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Poliovirus 1-3 Neutralization Antisera Suppliers

 EMAIL INQUIRY to  2 suppliers  
Centers for Disease Control and Prevention | Address: 1600 Clifton Rd., Atlanta, Georgia 30333, USA USA
www.cdc.gov | Send Inquiry | Phone: +1-(888)-232-6348
FDA Registration: 1050190  Employee Count: ~180
Products: Healthcare Service, Arizona Spp Antiserum (FDA Code: GTE), Fluorescent B. Pertussis Antisera (FDA Code: GOZ), Brucella Spp Agglutination Antigen (FDA Code: GSO), Escherichia Coli Antisera (FDA Code: GNA), Positive and Negative Febrile Antigen Control Serum (FDA Code: GSN), ...
Centers for Disease Control and Prevention is an online source for health information. more...
 
Alfa Biotech Spa | Address: Via Castagnetta 7, Pomezia 00040, Italy
Phone: +39-(6)-9195735
Products: C-Reactive Protein Test System (FDA Code: DCN), Rheumatoid Factor Test System (FDA Code: DHR), 2 Herpesvirus Hominis 1 CF Antigen (FDA Code: GQN), 2 Herpesvirus Hominis 1 Cf Antisera (FDA Code: GQO), Adenovirus 1-33 CF Antigen (FDA Code: GOD), Adenovirus 1-33 CF Antisera (FDA Code: GOA), ...
Alfa Biotech Spa specializes in offering vaccines, blood products and diagnostic products for laboratory & medical use. more...
 EMAIL INQUIRY to  2 Poliovirus 1-3 Neutralization Antisera suppliers  
FDA Code / Regulation: GOF / 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.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 866.9.

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