Technical specifications
The principle:
- Antigen detection
Approval from the Federal Institute for Drugs & amp; Medical device
No cross reactions
- No cross-reactions with other coronaviruses SARS, MERS, NL13, 229E, OC433)
- Many other microorganisms tested
Accuracy in the areas:
- Specificity 99.28%
- Low detection limit of 1.11 x 10² TCID50 / mL.
- Sensitivity 96.0%
-
reliable results in 15 minutes:
PPA: 86.54%
NPA: 100%(Positive / Negative Percent Agreement)
qualitative immunoassay
- no instruments or special equipment required
User skills:
- normal
Procedure:
- Nose or throat swab
Test capacities.
- Possibility of mass testing
Number of individual tests per box:
- 25 tests
Origin:
Made in South Korea
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