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Test Type
Visual Read
Time to Results
Human Whole Blood / Serum / Plasma Sample
UNSPSC Code
Cassette Format
Lateral Flow Method
COVID-19 IgG / IgM
Antibody Test
15 Minute Results
41116126
Features
The Assure COVID-19 IgG/IgM Rapid Test Device is for use under FDA Emergency Use Authorization: https:www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
Use of this test with all authorized specimen types is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA)
42 U.S.C. 263a
that meet requirements to perform moderate or high complexity tests; this test is also authorized for use with fingerstick whole blood specimens only 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
The Assure COVID-19 IgG/IgM Rapid Test Device is a rapid lateral flow chromatographic immunoassay intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA)
serum
plasma (sodium EDTA) and fingerstick whole blood
The Assure COVID-19 IgG/IgM Rapid Test Device is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2
indicating recent or prior infection - at this time
it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity
Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities
False positive results for Assure COVID-19 IgG/IgM Rapid Test Device 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 second
different IgG or IgM assay
This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 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
