March 18, 2008

    GENTLE TOUCH

    FDA Adverse Event
    Injury ·WESLEY JESSEN/PBH·Product code LPM·September 9, 1997

    MATTRIX

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code GZF·September 13, 2011

    ETEST ® METRONIDAZOLE (MZH 256) US

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code JWY·September 25, 2015

    PUMP, INFUSION, ENTERAL PRODUCT CODE: LZH

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LZH·January 1, 2020

    CSI, DAILY WEAR, SPHERE

    FDA Adverse Event
    Other ·WESLEY JESSEN/PBH LTD.·Product code LPL·June 29, 1999

    CSI LOCATOR TINT

    FDA Adverse Event
    Injury ·WESLEY JESSEN/PBH LTD.·Product code LPL·September 2, 1999

    PRECISION UV CONTACT LENS

    FDA Adverse Event
    Injury ·WESLEY JESSEN/PBH LTD.·Product code LPL·January 9, 1998

    NATURAL TOUCH BABY BLUE

    FDA Adverse Event
    Other ·WESLEY JESSEN/PBH LTD.·Product code LPL·January 27, 1999

    DUROM ACETABULAR COMPONENT

    FDA Adverse Event
    Injury ·DURON ACETABULAR COMPONENT AND METASUL LZH·Product code KWA·July 20, 2012

    SINGLE USE BIOPSY VALVE (STERILE)

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·March 4, 2021

    SINGLE USE BIOPSY VALVE (STERILE)

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·March 4, 2021