BEUDAMED
    287 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    MAQUET CARDIOPULMONARY AG

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 6, 2013

    MAQUET CARDIOPULMONARY AG

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 6, 2013

    MAQUET CARDIOPULMONARY AG

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 6, 2013

    MAQUET CARDIOPULMONARY AG

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 6, 2013

    MAQUET CARDIOPULMONARY AG

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 6, 2013

    MAQUET CARDIOPULMONARY AG

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 6, 2013

    MAQUET CARDIOPULMONARY AG

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 6, 2013

    MAQUET CARDIOPULMONAY AG

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 6, 2013

    HEMOCONCENTRATOR 20

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KDI·July 28, 2015

    8010762-2008-00003

    FDA Adverse Event
    Malfunction ·Product code KFM·September 11, 2008

    8010762-2019-00073

    FDA Adverse Event
    Malfunction ·March 19, 2019

    8010762-2019-00063

    FDA Adverse Event
    Malfunction ·March 7, 2019

    8010762-2019-00078

    FDA Adverse Event
    Malfunction ·March 25, 2019

    8010762-2019-00043

    FDA Adverse Event
    Malfunction ·February 25, 2019

    8010762-2008-00001

    FDA Adverse Event
    Malfunction ·Product code DTQ·February 20, 2008

    HEMOCONCENTRATOR 20

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KDI·July 28, 2015

    MAQUET HCU30 DEVICE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWC·October 7, 2016

    HEMOCONCENTRATOR 20

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KDI·July 28, 2015

    HEMOCONCENTRATOR 20

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KDI·July 28, 2015

    HEMOCONCENTRATOR 20

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KDI·July 28, 2015