Lymphocytic Choriomeningitis Virus CF Antigen Test Suppliers @ MedicRegister.com

EMAIL INQUIRY to 2 suppliers

Diesse Diagnostica Senese S.p.A | Address: Via Del Pozzo 5, Loc. S. Martino, Monteriggioni 53035, Italy
www.diesse.it | Send Inquiry | Phone: +39-(577)-319560
FDA Registration: 9615056 Year Established: 1982 Quality: ISO 9001, ISO 13485 and CE Mark Certified
Products: Erythrocyte Sedimentation Rate Test (FDA Code: JPH), Specimen Collection Device (FDA Code: LIO), Automated Sedimentation Rate Device (FDA Code: GKB), Aerobic Transport System (FDA Code: JTW), Mumps Virus Enzyme Linked Immunoabsorbent Assay (FDA Code: LJY), Rubeola Enzyme Linked Immunoabsorbent Assay (FDA Code: LJB), ...
Diesse Diagnostica Senese S.p.A is a manufacturer of instrument systems and reagents for infectious diseases testing. We offer Ves Matic® - line of instruments and system for blood collection & an 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 Lymphocytic Choriomeningitis Virus CF Antigen Test suppliers

FDA Code / Regulation: 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.

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.