FTD SARS-CoV-2 Assay1For the specific detection of the coronavirus causing COVID-19
Clinical Use
Respiratory Testing
In late 2019, China notified the World Health Organization (WHO) of a novel strain of coronavirus. This virus, now named SARS-CoV-2, targets the epithelial cells of the respiratory tract and causes infection that can lead to Coronavirus disease 2019 (COVID-19). Siemens Healthineers new molecular assay uses real-time PCR to detect RNA from this virus.
Emergent SARS-CoV-2 Variants
In silico analysis has shown that the FTD SARS-CoV-2 Assay detects the emergent SARS-CoV-2 variants, first identified in the UK and South Africa, at a rate of 100%.*
Features & Benefits
- Kit comprised of a single-well dual target assay for the specific detection of SARS-CoV-2 (COVID-19)
- Designed for high sensitivity, specificity, and inclusivity
- Covers highly conserved regions within ORF1ab and N gene
- Uses the same assay setup protocol and thermal-cycling profile as all FTD respiratory disease kits
Product availability varies by country and is subject to local regulatory requirements.
*Data on file at Fast Track Diagnostics, A Siemens Healthineers Company, Luxembourg
CE-IVD labelled for diagnostic use in the EU. This test has not been FDA cleared or approved. This test has been authorized by FDA under an EUA for use by authorized laboratories. This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics 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.