-
,for, Item ID-
- #1180548
- Ortho Clinical Diagnostics #6199944
Antigen Extraction Buffer Vitros® For use to Extract the Viral Load from Swab Samples Placed in Appropriate Transport Media / For use on the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems
BUFFER, ANTIGEN EXTRACTION SARS-COV-2 (1000T/EA) D/S
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Features
- The Vitros SARS-CoV-2 Antigen Reagent Pack used in combination with the Vitros SARS-CoV-2 Antigen Calibrator is for use under an FDA EUA only: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
- Authorized Laboratories: Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C 263a, that meet the requirements to perform moderate or high complexity tests
- The VITROS Immunodiagnostic Products SARS-CoV-2 Antigen test is a chemiluminescent immunoassay intended for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in nasopharyngeal (NP) specimens from individuals who are suspected of COVID-19 by their healthcare provider within one to six days of the onset of symptoms using the VITROS 3600 Immunodiagnostic System and the VITROS 5600/XT 7600 Integrated Systems
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Product Details Email
Product Specifications
| McKesson # | 1180548 |
|---|---|
| Manufacturer # | 6199944 |
| Brand | Vitros® |
| Manufacturer | Ortho Clinical Diagnostics |
| Country of Origin | United Kingdom |
| Application | Antigen Extraction Buffer |
| Buy American Act (BAA) Compliant | Yes |
| For Use With | For use to Extract the Viral Load from Swab Samples Placed in Appropriate Transport Media / For use on the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems |
| Specifications | 28 mL |
| Trade Agreement Act (TAA) Compliant | Yes |
| UNSPSC Code | 41116128 |
Features
- The Vitros SARS-CoV-2 Antigen Reagent Pack used in combination with the Vitros SARS-CoV-2 Antigen Calibrator is for use under an FDA EUA only: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
- Authorized Laboratories: Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C 263a, that meet the requirements to perform moderate or high complexity tests
- The VITROS Immunodiagnostic Products SARS-CoV-2 Antigen test is a chemiluminescent immunoassay intended for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in nasopharyngeal (NP) specimens from individuals who are suspected of COVID-19 by their healthcare provider within one to six days of the onset of symptoms using the VITROS 3600 Immunodiagnostic System and the VITROS 5600/XT 7600 Integrated Systems
- Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status; positive results do not rule out bacterial infection or co-infection with other viruses
- Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities
- Negative results from patients with symptom onset outside of one to six days should be treated as presumptive
- Negative results do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions
- Negative results should be considered in the context of a patient’s recent exposures, history and the presence of clinical signs and symptoms consistent with COVID-19
- 1 extraction buffer pack containing: 4 bottles of VITROS SARS-CoV-2 Antigen Extraction Buffer (28 mL) with antimicrobial agent
- Rx only; For in vitro diagnostic and laboratory professional use
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