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HEALTH CANADA APPROVED

Rapid Test for Covid-19

Easy to use

The tests can be applied in any environment without the need for additional tools. Easy to carry, no special storage requisites, and easy to use. Get your kit and test yourself in a manner of minutes.

High accuracy

Straight forward nasopharyngeal swab collection with proven high accuracy results

Rapid result

Boson Antigen testers show results within less than 20 minutes, while standard RT PCR tests can take up 3 days to do so.

HOW IT WORKS

Rapid SARS-CoV-2 Antigen Test Card is a lateral flow immunoassay able to detect the nucleocapsid protein from SARS-CoV-2 in nasopharyngeal swab specimens from individuals who are suspected of COVID-19 by their healthcare provider within the first 7 days of symptom onset.

1. Sample collection

Carefully insert the swab into the nostril and swab over the surface of the posterior nasopharynx.

2. Sample preparation

Add 8 drops of extraction buffer into the extraction tube. Leave the swab in the extraction buffer for 1 minute.

3. Procedure

Add 2-3 drops of test specimen from the extraction tube on the test card and read the results at 15-20 minutes.

4. Result interpretation

See IFU (Instructions For Use) sheet inside the device kit for more details.

Download reports

Please refer to the IFU information sheet and Full User Product Training document for detailed device information.

English IFU

Health Canada Interim Order Authorization

Clinical Evaluation Report

FAQ

For answers to commonly asked questions and more information about the Boson Rapid SARS Co-V2 device, please visit our FAQs page

It was so much easier doing my own test at home, instead of waiting in line.

Mike

Thank you! This has given our family peace of mind to know right away if are sick. Sometimes it might just be a cold, but now we know for sure.

Jeannette

I didn't want to leave the house to get tested in case I gave it to someone in my elevator. This was much safer.

Allen

Performance Statistics

For more details, please download the clinical study report.