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Osmetech, Inc.

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Web: http://www.osmetech.com
E-Mail:
Address: 757 S. Raymond Avenue, Pasadena, California 91105, USA
Phone: +1-(770)-510-4444 | Fax: +1-(770)-510-4445 | Map/Directions >>
 
 

Profile: Osmetech focuses on providing cutting-edge, cost effective molecular diagnostic technologies. We offer products like eSensorr XT-8, eSensorr CFCD & SensiTubeT. The FDA cleared eSensorr CF carrier detection (CFCD) system offers highly accurate and reproducible cystic fibrosis carrier results delivered in an easy to interpret report. Each kit includes all reagents necessary for PCR amplification and mutation detection in a single box. Our products are primarily used in the emergency room, operating room, cardiac monitoring area and any location where time critical diagnostic testing is performed within the hospital setting. Our OPTI analyzers utilize a sensor technology based on optical fluorescence sensors and the process of optical reflectance.

The company was founded in 1993. LON:OMH (SEC Filings)

41 Products/Services (Click for related suppliers)  
• Arterial Catheters
• Automated Hemoglobin System (FDA Code: GKR / 864.5620)
An automated hemoglobin system is a fully automated or semi-automated device which may or may not be part of a larger system. The generic type of device consists of the reagents, calibrators, controls, and instrumentation used to determine the hemoglobin content of human blood.
• Blood Gas & Electrolyte Analyzers
• Blood Gas Analyzers
• Blood Gas and Ph Electrode Measurement (FDA Code: CHL / 862.1120)
A blood gases (PCO2, PO2) and blood pH test system is a device intended to measure certain gases in blood, serum, plasma or pH of blood, serum, and plasma. Measurements of blood gases (PCO2, PO2) and blood pH are used in the diagnosis and treatment of life-threatening acid-base disturbances.
• Blood Gas Data Management Software
• Blood Gas Monitors
• Blood glucose testing
• Blood Sample Collection Kits
• Calcium Ion Specific Electrode (FDA Code: JFP / 862.1145)
A calcium test system is a device intended to measure the total calcium level in serum. Calcium measurements are used in the diagnosis and treatment of parathyroid disease, a variety of bone diseases, chronic renal disease and tetany (intermittent muscular contractions or spasms).
• Catheters
• Chloride Ion Specific Electrode (FDA Code: CGZ / 862.1170)
A chloride test system is a device intended to measure the level of chloride in plasma, serum, sweat, and urine. Chloride measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders such as cystic fibrosis and diabetic acidosis.
• Cytochrome P450 2c9 (Cyp450 2c9) Drug Metabolizing Enzyme Genotyping System (FDA Code: ODW / 862.3360)
A drug metabolizing enzyme genotyping system is a device intended for use in testing deoxyribonucleic acid (DNA) extracted from clinical samples to identify the presence or absence of human genotypic markers encoding a drug metabolizing enzyme. This device is used as an aid in determining treatment choice and individualizing treatment dose for therapeutics that are metabolized primarily by the specific enzyme about which the system provides genotypic information.
• Electrolyte Analyzers
• Gas Administration Devices
• Gene Mutation Detection, Cystic Fibrosis Transmembrane Conductance Regulator System (FDA Code: NUA / 866.5900)
• Genomic Dna Pcr 10-Methylenetetrahydrofolate Reductase Mutations Test 5 (FDA Code: OMM / 864.7280)
Factor V Leiden deoxyribonucleic acid (DNA) mutation detection systems are devices that consist of different reagents and instruments which include polymerase chain reaction (PCR) primers, hybridization matrices, thermal cyclers, imagers, and software packages. The detection of the Factor V Leiden mutation aids in the diagnosis of patients with suspected thrombophilia.
• Genomic Dna Pcr Factor Ii G20210a Mutations Test (FDA Code: NPR / 864.7280)
• Genomic Dna Pcr Factor V Leiden Mutations Test (FDA Code: NPQ / 864.7280)
• Glucose
• Glucose Analyzers
• Glucose Kits
• Glucose Oxidase, Glucose (FDA Code: CGA / 862.1345)
A glucose test system is a device intended to measure glucose quantitatively in blood and other body fluids. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia, and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma.
• Glucose Test Kits
• Instrumentation For Clinical Multiplex Test Systems (FDA Code: NSU / 862.2570)
• Instruments, Blood Gas & Electrolytes
• Multi Analyte Control (FDA Code: JJY / 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.
• Multianalyte Systems
• Oximeters (FDA Code: DQA / 870.2700)
An oximeter is a device used to transmit radiation at a known wavelength(s) through blood and to measure the blood oxygen saturation based on the amount of reflected or scattered radiation. It may be used alone or in conjunction with a fiberoptic oximeter catheter.
• Oximeters & Hemoximeters
• Point-of-care Testing, Blood Gas Kits
• Potassium Ion Specific Electrode (FDA Code: CEM / 862.1600)
A potassium test system is a device intended to measure potassium in serum, plasma, and urine. Measurements obtained by this device are used to monitor electrolyte balance in the diagnosis and treatment of diseases conditions characterized by low or high blood potassium levels.
• QA Programs
• Reagents
• Refurbished Equipment
• Respiratory Analyzers, Carbon Dioxide
• Sodium Ion Specific Electrode (FDA Code: JGS / 862.1665)
A sodium test system is a device intended to measure sodium in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of aldosteronism (excessive secretion of the hormone aldosterone), diabetes insipidus (chronic excretion of large amounts of dilute urine, accompanied by extreme thirst), adrenal hypertension, Addison's disease (caused by destruction of the adrenal glands), dehydration, inappropriate antidiuretic hormone secretion, or other diseases involving electrolyte imbalance.
• Software Programs
• Softwares
• Vitamin K Epoxide Reductase Complex Subunit One (Vkorc1) Genotyping System (FDA Code: ODV / 864.7750)
A prothrombin time test is a device used as a general screening procedure for the detection of possible clotting factor deficiencies in the extrinsic coagulation pathway, which involves the reaction between coagulation factors III and VII, and to monitor patients receiving coumarin therapy (the administration of one of the coumarin anticoagulants in the treatment of venous thrombosis or pulmonary embolism).
• Whole Blood Oximeter (FDA Code: GLY / 864.7500)
A whole blood hemoglobin assay is a device consisting or reagents, calibrators, controls, or photometric or spectrophotometric instrumentation used to measure the hemoglobin content of whole blood for the detection of anemia. This generic device category does not include automated hemoglobin systems.

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