595 results · 43ms · Sources: EU EUDAMED, US FDA

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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

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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