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Calbiotech, Inc.

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Web: http://www.calbiotech.com
E-Mail:
Address: 10461 Austin Drive, Spring Valley, California 91978, USA
Phone: +1-(619)-660-6162 | Fax: +1-(619)-660-6970 | Map/Directions >>
 
 

Profile: Calbiotech Inc. offers a wide range of diagnostic products, OEM manufacturing, R&D and method validation. We are accredited with ISO 9002 and ISO 13488 certification. We market a wide range of elisa & rapid test products in the areas of infectious diseases, autoimmune disorders, endocrine markers, tumor markers, thyroid markers, fertility markers and steroid markers. Our EZ-elisa line for infectious diseases and autoimmune disorders utilizes a single procedure to perform more than 60 different tests.

FDA Registration Number: 2090110

51 to 91 of 91 Products/Services (Click for related suppliers)  Page: << Previous 50 Results 1 [2]
• LH Chemiluminescent ELISA Kit
• Luteinizing Hormone (LH)
• Luteinizing Hormone Radioimmunoassay (FDA Code: CEP / 862.1485)
A luteinizing hormone test system is a device intended to measure luteinizing hormone in serum and urine. Luteinizing hormone measurements are used in the diagnosis and treatment of gonadal dysfunction.
• Molecular Analyte Specific Reagents (ASR)
• Morphine Specific ELISA Kits
• Mumps Virus Enzyme Linked Immunoabsorbent Assay (FDA Code: LJY / 866.3380)
Mumps virus serological reagents consist of antigens and antisera used in serological tests to identify antibodies to mumps virus in serum. Additionally, some of these reagents consist of antisera conjugated with a fluorescent dye (immunofluorescent reagents) used in serological tests to identify mumps viruses from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of mumps and provides epidemiological information on mumps. Mumps is an acute contagious disease, particularly in children, characterized by an enlargement of one or both of the parotid glands (glands situated near the ear), although other organs may also be involved.
• Mycoplasma Spp Enzyme Linked Immunoabsorbent Assay (FDA Code: LJZ / 866.3375)
• Myoglobin (FDA Code: DDR / 866.5680)
A myoglobin immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the myoglobin (an oxygen storage protein found in muscle) in serum and other body fluids. Measurement of myoglobin aids in the rapid diagnosis of heart or renal disease.
• Myoglobin Enzyme Immunoassay Test Kit
• Myoglobin Radioimmunoassay Reagent Kits
• Myoglobin Ria Test Kit
• Natural Progesterone
• Opiates ELISA Kit
• Oral Insulin Kit
• Progesterone
• Progesterone - 17-OH Testing Kit
• Progesterone Hormone
• Progesterone Injections
• Progesterone Pills
• Progesterone Radioimmunoassay Test (FDA Code: JLS / 862.1620)
A progesterone test system is a device intended to measure progesterone (a female hormone) in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of disorders of the ovaries or placenta.
• Progesterone Supplements
• Progestrone ELISA Kit
• Prolactin Kit
• Prolactin Radioimmunoassay (FDA Code: CFT / 862.1625)
A prolactin (lactogen) test system is a device intended to measure the anterior pituitary polypeptide hormone prolactin in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of disorders of the anterior pituitary gland or of the hypothalamus portion of the brain.
• Radioimmunoassay for Dehydroepiandrosterone Sulfate (FDA Code: JKC / 862.1245)
A dehydroepiandrosterone (free and sulfate) test system is a device intended to measure dehydroepiandrosterone (DHEA) and its sulfate in urine, serum, plasma, and amniotic fluid. Dehydroepiandrosterone measurements are used in the diagnosis and treatment of DHEA-secreting adrenal carcinomas.
• Rubeola Enzyme Linked Immunoabsorbent Assay (FDA Code: LJB / 866.3520)
Rubeola (measles) virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to rubeola virus in serum. The identification aids in the diagnosis of measles and provides epidemiological information on the disease. Measles is an acute, highly infectious disease of the respiratory and reticuloendothelial tissues, particularly in children, characterized by a confluent and blotchy rash.
• Salivary Estradiol Enzyme Immunoassay Kit
• Salivary Testosterone Enzyme IMMUNOASSAY Kit
• Salmonella Spp Antigen (FDA Code: GRL / 866.3550)
• Sensitive Rat Insulin RIA Kit
• Testosterone
• Testosterone Detection Kit
• Testosterone EIA Test Kit
• Testosterone ELISA Kit
• Testosterone Kits
• Testosterone Radioimmunoassay Test Kits
• Total Triiodothyronine Radioimmunoassay (FDA Code: CDP / 862.1710)
A total triiodothyronine test system is a device intended to measure the hormone triiodothyronine in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of thyroid diseases such as hyperthyroidism.
• Treponima pallidum IgG ELISA Kit
• Treponima pallidum IgM ELISA Kit
• Triiodothyronine Uptake Radioassay (FDA Code: KHQ / 862.1715)
A triiodothyronine uptake test system is a device intended to measure the total amount of binding sites available for binding thyroid hormone on the thyroxine-binding proteins, thyroid-binding globulin, thyroxine-binding prealbumin, and albumin of serum and plasma. The device provides an indirect measurement of thyrkoxine levels in serum and plasma. Measurements of triiodothyronine uptake are used in the diagnosis and treatment of thyroid disorders.
• Ultrasensitive Mouse Insulin kit

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