Description
Unit: 1 Box (40 Tests)
Regulatory Status: CLIA Waived/Professional Use Only
Contents: (40) Test devices, (2×20) Nasal swab specimen collection & dispensing tube containing OSOM Antigen Buffer, (40) sterile swabs, (1) package insert with test procedure page
Sample Type: Nasal Swab
Storage Requirements: 59 F – 86 F
OSOM® COVID-19 Antigen Rapid Test is a lateral flow chromatographic immunoassay intended for the qualitative detection of the SARS-CoV-2 nucleocapsid protein antigen in direct midturbinate (MT) nasal swab specimens from individuals who are suspected of COVID-19
As with other OSOM Rapid Tests, it is made in the USA and supported by a highly skilled technical support team of medical technologists/professionals.
The OSOM COVID-19 Antigen Rapid Test is intended for use by healthcare professionals or operators who are proficient in performing tests in point of care settings. The OSOM COVID-19 Antigen Rapid Test is only for in vitro diagnostic use under the Food and Drug Administration’s Emergency Use Authorization.
