Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Inst
Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems,Manual Antimicrobial Susceptibility Test Systems,Panels, Test, Susceptibility, Antimicrobial
Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Inst
Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems,Manual Antimicrobial Susceptibility Test Systems,Panels, Test, Susceptibility, Antimicrobial
Manual Antimicrobial Susceptibility Test Systems,Instrument For Auto Reader & In
Manual Antimicrobial Susceptibility Test Systems,Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems,Panels, Test, Susceptibility, Antimicrobial,Susceptibility Test Cards, Antimicrobial,Gram Negative Identification Panel
Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Pane
Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Panels, Test, Susceptibility, Antimicrobial,Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems,Manual Antimicrobial Susceptibility Test Systems
The Access SARS-CoV-2 IgG II Calibrators are intended to calibrate the Access SA
The Access SARS-CoV-2 IgG II Calibrators are intended to calibrate the Access SARS-CoV-2 IgG II assay for the in vitro semi-quantitative and qualitative detection of SARS-CoV-2 IgG antibodies in human plasma (lithium heparin, dipotassium EDTA, tripotassium EDTA, and sodium citrate) for use on the Access Immunoassay Systems only.The Access SARS-CoV-2 IgG II calibrators are only for use under the Food and Drug Administration's Emergency Use Authorization.
The Access Toxo IgG QC is intended for monitoring system performance of the Acce
The Access Toxo IgG QC is intended for monitoring system performance of the Access Toxo IgG assay.
The Access CEA QC (BSA matrix) controls are intended for monitoring the system p
The Access CEA QC (BSA matrix) controls are intended for monitoring the system performance of immunoenzymatic procedures for the quantitative measurement of Carcinoembryonic Antigen (CEA) using Access CEA reagents.
The epoc Blood Analysis System, is intended for use by trained medical professio
The epoc Blood Analysis System, is intended for use by trained medical professionals as an in vitro diagnostic device for thequantitative testing of samples of heparinized or un-anticoagulated arterial, venous or capillary whole blood in the laboratory orat the point of care in hospitals, nursing homes or other clinical care institutions.
The epoc Blood Analysis System, is intended for use by trained medical professio
The epoc Blood Analysis System, is intended for use by trained medical professionals as an in vitro diagnostic device for thequantitative testing of samples of heparinized or un-anticoagulated arterial, venous or capillary whole blood in the laboratoryor at the point of care in hospitals, nursing homes or other clinical care institutions.
NA+/K+/CA++/CL- Electrode fill solution. In vitro diagnostics material for use w
NA+/K+/CA++/CL- Electrode fill solution. In vitro diagnostics material for use with RAPIDLab® 1200 electrodes.
pH electrode fill soultion, in vitro diagnostics material for use with RAPIDLab®
pH electrode fill soultion, in vitro diagnostics material for use with RAPIDLab® 1200 series electrodes
Ready Sensor™ Chloride Biosensor. An in vitro diagnostic device for use on the R
Ready Sensor™ Chloride Biosensor. An in vitro diagnostic device for use on the RapidLab® 1200 series instruments
Ready Sensor™ Potassium Biosensor. An in vitro diagnostic device for use on the
Ready Sensor™ Potassium Biosensor. An in vitro diagnostic device for use on the RapidLab® 1200 series instruments
Ready Sensor™ Sodium Biosensor. An in vitro diagnostic device for use on the Rap
Ready Sensor™ Sodium Biosensor. An in vitro diagnostic device for use on the RapidLab® 1200 series instruments
Ready Sensor™ pH Biosensor. An in vitro diagnostic device for use on the RapidLa
Ready Sensor™ pH Biosensor. An in vitro diagnostic device for use on the RapidLab® 1200 series instruments
RAPIDPOINT® 340 Sampler Module, an in vitro diagnostics device to be used on the
RAPIDPOINT® 340 Sampler Module, an in vitro diagnostics device to be used on the RAPIDPOINT® 340 analyzer
RAPIDPOINT® 350 Sensor Module, an in vitro diagnostics device to be used on the
RAPIDPOINT® 350 Sensor Module, an in vitro diagnostics device to be used on the RAPIDPOINT® 350 analyzer
RAPIDPOINT® 350 Sampler Module, an in vitro diagnostics device to be used on the
RAPIDPOINT® 350 Sampler Module, an in vitro diagnostics device to be used on the RAPIDPOINT® 350 analyzer
RAPIDPOINT® 340 Sensor Module, an in vitro diagnostics device to be used on the
RAPIDPOINT® 340 Sensor Module, an in vitro diagnostics device to be used on the RAPIDPOINT® 340 analyzer
RAPIDLab 1200 systems are intended for in vitro diagnostic use by healthcare pro
RAPIDLab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human blood. The 1265 can determine pH, pCO2, pO2, Na+, K+, Ca++, Cl-, glucose, lactate, tHb, nBili, FO2Hb, FCOHb, FMetHb, FHHb parameters
RAPIDLab 1200 systems are intended for in vitro diagnostic use by healthcare pro
RAPIDLab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human whole blood. The 1260 can determine pH, pCO2, pO2, Na+, K+, Ca++, Cl-, glucose, lactate parameters
RAPIDLab 1200 systems are intended for in vitro diagnostic use by healthcare pro
RAPIDLab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human whole blood. The 1245 can determine pH, pCO2, pO2, tHb, nBili, FO2Hb, FCOHb, FMetHb, FHHb parameters
RAPIDLab 1200 systems are intended for in vitro diagnostic use by healthcare pro
RAPIDLab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human whole blood. The 1240 can determine pH, pCO2, pO2 parameters
Ready Sensor™ Calcium Biosensor. An in vitro diagnostic device for use on the Ra
Ready Sensor™ Calcium Biosensor. An in vitro diagnostic device for use on the RapidLab® 1200 series instruments
Ready Sensor™ pCO2 Biosensor. An in vitro diagnostic device for use on the Rapid
Ready Sensor™ pCO2 Biosensor. An in vitro diagnostic device for use on the RapidLab® 1200 series instruments
Ready Sensor™ pO2 Biosensor. An in vitro diagnostic device for use on the RapidL
Ready Sensor™ pO2 Biosensor. An in vitro diagnostic device for use on the RapidLab® 1200 series instruments
Reference Electrode Refill. An in vitro diagnostic device for use on the RAPIDLa
Reference Electrode Refill. An in vitro diagnostic device for use on the RAPIDLab® 1200 series instruments
Ready Sensor™ Reference Biosensor. An in vitro diagnostic device for use on the
Ready Sensor™ Reference Biosensor. An in vitro diagnostic device for use on the RapidLab® 1200 series instruments
RAPIDLab® 1200 Systems Wash Cartridge, for in vitro diagnostic use with RAPIDLab
RAPIDLab® 1200 Systems Wash Cartridge, for in vitro diagnostic use with RAPIDLab® 1200 series systems
RAPIDLab® 1200 Systems Reagent Cartridge for in vitro diagnostics use with the R
RAPIDLab® 1200 Systems Reagent Cartridge for in vitro diagnostics use with the RAPIDLab 1200 series systems.
RAPIDChem® 754, RAPIDPoint® 340/350 Daily Cleaner Kit, for in vitro diagonstic u
RAPIDChem® 754, RAPIDPoint® 340/350 Daily Cleaner Kit, for in vitro diagonstic use with Rapidchem® 754, Rapidpoint® 340/350 systems
Li+ Sensor module, an in vitro diagnostics device to be used on the RAPIDChem® 7
Li+ Sensor module, an in vitro diagnostics device to be used on the RAPIDChem® 754 analyzer
RAPIDPoint® 400/405/500 Wash/Waste Cartridge, for in vitro diagnostics use with
RAPIDPoint® 400/405/500 Wash/Waste Cartridge, for in vitro diagnostics use with the RAPIDPoint® 400/405/500 series systems.
The Rapidchem® 744 analyzer is designed for clinical laboratory use, making dire
The Rapidchem® 744 analyzer is designed for clinical laboratory use, making direct quantitative measurements of Na+ (sodium), K+ (potassium), and Cl- (chloride) or Lithium (Li+) in serum, plasma, whole blood and urine (not applicable for Lithium) samples.
For in vitro diagnostic use for multi-level quality control of RAPIDPoint 400/50
For in vitro diagnostic use for multi-level quality control of RAPIDPoint 400/500 series and RAPIDLab 1200 series systems.
RAPIDChem® 700 RAPIDPoint® 350 K+ Sensor, for in vitro diagnostics use with Rapi
RAPIDChem® 700 RAPIDPoint® 350 K+ Sensor, for in vitro diagnostics use with Rapidchem® 700, Rapidpoint 350 systems.
RAPIDChem® 700 Urine Diluent for in vitro use with Rapidchem® 700 systems. Conta
RAPIDChem® 700 Urine Diluent for in vitro use with Rapidchem® 700 systems. Contains: buffers & presevatives
RAPIDChem® 744 Daily Cleaner Kit, for in vitro diagnostics use with Rapidchem® 7
RAPIDChem® 744 Daily Cleaner Kit, for in vitro diagnostics use with Rapidchem® 744 systems.
RAPIDChem® 700 RAPIDPoint® 340/350 Reference Sensor for in vitro diagnostics use
RAPIDChem® 700 RAPIDPoint® 340/350 Reference Sensor for in vitro diagnostics use with Rapidchem® 700, Rapidpoint ® 340/350 systems.
RAPIDChem® 700 Lithium Sensor for in vitro diagnostics use with the Rapidchem ®
RAPIDChem® 700 Lithium Sensor for in vitro diagnostics use with the Rapidchem ® 700 systems
RAPIDChem® 700 Chloride Sensor for in vitro diagnostics use with the Rapidchem ®
RAPIDChem® 700 Chloride Sensor for in vitro diagnostics use with the Rapidchem ® 700 systems