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Euroimmun Us Inc.

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Contact: Kathryn Kohl
Web: http://www.euroimmunus.com
E-Mail:
Address: 429 Rockaway Valley Road, Bld. No 12, Boonton Twp., New Jersey 07005, USA
Phone: +1-(973)-402-6101 | Fax: +1-(973)-402-2551 | Map/Directions >>
 
 

Profile: Euroimmun Us Inc manufactures medical diagnostic products. Our medical products include fluorescence-labeled antibodies, controls for indirect immunofluorescence, and test systems or single slides for indirect immunofluorescence products. We offer auto immune and infectious serology products.

FDA Registration Number: 3007118747

45 Products/Services (Click for related suppliers)  
• Adenovirus 1-33 CF Antisera (FDA Code: GOA / 866.3020)
Adenovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to adenovirus in serum. Additionally, some of these reagents consist of adenovirus antisera conjugated with a fluorescent dye and are used to identify adenoviruses directly from clinical specimens. The identification aids in the diagnosis of disease caused by adenoviruses and provides epidemiological information on these diseases. Adenovirus infections may cause pharyngitis (inflammation of the throat), acute respiratory diseases, and certain external diseases of the eye (e.g., conjunctivitis).
• Allergy Test
• Allergy Testing
• Anti-Cyclic Citrullinated Peptide (Ccp) Antibodies (FDA Code: NHX / 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.
• Antibody Detection Candida Species (FDA Code: LSG / 866.3165)
• 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)
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).
• Automated Immunoassay Analyzers
• Automated Slide Stainer (FDA Code: KPA / 864.3800)
An automated slide stainer is a device used to stain histology, cytology, and hematology slides for diagnosis.
• B 1-6 Coxsackievirus A 1-24 Fluorescent Antisera Test (FDA Code: GNM / 866.3145)
Coxsackievirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to coxsackievirus in serum. Additionally, some of these reagents consist of coxsackievirus antisera conjugated with a fluorescent dye that are used to identify coxsackievirus from clinical specimens or from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of coxsackievirus infections and provides epidemiological information on diseases caused by these viruses. Coxsackieviruses produce a variety of infections, including common colds, meningitis (inflammation of brain and spinal cord membranes), herpangina (brief fever accompanied by ulcerated lesions of the throat), and myopericarditis (inflammation of heart tissue).
• B.Pertussis Antigen (FDA Code: GOX / 866.3065)
• Beta 2-Glycoprotein I (FDA Code: DDN / 866.5430)
Abeta -2-glycoprotein I immunological test system is a device that consists of the reagents used to measure by immunochemical techniques thebeta -2-glycoprotein I (a serum protein) in serum and other body fluids. Measurement ofbeta -2-glycoprotein I aids in the diagnosis of an inherited deficiency of this serum protein.
• Brucella Spp Fluorescent Antisera (FDA Code: GSM / 866.3085)
• Diagnostic Aids
• Echinococcus Granulosus Indirect Fluorescent Antibody Test Antigen (FDA Code: GPD / 866.3200)
• Echinococcus Spp. Positive Control Antisera (FDA Code: GPE / 866.3200)
• Echovirus 1-34 Fluorescent Antisera Test (FDA Code: GRK / 866.3205)
Echovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to echovirus in serum. Additionally, some of these reagents consist of echovirus antisera conjugated with a fluorescent dye used to identify echoviruses from clinical specimens or from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of echovirus infections and provides epidemiological information on diseases caused by these viruses. Echoviruses cause illnesses such as meningitis (inflammation of the brain and spinal cord membranes), febrile illnesses (accompanied by fever) with or without rash, and the common cold.
• Endomysial Autoantibodies (FDA Code: MVM / 866.5660)
• Enzyme Immunoassay
• Enzyme Labeled Anti-DNA Antibody (FDA Code: LRM / 866.5100)
• Fluorescence Microscope Aids
• Fluorescent Adenovirus 1-33 Antisera (FDA Code: GNY / 866.3020)
• Fluorescent B. Pertussis Antisera (FDA Code: GOZ / 866.3065)
• 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.
• HSV-1 Herpes Simplex Virus Enzyme-Linked Immunosorbent Assay (FDA Code: MXJ / 866.3305)
• HSV-2 Herpes Simplex Virus Enzyme-Linked Immunosorbent Assay (FDA Code: MYF / 866.3305)
• IFA Antibody Antigen Respiratory Syncytial Virus (FDA Code: LKT / 866.3480)
Respiratory syncytial virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to respiratory syncytial virus in serum. Additionally, some of these reagents consist of respiratory syncytial virus antisera conjugated with a fluorescent dye (immunofluorescent reagents) and used to identify respiratory syncytial viruses from clinical specimens or from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of respiratory syncytial virus infections and provides epidemiological information on diseases caused by these viruses. Respiratory syncytial viruses cause a number of respiratory tract infections, including the common cold, pharyngitis, and infantile bronchopneumonia.
• Immunofluorescence Assay Reagents
• Infectious Disease Serology Test
• Influenza Virus Antisera (FDA Code: GNS / 866.3330)
Influenza virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to influenza in serum. The identification aids in the diagnosis of influenza (flu) and provides epidemiological information on influenza. Influenza is an acute respiratory tract disease, which is often epidemic.
• Klebsiella Spp. Fluorescent Antisera (FDA Code: GTB / 866.3340)
• Legionella Direct & Indirect Fluorescent Antibody Regents (FDA Code: LHL / 866.3300)
• Legionella Spp. ELISA (FDA Code: MJH / 866.3300)
• Microplate ELISA Test Systems
• Microscope Condenser (FDA Code: KEI / 864.3600)
Microscopes and accessories are optical instruments used to enlarge images of specimens, preparations, and cultures for medical purposes. Variations of microscopes and accessories (through a change in the light source) used for medical purposes include the following:
• 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.
• Mumps Virus Fluorescent Antiserum Test (FDA Code: GRA / 866.3380)
• Mycoplasma Spp Enzyme Linked Immunoabsorbent Assay (FDA Code: LJZ / 866.3375)
• Mycoplasma Spp. Fluorescent Antisera (FDA Code: GRZ / 866.3375)
• Parainfluenza Virus 1-4 CF Antisera (FDA Code: GQT / 866.3400)
Parainfluenza virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to parainfluenza virus in serum. The identification aids in the diagnosis of parainfluenza virus infections and provides epidemiological information on diseases caused by these viruses. Parainfluenza viruses cause a variety of respiratory illnesses ranging from the common cold to pneumonia.
• Pipetting and Diluting Station (FDA Code: JQW / 862.2750)
A pipetting and diluting system for clinical use is a device intended to provide an accurately measured volume of liquid at a specified temperature for use in certain test procedures. This generic type of device system includes serial, manual, automated, and semi-automated dilutors, pipettors, dispensers, and pipetting stations.
• Respiratory Syncytial Virus - Elisa (FDA Code: MCE / 866.3480)
• 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.
• Rubeola Fluorescent Antiserum (FDA Code: GRE / 866.3520)
• Skin (Bullous Pemphigoid 180 And Bullous Pemphigoid 230 Autoantibodies (FDA Code: OEG / 866.5660)

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