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,for, Item ID-
- #1253219
- Providers like you icon 36
- Sekisui Diagnostics #1080
Respiratory Test Kit OSOM® Flu A + B / SARS-CoV-2 Combo 25 Tests
TEST, RAPID ANTIGEN OSOM FLU SARS COV-2 COMBO (25/KT)
Features
- The OSOM® Flu SARS-CoV-2 Combo Test is under 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 OSOM® Flu SARS-CoV-2 Combo 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 four (4) days of symptom onset when tested at least twice over three days with at least 48 hours between tests
- 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
- More …
Product Details Email
Product Specifications
McKesson # | 1253219 |
---|---|
Manufacturer # | 1080 |
Brand | OSOM® |
Manufacturer | Sekisui Diagnostics |
Country of Origin | United States |
Application | Respiratory Test Kit |
Contents 1 | Each Kit contains: (25) Sterile Nasal Swabs, (27) Test Sticks, (1) Flu A / Flu B / SARS-CoV-2 Positive Control Swab, (1) Flu A / Flu B / SARS-CoV-2 Negative Control Swab, (2) Result Interpretation Cards, IFU, Quick Reference Guide, (1) Workstation |
HCPCS | K1034 |
Is_ECAT | N |
Is_GSA | Y |
Is_VA | N |
Number of Tests | 25 Tests |
Purchase Program Type | Standard Purchase |
Reading Type | Visual Read |
Sample Type | Anterior Nasal Swab Sample |
Specialty | Immunoassay |
Test Format | Test Device Format |
Test Kit Type | Rapid |
Test Method | Lateral Flow |
Test Name | Flu A + B / SARS-CoV-2 Combo |
Test Type | Antigen Test |
Time to Results | 10 Minute Results |
UNSPSC Code | 41116144 |
Features
- The OSOM® Flu SARS-CoV-2 Combo Test is under 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 OSOM® Flu SARS-CoV-2 Combo 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 four (4) days of symptom onset when tested at least twice over three days with at least 48 hours between tests
- 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
- Results are for the simultaneous in vitro detection and differentiation of SARS-CoV-2, influenza A virus, and influenza B virus protein antigen, but does not differentiate, between SARS-CoV and SARS-CoV-2 viruses and is not intended to detect influenza C antigens
- Positive results do not rule out bacterial infection or co-infection with other viruses; the agent detected may not be the definitive cause of disease
- All negative results are presumptive, and should be confirmed with a molecular assay, if necessary, for patient management
- Negative results do not rule out influenza or SARS-CoV-2 infection, and should not be used as the sole basis for treatment or patient management decisions, including infection control measures such as isolating from others and wearing masks
- Negative results should be considered in the context of an individual’s recent exposures, history and the presence of clinical signs and symptoms consistent with each respiratory infection
- Rapid: Differentiate between three viral infections (COVID-19, Flu A, & Flu B) in only 10 minutes at the point-of-care
More Information
- OSOM Flu A + B and SARS-CoV-2 Combo FDA EUA Letter
- OSOM Flu A + B and SARS-CoV-2 Combo IFU
- OSOM Flu A + B and SARS-CoV-2 Combo Patients Fact Sheet
- OSOM Flu A + B and SARS-CoV-2 Combo Healthcare Providers Fact Sheet
- OSOM Flu A + B and SARS-CoV-2 Combo Quick Ref Guide
- OSOM Flu A + B and SARS-CoV-2 Combo Kit Expiry Extension Letter
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