BEUDAMED
    662 results · 42ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    MAQUET INC.

    FDA Adverse Event
    Malfunction ·MAQUET, INC.·Product code CBK·April 12, 2011

    CASTLE

    FDA Adverse Event
    Other ·MAQUET INC.·Product code FSY·March 20, 2009

    GETINGE/CASTLE

    FDA Adverse Event
    Malfunction ·MAQUET, INC.·Product code FQO·April 1, 2010

    9710055-2008-00010

    FDA Adverse Event
    Other ·Product code FSY·September 5, 2008

    CASTLE

    FDA Adverse Event
    Malfunction ·MAQUET, INC. (F.K.A. GETINGEUSA)·Product code FSY·January 15, 2010

    MAQUET

    FDA Adverse Event
    Injury ·MAQUET GMBH AND CO. KG·Product code HBL·April 26, 2010

    MAQUET

    FDA Adverse Event
    Injury ·MAQUET GMBH & CO. KG·Product code HBL·April 26, 2010

    SHAMPAINE

    FDA Adverse Event
    Other ·MAQUET, INC.·Product code FQO·January 27, 2010

    MAQUET

    FDA Adverse Event
    Other ·MAQUET SUZHOU COMPANY LTD·Product code BYX·March 10, 2010

    8010042-2007-00153

    FDA Adverse Event
    Malfunction ·Product code CBK·July 6, 2007

    *

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·May 28, 2008

    8010042-2008-00045

    FDA Adverse Event
    Malfunction ·Product code CBK·April 4, 2008

    8010042-2008-00046

    FDA Adverse Event
    Malfunction ·Product code CBK·April 4, 2008

    8010042-2008-00044

    FDA Adverse Event
    Malfunction ·Product code CBK·April 4, 2008

    8010042-2008-00014

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

    8010042-2008-00022

    FDA Adverse Event
    Malfunction ·Product code CBK·February 26, 2008

    8010042-2008-00041

    FDA Adverse Event
    Malfunction ·Product code CBK·March 27, 2008

    8010762-2008-00001

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

    8010042-2008-00024

    FDA Adverse Event
    Malfunction ·Product code CBK·February 15, 2008

    8010042-2008-00019

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