Albumin reagent is used for the quantitative determination of albumin concentration in human serum.

For the quantitative determination of alkaline phosphatase in human serum.

For the quantitative determination of alanine aminotransferase in serum used in routine examination and monitoring of therapy and relapses.

For the quantitative determination of aspartate aminotransferase (AST) in human serum. The reagents are used in routine examination and monitoring of therapy and relapses.

For the quantitative determination of direct bilirubin in human serum. For in vitro diagnostic use.

Urea nitrogen (BUN) liquid reagent is used for the kinetic quantitative determination of Urea Nitrogen (BUN) in human serum used in routine examination and monitoring of therapy and relapses.

For the quantitative determination of calcium concentration in serum or plasma.

For the quantitative determination of total cholesterol in serum

For the quantitative determination of Creatine Kinase in human serum.

Creatinine reagent is used for the quantitative determination of creatinine in human serum.

For the In Vitro quantitative determination of glucose in human serum or plasma.

Inorganic phosphorus (UV method) reagent is for the quantitative determination of inorganic phosphorus in human serum.

Lactate Dehydrogenase LS (LDH-L) liquid reagent is intended to use for the In Vitro quantitative kinetic determination of Lactate Dehydrogenase activity in serum.

For the quantitative determination of total protein concentration in human serum.

For the in vitro quantitative determination of Triglycerides in serum or plasma.

For the in vitro quantitative determination of Uric Acid in serum.

The IDG HDL-Cholesterol reagent is intended for the in vitro quantitative determination of High Density Lipoprotein Cholesterol in human serum or plasma. The reagent can assist in the diagnosis and treatment of patients at risk for developing coronary heart disease.

The IDG PT-HS reagent is an in vitro diagnostic assay intended for use in performing the one stage prothrombin time (PT) test and assays which are based on a modified prothrombin time.

The IDG APTT-EA reagent is an in vitro diagnostic assay intended for use in determining activated partial thromboplastin time (APTT) and coagulation factor assays that are based on a modified APTT.

Calcium Chloride 0.020 M is a reagent for use only in the in vitro determination of Prothrombin Time (PT), Activated Partial Thromboplastin Time (APTT) and recalcification (plasma clotting) time, as well as in various coagulation factor assays

The IDG Control Level 1 Normal is intended for use in quality assurance of in vitro diagnostic coagulation tests (1-3). The reagent is suitable for use as a normal coagulation time control in the one-stage prothrombin time (PT) assay and in the activated partial thromboplastin time (APTT) assay.

The IDG Control Level 2 Low Abnormal is intended for use for quality assurance of in vitro diagnostic coagulation tests (1-3). The reagent is suitable for use as a low abnormal coagulation time control in the one-stage prothrombin time (PT) assay and in the activated partial thromboplastin time (APTT) assay

For in vitro diagnostic use only. The Chemistry Control is to be used for monitoring the accuracy and precision of clinical chemistry procedures. This control contains constituents commonly of interest in a general chemistry control, including common drugs and thyroids.. The assayed multi-analyte control product is packaged with one level of analytes.

For in vitro diagnostic use only. The Chemistry Control is to be used for monitoring the accuracy and precision of clinical chemistry procedures. This control contains constituents commonly of interest in a general chemistry control, including common drugs and thyroids. The assayed multi-analyte control product is packaged with one level of analytes.

The Multi-Analyte Chemistry calibrator is for use as a calibrator of IDG Clinical chemistry assays. This calibrator material is well suited for automated and semi-automated analytical procedures.

The HDL-LDL calibrator is used to establish the value of high density lipoprotein cholesterol and low-density lipoprotein cholesterol for IDG HDL Cholesterol Enzymatic and LDL Cholesterol Enzymatic Assays, respectively. The calibrator isfor in vitro diagnostic use only.