468 results · 42ms · Sources: EU EUDAMED, US FDA

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MAQUET INC.

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

GETINGE/CASTLE

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

CASTLE

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

ROTAFLOW CENTRIFUGAL PUMP

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code DWA·November 9, 2006

8010042-2008-00047

FDA Adverse Event
Malfunction ·Product code IOY·April 11, 2008

8010042-2008-00050

FDA Adverse Event
Malfunction ·Product code CBK·April 16, 2008

8010042-2008-00029

FDA Adverse Event
Malfunction ·Product code CBK·March 13, 2008

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FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·February 13, 2008

8010042-2008-00031

FDA Adverse Event
Malfunction ·Product code CBK·February 29, 2008