Test
For rapid differential diagnosis of acute influenza A and influenza B viral infections.
Specificity | 95.1.% / 99.3% (culture) 96.8%/98.9% (PCR) |
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Sensitivity | 98.6.%/100.0% (Culture), 97.2%/100% (PCR) |
Content And Storage | 2°C to 8°C |
Control Sets | M106 |
Detectable Analytes | Influenza A and B |
Shelf Life | 12 Months from DOM |
CE Marker | Yes |
CPT Code | 87502 |
Clia Complexity | Moderate |
Test Time | ≈45 min. |
The Solana RSV + hMPV Assay is a rapid qualitative in vitro diagnostic test for the detection and differentiation of Respiratory Syncytial Virus (RSV) and Human Metapneumovirus (hMPV) viral RNA in nasal and nasopharyngeal swabs from patients with signs and symptoms of respiratory infection.
An isothermal Reverse Transcriptase - Helicase-Dependent Amplification (RT-HDA) assay intended for the qualitative detection of nucleic acid from SARS-CoV-2 in nasopharyngeal (NP) and nasal (NS) swab specimens from individuals suspected of COVID-19.
Disposable | Yes |
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CE Marker | CE-IVD |
For Use With (Application) | RT-PCR, Rapid PCR |
Sterility | Non-sterile |
Clia Complexity | Moderate |
Included with kit, additional may be ordered separately
Isothermal Reverse Transcriptase-Helicase-Dependent Amplification (RT-HDA) assay intended for the qualitative detection of nucleic acid from SARS-CoV-2 in nasopharyngeal & nasal swab specimens from individuals suspected of COVID-19 by their healthcare provider.
Includes | Universal Transport Media |
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Quantity | 96/Kit |
Shelf Life | At least 4 months from date of manufacture |
Certifications/Compliance | Emergency Use Authorization (EUA) |
For Use With (Application) | Solana Instrument |
Sterility | Non-sterile |
Included with kit, additional may be ordered separately