CareStart COVID-19 Antigen Rapid At-Home Test, 2/Box

Vendor direct - Longer Lead times Apply
Expected to ship within 7-14 days

The CareStart™ COVID-19 Antigen Home Rapid Self-Test is a non-invasive and easy-to-use antigen test, designed for home use or point-of-care testing, to determine active COVID-19 infection in a patient through nasal swabbing. Fast and precise results can be obtained within 10 minutes, which can help individuals and healthcare professionals provide proper diagnosis and action.

Simple and Efficient Testing

  • This COVID-19 Antigen Rapid Test was made to quickly detect Sars-CoV-2 nucleocapsid protein antigen in a person
  • Any symptomatic person, age 2 and above, within the first 7 days of their symptoms, can be tested
  • This test can also be used for an individual without symptoms or for a person who has other epidemiological reasons to suspect COVID-19 infection, when tested twice over three days (with a 24-hour interval)
  • Packaged (2) tests per box

Quick and Easy to Use

  • A sample can be obtained (either self-collected or adult-collected) by brushing the nasal swab 5 times against the inner wall of both nostrils of a patient
  • The specimen is then mixed with the solution inside the extraction vial, thoroughly mixing 5 times to make sure that all the samples collected are incorporated with the buffer solution

Fast and Accurate Results

  • Accurate results will be shown 10 minutes after applying the sample and should not exceed 15 minutes to avoid reading false positive or negative results

Digitally Compatible Rapid Test

  • This rapid test can also be administered with the step-by-step guidance of the user-friendly On/Go mobile application, which can be downloaded through the user’s app store or by scanning the QR code provided in the package box and the user manual

FDA Disclaimer

This swab test kit is not FDA cleared or approved, but only authorized under an Emergency Use Authorization for home use or point of care use. It is authorized for the rapid detection of proteins from SARS-CoV-2 and not for any other viruses or pathogens. The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(2), unless the declaration is terminated or authorization is revoked sooner.

More Information
Part Number 02-72-0271
Country of Origin US
UNSPSC Category 42301504
Harmonization Code 9023.00.00.00
Mfg# RCPM00271
Warranty No Warranty
Promo Message Expected to ship within 7-14 days
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