-
,for, Item ID-
- #1179188
- Abbott #06R9110
Antibody Test Control Set AdviseDx SARS-CoV-2 IgM Positive Level / Negative Level 2 X 4.0 mL
CONTROL, SARS-COV-2 IGM ALINITY (1/BX) D/S
Features
- The AdviseDx SARS-CoV-2 IgM Assay is for use under an FDA EUA only: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
- Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C 263a, that meet requirements to perform moderate or high complexity tests
- The AdviseDx SARS-CoV-2 IgM Control Kit is for the estimation of test precision and the detection of systematic analytical deviations of the Alinity i system when used for the qualitative detection of IgM antibodies to SARS-CoV-2 in human serum, serum separator tube, and plasma (dipotassium EDTA, tripotassium EDTA, lithium heparin, lithium heparin separator tube, sodium heparin)
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Product Details Email
Product Specifications
| McKesson # | 1179188 |
|---|---|
| Manufacturer # | 06R9110 |
| Brand | AdviseDx |
| Manufacturer | Abbott |
| Country of Origin | Unknown |
| Application | Control Set |
| Buy American Act (BAA) Compliant | No |
| Container Type | Vial |
| For Use With | For the Estimation of Test Precision and the Detection of Systematic Analytical Deviations of the Alinity i System when used for the Qualitative Detection of IgM Antibodies to SARS-CoV-2 |
| Levels | Positive Level / Negative Level |
| Product Dating | McKesson Acceptable Dating: we will ship >= 30 days |
| Storage Requirements | Requires Refrigeration |
| Test Category | Respiratory |
| Test Name | SARS-CoV-2 IgM |
| Test Type | Antibody Test |
| Trade Agreement Act (TAA) Compliant | Yes |
| UNSPSC Code | 41116128 |
| Volume | 2 X 4.0 mL |
Features
- The AdviseDx SARS-CoV-2 IgM Assay is for use under an FDA EUA only: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
- Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C 263a, that meet requirements to perform moderate or high complexity tests
- The AdviseDx SARS-CoV-2 IgM Control Kit is for the estimation of test precision and the detection of systematic analytical deviations of the Alinity i system when used for the qualitative detection of IgM antibodies to SARS-CoV-2 in human serum, serum separator tube, and plasma (dipotassium EDTA, tripotassium EDTA, lithium heparin, lithium heparin separator tube, sodium heparin)
- At this time, it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity; AdviseDx SARSCoV-2 IgM assay should not be used to diagnose acute SARS-CoV-2 infection
- Laboratories within the United States and its territories are required to report all results to the appropriate public health authorities
- Negative results do not preclude acute SARSCoV-2 infection; if acute infection is suspected, direct testing for SARS-CoV-2 is necessary
- False positive results for the AdviseDx SARS-CoV-2 IgM assay may occur due to cross-reactivity from pre-existing antibodies or other possible causes
- Due to the risk of false positive results, confirmation of positive results should be considered using a second, different IgM assay
- 1 X 4.0 mL Positive control; 1 X 4.0 mL Negative Control
- Negative control contains human plasma
- Positive control contains inactivated, cell-free, human blood-derived material, reactive for anti-SARS-CoV-2 IgM
More Information
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