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T. gondii IgM Test System

Intended Use

The ZEUS IFA Toxoplasma gondii IgM Test System is an indirect fluorescent antibody assay intended for the presumptive qualitative detection of IgM antibodies to T. gondii in human serum, and for the presumptive diagnosis of acute, recent, or reactive T. gondii infection. To adquately assess a patient's serological status, testing must be performed in conjunction with an anti-T. gondii IgG antibody assay.

Registration / Clearance

FDA Cleared

Health Canada Licensed

Product Code: FA8001M

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Ancillary Products:

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