INDICAID PoC (Professional) COVID-19 RAPID ANTIGEN TESTS (25 TESTS)

$200.00

USA SALES ONLY 

A VALID CLIA NUMBER IS REQUIRED FOR PURCHASE.
ENTER CLIA NUMBER IN THE SHOPPING CART AT THE TIME OF PURCHASE.

*ONLINE PURCHASES ARE LIMITED TO 40 BOXES CONTAINING 1000 Tests. FOR ORDERS OVER 40 BOXES, PLEASE CONTACT OUR SALES PROFESSIONALS.

At only $8.00 per test, INDICAID® is a fast, reliable, and affordable Professional  COVID-19 Rapid Antigen Test for use by laboratories, pharmacies, urgent care clinics, nursing homes, hospitals, businesses/employers, schools, sports, events, and more, that have a CLIA certified technician to administer and/or supervise the tests.

  • The INDICAID COVID-19 Antigen Test is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-coV-2 indirect anterior nasal swab specimens from individuals who are suspected of COVID-19.
  • For use with direct anterior nasal and nasopharyngeal swab specimens, non-invasive test procedures
  • Rapid results within 20 minutes
  • Detect SARS-CoV-2 nucleocapsid protein antigen
  • Effective in Detecting Omicron Variant (B.1.1.529) and specific variants of new coronavirus.*
  • Accuracy: Sensitivity 88.9%; Specificity 96.8%; Overall accuracy 95.6%
  • Fact Sheet for Healthcare Providers... View/Download Here
  • For additional information, view our Resource/Download page.

*Detectable variants include Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), Delta (B.1.617.2), Delta Plus (AY.1 and AY.2) and Omicron (B.1.1.529)
View Our Statement.

For complete product information, please refer to our full product page, located on our corporate site.

Quality Controls

It is the responsibility of each laboratory or healthcare setting to ensure quality assurance. Check out our Quality Control product option. Quality control requirements should be followed in conformance with local, state, and federal regulations or accreditation requirements and the user laboratory’s standard quality control procedures.

(Controls sold separately)

EXPIRATION DATE

NOTE: Expiration Date: If you receive a box that has an expiration date that has passed, please do not be concerned. The FDA has granted an extended expiration life by 6 months from the expiration date printed on the back of the box for these tests.

Read the FDA EUA Expiration Extension Update Document.

The shelf-life for all lots of INDICAID with initial prefix 21SXXXX ND LOTS 22S0001 - 22S0100 may be  extended by (6) months from the  expiration dating printed on the product packaging.

Review the Memo Discussing Specific Impacted INDICAID PoC Lot Numbers.

 

CLIA INFORMATION

The Clinical Laboratory Improvement Amendments of 1988 (CLIA) regulations include federal standards applicable to all U.S. facilities or sites that test human specimens for health assessment or to diagnose, prevent, or treat disease. CDC, in partnership with CMS and FDA, supports the CLIA program and clinical laboratory quality. Learn more about CLIA.