-
,for, Item ID-
- #1236252
- Providers like you icon 21
- Visby Medical #PS-400532
Respiratory Test Kit Visby Medical™ COVID-19 / Influenza A + B Starter Kit 40 Tests CLIA Waived
STARTER KIT, 2 RESPIRATORY TEST W/ACCESS (40TEST/KIT) D/S
Features
- One-Time ONLY Starter Kit, Respiratory: (2) 20 Test Respiratory Kits (40 tests), (1) Power Adapter, (1) Visby Resp Control Kit (2 pos / 2 neg), (1) Staff Training Event, (1) Provider to Provider Discussion
- Limited to 1 per customer
- The Visby Medical Respiratory Health Test is authorized for Emergency Use by FDA under an EUA for use by Authorized Labs: https://www.fda.gov/medical-devices/covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-molecular-diagnostic-tests-sars-cov-2
- More …
Product Details Email
Product Specifications
McKesson # | 1236252 |
---|---|
Manufacturer # | PS-400532 |
Brand | Visby Medical™ |
Manufacturer | Visby Medical |
Country of Origin | China |
Application | Respiratory Test Kit |
CLIA Classification | CLIA Waived |
CLIA Classified | CLIA Waived |
Contents 1 | One-Time ONLY Starter Kit, Respiratory: (2) 20 Test Respiratory Kits (40 tests), (1) Power Adapter, (1) Visby Resp Control Kit (2 pos / 2 neg), (1) Staff Training Event, (1) Provider to Provider Discussion |
Number of Tests | 40 Tests |
Purchase Program Type | Starter Kit |
Reading Type | Visual Read |
Sample Type | Anterior Nasal / Nasopharyngeal Swab Sample |
Specialty | Molecular |
Technology | Colorimetric |
Test Format | Test Device Format |
Test Kit Type | Rapid |
Test Name | COVID-19 / Influenza A + B Starter Kit |
Test Type | RT-PCR |
Time to Results | 30 Minute Results |
UNSPSC Code | 41106302 |
Volume | 5.9 mL |
Features
- One-Time ONLY Starter Kit, Respiratory: (2) 20 Test Respiratory Kits (40 tests), (1) Power Adapter, (1) Visby Resp Control Kit (2 pos / 2 neg), (1) Staff Training Event, (1) Provider to Provider Discussion
- Limited to 1 per customer
- The Visby Medical Respiratory Health Test is authorized for Emergency Use by FDA under an EUA for use by Authorized Labs: https://www.fda.gov/medical-devices/covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-molecular-diagnostic-tests-sars-cov-2
- Visby Medical Respiratory Health Test is a single-use (disposable), fully integrated, rapid, automated RT-PCR in vitro diagnostic test intended for the simultaneous qualitative detection and differentiation of SARS-CoV-2, influenza A, and influenza B viral RNA in healthcare provider-collected nasopharyngeal and anterior nasal swab specimens, and healthcare provider-instructed self-collected anterior nasal swab specimens (collected on site) from individuals with signs and symptoms of respiratory tract infection consistent with COVID-19
- Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, that meet requirements to perform high, moderate, or waived complexity tests
- The Visby Medical Respiratory Health Test is authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation
- Positive results are indicative of the presence of SARS-CoV-2, influenza A, and/or influenza B nucleic acid, but do not rule out bacterial infection or co-infection with other pathogens not detected by the test
- Negative results for influenza B are presumptive and should be confirmed with an alternative molecular FDA-cleared or authorized assay, if necessary for patient management
- Negative results do not preclude SARS-CoV-2, influenza A, and/or influenza B infection and should not be used as the sole basis for patient management decisions
- True PCR results that detect and differentiate RNA from the viruses that cause flu and COVID-19, in under 30 minutes with lab accuracy in the palm of your hands
More Information
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