-
,for, Item ID-
- #1289010
- Nuclein LLC #CN-0006
Respiratory Test Kit DASH® SARS-CoV-2 & Flu A + B 20 Tests CLIA Waived
TEST KIT, SARS-COV-2 & FLU A/BDASH (20/KT) D/S
Features
- The DASH SARS-CoV-2 & Flu A/B Test is a rapid reverse transcription polymerase chain reaction (RT-PCR) assay performed on the DASH Rapid PCR Instrument and is intended for the simultaneous in vitro qualitative detection and differentiation of SARS-CoV-2, influenza A and inflenza B virus ribonucleic acid (RNA) in anterior nasal swab specimens from patients with signs and symptoms of respiratory tract infection
- The test is intended to aid in the differential diagnosis of SARS-CoV-2, influenza A, and influenza B in humans in conjunction with other clinical, epidemiologic and laboratory findings
- Positive results of a specific target are indicative of the presence of that viral RNA and may not be the definite cause of disease
- More …
Product Details Email
Product Specifications
| McKesson # | 1289010 |
|---|---|
| Manufacturer # | CN-0006 |
| Brand | DASH® |
| Manufacturer | Nuclein LLC |
| Country of Origin | United States |
| Application | Respiratory Test Kit |
| Buy American Act (BAA) Compliant | Yes |
| CLIA Classification | CLIA Waived |
| CLIA Classified | CLIA Waived |
| Contents 1 | (20) Test Cartridges, (20) Swabs |
| For Use With | For DASH Rapid PCR Instrument |
| Number of Tests | 20 Tests |
| Product Dating | McKesson Acceptable Dating: we will ship >= 60 days |
| Purchase Program Type | Standard Purchase |
| Reading Type | Machine Read |
| Sample Type | Anterior Nasal Swab Sample |
| Specialty | Molecular |
| Test Format | Cartridge Format |
| Test Kit Type | Rapid |
| Test Name | SARS-CoV-2 & Flu A + B |
| Test Type | RT-PCR |
| Time to Results | 15 Minute Results |
| Trade Agreement Act (TAA) Compliant | Yes |
| UNSPSC Code | 41116144 |
Features
- The DASH SARS-CoV-2 & Flu A/B Test is a rapid reverse transcription polymerase chain reaction (RT-PCR) assay performed on the DASH Rapid PCR Instrument and is intended for the simultaneous in vitro qualitative detection and differentiation of SARS-CoV-2, influenza A and inflenza B virus ribonucleic acid (RNA) in anterior nasal swab specimens from patients with signs and symptoms of respiratory tract infection
- The test is intended to aid in the differential diagnosis of SARS-CoV-2, influenza A, and influenza B in humans in conjunction with other clinical, epidemiologic and laboratory findings
- Positive results of a specific target are indicative of the presence of that viral RNA and may not be the definite cause of disease
- Positive results do not rule out co-infection with other pathogens. Negative results do not preclude SARS-CoV-2, influenza A or influenza B infection and should not be used as the sole basis for patient management decisions
- Anterior nasal swab sample collection rather than more invasive nasopharyngeal swabs
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