898 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·August 18, 2009
ANALYTICAL E MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code DHA·February 14, 2013
ANALYTICAL P MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·June 28, 2013
COBAS 8000 E602 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·December 15, 2014
COBAS 8000 C 702 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·June 28, 2022
ANALYTICAL E MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·February 26, 2014
1823260-2017-02175
FDA Adverse Event
Malfunction
·October 3, 2017
COBAS 8000 C701 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·September 22, 2014
ANALYTICAL E MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code DHA·February 5, 2013
REST ASSURED, GEN II ORIGINAL
FDA Adverse Event
Malfunction
·RANIR, LLC·Product code OBR·December 18, 2014
1823260-2017-01054
FDA Adverse Event
Malfunction
·May 19, 2017
MAILMAN GUIDE WIRE
FDA Adverse Event
Injury
·SCIMED A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code DQX·November 26, 1997
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 8, 2008
SYNERGY
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 7, 2011
CAREFUSION
FDA Adverse Event
Malfunction
·CAREFUSION·Product code LSZ·May 1, 2015
COBAS E411 SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBC·February 28, 2013
1823260-2017-01788
FDA Adverse Event
Malfunction
·August 22, 2017
ANALYTICAL E MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·October 25, 2013
COBAS 6000 C (501) MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·January 2, 2018
CADD LEGACY
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FRN·September 21, 2018