Typhoid IgG/IgM Rapid Test Device

Model RT-105

Lateral flow test for differential detection of anti-Salmonella typhi IgG and IgM in serum, plasma or whole blood.

Differentiates IgG from IgM
Serum, plasma or whole blood
Result in 15 to 20 minutes
Stable at 2–36 °C for 24 months

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For in vitro diagnostic use by laboratory and healthcare professionals only. Please refer to the instructions for use supplied with each product for complete protocol and performance details.

Overview

A lateral flow immunoassay for the qualitative detection and differentiation of anti-Salmonella typhi IgG and IgM antibodies in human whole blood, serum or plasma, as an aid in the diagnosis of typhoid fever. Alternative methods should be used to confirm the result. Results should not be the sole basis for a clinical decision.

Intended use: Qualitative detection and differentiation of anti-Salmonella typhi IgG and IgM antibodies in human serum, plasma or whole blood.

Specifications

Specifications for Typhoid IgG/IgM Rapid Test Device
Shelf life	24 months
Catalogue number	105
Specimen type	Serum, plasma or whole blood
Specimen volume	1 drop (25 µL) sample plus 2 drops (50 µL) of assay buffer
Storage	2–36 °C
Time to result	15–20 minutes
Sensitivity (manufacturer-stated)	99.5 %
Specificity (manufacturer-stated)	99.9 %