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Alfa Biotech Spa


Address: Via Castagnetta 7, Pomezia 00040, Italy
Phone: +39-(6)-9195735 | Map/Directions >>
 
 

Profile: Alfa Biotech Spa specializes in offering vaccines, blood products and diagnostic products for laboratory & medical use.

46 Products/Services (Click for related suppliers)  
• 2 Herpesvirus Hominis 1 CF Antigen (FDA Code: GQN / 866.3305)
• 2 Herpesvirus Hominis 1 Cf Antisera (FDA Code: GQO / 866.3305)
• Adenovirus 1-33 CF Antigen (FDA Code: GOD / 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).
• Adenovirus 1-33 CF Antisera (FDA Code: GOA / 866.3020)
• Adenovirus 1-33 Neutralization Antisera (FDA Code: GNZ / 866.3020)
• B 1-6 Coxsackievirus A 1-24 CF Antisera (FDA Code: GNO / 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 1-6 Coxsackievirus A 1-24 Neutralization Antiserum (FDA Code: GNN / 866.3145)
• B. Parapertussis Agglutinating Antisera (FDA Code: GOW / 866.3065)
• Brucella Spp Agglutination Antigen (FDA Code: GSO / 866.3085)
• C-Reactive Protein Test System (FDA Code: DCN / 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.
• Coxsackievirus A 1-24 CF Antigen (FDA Code: GNG / 866.3145)
• Cytomegalovirus CF Antigen (FDA Code: GQH / 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.
• Echinococcus SPP Agglutinating Antigen (FDA Code: GPF / 866.3200)
• Echovirus 1-34 CF Antigen (FDA Code: GNL / 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.
• Echovirus 1-34 CF Antisera (FDA Code: GNK / 866.3205)
• Echovirus 1-34 Neutralization Antisera (FDA Code: GNI / 866.3205)
• Equine Encephalitis CF Antigen (FDA Code: GQD / 866.3240)
Equine encephalomyelitis virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antobodies to equine encephalomyelitis virus in serum. The identification aids in the diagnosis of diseases caused by equine encephalomyelitis viruses and provides epidemiological information on these viruses. Equine encephalomyelitis viruses are transmitted to humans by the bite of insects, such as mosquitos and ticks, and may cause encephalitis (inflammation of the brain), rash, acute arthritis, or hepatitis.
• Febrile Antigens Slide/Tube Test (FDA Code: GNC / 866.3550)
• Herpes Virus Hominis Neutralization Antisera (FDA Code: GQM / 866.3305)
• Influenza Virus (A, B, C) Antisera (FDA Code: GNW / 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.
• Influenza Virus CF Antigen (FDA Code: GNX / 866.3330)
• Listeria Monocytogenes Slide and Tube Antigen (FDA Code: GSI / 866.3355)
• Lymphocytic Choriomeningitis Virus CF Antigen Test (FDA Code: GQK / 866.3360)
Lymphocytic choriomeningitis virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to lymphocytic choriomeningitis virus in serum. The identification aids in the diagnosis of lymphocytic choriomeningitis virus infections and provides epidemiological information on diseases caused by these viruses. Lymphocytic choriomeningitis viruses usually cause a mild cerebral meningitis (inflammation of membranes that envelop the brain) and occasionally a mild pneumonia, but in rare instances may produce severe and even fatal illnesses due to complications from cerebral meningitis and pneumonia.
• Mycobacterium Tuberculosis Fluorescent Antiserum Test (FDA Code: GRT / 866.3370)
• Mycoplasma Spp Antiserum (FDA Code: GSA / 866.3375)
• Mycoplasma Spp CF Antigen (FDA Code: GSB / 866.3375)
• Neisseria Gonorrhoeae Identification Kit (FDA Code: JSX / 866.2660)
A microorganism differentiation and identification device is a device intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease.
• Non-Treponemal Antigen (FDA Code: GMQ / 866.3820)
• 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.
• Parainfluenza Virus 1-4 Neutralization Antisera (FDA Code: GQP / 866.3400)
• Parainfluenza Virus CF Antigen (FDA Code: GQS / 866.3400)
• Poliovirus 1-3 CF Antigen (FDA Code: GOH / 866.3405)
Poliovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to poliovirus in serum. Additionally, some of these reagents consist of poliovirus antisera conjugated with a fluorescent dye (immunofluorescent reagents) used to identify polioviruses from clinical specimens or from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of poliomyelitis (polio) and provides epidemiological information on this disease. Poliomyelitis is an acute infectious disease which in its serious form affects the central nervous system resulting in atrophy (wasting away) of groups of muscles, ending in contraction and permanent deformity.
• Poliovirus 1-3 CF Antisera (FDA Code: GOG / 866.3405)
• Poliovirus 1-3 Neutralization Antisera (FDA Code: GOF / 866.3405)
• Psittacosis CF Antigen (FDA Code: GPW / 866.3120)
Chlamydia serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to chlamydia in serum. Additionally, some of these reagents consist of chlamydia antisera conjugated with a fluorescent dye used to identify chlamydia directly from clinical specimens or cultured isolates derived from clinical specimens. The identification aids in the diagnosis of disease caused by bacteria belonging to the genusChlamydia and provides epidemiological information on these diseases. Chlamydia are the causative agents of psittacosis (a form of pneumonia), lymphogranuloma venereum (a venereal disease), and trachoma (a chronic disease of the eye and eyelid).
• Psittacosis CF Antiserum (FDA Code: GPT / 866.3120)
• Q Fever CF Antigen Test (FDA Code: GPS / 866.3500)
Rickettsia serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to rickettsia in serum. Additionally, some of these reagents consist of rickettsial antisera conjugated with a fluorescent dye (immunofluorescent reagents) used to identify rickettsia directly from clinical specimens. The identification aids in the diagnosis of diseases caused by virus-like bacteria belonging to the genusRickettsiae and provides epidemiological information on these diseases. Rickettsia are generally transmitted by arthropods (e.g., ticks and mosquitoes) and produce infections in humans characterized by rash and fever (e.g., typhus fever, spotted fever, Q fever, and trench fever).
• Q Fever CF Antiserum Test (FDA Code: GPR / 866.3500)
• Reovirus 1-3 CF Antigen (FDA Code: GQB / 866.3470)
Reovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to reovirus in serum. The identification aids in the diagnosis of reovirus infections and provides epidemiological information on diseases caused by these viruses. Reoviruses are thought to cause only mild respiratory and gastrointestinal illnesses.
• Reovirus 1-3 Neutralizing Antisera (FDA Code: GPX / 866.3470)
• Respiratory Syncytial Virus Neutralization Antiserum Test (FDA Code: GQF / 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.
• 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.
• Rubeola CF Antigen (FDA Code: GRJ / 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.
• Spectacle Frame (FDA Code: HQZ / 886.5842)
A spectacle frame is a device made of metal or plastic intended to hold prescription spectacle lenses worn by a patient to correct refractive errors.
• Toxoplasma Gondii CF Antigen Test (FDA Code: GMN / 866.3780)
• Toxoplasma Gondii IHA Antigen Test (FDA Code: GMM / 866.3780)

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