The device is intended for use in the quality control of CK-MB assays on clinical chemistry systems.

The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma.

The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma.

The device is intended for use in the calibration of CK-MB assays in clinical chemistry systems.

The CK method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of creatine kinase activity in serum or plasma.

The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.

The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.

The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.

The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.

The device is intended for the quantitative in vitro determination of creatine kinase activity in serum or plasma.

The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems.

Randox High Sensitivity CRP Control Level I is a ready to use control in a stabilised protein base. It is intended for use with the Randox High Sensitivity CRP Assay (Catalogue No. CP3885) for the control of accuracy and the control of reproducibility.

Randox High Sensitivity CRP Control Level II is a ready to use control in a stabilised protein base. It is intended for use with the Randox High Sensitivity CRP Assay (Catalogue No. CP3885) for the control of accuracy and the control of reproducibility.

The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems.

The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems.

This product is intended for in vitro diagnostic use in the quality control of CRP on clinical chemistry systems.

This product is intended for in vitro diagnostic use, in the quality control of CRP on clinical chemistry systems.

The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems.

This product is intended for in vitro diagnostic use, in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems.

This product is intended for in vitro diagnostic use in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems.

The CREA method used on the Dimension clinical chemistry system is an in vitro diagnostic device intended for the quantitative determination of Creatinine in serum, plasma or urine

The is intended for the quantitative in vitro diagnostic determination of Creatinine in serum, plasma or urine

The device intended for the quantitative in vitro determination of Creatinine in serum, plasma or urine

The is intended for the quantitative in vitro diagnostic determination of Creatinine in serum, plasma or urine

Randox Cytokine high sensitivity controls are intended for use as an assayed quality control in the routine monitoring of accuracy and precision for the analytes listed in this insert. The Randox Cytokine high sensitivity controls are multi-analyte. Each control contains all of the analytes listed overleaf. There are 3 levels of control: low, medium and high; Level 1, 2 and 3 respectively.

"Randox Cytokine controls are intended for use as an assayed quality control in the routine monitoring of accuracy and precision for the analytes listed in this insert.The Randox Cytokine Controls are multi-analyte. Each control contains all of the analytes listed overleaf. There are 3 levels of control: low, medium and high; Level 1, 2 and 3 respectively. "

The Randox Ammonia Ethanol Control Level 1 is intended for in vitro diagnostic use, in the quality control of Ammonia and Alcohol Assays to monitor precision and to detect systematic analytical deviations on clinical chemistry systems.

The Randox Ammonia Ethanol Control - Level 2 is intended for in vitro diagnostic use, in the quality control of Ammonia and Alcohol Assays to monitor precision and to detect systematic analytical deviations on clinical chemistry systems.

The Randox Ammonia Ethanol Control - Level 3 is intended for in vitro diagnostic use, in the quality control of Ammonia and Alcohol Assays to monitor precision and to detect systematic analytical deviations on clinical chemistry systems.

Chemiluminescent substrate comprised of 1 bottle of Luminol Reagent - EV805 and 1 bottle of Peroxide Reagent. The analyser uses a 1:1 mixture of the two solutions as a working signal reagent to generate a chemiluminescent signal which can be detected by the imaging module of the Evidence™ analyser.

Diluted displacement fluid is used to wash the Evidence™ reagent tubing between dispenses.

Diluted wash buffer is used for washing the biochips between assay steps to remove all unbound materials.

Chemiluminescent substrate comprised of 1 bottle of Luminol Reagent - EV701 and 1 bottle of Peroxide Reagent. The analyser uses a 1:1 mixture of the two solutions as a working signal reagent - EV701 to generate a chemiluminescent signal which can be detected by the imaging module of the Evidence™ analyser.

This product is intended for in vitro diagnostic use in the calibration of the Randox Liquid Fructosamine assay on clinical chemistry systems.

This product is intended for in vitro diagnostic use in the quality control of the Randox Liquid Fructosamine assay on clinical chemistry systems.

This product is intended for in vitro diagnostic use in the quality control of the Randox Liquid Fructosamine assay on clinical chemistry systems.

A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine

A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, plasma and urine

A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine

A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine

A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, plasma and urine

A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine

A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine

A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine

A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, lithium plasma and urine

A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, lithium plasma and urine

A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine