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T. gondii IgG Test System

Intended Use

The ZEUS IFA Toxoplasma gondii IgG Test System is an indirect fluorescent antibody assay intended to detect the presence of circulating T. gondii antibodies in human sera and is for in vitro diagnostic use.

Registration / Clearance

FDA Cleared

Health Canada Licensed

Product Code: FA8001G

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Ancillary Products:

  • (1017P) Blotter Paper (Package of 10)
  • (FA0008) PBS