InBios CL Detect Rapid Test for Cutaneous Leishmaniasis

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Product Details:

Shelf Life 18 months from manufacturing date
Storage Instructions Store at 230C, do not freeze
Display Type Visual (color change/result lines)
Function Detection of Cutaneous Leishmaniasis
Features Rapid results, Easy to use, Minimal equipment required, Field usable
Measurement Range Qualitative (Positive/Negative)
Instruments Type Diagnostic Rapid Test
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InBios CL Detect Rapid Test for Cutaneous Leishmaniasis Price And Quantity

InBios CL Detect Rapid Test for Cutaneous Leishmaniasis Product Specifications

Material Test Strip, Plastic Cassette, Buffer Solution, Swab
Display Type Visual (color change/result lines)
Wall Mounted No
Equipment Type Rapid Diagnostic Test Kit
Use In vitro diagnostic detection of Leishmania antigen in skin lesions
Storage Instructions Store at 230C, do not freeze
Usage Type Single Use
Real-Time Operation Yes
Accuracy >90% (variable depending on study)
Technology Lateral Flow Immunoassay
Noise Level Silent
Portable Yes
Color White cassette, color indicator on result window
Shelf Life 18 months from manufacturing date
Condition New
Weight Approx. 12 g per test kit
Measurement Range Qualitative (Positive/Negative)
Features Rapid results, Easy to use, Minimal equipment required, Field usable
Instruments Type Diagnostic Rapid Test
Function Detection of Cutaneous Leishmaniasis
Dimension (L*W*H) Individual test device: Approx. 8 x 2 x 0.5 cm
Operating Type Manual
Power Source None (Manual/Non-electric)

Intended User Healthcare professional or trained personnel
Test Principle Detection of Leishmania antigen in lesion sample via lateral flow
Sensitivity Varying by geography and sample type; generally high for L. major
Specificity Varying by geographical area; generally >85%
Time to Result 30 minutes
Sample Type Skin lesion exudate or tissue
Kit Components Test device, extraction buffer, swab, instructions

InBios CL Detect Rapid Test for Cutaneous Leishmaniasis Trade Information

Supply Ability 100 Unit Per Day
Delivery Time 1-7 Days

Product Description

Brand	InBios
Sample Type	Ulcerative skin lesions
Pack Size	25T
CAT No	CL025

The CLDetect Rapid Test is a qualitative,in vitroimmunochromatographic assay for the rapid detection of Leishmania species antigen in ulcerative skin lesions. The test is intended for use with dental broach samples from less than four month old ulcerative skin lesions that are obtained from patients with suspected cutaneous leishmaniasis (CL). The test targets the peroxidoxin antigen of Leishmania species that may cause CL.

Fast and Reliable Leishmaniasis Detection

The InBios CL Detect Rapid Test offers results in just 30 minutes, enabling swift clinical decision-making. Its lateral flow technology ensures dependable detection of Leishmania antigens in skin lesion samples. With sensitivity and specificity that generally exceed 85%, especially for L. major, clinicians can trust the accuracy for various geographic regions.

Designed for Field and Clinic Use

This rapid test kit is specifically built for deployment in both remote and clinical settings. Its manual operation requires no electricity or advanced apparatus, while its portable and robust design makes it exceptionally field-friendly. The kit's clear visual results ensure usability in diverse environments.

User-Friendly and Safe

Each kit contains all necessary components for single-use testing: a test device, buffer solution, swab, and clear instructions. The process involves minimal steps to reduce errors, and the compact, sealed packaging strengthens biosafety and simplifies transport or storage for up to 18 months.

FAQ's of InBios CL Detect Rapid Test for Cutaneous Leishmaniasis:

Q: How is the InBios CL Detect Rapid Test performed?

A: To use the test, a healthcare professional collects a sample from the lesion using the provided swab, mixes it with the supplied buffer, and applies the mixture to the test device. After 30 minutes, results are determined by the appearance of color lines on the test cassette.

Q: What samples are suitable for the InBios CL Detect Rapid Test?

A: The test is validated for skin lesion exudate or tissue samples taken directly from suspected cutaneous leishmaniasis lesions.

Q: When should this rapid test be used?

A: This test is intended for situations where quick on-site diagnosis is needed, such as in clinics, field surveys, or remote healthcare facilities where Cutaneous Leishmaniasis is suspected.

Q: Where can the test be deployed or stored?

A: The kit is portable and can be used in a clinic, hospital, or the field. It must be stored at temperatures between 2-30C, and should not be frozen.

Q: What is the benefit of using this test compared to traditional methods?

A: The InBios CL Detect Rapid Test provides fast, reliable results without the need for complex laboratory infrastructure, making it ideal for early diagnosis and timely management of Cutaneous Leishmaniasis.

Q: How accurate is the test for diagnosing Cutaneous Leishmaniasis?

A: The test generally offers more than 90% accuracy, with sensitivity and specificity varying by region and sample type, being especially high for cases of L. major.

Q: What is included in the test kit and is it reusable?

A: Each kit includes a test device, extraction buffer, swab, and instructions. The test is designed for single use only and should be properly disposed of after use.

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