For the Quantitative Determination of Magnesium in Serum, Plasma or Urine.

For the Quantitative Colorimetric determination of Total Calcium in serum, plasma or urine.

For the Quantitative Colorimetric determination of Total Calcium in serum.

Quantitative Colorimetric Determination of Chloride in Serum, Plasma, Urine and CSF.

The Stanbio Total Bilirubin LiquiColor® test system is a device intended to measure the levels of bilirubin (total) in serum and plasma. Measurements of the levels of bilirubin, an organic compound formed during the normal and abnormal destruction of red blood cells, is used in the diagnosis and treatment of liver, hemolytic, hematological, and metabolic disorders, including hepatitis and gall bladder block.

For the quantitative colorimetric determination of Direct Bilirubin in Serum and Plasma.

For the Quantitative Colorimetric Determination of Total Bilirubin in Serum or Plasma.

For the Quantitative Colorimetric Determination of Direct Bilirubin in Serum or Plasma.

For the Quantitative Colorimetric Determination of Total and Direct Bilirubin in Serum or Plasma.

For the Quantitative Colorimetric Determination of Iron and Unsaturated Iron-Binding Capacity in Serum.

Quantitative Kinetic Determination of Creatinine in Serum or Urine.

For the quantitative enzymatic determination of creatinine in serum and urine.

For the quantitative enzymatic determination of creatinine in serum and urine.

For the Quantitative Determination of High Density Lipoprotein (HDL) Cholesterol in Human Serum.

For the Quantitative Determination of High Density Lipoprotein (HDL) Cholesterol in Human Serum.

For the Quantitative Determination of High Density Lipoprotein (HDL) Cholesterol in Human Serum.

For the Calibration of Stanbio HDL Cholesterol and LDL Cholesterol LiquiColor® Reagent Kits.

For Use in the Determination of High Density Lipoprotein (HDL) Cholesterol in Serum or Plasma.

For the Quantitative Determination of Low Density Lipoprotein (LDL) Cholesterol in Human Serum or Plasma.

For the Quantitative Determination of Creatine Kinase-MB (CK-MB) in Serum for Manual and/or Automated Procedures.

For the Quantitative-Enzymatic-Colorimetric Determination of Total and HDL Cholesterol in Serum or Plasma.

For the Quantitative-Enzymatic-Colorimetric Determination of Total and HDL Cholesterol in Serum or Plasma.

For the Quantitative Determination of Glucose in Serum or Plasma.

For the Quantitative Determination of Glucose in Serum, Plasma or CSF.

For the Quantitative Determination of Glucose in Serum, Plasma or CSF.

For the Quantitative Determination of Glucose in Serum, Plasma or CSF.

STAT-Site® Diluent is intended to be used with the STAT-Site® M β-HB Test Strips or KetoSite® Test Cards to dilute specimens containing high levels of β-hydroxybutyrate into the test range of 0 – 2 mM. Additionally, the diluent helps to eliminate possible matrix effects caused by interfering substances such as acetoacetate.

Stanbio Glycated Serum Protein (GSP) Calibrator Kit is intended to be used for calibration of Stanbio Glycated Serum Protein LiquiColor® Assay (REF 2350-062).

Stanbio Glycated Serum Protein (GSP) Control Kit is intended to be used for quality control procedures in examining the accuracy and precision of Stanbio Glycated Serum Protein LiquiColor® Assay (REF 2350-062).

For the Quantitative Determination of ß-Hydroxybutyrate in Human Serum or Plasma.

For the Kinetic Quantitative Determination of Alkaline Phosphatase in Serum for Manual and/or Automated Procedures.

For the Kinetic Quantitative Determination of Alkaline Phosphatase in Serum for Manual and/or Automated Procedures.

For the Kinetic Quantitative Determination of Creatine Kinase in Serum.

For the Kinetic Quantitative Determination of AST/GOT in Serum for Manual and/or Automated Procedures.

For the Kinetic Quantitative Determination of AST/GOT in Serum for Manual and/or Automated Procedures.

For the Kinetic Quantitative Determination of ALT/ GPT in Serum for Manual and/or Automated Procedures.

For the Kinetic Quantitative Determination of ALT/ GPT in Serum for Manual and/or Automated Procedures.

For the Quantitative Determination of Lactate Dehydrogenase in Serum and EDTA Plasma.

For the Quantitative Determination of Lactate Dehydrogenase in Serum and EDTA Plasma.

For the Kinetic Quantitative Determination of γ-Glutamyl Transferase in Serum for Manual and/or Automated Procedures.

For the Kinetic Quantitative Determination of γ-Glutamyl Transferase in Serum for Manual and/or Automated Procedures.

For the Quantitative Determination of Amylase in Serum and Urine.

STAT-Site® Controls are intended to be used to verify the procedural reliability of the assay for β-hydroxybutyrate using STAT-Site® Mβ-HB Meter and Test Strips.

The STAT-Site® Linearity Check is intended to be used to perform a linearity evaluation of the STAT-Site® Mβ-HB Test Strips /KetoSite® Test Cards by making a series of dilutions using STAT-Site® Diluent (Catalog No. 202000). Both the STAT-Site® Mβ-HB Test Strips and KetoSite® Test Cards are used in the measurement of β-hydroxybutyrate with the STAT-Site® Mβ-HB and STAT-Site® Meter.

A bi-level reference control set intended for use on HemoPoint® H2 Hemoglobin testing system.

The STAT-Site® M β-HB Test is intended for the quantitative determination of the ketone body β-Hydroxybutyrate in serum or plasma using the STAT-Site® M β-HB Analyzer (Catalog #400400). The STAT-Site® M β-HB Test may be used with adults, infants, and children. For laboratory use only.

The STAT-Site® Mß-HB Meter is a dedicated reflectance photometer designed to accept only STAT-Site® Mß-HB CODE Keys and STAT-Site® Mß-HB Test Strips. This test system is intended or the quantitative determination of ß-hydroxybutyrate in serum or plasma.

For the Quantitative Determination of ß-Hydroxybutyrate in Serum or Plasma.

This instrument is intended to be used to read and calculate the results of in-vitro clinical diagnostic assays, as well as any other application requiring absorbance or concentration readings at or near the available wavelengths. This general purpose instrument is intended to be used by laboratory professionals capable of selecting the appropriate features and options for each specific clinical application.

This instrument is intended to be used to read and calculate the results of in-vitro clinical diagnostic assays, as well as any other application requiring absorbance or concentration readings at or near the available wavelengths. This general purpose instrument is intended to be used by laboratory professionals capable of selecting the appropriate features and options for each specific clinical application.