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Finecare LH Rapid Quantitative Test

105 INR/Kit

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Product Details:

Shelf Life 18 months from date of manufacture
Frequency Single use per test
Usage Type Diagnostic Test for Laboratory or Point-of-Care use
Features Rapid results, quantitative LH measurement, easy operation, compatible with Finecare FIA Meters
Function Quantitative detection of LH
Storage Instructions Store at 2-30C, keep away from direct sunlight and moisture
Measurement Range 2200 mIU/mL
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Finecare LH Rapid Quantitative Test Price And Quantity

Price 105 INR/Kit
Minimum Order Quantity 2 Box

Finecare LH Rapid Quantitative Test Product Specifications

Instruments Type Immunofluorescence Analyzer Test
Portable Yes
Power Consumption Depends on analyzer
Display Type Requires Finecare Fluorescence Immunoassay Analyzer
Equipment Type LH Rapid Quantitative Test
Accuracy >=95%
Condition New
Technology Lateral Flow Immunofluorescence Assay (LFIA)
Power Source Battery or External Power Adapter (Analyzer required)
Dimension (L*W*H) Individual cassette: approx. 80 mm x 20 mm x 6 mm
Weight Approx. 10g (per test cassette)
Measurement Range 2200 mIU/mL
Voltage As per analyzer specification
Real-Time Operation Yes
Usage Type Diagnostic Test for Laboratory or Point-of-Care use
Features Rapid results, quantitative LH measurement, easy operation, compatible with Finecare FIA Meters
Material Test cassette and buffer (medical grade plastics, reagents)
Function Quantitative detection of LH
Color White cassette
Use Testing Luteinizing Hormone (LH) levels in human blood/serum/plasma
Storage Instructions Store at 2-30C, keep away from direct sunlight and moisture
Wall Mounted No
Noise Level Silent
Operating Type Manual with Analyzer
Shelf Life 18 months from date of manufacture
Frequency Single use per test

Finecare LH Rapid Quantitative Test Trade Information

FOB Port JAIPUR
Delivery Time 10 Days
Sample Policy Contact us for information regarding our sample policy
Main Domestic Market All India

Product Description

The Finecare LH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare FIA System for quantitative determination of Luteinizing hormone (LH) in human whole blood, serum or plasma. This test is used as an aid to diagnose the ovulation cycle, premature ovarian failure and gonadal hypoplasia.

. Store the test kit at 430 up to the expiration date printed on package.
2. If removed from refrigerator, allow the test kit for 30 minutes to return to room temperature before testing.
3. Do not remove the Test Cartridge from the pouch until use. The Test Cartridge should be used within 1 hour once opened.

Technical Details

Rapid and Precise LH Detection

With a swift turnaround of just 15 minutes, the Finecare LH Rapid Quantitative Test offers healthcare professionals a reliable method for monitoring Luteinizing Hormone levels. Leveraging advanced immunofluorescence technology, the test ensures high sensitivity, enabling accurate quantification necessary for clinical assessments and fertility evaluations.

Seamless Compatibility and Simple Use

Designed for compatibility with the Finecare Fluorescence Immunoassay Analyzer, this test fits effortlessly into existing diagnostic workflows. Its straightforward manual operation is optimized for healthcare environments, offering clear instructions and user-friendly features for precise and repeatable results.

Robust and Flexible Storage

Each cassette, fashioned from medical-grade plastics, is easy to handle and can be stored conveniently at temperatures from 2C to 30C, with a shelf life of 18 months. The compact, portable design makes it ideal for both laboratory and point-of-care testing scenarios, ensuring flexibility in deployment.

FAQ's of Finecare LH Rapid Quantitative Test:

Q: How is the Finecare LH Rapid Quantitative Test performed?

A: To perform the test, a healthcare professional collects 75 L of whole blood, serum, or plasma, dispenses it into the sample well of the test cassette using the provided pipette, adds the buffer, and inserts the cassette into a Finecare FIA Meter. The analyzer interprets the fluorescent signal, generating quantitative LH results within 15 minutes.

Q: What are the sample types accepted for this test?

A: The Finecare LH Rapid Quantitative Test can analyze human whole blood, serum, or plasma samples, offering flexibility for healthcare professionals to choose the most suitable sample type for their clinical needs.

Q: Where are the results displayed and how are they read?

A: Results are displayed on the Finecare Fluorescence Immunoassay Analyzer. The analyzer interprets the test cassette's fluorescent signal, providing a quantitative measurement of LH in the sample, expressed in mIU/mL.

Q: When should the test be used and who is it intended for?

A: This test is intended for use by healthcare professionals in diagnostic laboratories or point-of-care settings, whenever quantitative measurement of LH levels is clinically required, such as in fertility assessments or hormonal evaluations.

Q: What are the storage and handling requirements for the test kit?

A: Store the test kit at temperatures between 2C and 30C, away from direct sunlight and moisture. The kit has a shelf life of 18 months from the date of manufacture, and should be kept sealed until use to maintain integrity.

Q: What benefits does the Finecare LH Rapid Quantitative Test provide?

A: The test offers rapid, highly accurate, and quantitative LH measurement. Its portability, ease of use, and compatibility with Finecare FIA Meters allow healthcare providers to deliver timely, informed clinical decisions at both the bedside and in laboratory settings.

Q: Is the test suitable for in-home use or by laypersons?

A: No, the Finecare LH Rapid Quantitative Test is intended strictly for professional and in vitro diagnostic use. It requires specialized equipment and interpretation, and must be administered by trained healthcare personnel.

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