Ortho is expanding access to testing with the addition of a high-throughput, highly accurate test for acute detection of the SARS-CoV-2 virus.
Meeting the demands of the pandemic with reliable, high-throughput testing solutions for both SARS-CoV-2 infection and antibody detection. Ortho’s integrated VITROS® system allows labs to concurrently run routine and COVID-19 tests, confidently delivering trusted results.
Ortho’s Antigen Test is a high-throughput, highly accurate test that detects acute infection of SARS-CoV-2.
Learn More >Ortho’s Antibody Test detects antibodies to the S1 protein, a primary target for neutralizing antibodies against SARS-CoV-2.
Visualizing SARS-CoV-2 Testing Data across your network of labs.
Learn More >Ortho has three VITROS® COVID-19 Testing Solutions that can be run on the same high-throughput system: VITROS® COVID-19 Total, VITROS® COVID-19 IgG and VITROS® COVID-19 Antigen Test.
Disposable tips, microsensor quality control, and Intellicheck Error-Reducing technology all work together to ensure you always get the most reliable results, every single time.
VITROS® doesn’t require plumbing, which means you can adapt and enhance your lab’s workflow to the changing needs of the pandemic.
Ready when you need it with 24-hour ready mode and long calibration intervals at 28 days.
Content for New div Tag Goes HereOrtho Care™ holistic support program is #1 in service, virtual training, with a 98% uptime guarantee*.
Content for New div Tag Goes Here*Ortho Care™ is Ortho’s global award-winning service and support program that allows you to focus on patient care, not analyzer care. Ortho Care™ holistic support program is #1 in service, virtual training, with a 98% uptime guarantee*. Training: Gain access to unlimited Virtual Key Operator, General Operator and Continuing Education Training – enabling you to leverage Ortho’s solutions wherever you are.
High throughputs, short turnaround times, up-to-date data, and easy-to-use automated systems will help improve the efficiency of your lab during this tumultuous time.
The latest COVID-19 data and insights, fast, reliable results, and our VITROS® system’s unique technology will help position your hospital as a leader in your community during this pandemic.
Fast, reliable COVID-19 testing for both virus and antibody detection can help community leaders make informed decisions about public health.
Content for New div Tag Goes HereOur VITROS® COVID-19 Solutions are just our newest way to help you overcome today’s challenges and provide better care for your patients and your community. But all of Ortho’s solutions, from COVID-19 and beyond, are designed with you and your patient in mind. Because every test is a life.
This website contains information that is targeted to a wide range of audiences and could contain product details or information otherwise not valid or applicable to your country. Please remember to consult your local legal restrictions, regulations, registrations or intended uses in the country of your origin. Product availability may vary from country to country and is subject to varying regulatory requirements.
The VITROS Anti-SARS-CoV-2 Total and IgG Antibody tests and the VITROS SARS-CoV-2 Antigen Test have not been FDA cleared or approved. They have been authorized by the FDA under an Emergency Use Authorization and testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, to perform moderate or high complexity tests. The VITROS Antibody tests have been authorized only for the detection of either Total or IgG antibodies from SARS-CoV-2, not for any other viruses or pathogens, and results should not be used as the sole basis for diagnosis. The VITROS Antigen test has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens. These tests are only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests 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.
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