Uh-Oh Labs Dx Pro 1.2

Uh-Oh Labs Dx Pro assists users in navigating the process of conducting the UOL COVID-19 Test and provides results in a clear and understandable manner.

The UOL COVID-19 Test necessitates the use of the Uh-Oh Labs Dx Pro application and includes the UOL COVID-19 Instrument and UOL COVID-19 Test Kit, both accessible on www.uhohlabs.com.

The UOL COVID-19 Test can identify COVID-19 within 40 minutes with a 96.1% overall accuracy, in comparison to PCR tests, without presenting any false positives.

Designed for trained professionals who are adept at performing UOL COVID-19 Tests, this diagnostic tool is authorized under the Food and Drug Administration’s Emergency Use Authorization.

The purpose of the UOL COVID-19 Test is to qualitatively detect nucleic acid from SARS-CoV-2, the virus responsible for causing COVID-19, in individuals suspected of being infected according to healthcare provider recommendations. Testing is restricted to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, that fulfill obligations to handle high, moderate, or waived complexity tests. The UOL COVID-19 Test is sanctioned for application at the Point of Care (PoC), such as in healthcare settings with a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.

It is crucial to remember that findings from the UOL COVID-19 Test ought not to be utilized as the sole grounds for medical treatment or patient care decisions. Such results should be supplemented with clinical evaluations, patient records, and/or epidemiological data for comprehensive patient management.