Respiratory Test Kit – Optimal Medical Supplies

OneStep Plus Strep A Dipstick Test Kit CLIA Waived Box of 25

user — Thu, 06 Nov 2025 15:18:20 +0000

OneStep Pro+ Strep A Cassette Test CLIA Waived Box of 25

user — Thu, 06 Nov 2025 15:17:03 +0000

Respiratory Test Kit Consult Strep A Test 25 Tests CLIA Waived

user — Thu, 30 Oct 2025 19:36:41 +0000

Respiratory Test Kit Tyfast Flu A+B / COVID-19 Multiplex Rapid Test Box of 10

user — Fri, 10 Oct 2025 14:20:50 +0000

Features

The CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test is only for in vitro diagnostic use under the Food and Drug Administration’s Emergency Use Authorization:
Product ships with minimum 60 days dating
The CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test is a lateral flow immunochromatographic assay intended for in vitro rapid, simultaneous qualitative detection and differentiation of influenza A and influenza B nucleoprotein antigens and SARS-CoV-2 nucleocapsid antigen directly from anterior nasal swab specimens of individuals with signs and symptoms of respiratory infection consistent with COVID-19 by their healthcare provider within the first five (5) days of symptom onset when tested at least twice over three days with at least 48 hours between tests

Respiratory Test Kit RSV CLIA Waived Box of 20

user — Fri, 10 Oct 2025 14:19:37 +0000

Features

Rapid detection of RSV in patients <6 years old or >60 years old

Built in control features in cassette (Liquid positive and negative controls provided)

Can use nasopharyngeal swabs or nasal aspirates for testing

Respiratory Test Kit Advin COVID-19 Antigen Test 25 Tests

user — Fri, 10 Oct 2025 14:18:28 +0000

Features

The Advin COVID-19 Antigen Test @Home is For FDA Emergency Use Authorization (EUA) only: https://www.fda.gov/medical-devices/covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-antigen-diagnostic-tests-sars-cov-2

The Advin COVID-19 Antigen Test @ Home is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigens from SARS-CoV-2

This test is authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or with adult-collected anterior nasal (nares) samples from individuals aged 2 years or older

Respiratory Test Kit COVID-19 / Flu A&B Antigen Home Test (OTC) CLIA Waived Box of 2 tests

user — Fri, 10 Oct 2025 14:16:56 +0000

Simultaneously detects 3 viruses (SARS-CoV-2, Flu A&B)
Results in 15 minutes
No repeat testing necessary

Respiratory Test Kit BinaxNOW COVID-19 / Flu A&B (Professional) CLIA Waived Box of 25

user — Fri, 10 Oct 2025 14:15:45 +0000

The BinaxNOW COVID-19/Flu A&B is a lateral flow immunochromatographic assay intended for the qualitative detection and differentiation of influenza A, and influenza B nucleoprotein antigens and SARS-CoV-2 nucleocapsid protein directly in anterior nasal swab samples from individuals with signs and symptoms of respiratory tract infection
For Professional use

All negative results are presumptive and should be confirmed with an FDA-cleared molecular assay when determined to be appropriate by a healthcare provider

Respiratory Test Kit Tyfast Flu A+B / COVID-19 Multiplex Rapid Test Box of 25

user — Fri, 10 Oct 2025 14:14:31 +0000

Features

The CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test is only for in vitro diagnostic use under the Food and Drug Administration’s Emergency Use Authorization: https://www.fda.gov/medical-devices/covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-antigen-diagnostic-tests-sars-cov-2
Product ships with minimum 90 days dating

The CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test is a lateral flow immunochromatographic assay intended for in vitro rapid, simultaneous qualitative detection and differentiation of influenza A and influenza B nucleoprotein antigens and SARS-CoV-2 nucleocapsid antigen directly from anterior nasal swab specimens of individuals with signs and symptoms of respiratory infection consistent with COVID-19 by their healthcare provider within the first five (5) days of symptom onset when tested at least twice over three days with at least 48 hours between tests

Respiratory Test Kit Strep A Test 50 Tests CLIA Waived

user — Fri, 10 Oct 2025 14:09:56 +0000

A rapid test for the qualitative detection of Strep A antigen in throat swab specimens
Accurate – 97% sensitivity and 95% specificity
Results in five minutes