The OnSite Toxo IgG/IgM Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum or plasma.
For In Vitro Diagnostic Use :
1. Read these Instructions for Use completely before performing the test. Failure to follow the
instructions could lead to inaccurate test results.
2. Do not open the sealed pouch until ready to conduct the assay.
3. Do not use expired devices or components.
4. Bring all reagents to room temperature (15-30°C) before use.
5. Do not use components from another test kit to substitute for components of this kit.
6. Do not use hemolyzed blood specimens for testing.
7. Wear protective clothing and disposable gloves while handling the kit reagents and clinical
specimens. Wash hands thoroughly after performing the test.
8. Users of this test should follow the US CDC Universal Precautions for prevention of transmissionof HIV, HBV and other blood-borne pathogens.
9. Do not smoke, drink or eat in areas where specimens or kit reagents are being handled.
10. Dispose of all specimens and materials used to perform the test as bio-hazardous waste.
11. Handle negative and positive controls in the same manner as patient specimens.
12. The test result should be read 10-15 minutes after a specimen is applied to the sample well or
sample pad of the device. Any results interpreted outside of the 10-15 minute window should
be considered invalid and must be repeated.
13. Do not perform the test in a room with strong air flow, e.g. an electric fan or strong air
conditioning.
Catalog# |
Product |
Quantity |
Specimen |
| R0234C | Toxo IgG/IgM Combo Rapid Test | 30/kit | S/P |
Catalog# |
Product |
Quantity |
Specimen |
| R0233C | Toxo IgG/IgM Rapid Test | 30/kit | S/P |
| R0233S | Toxo IgG/IgM Rapid Test (strip) | 50/kit | S/P |
