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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