CL Detect™ Rapid Test for Cutaneous Leishmaniasis
FDA Cleared for In Vitro Diagnostic Use

The CL Detect™ Rapid Test is a qualitative, in vitro immunochromatographic assay for the rapid detection of Leishmania species antigen in ulcerative skin lesions.

Resources
- US FDA Cleared
- 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
Catalog No. | CL025 |
Format | ICT (strip) |
Quantity/Kit | 25 tests |
Time to Result | 20 minutes |
Sample Type | Skin lesions |
Storage | Room Temperature (20°C-30°C) |
Shelf Life | 24 months |
For more information, download the instructions for use via the “Downloads” tab.
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