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.


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
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For more information, download the instructions for use via the “Downloads” tab.

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