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InBios International Inc. CL Detect™ Rapid Test for Cutaneous Leishmaniasis

Description
- FDA 510(k) Cleared and CE Marked
- Relative Specificity in non-endemic population: 96%
- Relative Sensitivity and Specificity in endemic population: 100% and 84% respectively
- Kit includes 25 tests, controls, buffers and sterile dental broaches
Specifications
Specifications
| Content And Storage | Room Temp, 20°C to 30°C |
| Detectable Analytes | Leishmania species antigen |
| Detection Method | Rapid Test |
| Type | Rapid Test |
| Immunoassay Kit Format | ICT (Strip) |
| Quantity | 25 Tests/Kit |
| Analysis Time | 20 min. |
| Form | Ready-to-Use (RTU) |
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