BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    H 105700#TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·May 5, 2015

    HQV 32902#INTEGRATED ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·June 22, 2015

    BD ECLIPSE¿ BLOOD COLLECTION NEEDLE WITH LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·December 6, 2017

    FEMOSTOP

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS, INC.·Product code MGB·November 21, 2003

    VERTEBRAL BODY SPREADER- ANGLED

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTD·March 20, 2013

    ADVIA CENTAUR XP

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MOI·August 15, 2014

    DLT TS CER HD 12/14 40MM +8.5

    FDA Adverse Event
    Injury ·DEPUY INT'L., LTD.·Product code LZO·February 24, 2011

    FEMOSTOP

    FDA Adverse Event
    Injury ·RADI MEDICAL SYSTEMS·Product code DXC·August 20, 2003