![COV-13C25 Box Pouch and Cassette](https://strategicstrike.blob.core.windows.net/lochness-products/staging/COV-13C25_1.png)
![COV-13C25 Pouch and Cassette](https://strategicstrike.blob.core.windows.net/lochness-products/staging/COV-13C25_2.png)
![COV-13C25 Box Pouch and Cassette](https://strategicstrike.blob.core.windows.net/lochness-products/staging/COV-13C25_1.png)
![COV-13C25 Pouch and Cassette](https://strategicstrike.blob.core.windows.net/lochness-products/staging/COV-13C25_2.png)
![](https://img.youtube.com/vi/m4iDoR0PwYM/default.jpg)
![](https://img.youtube.com/vi/c3dwop5KOns/default.jpg)
The Rapid Response™ COVID-19 IgG/IgM Rapid Test Device is an in vitro immunoassay for the direct and qualitative detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood (including venous whole blood and capillary whole blood), serum, or plasma.
At the Point of Care setting, this test is only authorized for use with fingerstick whole blood specimens.
The test is for professional use only. This assay is not intended for home testing (or self-testing).
Pursuant to section 5 of the Interim Order Respecting the Importation and Sale of Medical Devices for Use in Relation to COVID-19, made by the Minister of Health on March 18, 2020, the Rapid Response™ COVID-19 IgG/IgM Rapid Test Device is now authorized for sale or importation in Canada.
- 25 Test Cassettes
- 25 Disposable Pipettes
- 25 Buffer Vials
- Product Insert
The Rapid Response™ COVID-19 IgG/IgM Rapid Test Device is an in vitro immunoassay for the direct and qualitative detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood (including venous whole blood and capillary whole blood), serum, or plasma.
At the Point of Care setting, this test is only authorized for use with fingerstick whole blood specimens.
The test is for professional use only. This assay is not intended for home testing (or self-testing).
Pursuant to section 5 of the Interim Order Respecting the Importation and Sale of Medical Devices for Use in Relation to COVID-19, made by the Minister of Health on March 18, 2020, the Rapid Response™ COVID-19 IgG/IgM Rapid Test Device is now authorized for sale or importation in Canada.
- Please note that certain products may only be available in specific regions; kindly consult with a sales representative for further information regarding product availability.
- The information provided on this website is for educational purposes only and should not be construed as medical advice. Always consult with a qualified healthcare professional regarding any medical concerns or conditions.
- Our products are intended for use as specified in the product documentation. It is important to carefully read and follow all instructions provided with the product.