The Piccolo® Lipid Panel reagent disc, used with the Piccolo® blood chemistry analyzer or the Piccolo Xpress® Chemistry analyzer, is intended for the in vitro quantitative determination of total cholesterol (CHOL), high-density lipoprotein cholesterol (HDL), and triglycerides (TRIG) in capillary (fingerstick) lithium heparinized whole blood, venous lithium heparinized whole blood, lithium heparinized plasma, or serum in a clinical laboratory setting or point-of-care location. From these determinations low-density lipoprotein cholesterol (LDL), very low-density lipoprotein cholesterol (VLDL), non-HDL cholesterol, and a total cholesterol/high-density lipoprotein cholesterol ratio (TC/H) are calculated by the analyzer.Lipid measurements are used in the diagnosis and treatment of lipid and lipoprotein disorders, atherosclerosis, various liver and renal diseases, diabetes mellitus, and other diseases involving lipid metabolism or various endocrine disorders.This test is waived under CLIA ’88 regulations. If a laboratory modifies the test system instructions, then the test is considered high complexity and subject to all CLIA requirements. For CLIA waived labs, only lithium heparin whole blood (venous or capillary) may be tested. For use in moderate complexity labs, lithium heparinized whole blood, lithium heparinized plasma, or serum may be used.

The Piccolo® Lipid Panel Plus, used with the Piccolo® blood chemistry analyzer or the Piccolo Xpress® chemistry analyzer, is intended for the in vitro quantitative determination of total cholesterol (CHOL), high-density lipoprotein cholesterol (HDL), triglycerides (TRIG), alanine aminotransferase (ALT), aspartate aminotransferase (AST), and glucose (GLU) in capillary (fingerstick) lithium heparinized whole blood, venous lithium heparinized whole blood, lithium heparinized plasma, or serum in a clinical laboratory setting or point-of-care location. From the CHOL, HDL and TRIG determinations, low-density lipoprotein cholesterol (LDL), very low-density lipoprotein cholesterol (VLDL), non-HDL cholesterol, and a total cholesterol/high-density lipoprotein cholesterol ratio (TC/H) are calculated by the analyzer.Lipid measurements are used in the diagnosis and treatment of lipid and lipoprotein disorders, atherosclerosis, various liver and renal diseases, diabetes mellitus, and other diseases involving lipid metabolism or various endocrine disorders.The tests on this panel are waived under CLIA ’88 regulations. If a laboratory modifies the test system instructions, then the tests are considered high complexity and subject to all CLIA requirements. For CLIA waived labs, only lithium heparin whole blood (venous or capillary) may be tested. For use in moderate complexity labs, lithium heparinized whole blood, lithium heparinized plasma, or serum may be used.

Alere Cholestech LDX® TC HDL

Alere Cholestech LDX® Lipid Profile

Alere Cholestech LDX® TC HDL GLU

Alere Cholestech LDX® Lipid Profile GLU

Alere Cholestech LDX® Lipid Profile GLU

Alere Cholestech LDX® Lipid Profile

Alere Cholestech LDX® Lipid Profile GLU

HDL-C Reagent

HDL-C Reagent

HDL Cholesterol Reagent HDL 2 x 200

HDL-Cholesterol

LDL-Cholesterol

HDL-Cholesterol

LDL-Cholesterol

HDLD (High Density Lipoprotein Direct) w/ cal 3 x 250 tests

HDLD (High Density Lipoprotein Direct) w/ cal 3 x 100 tests

HDLD W/CALIBRATOR, 2 X 200 tests

HDLD (HDL Cholesterol Direct) w/ calibrator 4 x 250 tests

HDLD (HDL Cholesterol Direct) w/ cal 2 x 250 tests

In Vitro Diagnostics testing kit R1:3X45mL, R2:3X15mL

The HDL-Cholesterol Reagent Set 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.

HDL CHOLESTEROL (2 x 30mL R1, 2 x 10mL R2, 1 x 3mL Standard)

HDL CHOLESTEROL (2x 125mL R1, 2x 42mL R2)

HDL CHOLESTEROL (4x 125mL R1, 4x 42mL R2)

HDL CHOLESTEROL (2x 30mL R1, 2x 10mL R2)

HDL CHOLESTEROL Bulk

HDL, CHOLESTEROL (4x 40mL R1, 2x 45mL R2)

HDL-Cholesterol Reagent 2 X 66 mL + 1 X 44 mL

HDL-Cholesterol Reagent 1 X 240 mL + 1 X 80 mL

HDL-Cholesterol Reagent 1 X 25 mL + 1 X 8.4 mL

HDL-Cholesterol Reagent 1 X 60 mL + 1 X 20 mL

Clinical Analyzer

WASH Solution used for the Vantera Clinical Analyzer

Sample Diluent 1 used for the Vantera Clinical Analyzer.

NMR Reference Standard used for the Vantera Clinical Analyzer.

VITROS Chemistry Products dHDL Slides

VITROS Chemistry Products dHDL Slides

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

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

An HDL-cholesterol test system is a device intended for the quantitative in vitro determination of HDL-cholesterol concentration in human serum and plasma.

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

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