Siemens Healthineers propose un large éventail de tests des maladies infectieuses (ID), dans toutes les disciplines, du diagnostic, dépistage et génotypage, à la thérapie et la surveillance.
*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 detecting the presence of antibodies against 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. Product availability may vary by country and is subject to regulatory requirements.
1For research use only (RUO). Pursuing FDA emergency use authorization (EUA). Pursuing WHO emergency use assessment and listing (EUAL) certification.