10,000 results
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40ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SODIUM/POTASSIUM 140/5 MEQ/L)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SODIUM/POTASSIUM (100/100 MEQ/E)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
LITHIUM INTERNAL STANDARD 1 MEQ/L #60085
FDA 510(k)
FDA Class 2
·Clinical Chemistry
LITHIUM INTERNAL STANDARD 1500 MEQ/L #60086
FDA 510(k)
FDA Class 2
·Clinical Chemistry
LITHIUM INTERNAL STANDARD 3000 MEQ/L #60084
FDA 510(k)
FDA Class 2
·Clinical Chemistry
COBAS INTEGRA 800
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·May 15, 2008
SOLUTION B- NA 50MEQ/L, K 40 MEQ/L
FDA 510(k)
FDA Class 2
·Clinical Chemistry
MODULAR ANALYTICS CORE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·November 18, 2010
COBAS PRO ISE ANALYTICAL UNIT
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·June 14, 2024
OMNI 6
FDA Adverse Event
Malfunction
·AVL GMBH·Product code JJC·September 5, 2002
COBAS 6000 C501 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CGA·July 31, 2012
HITACHI 917 DISK
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·August 14, 2008
ALINITY C PROCESSING MODULE
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code JJE·June 2, 2023
917 DISK SYSTEM W/CO2
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·November 13, 2007
COBAS INTEGRA 400
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·May 8, 2007
COBAS 6000 C501 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JGS·February 20, 2012
COBAS INTERGRA 800
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·December 20, 2007
COBAS INTEGRA 800
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·March 21, 2008
I-STAT CHEM8+ CARTRIDGE
FDA Adverse Event
Other
·ABBOTT POINT OF CARE INC.·Product code MMI·April 10, 2007
ALINITY C PROCESSING MODULE
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code JJE·September 23, 2025