The Human Assayed Multi-sera is supplied at 2 levels, level 2 and 3. Target values and ranges are supplied for the analytes listed in the values section at both levels.

The Human Assayed Multi-sera is supplied at 2 levels, level 2 and 3. Target values and ranges are supplied for the analytes listed in the values section at both levels.

The product is intended for the quantitative in vitro determination of IgA in serum or plasma.

This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility ofanalytes listed in the package insert.

This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.

This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.

This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.

The product is intended for the quantitative in vitro determination of IgA in serum or plasma.

The product is intended for the quantitative in vitro determination of IgA in serum or plasma.

The product is intended for the quantitative in vitro determination of IgA in serum or plasma.

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

An IgE test system is a device intended for the quantitative in vitro determination of immunoglobulin E (IgE) concentration in human serum or plasma

The IgG test system is a device intended for the quantitative in vitro determination of immunoglobulin G (IgG) concentration in serum and plasma

The IgG test system is a device intended for the quantitative in vitro determination of immunoglobulin G (IgG) concentration in serum and plasma

The IgG test system is a device intended for the quantitative in vitro determination of immunoglobulin G (IgG) concentration in serum and plasma

For the quantitative in vitro determination of IgM in serum and plasma

For the quantitative in vitro determination of IgM in serum and plasma

Liquid Protein Calibrators are an in vitro diagnostic product used for the calibration of ASO, Complement C3, Complement C4, Ceruloplasmin, CRP, Ferritin, Haptoglobin, IgA, IgG, IgM, Prealbumin, RF and Transferrin assays.

Liquid Protein Calibrators are an in vitro diagnostic product used for the calibration of Alpha-1-Antitrypsin, Alpha-1-Acid glycoprotein, IgA, IgG and IgM assays that require sample pre-dilution.

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

A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum or plasma.

A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum.

A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum or plasma.

A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum or plasma.

This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.

This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.

This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.

This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.

This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.

This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.

A Lipase test system is a device intended for the quantitative in vitro determination of Lipase in human serum and plasma

For the quantitative in vitro determination of Lipase in human serum and plasma.

Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma

An APO B test system is a device intended for the quantitative in vitro determination of Apolipoprotein B (APO B) in serum and plasma.

Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma

Immunoturbidimetric assay for the quantitative in vitro determination of Apolipoprotein B in human serum.

For the quantitative in vitro determination of Lipoprotein (a) in human serum or plasma.

Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma

An APO B test system is a device intended for the quantitative in vitro determination of Apolipoprotein B (APO B) in serum and plasma.

This product is intended for in-vitro use in the calibration of Apolipoprotein A-I and Apolipoprotein B assays.