-
,for, Item ID-
- #1131782
- Beckman Coulter #A30945
Immunoassay Reagent Access® IL-6 For Access Immunoassay Systems 2 X 50 Tests
REAGENT, ACCESS IL 6 2X50ML D/S
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Features
- The Access IL-6 Immunoassay is only for use under the Food and Drug Administration’s Emergency Use: 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 of 1988 (CLIA), 42 U.S.C. §263a, to perform moderate or high complexity tests
- This test has been authorized only to assist in identifying severe inflammatory response, when used as an aid in determining the risk of intubation with mechanical ventilation in confirmed COVID-19 patients
- More …
Product Details Email
Product Specifications
McKesson # | 1131782 |
---|---|
Manufacturer # | A30945 |
Brand | Access® |
Manufacturer | Beckman Coulter |
Country of Origin | United States |
Application | Immunoassay Reagent |
Container Type | Bottle |
For Use With | For Access Immunoassay Systems |
Number of Tests | 2 X 50 Tests |
Product Dating | McKesson Acceptable Dating: we will ship >= 90 days |
Sample Type | Serum / Plasma Sample |
Specialty | Immunoassay |
Storage Requirements | Requires Refrigeration |
Test Category | Autoimmune |
Test Method | Chemiluminescent Immunoassay |
Test Name | IL-6 |
Time to Results | 35 Minute Results |
UNSPSC Code | 41116010 |
Volume | 2 X 50 mL |
WARNING: This product can expose you to chemicals which are known to the State of California to cause cancer and birth defects or other reproductive harm. For more information, go to www.p65Warnings.ca.gov.
Features
- The Access IL-6 Immunoassay is only for use under the Food and Drug Administration’s Emergency Use: 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 of 1988 (CLIA), 42 U.S.C. §263a, to perform moderate or high complexity tests
- This test has been authorized only to assist in identifying severe inflammatory response, when used as an aid in determining the risk of intubation with mechanical ventilation in confirmed COVID-19 patients
- This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of medical devices under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C § 360bbb- 3(b)(1), unless the authorization is terminated or revoked sooner
- The Access IL-6 assay is an in vitro diagnostic test for the quantitative measurement of IL-6 (Interleukin 6) in human serum and plasma (heparin)
- Normal IL-6 results do not preclude development of a severe inflammatory response, and IL-6 should not be used as the sole basis for patient management decision
- Results must be combined with clinical observations, patient history, other laboratory parameters, and epidemiological information
- The Access IL-6 assay is a paramagnetic particle, chemiluminescent immunoassay and is intended for use on Access immunoassay analyzers
- Approx 35 Minutes time to first result
- For use with Access Family of Immunoassay Systems: Access 2, UniCel DxC 600i, UniCel DxI 600, UniCel DxI 800, UniCel DxC 880i, UniCel DxC 860i, UniCel DxC 680i, UniCel DxC 660i
- WARNING: Cancer and Reproductive Harm – www.P65Warnings.ca.gov.
More Information
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