User Manual - Quidel
Dymo 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.
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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
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
www.quidel.comReference the Package Insert for Warnings and Precautions, Specimen Collection and Handling, and Quality Control. Study the Package Insert and User Manual thoroughly before using Quick Reference Instructions. This is not a complete Package Insert.
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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