-
,for, Item ID-
- #1249207
- Providers like you icon 13
- Germaine Laboratories Inc #GCRSV-502B-PBS
Respiratory Test Kit Rapid Check™ Respiratory Syncytial Virus Test (RSV) 20 Test CLIA Waived
TEST KIT, RSV RAPID CHECK ANTIGEN W/SWAB CLIA WAIVED (20/KT)
Features
- 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
- 510(k) Cleared and CLIA Waived for Prescription Use
- More …
Product Details Email
Product Specifications
| McKesson # | 1249207 |
|---|---|
| Manufacturer # | GCRSV-502B-PBS |
| Brand | Rapid Check™ |
| Manufacturer | Germaine Laboratories Inc |
| Country of Origin | United States |
| Application | Respiratory Test Kit |
| Buy American Act (BAA) Compliant | No |
| CLIA Classification | CLIA Waived |
| CLIA Classified | CLIA Waived |
| Contents 1 | (20) Individually Packaged Test Devices, (20) Nasopharyngeal Swabs, 2 mL Extraction Reagent Solution, (20) Extraction Tubes, (20) Phosphate Buffered Saline (PBS) Vials, (40) Disposable Pipettes, 1 mL Positive Control Reagent, 1 mL Negative Control Reagent, Instructions for Use |
| Number of Tests | 20 Test |
| Purchase Program Type | Standard Purchase |
| Reading Type | Visual Read |
| Sample Type | Nasopharyngeal Swab / Nasal Aspirate Sample |
| Specialty | Immunoassay |
| Test Format | Test Device Format |
| Test Kit Type | Rapid |
| Test Name | Respiratory Syncytial Virus Test (RSV) |
| Test Type | Antigen Test |
| Time to Results | 15 Minute Results |
| Trade Agreement Act (TAA) Compliant | No |
| UNSPSC Code | 41116126 |
Features
- 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
- 510(k) Cleared and CLIA Waived for Prescription Use
- Detection of fusion protein of respiratory syncytial virus
- Nasopharyngeal swab and nasal aspirate specimen
- Positive% Agreement: 93. 9%
- Negative% Agreement: 97.7%
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