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CareStart COVID-19 Rapid Antigen Tests AN (Box of 20)
COVID-19 Rapid Antigen Tests

CareStart COVID-19 Rapid Antigen Tests AN (Box of 20)

Your Price: $289.00
Part Number: RCHM-02071-AN
Availability: In Stock and Ships Same or Next Day!

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Quantity Pricing

Quantity Price
5 - 9 $269.00
10 - 20 $264.00
21 - 49 $259.00
50+ $244.00

Access Bio's CARESTART COVID-19 Antigen Rapid Test (Anterior Nasal Swab [Shallow Swab])


UPDATED 3/15/21: FDA authorized a 9-month shelf life for this product. VIEW THE NOTICE HERE
The shelf-life expiration date for the CareStart COVID-19 ANTIGEN tests have been extended per the manufacturer.  The current inventory shipping will show it expires 6/30/2021, however the lot letter provided by the manufacturer extends this product to expire 9/30/2021.


Informational Brochure


 RAPID Point Of Care Test

The continuing spread of COVID-19 has raised the importance of rapid screening.  Demand for rapid test kits is rising because unlike polymerase chain reaction (PCR) tests, they require no special equipment.  Access Bio, Inc., the world's leading manufacturer of rapid test kits for malaria, developed CareStart™ COVID-19 Ag to rapidly detect antigens of SARS-CoV-2, the virus which causes COVID-19. 

The CareStart™ COVID-19 Antigen Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from individuals who are suspected of COVID-19 by their healthcare providers. This product is available under FDA/EUA authorization.

  • Lateral flow assay
  • Rapid results in 10 minutes
  • Minimally invasive specimen collection (nasopharyngeal or anterior nasal)
  • Intended at POC setting (i.e., in patient care settings) by medical professionals
  • For in-vitro use only
  • Detect SARS-CoV-2 nucleocapsid protein antigen
  • For prescription use only
  • Anterior nasal swab (Shallow swab)

The CareStart™ COVID-19 Antigen Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from individuals who are suspected of COVID-19 by their healthcare providers.

Important Information

  • This test has been authorized by FDA under an EUA for professional use.
  • This test has not been FDA cleared or approved.
  • This test 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 Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.
  • Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains, such as coronavirus HKU1, NL63, OC43, or 229E.
  • This product is intended for professional use and not for home use.

This test is authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.



Important Information:

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