Biocheck, Inc.

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Web: http://www.biocheckinc.com
E-Mail:
Address: 323 Vintage Park Dr., Foster City, California 94404, USA
Phone: +1-(650)-573-1968 | Fax: +1-(650)-573-1969 | Map/Directions >>
 
 

Profile: Biocheck, Inc. develops and distributes immunodiagnostic test kits for the healthcare markets. We are an ISO 9001, CE certified company. We offer products such as tumor markers, thyroid, steroids, cardiac markers, fertility, hepatitis, & antibody purification. Our troponin I is used for the in vitro quantitative determination of cardiac troponin I in human serum. Our C-reactive protein is used for the in vitro quantitative determination of C-reactive protein (CRP) concentration in human serum or plasma.

The company was founded in 1997, has revenues of USD 1-5 Million, has ~20 employees and is ISO, CE certified.

FDA Registration Number: 2953756

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• 11-keto Testosterone EIA Kit
• Alpha-Fetoprotein for Testicular Cancer Test Kit (FDA Code: LOJ / 866.6010)
A tumor-associated antigen immunological test system is a device that consists of reagents used to qualitatively or quantitatively measure, by immunochemical techniques, tumor-associated antigens in serum, plasma, urine, or other body fluids. This device is intended as an aid in monitoring patients for disease progress or response to therapy or for the detection of recurrent or residual disease.
• Beta-2-Microglobulin Immunological Test System (FDA Code: JZG / 866.5630)
Abeta -2-microglobulin immunological test system is a device that consists of the reagents used to measure by immunochemical techniquesbeta -2-microglobulin (a protein molecule) in serum, urine, and other body fluids. Measurement ofbeta -2-microglobulin aids in the diagnosis of active rheumatoid arthritis and kidney disease.
• Biopotential Amplifier and Signal Conditioner (FDA Code: DRR / 870.2050)
A biopotential amplifier and signal conditioner is a device used to amplify or condition an electrical signal of biologic origin.
• C-Reactive Protein (CRP), FITC Conjugate (FDA Code: DCK / 866.5270)
A C-reactive protein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the C-reactive protein in serum and other body fluids. Measurement of C-reactive protein aids in evaluation of the amount of injury to body tissues.
• C-Reactive Protein Test System (FDA Code: DCN / 866.5270)
• Campylobacter Pylori (FDA Code: LYR / 866.3110)
• Cancer 549 Antigen (FDA Code: MJB)
• Carcinoembryonic Antigen Test System (FDA Code: DHX / 866.6010)
• Cytomegalovirus Enzyme Linked Immunoabsorbent Assay (FDA Code: LFZ / 866.3175)
Cytomegalovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to cytomegalovirus in serum. The identification aids in the diagnosis of diseases caused by cytomegaloviruses (principally cytomegalic inclusion disease) and provides epidemiological information on these diseases. Cytomegalic inclusion disease is a generalized infection of infants and is caused by intrauterine or early postnatal infection with the virus. The disease may cause severe congenital abnormalities, such as microcephaly (abnormal smallness of the head), motor disability, and mental retardation. Cytomegalovirus infection has also been associated with acquired hemolytic anemia, acute and chronic hepatitis, and an infectious mononucleosis-like syndrome.
• Enzyme Immunoassay (EIA) Kits
• Estradiol
• Estradiol ELISA Kit
• Estradiol Kits
• Estradiol Radioimmunoassay Test (FDA Code: CHP / 862.1260)
An estradiol test system is a device intended to measure estradiol, an estrogenic steroid, in plasma. Estradiol measurements are used in the diagnosis and treatment of various hormonal sexual disorders and in assessing placental function in complicated pregnancy.
• Ferritin (FDA Code: DBF / 866.5340)
A ferritin immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the ferritin (an iron-storing protein) in serum and other body fluids. Measurements of ferritin aid in the diagnosis of diseases affecting iron metabolism, such as hemochromatosis (iron overload) and iron deficiency amemia.
• FerritiN EliSA Test Kit
• Ferritin Enzyme Immunoassay Test Kit
• Ferritin Radioimmunoassay Test (FDA Code: JMG / 866.5340)
• Ferritin Testing Kit
• Fertility ELISA Kits
• Follicle Stimulating Hormone Radioimmunoassay (FDA Code: CGJ / 862.1300)
A follicle-stimulating hormone test system is a device intended to measure follicle-stimulating hormone (FSH) in plasma, serum, and urine. FSH measurements are used in the diagnosis and treatment of pituitary gland and gonadal disorders.
• Gamma Dab Ferritin Kit
• Herpes Simplex Virus Enzyme Linked Immunoabsorbent Assay (FDA Code: LGC / 866.3305)
• Human Chorionic Gonadotropin (hCG)
• Human Chorionic Gonadotropin (HCG) ELISA Kit
• Human Chorionic Gonadotropin (hCG) Enzyme Immunoassay Test Kit
• Human Chorionic Gonadotropin Radioimmunoassay (FDA Code: JHI / 862.1155)
A human chorionic gonadotropin (HCG) test system is a device intended for the early detection of pregnancy is intended to measure HCG, a placental hormone, in plasma or urine.
• Human Growth Hormone Radioimmunoassay (FDA Code: CFL / 862.1370)
A human growth hormone test system is a device intended to measure the levels of human growth hormone in plasma. Human growth hormone measurements are used in the diagnosis and treatment of disorders involving the anterior lobe of the pituitary gland.
• IgE Control (FDA Code: DGC / 866.5510)
An immunoglobulins A, G, M, D, and E immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the immunoglobulins A, G, M, D, an E (serum antibodies) in serum. Measurement of these immunoglobulins aids in the diagnosis of abnormal protein metabolism and the body's lack of ability to resist infectious agents.
• Immunodiagnostic Test Kits
• Immunoglobulins D Radioimmunoassay Test (FDA Code: JHR / 866.5510)
• 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.
• Ovarian Tumor-Associated Antigen(Ca 125) Test (FDA Code: LTK / 866.6010)
• 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.
• 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.
• Prostate-Specific Antigen for Management of Prostate Cancers (FDA Code: LTJ / 866.6010)
• RIA Gnost Ferritin Kit
• Rubella Enzyme Linked Immunoabsorbent Assay (FDA Code: LFX / 866.3510)
Rubella virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to rubella virus in serum. The identification aids in the diagnosis of rubella (German measles) or confirmation of a person's immune status from past infections or immunizations and provides epidemiological information on German measles. Newborns infected in the uterus with rubella virus may be born with multiple congenital defects (rubella syndrome).
• Salivary Estradiol Enzyme Immunoassay Kit
• Salivary Testosterone Enzyme IMMUNOASSAY Kit
• Steroid ELISA Kits
• Testosterone
• Testosterone Detection Kit
• Testosterone EIA Test Kit
• Testosterone ELISA Kit
• Testosterone Kits
• Testosterone Radioimmunoassay Test Kits

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