For coagulation tests and as a rinsing solution for the sample needles of the Sy
For coagulation tests and as a rinsing solution for the sample needles of the Sysmex® CA Systems
N/T Protein Control SL/M is a medium level, multi-analyte control for use as acc
N/T Protein Control SL/M is a medium level, multi-analyte control for use as accuracy and precision control in the determination of human serum proteins by immunonephelometry with the BN Systems
N/T Protein Control SL/H is a high level, multi-analyte control for use as accur
N/T Protein Control SL/H is a high level, multi-analyte control for use as accuracy and precision control in the determination of human serum proteins by immunonephelometry with the BN Systems
For the determination of the activity of coagulation factor X in human plasma by
For the determination of the activity of coagulation factor X in human plasma by coagulometric methods
For the determination of the activity of coagulation factor XI in human plasma b
For the determination of the activity of coagulation factor XI in human plasma by coagulometric methods
Quantitative determination of soluble transferrin receptor (sTfR) in human serum
Quantitative determination of soluble transferrin receptor (sTfR) in human serum and heparinized plasma on BN Systems
LA 1 Screening Reagent. Simplified DRVV reagent to screen for the presence of Lu
LA 1 Screening Reagent. Simplified DRVV reagent to screen for the presence of Lupus Anticoagulants
For use as a low level assayed control for the quantitative measurement of low m
For use as a low level assayed control for the quantitative measurement of low molecular weight heparin with Berichrom Heparin
For calibration of the Berichrom Heparin assay for measurement of low molecular
For calibration of the Berichrom Heparin assay for measurement of low molecular weight heparin
JPA
SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES
For use as a high level assayed control for the quantitative measurement of unfr
For use as a high level assayed control for the quantitative measurement of unfractionated heparin with Berichrom Heparin
Quantitative determination of homocysteine in human serum and plasma on BN II an
Quantitative determination of homocysteine in human serum and plasma on BN II and BN ProSpec® Systems
CYSC CON L is an assayed intralaboratory quality control for assessment of preci
CYSC CON L is an assayed intralaboratory quality control for assessment of precision and analytical bias in the determination of the CYSC method on the Dimension Vista® System
PROT1 CON M is an assayed, mid-level, intralaboratory, multi-analyte quality con
PROT1 CON M is an assayed, mid-level, intralaboratory, multi-analyte quality control for the assessment of precision and analytical bias on the Dimension Vista® System
For the quantitative measurement of immunoglobulin E in human serum and plasma (
For the quantitative measurement of immunoglobulin E in human serum and plasma (heparin or EDTA) on the Dimension Vista® System
DGC
IGE, ANTIGEN, ANTISERUM, CONTROL
DImension Vista® Immunoglobulin E Flex® reagent cartridge
For the quantitative measurement of C-reactive protein in human serum and plasma
For the quantitative measurement of C-reactive protein in human serum and plasma on the Dimension Vista® System
NQD
CARDIAC C-REACTIVE PROTEIN, ANTIGEN, ANTISERUM, AND CONTROL
For the quantitative measurement of total homocysteine in human serum and plasma
For the quantitative measurement of total homocysteine in human serum and plasma on the Dimension Vista® System
The DIMERTEST® Latex Assay is intended for the rapid qualitative or semiquantita
The DIMERTEST® Latex Assay is intended for the rapid qualitative or semiquantitative evaluation of circulating derivatives of cross-linked fibrin degradation products (XL-FDP) in human plasma
DAP
FIBRINOGEN AND FIBRIN SPLIT PRODUCTS, ANTIGEN, ANTISERUM, CONTROL
For differential staining in hematology that gives results similar to a Wright-G
For differential staining in hematology that gives results similar to a Wright-Giemsa stain
Assayed accuracy and precision controls in the determination of free light chain
Assayed accuracy and precision controls in the determination of free light chains (FLC) type kappa and type lambda on BN Systems.
Assayed accuracy and precision controls in the determination of free light chain
Assayed accuracy and precision controls in the determination of free light chains (FLC) type kappa and type lambda on BN Systems.
The BN ProSpec® is a system for the quantitative determination of proteins in se
The BN ProSpec® is a system for the quantitative determination of proteins in serum, plasma, urine and CSF
Quantitative determination of carbohydrate-deficient transferrin (CDT) in human
Quantitative determination of carbohydrate-deficient transferrin (CDT) in human serum on BN II and BN ProSpec® Systems
Qualitative detection or semi-quantitative determination of C-reactive protein (
Qualitative detection or semi-quantitative determination of C-reactive protein (CRP) in human serum
Qualitative detection or semi-quantitative determination of C-reactive protein (
Qualitative detection or semi-quantitative determination of C-reactive protein (CRP) in human serum
This product is intended for use in the calibration of Myoglobin immunoturbidime
This product is intended for use in the calibration of Myoglobin immunoturbidimetric assays.
Immunoturbidimetric assay for the quantitative in vitro determination of Myoglob
Immunoturbidimetric assay for the quantitative in vitro determination of Myoglobin in human serum.
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I, Myoglobin
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I, Myoglobin and Creatine kinase MB in human whole blood, serum and plasma
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I, Myoglobin,
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I, Myoglobin, Creatine kinase MB and Nt-proBNP in human serum and plasma
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I, Myoglobin
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I, Myoglobin and Creatine kinase MB in human whole blood, serum and plasma
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I and Myoglob
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I and Myoglobin in human whole blood, serum and plasma
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I, Myoglobin
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I, Myoglobin and Creatine kinase MB in human serum and plasma
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I and Myoglob
In Vitro Diagnostic Test kit for the detection of Cardiac Troponin I and Myoglobin in human serum and plasma
The Stratus® CS Acute Care(TM) Myoglobin Dilution Pak (MYO DilPak) is an in vitr
The Stratus® CS Acute Care(TM) Myoglobin Dilution Pak (MYO DilPak) is an in vitro diagnostic product intended to be used in conjunction with the Acute Care(TM) MYO TestPak for the measurement of samples with elevated levels of Myoglobin.
The Stratus® CS Acute Care(TM) Myoglobin Calibrator (MYO CalPak) is an in vitro
The Stratus® CS Acute Care(TM) Myoglobin Calibrator (MYO CalPak) is an in vitro diagnostic product intended to be used for the calibration of the Stratus® CS Acute Care(TM) MYO method.
The Stratus® CS Acute Care(TM) Myoglobin (MYO) method is an in vitro diagnostic
The Stratus® CS Acute Care(TM) Myoglobin (MYO) method is an in vitro diagnostic test for the quantitative measurement of myoglobin in heparinized plasma.
The Stratus® CS Acute Care™ Cardiac Troponin I Dilution Pak (cTNI DilPak) is an
The Stratus® CS Acute Care™ Cardiac Troponin I Dilution Pak (cTNI DilPak) is an in vitro diagnostic product intended to be used in conjunction with the Acute Care™ cTNI TestPak on the Stratus® CS analyzer for the measurement of samples with elevated levels of cardiac Troponin I.
The Stratus® CS Acute Care™ Troponin I Calibrator (cTNI CalPak) is an in vitro d
The Stratus® CS Acute Care™ Troponin I Calibrator (cTNI CalPak) is an in vitro diagnostic product intended to be used for the calibration of the Stratus® CS Acute Care™ cTNI method.
The Stratus® CS Acute Care™ Troponin I method (cTNI) is an in vitro diagnostic t
The Stratus® CS Acute Care™ Troponin I method (cTNI) is an in vitro diagnostic test for the measurement of cardiac troponin I in heparinized plasma.
The Stratus® CS Acute Care™ CKMB Dilution Pak (CKMB DilPak) is an in vitro diagn
The Stratus® CS Acute Care™ CKMB Dilution Pak (CKMB DilPak) is an in vitro diagnostic product intended to be used in conjunction with the Acute Care™ CKMB TestPak on the Stratus® CS analyzer for the measurement of samples with elevated CKMB levels.
The Stratus® CS Acute Care (TM) CKMB Calibrator (CKMB CalPak) is an in vitro dia
The Stratus® CS Acute Care (TM) CKMB Calibrator (CKMB CalPak) is an in vitro diagnostic product intended to be used for the calibration of the Stratus® CS Acute Care (TM) CKMB method.
The Stratus® CS Acute Care (TM) CKMB method is an in vitro diagnostic test for t
The Stratus® CS Acute Care (TM) CKMB method is an in vitro diagnostic test for the measurement of the MB isoenzyme of creatine kinase (ATP: Creatine N-Phosphostransferase, E. C. No. 2.7.3.2) in heparinized plasma.