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,for, Item ID-
- #1192948
- Ortho Clinical Diagnostics #6199976
Calibrator Vitros® Anti-SARS-CoV-2 Total N Antibody For VITROS ECi/ECiQ, 3600 Immunodiagnostic Systems, and VITROS 5600, XT 7600 Integrated Systems
CALIBRATOR, VITROS SARS-COV-2 TOTAL N AB (2/PK) D/S
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Features
- The Vitros Anti-SARS-CoV-2 Total N Antibody test is only for use under the Food and Drug Administration's Emergency Use Authorization: https://www.fda.gov/medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-serology-and-other-adaptive-immune-response-tests-sars-cov-2
- Testing is limited to 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
- VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total N Antibody Reagent Pack when used in combination with the VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total N Antibody Calibrators is a chemiluminescent immunoassay test intended for the qualitative detection of total antibody (including IgG, IgA and IgM) to SARS-CoV-2 nucleocapsid protein in human serum and plasma (K2 -EDTA)
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Product Details Email
Product Specifications
McKesson # | 1192948 |
---|---|
Manufacturer # | 6199976 |
Brand | Vitros® |
Manufacturer | Ortho Clinical Diagnostics |
Country of Origin | United Kingdom |
Application | Calibrator |
Container Type | Vial |
For Use With | For VITROS ECi/ECiQ, 3600 Immunodiagnostic Systems, and VITROS 5600, XT 7600 Integrated Systems |
Form | Lyophilized |
Product Dating | McKesson Acceptable Dating: we will ship >= 30 days |
Storage Requirements | Requires Refrigeration |
Test Category | Respiratory |
Test Name | Anti-SARS-CoV-2 Total N Antibody |
Test Type | Antibody Test |
UNSPSC Code | 41116145 |
Features
- The Vitros Anti-SARS-CoV-2 Total N Antibody test is only for use under the Food and Drug Administration's Emergency Use Authorization: https://www.fda.gov/medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-serology-and-other-adaptive-immune-response-tests-sars-cov-2
- Testing is limited to 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
- VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total N Antibody Reagent Pack when used in combination with the VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total N Antibody Calibrators is a chemiluminescent immunoassay test intended for the qualitative detection of total antibody (including IgG, IgA and IgM) to SARS-CoV-2 nucleocapsid protein in human serum and plasma (K2 -EDTA)
- Laboratories within the United States and its territories are required to report all results to the appropriate public health authorities
- The sensitivity of VITROS Anti-SARS-CoV-2 Total N Antibody test in early infection is unknown; negative results do not preclude acute SARS-CoV-2 infection; if acute infection is suspected, direct testing for SARS-CoV-2 is necessary
- False positive results for VITROS Anti-SARS-CoV-2 Total N Antibody test may occur due to cross-reactivity from pre-existing antibodies or other possible causes
- Negative results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus
- Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains, such as coronavirus HKU1, NL63, OC43, or 229E
- Kit contains: 2 vials of VITROS Anti‑SARS-CoV-2 Total N Antibody Calibrators (anti-SARS-CoV-2 in buffer with bovine serum albumin and antimicrobial agent, 1.0 mL)
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