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J.Mitra Advantage Typhi IgM & IgG Rapid Card - Pack of 50 Test
J.Mitra Advantage Typhi IgM & IgG Rapid Card - Pack of 50 Test: Image 1
J.Mitra Advantage Typhi IgM & IgG Rapid Card - Pack of 50 Test: Image 2
J.Mitra Advantage Typhi IgM & IgG Rapid Card - Pack of 50 Test: Image 3
J.Mitra Advantage Typhi IgM & IgG Rapid Card - Pack of 50 Test: Image 4

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Brand J. Mitra

What's in the Box

50 Typhi IgM & IgG Rapid Test Devices, Sample Droppers, Buffer Solution, Product Insert & Standard Diagnostic Kit Packaging.

The J.Mitra Advantage Typhi IgM & IgG Rapid Card is a diagnostic tool engineered for the rapid and qualitative differential detection of IgM and IgG antibodies specific to Salmonella Typhi and Salmonella Paratyphi. This test is crucial for the early diagnosis of typhoid fever, enabling healthcare professionals to initiate timely treatment and determine both recent and past infection stages.

This rapid card is a lateral flow immunochromatographic assay. It utilizes anti-human IgM and anti-human IgG antibodies immobilized on a nitrocellulose strip, with a conjugate containing colloidal gold complexed with S. typhi antigen. The device itself is constructed from plastic.

Designed for in vitro diagnostic use, this test is suitable for various clinical and point-of-care settings due to its ease of use and ability to provide swift results. The manufacturer, J. Mitra & Co. Pvt. Ltd., operates under ISO 9001:2015, ISO 13485:2016, and ICMED 13485 quality management system certifications.

Key Features : 

Qualitative differential and simultaneous detection of Salmonella typhi IgM and IgG antibodies in human serum, plasma, or whole blood.
Lateral flow immunochromatographic assay utilizing anti-human IgM and IgG antibodies on a nitrocellulose strip with colloidal gold conjugated to S. typhi antigen.
For in vitro diagnostic use, manufactured by an ISO 9001:2015, ISO 13485:2016, ICMED 13485 certified company.
Stable for storage at temperatures between 2-30°C.
Provides test results within 20 minutes.
Compatible with human serum, plasma, or whole blood specimens.

Material / Reagent TypeLateral flow immunochromatographic assay with anti-human IgM, anti-human IgG, and colloidal gold conjugated to S. typhi antigen on a nitrocellulose strip, housed in a plastic device.
Clinical / Analytical FunctionQualitative differential and simultaneous detection of Salmonella typhi (S. typhi) IgM and IgG antibodies in human serum / plasma for early diagnosis and determination of recent and past typhoid infection.
Regulatory ApprovalIn vitro diagnostic use; manufactured by an ISO 9001:2015, ISO 13485:2016, ICMED 13485 certified company.
Storage Conditions2-30°C
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