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Visceral Leishmaniasis Diagnostic Test

United States

Immunodiagnostic test for detection of antibodies to Leishmania donovani. Designed for diagnosis of visceral leishmaniasis in clinical laboratory settings.

Manufactured by

United States

Since 1996, InBios has been a leader in the development of diagnostic tests for emerging infectious diseases and biothreats. Products are designed for superior performance, efficiency and value. These include many FDA market authorized and CE marked assays for arboviruses, parasitic infections, biothreats, and more. InBios continues to anticipate and serve the growing global public health demand. Products in the pipeline include next generation platforms for tick-borne and respiratory diseases.

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