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MP Biomedical™ Rapid 2019-nCoV IgG/IgM Combo Diagnostic Test Cards to COVID-19 Product Code.: 16650272

MP Biomedical™ Rapid 2019-nCoV IgG/IgM Combo Diagnostic Test Cards to COVID-19

Product Code. 16650272 Shop All MP Biomedical Products
25 Tests, 25 tests
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Quantity:
25 Tests
Unit Size:
25 tests
This item is not returnable. View return policy

Product Code. 16650272

Brand: MP Biomedical™ 07RDCOV19

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This item is not returnable. View return policy

Rapid 2019-nCoV IgG/IgM Combo Diagnostic Test Cards to COVID-19 is a rapid immunochromatographic test designed for the qualitative determination of IgG and IgM antibodies to 2019 novel coronavirus (2019-nCoV, SARS-CoV-2) in human serum, plasma, or whole blood.

  • A rapid diagnostic test for the detection of IgG and IgM antibodies to COVID-19.
  • Rapid results in 15 minutes, and requires no instruments.
  • It is widely accepted that IgM provides the first line of defense during viral infections, followed by the generation of adaptive, high affinity IgG responses for long term immunity and immunological memory. Testing of COVID-19 IgM and IgG antibodies therefore, is an effective method for the rapid diagnosis of COVID-19 infection. Detection of COVID-19 IgM antibodies tend to indicate a recent exposure to COVID-19, whereas detection of COVID-19 IgG antibodies indicates a later stage of infection. Thus, this combined antibody test from MP Biomedicals could also provide information on the stage of infection.

Specifications

Accuracy 96.8%
Content And Storage Store the test device at 2 to 30°C in the original sealed pouch. Do Not Freeze.
CE Marker CE-IVD
Detectable Analytes COVID-19 IgG, IgM
Detection Method Immunochromatography
Sample Type Serum, Plasma, Whole Blood
Sensitivity 87.8%
Disposable Single-use
Includes MP Rapid 2019-nCoV IgG/IgM Combo Test Card (x25), Sample buffer, Capillary pipets, Instructions for Use
Packaging Type 1 Box of 25 Tests
Quantity 25 Tests
Sample Size 2 ÎĽL
Shipping Condition 2°C to 30°C
Specificity 0.99
Test Time 15 min.
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      MP Biomedicals - Rapid Test COVID-19

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    Lot Number Certificate TypeDeclaration of Conformity Date29/04/2020 Product Code
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