232 results
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36ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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KRATOS ANALYTICAL LTD.
FDA registration
KRATOS ANALYTICAL LTD.·1 product·🇬🇧 United Kingdom
Ibex Prostate Detect
FDA UDI
IBEX MEDICAL ANALYTICS LTD·07290019124016·Ibex Prostate Detect is a software only device ...
ANALYTICAL D MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·August 16, 2010
ANALYTICAL P MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·February 21, 2013
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·August 10, 2010
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·June 21, 2010
ANALYTICAL D MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·September 15, 2014
MPA
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JQP·December 14, 2010
ACCU-CHEK ® COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 19, 2010
COBAS INTEGRA 800
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·May 31, 2007
CALCIUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CIC·September 14, 2011
ALBUMIN BCG METHOD
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CIX·June 29, 2011
AST
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FET·May 11, 2011
COBAS C 303 ANALYTICAL UNIT
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·December 11, 2024
ANALYTICAL D MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·July 12, 2010
UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code GKZ·December 7, 2010
GLUCO-QUANT GLUCOSE/HK
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CFR·July 5, 2011
ANALYTICAL D MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·April 3, 2013
ANALYTICAL D MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·March 16, 2012
ANALYTICAL D MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CFR·March 5, 2012