| Click here to know more about extention of shelf-life expiration date under Health Canada Interim Order Authorization. |
Omicron Variant Update: Click Here to read our latest update on the impact of the Omicron variant of SARS-CoV-2 on COVID-19 Antigen Rapid Test Device - At Home.
The Rapid Response™ COVID-19 Antigen Rapid Test Cassette - At Home is an in vitro immunochromatographic assay intended to detect nucleocapsid protein antigen from SARS-CoV-2 virus that causes COVID-19 in nasal swab samples from individuals suspected of COVID-19 within 7 days of symptom onset and from individuals without symptoms or other epidemiological reasons to suspect COVID-19 infection. This device is authorized for home-use in a non-laboratory setting with direct anterior nasal (nares) swab samples for:
- Unobserved self-collection for individuals aged 18 years or older
- Adult supervised self-collection for individuals age 14 or older
- Adult collecting from children 2 years or older
This test is authorized for home use only under the Health Canada Interim Order.
| Click here to know more about extention of shelf-life expiration date under Health Canada Interim Order Authorization. |
Omicron Variant Update: Click Here to read our latest update on the impact of the Omicron variant of SARS-CoV-2 on COVID-19 Antigen Rapid Test Device - At Home.
The Rapid Response™ COVID-19 Antigen Rapid Test Cassette - At Home is an in vitro immunochromatographic assay intended to detect nucleocapsid protein antigen from SARS-CoV-2 virus that causes COVID-19 in nasal swab samples from individuals suspected of COVID-19 within 7 days of symptom onset and from individuals without symptoms or other epidemiological reasons to suspect COVID-19 infection. This device is authorized for home-use in a non-laboratory setting with direct anterior nasal (nares) swab samples for:
- Unobserved self-collection for individuals aged 18 years or older
- Adult supervised self-collection for individuals age 14 or older
- Adult collecting from children 2 years or older
This test is authorized for home use only under the Health Canada Interim Order.
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 Antigen Rapid Test Cassette – At Home is now authorized for sale or importation in Canada. Interim Authorization Number: 342928
For information on purchase orders please contact your local sales representative or contact us at covid19@btnx.com or 1-888-339-9964.
For service in French, please email covid19@btnx.com and we will connect you to one of our partners for assistance. - Pour un service en français, veuillez envoyer un e-mail à covid19@btnx.com et nous vous mettrons en contact avec l'un de nos partenaires pour obtenir de l'aide.
- 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.
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