CL Detect™ Rapid Test for Cutaneous Leishmaniasis

FDA Cleared for In Vitro Diagnostic Use

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

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  • 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

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

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