QUICK REFERENCE INSTRUCTIONS - Quidel Corporation
The Sofia 2 Flu + SARS Antigen FIA is intended for use on the Sofia 2 only and by medical professionals or trained operators who are proficient in performing tests using the Sofia 2 Instrument. The Sofia 2 Flu + SARS Antigen FIA test is only for use under the Food and Drug Administration’s Emergency Use Authorization.
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Influenza A+B FIA - Quidel
www.quidel.comPage 3 of 3 Will the Sofia Influenza A+B FIA show a positive test result after someone has had a nasally administered vaccine? Individuals who received nasally administered influenza vaccine may have a positive flu A and/or flu B test result
For Research Use Only. EIA Kit Not for Use in Diagnostic ...
www.quidel.comResearch has also associated levels of C5a with pathogenesis of a variety of disease states including myocardial infarction(10-14), stroke(15,16) ... For Research Use Only. Not for use in diagnostic procedures. 2. Treat specimen samples as potentially biohazardous material.
Quick, easy, accurate! - Quidel Corporation
www.quidel.comQuick, easy, accurate! Diagnosing and managing respiratory syncytial virus (RSV) is serious business. In the U.S., RSV is estimated to be responsible for 73,400 to 126,300 hospitalizations annually for bronchiolitis and pneumonia alone among children younger than one year.1 In children hospitalized
User Manual - Quidel
www.quidel.comDymo LabelWriter 450 Printer (Part #1752264) Page 12 of 43 Dymo Vinyl Label Roll, 2 5/16” x 4” (Part #30256) Replacement Battery Contact Quidel Technical Support for additional supplies at 800.874.1517 (in the U.S.). See page 3 for additional contact information.
Influenza A+B FIA - Quidel Corporation
www.quidel.comDoes the Sofia Influenza A+B FIA detect H5N1 or other strains of “avian” influenza viruses? The Sofia Influenza A+B FIA has been shown to detect cultured human isolates of H5N1; as with other rapid tests for influenza, the ability of the Sofia Influenza A+B FIA to detect influenza Type A in patients infected with H5N1 has not been established.
QUICK REFERENCE INSTRUCTIONS - Quidel Corporation
www.quidel.comquick reference instructions All clinical specimens must be at room temperature before beginning the assay. Performing the assay outside the time and temperature ranges provided may produce invalid results.
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www.hsa.gov.sgThe SARS-CoV-2 Antigen Rapid Test is for self-testing use only. The test should only be used for the detection of SARS-CoV-2 antigens in nasal swab specimens. The intensity of the test line does not necessarily relate to the SARS-CoV-2 viral load in the specimen. 2. A false-negative test may result if the level of antigen in a sample is ...
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