Diamedix Corporation

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Web: http://www.diamedix.com
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Address: 2140 North Miami Ave, Miami, Florida 33127, USA
Phone: +1-(305)-324-2300 | Map/Directions >>
 
 

Profile: Diamedix Corporation manufactures & supplies enzyme immunoassays that are used to detect the presence of autoimmune and infectious diseases. We are an ISO OTHER, CE MARK certified company. We offer products like Magor Plus, DSXT, DS2T, autoimmune disease test kits & infectious disease test kits. Our Apo-tek LP (a) ™ is intended for the quantitative determination of lipoprotein (a) [LP (a)] in human serum and plasma. Our EZ complement CH50 assay is used to determine the functional integrity of the entire classic complement pathway.

The company was founded in 1985, has revenues of USD 5-10 Million, has ~50 employees and is ISO, CE certified. AMEX:IVD (SEC Filings)

FDA Registration Number: 1044713

31 Products/Services (Click for related suppliers)  
• Anti-RNP Antibody (FDA Code: LKO / 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).
• Anti-SM-Antibody (FDA Code: LKP / 866.5100)
• Antigen and Control Anti-DNA Antibody (FDA Code: LSW / 866.5100)
• Antigen And Control Extractable Antinuclear Antibody (FDA Code: LLL / 866.5100)
• 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).
• B2 - Glycoprotein I Antibodies Test System (FDA Code: MSV / 866.5660)
• Campylobacter Pylori (FDA Code: LYR / 866.3110)
• Clinical Colorimeter (FDA Code: JJQ / 862.2300)
A colorimeter, a photometer, or a spectrophotometer for clinical use is an instrument intended to measure radiant energy emitted, transmitted, absorbed, or reflected under controlled conditions. The device may include a monochromator to produce light of a specific wavelength.
• Complement Reagent (FDA Code: KTQ / 866.4100)
A complement reagent is a device that consists of complement, a naturally occurring serum protein from any warm-blooded animal such as guinea pigs, that may be included as a component part of serological test kits used in the diagnosis of disease.
• 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 IHA Antigen Test (FDA Code: LJO / 866.3175)
• Enzyme Immunoassay
• Enzyme Labeled Anti-DNA Antibody (FDA Code: LRM / 866.5100)
• Epstein-Barr Virus (FDA Code: LSE / 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).
• Epstein-Barr Virus CF Antiserum (FDA Code: GNP / 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)
• Immunological Anticardiolipin Test System (FDA Code: MID / 866.5660)
• Lyme Disease Test
• Micro Chemistry Analyzer (FDA Code: JJF / 862.2170)
A micro chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. The distinguishing characteristic of the device is that it requires only micro volume samples obtainable from pediatric patients. This device is intended for use in conjunction with certain materials to measure a variety of analytes.
• 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)
• Rheumatoid Factor Test System (FDA Code: DHR / 866.5775)
A rheumatoid factor immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the rheumatoid factor (antibodies to immunoglobulins) in serum, other body fluids, and tissues. Measurement of rheumatoid factor may aid in the diagnosis of rheumatoid arthritis.
• Rubella and Torch Test Kits
• 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).
• 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.
• Thyroid Autoantibody Test System (FDA Code: JZO / 866.5870)
A thyroid autoantibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the thyroid autoantibodies (antibodies produced against the body's own tissues). Measurement of thyroid autoantibodies may aid in the diagnosis of certain thyroid disorders, such as Hashimoto's disease (chronic lymphocytic thyroiditis), nontoxic goiter (enlargement of thyroid gland), Grave's disease (enlargement of the thyroid gland with protrusion of the eyeballs), and cancer of the thyroid.
• Toxoplasma Gondii Enzyme Linked Immunoabsorbent Assay (FDA Code: LGD / 866.3780)
• Treponema Pallidum Enzyme Linked Immunoabsorbent Assay (FDA Code: LIP / 866.3830)
• Varicella-Zoster Enzyme Linked Immunoabsorbent Assay (FDA Code: LFY / 866.3900)
Varicella-zoster virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to varicella-zoster in serum. The identification aids in the diagnosis of diseases caused by varicella-zoster viruses and provides epidemiological information on these diseases. Varicella (chicken pox) is a mild, highly infectious disease, chiefly of children. Zoster (shingles) is the recurrent form of the disease, occurring in adults who were previously infected with varicella-zoster viruses. Zoster is the response (characterized by a rash) of the partially immune host to a reactivation of varicella viruses present in latent form in the patient's body.

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