Quantimetrix Corp

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Web: http://www.4qc.com
E-Mail:
Address: 2005 Manhattan Beach Boulevard, Redondo Beach, California 90278, USA
Phone: +001-(310)-536-0006 | Fax: +001-(310)-536-9977 | Map/Directions >>
 
 

Profile: Quantimetrix Corp manufactures clinical laboratory quality control products. Our Dipper™ urine dipstick control is designed to validate visual & instrumental readings of urine dipsticks by immersing the dipstick into the control. Ammonia/Alcohol Control is intended as a means of monitoring various ammonia and ethanol assay methods. Our pyrogallol red molybdate dye binding method provides a simple, ready-to-use colorimetric method for total protein quantitation with greater linearity, using microliter samples of urine or cerebrospinal fluid in manual or automated systems. Our Lipoprint System is a high resolution diagnostic test for cholesterol components which are not routinely tested by other methods. The Lipoprint test provides detailed results within the subfractions of low density lipoproteins (LDL).

The company is ISO, CE certified.

FDA Registration Number: 7000640

50 Products/Services (Click for related suppliers)  
• Alkaline Phosphatase Isoenzymes Electrophoretic Separation Test (FDA Code: CIN / 862.1050)
An alkaline phosphatase or isoenzymes test system is a device intended to measure alkaline phosphatase or its isoenzymes (a group of enzymes with similar biological activity) in serum or plasma. Measurements of alkaline phosphatase or its isoenzymes are used in the diagnosis and treatment of liver, bone, parathyroid, and intestinal diseases.
• 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.
• Blood Collect Tubes
• Blood glucose testing
• Cardiac Markers
• Cardiac Markers Control
• Cardiac Markers kits
• Coding, Compliance Resources
• Compliance Resources, Clinical Lab
• Compliance Service, FDA
• Controls for Diagnostic Equipment
• Diabetic Monitoring
• Diagnostic Test Kits For Pregnancy
• Drug Mixture Control Materials (FDA Code: DIF / 862.3280)
A clinical toxicology control material is a device intended to provide an estimation of the precision of a device test system and to detect and monitor systematic deviations from accuracy resulting from reagent or instrument defects. This generic type of device includes various single, and multi-analyte control materials.
• Drug Specific Control Test (FDA Code: LAS / 862.3280)
• Drugs Of Abuse Test Kits
• Drugs Of Abuse Testing Kits
• Early Pregnancy Testing Kit
• Electrolyte Control (FDA Code: JJR / 862.1660)
• Electrophoresis Calibrators & Controls
• Electrophoresis Instruments
• Enzyme Controls (FDA Code: JJT / 862.1660)
• General Chemistry Calibrators
• General Chemistry Test Kits
• General Diagnostic Supplies
• General Examination Supplies
• General Medical Supplies
• Glucose
• Glucose Analyzers
• Glucose Kits
• Glucose Test Kits
• Hematology Kits
• Hematology Quality Control Mixture (FDA Code: JPK / 864.8625)
A hematology quality control mixture is a device used to ascertain the accuracy and precision of manual, semiautomated, and automated determinations of cell parameters such as white cell count (WBC), red cell count (RBC), platelet count (PLT), hemoglobin, hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC).
• Hemoglobin Control (FDA Code: GGM / 864.8625)
• Home pregnancy test kits, Hcg
• Lipid Analyzers
• Lipids Test Kits
• Lipoproteins Electrophoretic Separation Test (FDA Code: JHO / 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.
• Multi Analyte Control (FDA Code: JJY / 862.1660)
• POC Rapid Cardiac Markers
• Pregnancy Kits
• Pregnancy Testing Kits
• Publications Service
• Quality Assessment Programs
• Sensitive Pregnancy Tests
• Specialty Diagnostic Supplies
• Total Protein Biuret Method (FDA Code: CEK / 862.1635)
A total protein test system is a device intended to measure total protein(s) in serum or plasma. Measurements obtained by this device are used in the diagnosis and treatment of a variety of diseases involving the liver, kidney, or bone marrow as well as other metabolic or nutritional disorders.
• Urinalysis Controls (FDA Code: JJW / 862.1660)
• Urinalysis Kits
• Urine Dipstick Control

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