Profile: Creative Laboratory Products, Inc. specializes in manufacturing lipid additives. Our products are widely used by the manufacturers of liquid and lyophilized lipid controls. We produce lipid quality control products for the OEM market,and cholesterol / triglyceride lipoprotein additives for the diagnostic industry. Our lipid control is a human serum based multivariate control to be used as the liquid control for total cholesterol, total triglyceride, HDL cholesterol, LDL cholesterol, and apolipoproteins. Our iron control is a human serum control to be used to control total iron binding capacity, total serum iron, and unbound iron binding capacity assays.
The company was founded in 1987, has revenues of < USD 1 Million.
FDA Registration Number: 1832818
16 Products/Services (Click for related suppliers)
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• Abnormal Hemoglobin Control (FDA Code: JCM / 864.7415) |
• Assayed and Unassayed Single (Specified) Analyte Controls (FDA Code: JJX / 862.1660) A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls. |
• Control Antiserum Antigen Cholinesterase |
• Egg Triglyceride Concentrates |
• Electrophoretic, Lactate Dehydrogenase Isoenzymes (FDA Code: CFE / 862.1445) A lactate dehydrogenase isoenzymes test system is a device intended to measure the activity of lactate dehydrogenase isoenzymes (a group of enzymes with similar biological activity) in serum. Measurements of lactate dehydrogenase isoenzymes are used in the diagnosis and treatment of liver diseases, such as viral hepatitis, and myocardial infarction. |
• HDL Precipitation Method (FDA Code: LBR / 862.1475) A lipoprotein test system is a device intended to measure lipoprotein in serum and plasma. Lipoprotein measurements are used in the diagnosis and treatment of lipid disorders (such as diabetes mellitus), atherosclerosis, and various liver and renal diseases. |
• Human Lipoprotein Cholesterol Concentrates |
• Human Serum Controls |
• LDL & VLDL Precipitation Method (FDA Code: LBR / 862.1475) |
• Lipid Constituents Controls. |
• Lipid Standard |
• Lipoprotein Electrophoresis Controls |
• Low Density Lipoprotein (FDA Code: DFC / 866.5600) A low-density lipoprotein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the low-density lipoprotein in serum and other body fluids. Measurement of low-density lipoprotein in serum may aid in the diagnosis of disorders of lipid (fat) metabolism and help to identify young persons at risk from cardiovascular diseases. |
• Multi Analyte Control (FDA Code: JJY / 862.1660) |
• Porcine LDL Cholesterol Concentrates |
• Sickle Cell Test (FDA Code: GHM / 864.7825) A sickle cell test is a device used to determine the sickle cell hemoglobin content of human blood to detect sickle cell trait or sickle cell diseases. |