Profile: Zeus Scientific, Inc. is a global healthcare company that provides diagnostic products for the enhancement of patient care. We are an ISO 9001 certified company. We offer products like Athena, elisa & IFA. Our Athena Multi-Lyte® test system is a multiplexed, fluorescent, bead-based system designed to perform multiple assays. Our tissue fixative and wash solution is intended for transporting & processing fresh skin, kidney tissue, muscle & benign or malignant lymphoid tissue when performing immunohistochemical examinations & is intended for vitro diagnostic use.

The company was founded in 1976, has revenues of USD 10-25 Million, has ~60 employees and is ISO 9001 certified.

FDA Registration Number: 2242436

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• 2 Herpesvirus Hominis 1 Fluorescent Antisera (FDA Code: GQL / 866.3305)

• Acid Containing Fixative (FDA Code: LDW / 864.4010)

• ANA (Antinuclear antibodies)

• ANA Screen IgG EIA Kit

• Anti-Gliadin (Ab)

• Anti-Gliadin (Ab) IgA Kit

• Anti-Gliadin (Ab) IgG Kit

• Anti-MPO ANCA

• Anti-MPO ANCA EIA Auto-Immune Markers Testing Kit

• Antigen And Control Extractable Antinuclear Antibody (FDA Code: LLL / 866.5100) An antinuclear antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoimmune antibodies in serum, other body fluids, and tissues that react with cellular nuclear constituents (molecules present in the nucleus of a cell, such as ribonucleic acid, deoxyribonucleic acid, or nuclear proteins). The measurements aid in the diagnosis of systemic lupus erythematosus (a multisystem autoimmune disease in which antibodies attack the victim's own tissues), hepatitis (a liver disease), rheumatoid arthritis, Sjogren's syndrome (arthritis with inflammation of the eye, eyelid, and salivary glands), and systemic sclerosis (chronic hardening and shrinking of many body tissues).

• Antimicrobial Susceptibility Test Culture Media (FDA Code: JSO / 866.1700) A culture medium for antimicrobial susceptibility tests is a device intended for medical purposes that consists of any medium capable of supporting the growth of many of the bacterial pathogens that are subject to antimicrobial susceptibility tests. The medium should be free of components known to be antagonistic to the common agents for which susceptibility tests are performed in the treatment of disease.

• Antineutrophil Cytoplasmic Antibodies (ANCA) Test System (FDA Code: MOB / 866.5660) A multiple autoantibodies immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoantibodies (antibodies produced against the body's own tissues) in serum and other body fluids. Measurement of multiple autoantibodies aids in the diagnosis of autoimmune disorders (disease produced when the body's own tissues are injured by autoantibodies).

• Antinuclear Antibody, Indirect Immunofluorescen (FDA Code: DHN / 866.5100)

• Autoantibody Screen IFA Kit

• Borrelia Serological Reagent (FDA Code: LSR / 866.3830)

• Campylobacter Pylori (FDA Code: LYR / 866.3110)

• Capsid Epstein-Barr Virus Antigen (FDA Code: MCD / 866.3235) Epstein-Barr virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to Epstein-Barr virus in serum. The identification aids in the diagnosis of Epstein-Barr virus infections and provides epidemiological information on diseases caused by these viruses. Epstein-Barr viruses are thought to cause infectious mononucleosis and have been associated with Burkitt's lymphoma (a tumor of the jaw in African children and young adults) and postnasal carcinoma (cancer).

• Cardiolipin IgA EIA Kit

• Cardiolipin IgG EIA Kit

• Cardiolipin IgM EIA Kit

• Control Antigen Antinuclear Antibody (FDA Code: LKJ / 866.5100)

• 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.

• Cytomegalovirus Virus IF Antibody Igm Test (FDA Code: LKQ / 866.3175)

• Enzyme Labeled Antinuclear Antibody (FDA Code: LJM / 866.5100)

• Epstein-Barr Virus (FDA Code: LSE / 866.3235)

• Epstein-Barr Virus Fluorescent Antiserum (FDA Code: JRY / 866.3235)

• Epstein-Barr Virus IF Antibody IGM (FDA Code: LJN / 866.3235)

• Epstein-Barr Virus Nuclear Antigen Test (FDA Code: LLM / 866.3235)

• Gliadin Antibodies (FDA Code: MST / 866.5750) A radioallergosorbent immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the allergen antibodies (antibodies which cause an allergic reaction) specific for a given allergen. Measurement of specific allergen antibodies may aid in the diagnosis of asthma, allergies, and other pulmonary disorders.

• Herpes Simplex Virus Enzyme Linked Immunoabsorbent Assay (FDA Code: LGC / 866.3305)

• Herpes Virus Antibody

• Herpes Virus Hominis Neutralization Antisera (FDA Code: GQM / 866.3305)

• IgG Control (FDA Code: DEW / 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.

• Immunological Anticardiolipin Test System (FDA Code: MID / 866.5660)

• Indirect Immunofluorescent Anti-Smooth Muscle Antibody Test (FDA Code: DBE / 866.5120) An antismooth muscle antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the antismooth muscle antibodies (antibodies to nonstriated, involuntary muscle) in serum. The measurements aid in the diagnosis of chronic hepatitis (inflammation of the liver) and autoimmune connective tissue diseases (diseases resulting from antibodies produced against the body's own tissues).

• Indirect Immunofluorescent Antimitochondrial Antibody Test (FDA Code: DBM / 866.5090) An antimitochondrial antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the antimitochondrial antibodies in human serum. The measurements aid in the diagnosis of diseases that produce a spectrum of autoantibodies (antibodies produced against the body's own tissue), such as primary biliary cirrhosis (degeneration of liver tissue) and chronic active hepatitis (inflammation of the liver).

• Indirect Immunofluorescent Multiple Auto Antibody (FDA Code: DBL / 866.5660)

• Legionella Antibody IFA Test Kit

• Legionella Direct & Indirect Fluorescent Antibody Regents (FDA Code: LHL / 866.3300)

• Legionella Spp. ELISA (FDA Code: MJH / 866.3300)

• Lyme Disease Test

• Mouse Rheumatoid Factor (RF) ELISA Kit

• Mumps IgG EIA Kit

• 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 Detection Media (FDA Code: KIX / 864.2360) Mycoplasma detection media and components are used to detect and isolate mycoplasma pleuropneumonia-like organisms (PPLO), a common microbial contaminant in cell cultures.

• Mycoplasma IgG EIA Kit

• Mycoplasma IgM EIA Kit

• Mycoplasma SPP Antibody

• Mycoplasma Spp Enzyme Linked Immunoabsorbent Assay (FDA Code: LJZ / 866.3375)

• Mycoplasma Spp. Fluorescent Antisera (FDA Code: GRZ / 866.3375)