An Albumin test system is a device intended for the quantitative in vitro determination of Albumin concentration in serum.

The paracetamol test system is intended for the quantitative in vitro determination of Acetaminophen in human serum.

The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.

The device is intended for the quantitative in vitro determination of total bilirubin in serum or plasma.

The device is intended for the quantitative in vitro determination of direct bilirubin in serum or plasma.

The device is intended for the quantitative in vitro determination of direct bilirubin in serum or plasma.

The device is intended for the quantitative in vitro determination of total bilirubin in serum or plasma.

The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.

Enzymatic Clearance assay for the in vitro quantitative determination of HDL-cholesterol in human serum and plasma.

For the quantitative in vitro determination of cholesterol in serum and plasma.

For the quantitative in vitro determination of HDL Cholesterol in serum and plasma.

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

The device is intended for the quantitative in vitro determination of Cystatin C in serum or plasma.

The Opiates assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of Opiates in human urine.

The EDDP assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) in human urine.

The MDMA assay is an in vitro diagnostic reagent. For the qualitative and semi-quantitative analysis of MDMA in human urine.

The ethanol assay is an in vitro diagnostic test for the quantitative analysis of ethanol in human urine and serum.

The Methadone assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of methadone in human urine.

Enzymatic assay for the quantitative in vitro determination of glycated protein (fructosamine) in human serum or plasma.

The product is intended for the quantitative in vitro determination of Glucose in serum or urine.

A Gamma GT test system is a device intended for the quantitative in vitro determination of L Gamma Glutamyltransferase (GGT) activity in serum.

This product is intended for in vitro diagnostic use in the quality control of HbA1c on clinical chemistry systems.

The product is intended for the quantitative in vitro determination of Haemoglobin A1c concentration in whole blood.

A homocysteine test system is a device intended for the quantitative in vitro determination of homocysteine concentration in human serum.

This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Liquid Assayed Chemistry Control Premium Plus is for the control of accuracy.

This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Liquid Assayed Chemistry Control Premium Plus is for the control of accuracy.