Test
Rapid, one-step lateral flow test for Respiratory Syncytial Virus (RSV)
Type | RSV Test Kit |
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Format | Patented Card |
Sample Type | Nasal wash and nasopharyngeal swab |
Detectable Analytes | Respiratory Syncytial Virus (RSV) |
Test Time | 15 min. |
For rapid qualitative detection of respiratory syncytial virus (RSV) nucleoprotein antigens
Includes | Individually packaged cassettes 25, reagent tubes 25, reagent solution 25, sterile nasopharyngeal swabs 25, large, pink fixed volume pipettes 25, small, clear fixed volume pipettes 25, RSV positive control swab 1, negative control swab 1, package insert 1, quick reference instructions 1, QC card, printer Paper 1 |
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Type | Sofia™ RSV FIA Immunofluorescence Test Kit |
Sample Type | Nasopharyngeal swab and nasopharyngeal aspirate/wash specimens |
Detectable Analytes | Respiratory Syncytial Virus (RSV) Antigen |
For Use With (Application) | IVD |
Clia Complexity | Waived |
Test Time | >15 min. |
Provides objective results on an easy to read digital display, unlike current rapid RSV tests, which requires subjective visual test interpretation to determine positive or negative test result
Detectable Analytes | RSV |
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For rapid, qualitative detection of RSV antigen directly from nasopharyngeal swab or aspirate specimens from symptomatic pediatric patients
Remel Xpect RSV Control Kit is an Xpect RSV liquid control set.
Intended for the rapid, qualitative detection of respiratory syncytial virus (RSV) directly from nasopharyngeal swab and nasal aspirate specimens in those under the age of 6 or over the age of 60. Intended for use as an aid in the diagnosis of patients with symptoms consistent with RSV infection.
Use PathoDx™ Respiratory Virus Panel Control Slide along with RVP kit to perform direct immunofluorescence test.
For use with ImmunocardSTAT Flu/RSV
An in vitro rapid lateral flow test intended for the qualitative detection of Streptococcus pneumoniae and Legionella pneumophila antigens in urine specimens from patients with symptoms of pneumonia.
Can be used to determine a limit of detection (LOD), in diagnostic assay development or cross-reactivity studies
Rapid, qualitative detection of respiratory syncytial virus fusion protein in nasopharyngeal swabs/nasal aspirate specimens in children less than 6 years and adults over 60. Intended as an aid in the rapid laboratory diagnosis of acute respiratory syncytial virus infection in patients with such symptoms.