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Typhus Fever Antiserum Test Suppliers

 EMAIL INQUIRY to  2 suppliers  
Focus Diagnostics, Inc. | Address: 13665 Dulles Technology Drive, Herndon, Virginia 20171-4603, USA USA
www.focusdx.com | Phone: +1-(703)-480-2500
FDA Registration: 2023365
Products: Publications, HIV Antibody Test Kits, Helicobacter pylori Urease Test Kits, Gastric pH Test Kits, Gastric Occult Blood and Gastric pH Test Kits, Fecal Occult Blood Test Kits, ...
Focus Diagnostics, Inc. develops & markets quality services for rare, unusual and emerging infectious & immunologic diseases. We are an ISO 13485 certified company. We offer products like HerpeSelectr more...
 
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, Adenovirus 1-33 CF Antigen (FDA Code: GOD), Adenovirus 1-33 CF Antisera (FDA Code: GOA), Adenovirus 1-33 Neutralization Antisera (FDA Code: GNZ), Histoplasma Capsulatum Antigen (FDA Code: GMJ), Arizona Spp Antiserum (FDA Code: GTE), ...
Centers for Disease Control and Prevention is an online source for health information. more...
 EMAIL INQUIRY to  2 Typhus Fever Antiserum Test suppliers  
FDA Code / Regulation: GPN / 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).

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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