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

Catalog No. 21931260
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CL Rapid Test
This item is not returnable. View return policy
This item is not returnable. View return policy

Description

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

  • 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

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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