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Finecare Progesterone Rapid Quantitative Test

208 INR/Kit

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Product Details:

Display Type Digital (With Finecare FIA Meter)
Accuracy 95%
Features Quick Results, High Sensitivity and Accuracy, Quantitative Measurement, Easy to Use, Requires Finecare FIA Meter
Instruments Type Diagnostic Test Kit
Frequency Single Use/Test
Measurement Range 0.5~60 ng/mL
Function Progesterone Level Quantification
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Finecare Progesterone Rapid Quantitative Test Price And Quantity

Minimum Order Quantity 2 Box
Price 208 INR/Kit

Test Time Within 15 Minutes
Specimen Types Serum, Plasma, or Whole Blood
Sample Volume Required 75 L Serum/Plasma/Whole Blood
Sensitivity <0.5 ng/mL (varies as per lot)
Packing 25 Tests per Kit
Lot Traceability Each Cassette Individually Marked
Result Type Numerical Value on Digital Display
Analyzer Compatibility Finecare FIA Meter (Model Specified by Manufacturer)
Intended Users Professional Use Only
Expiry Date Marking Available on Individual Kit
Internal Quality Control Built-In Control Line on Each Test Cassette

Finecare Progesterone Rapid Quantitative Test Product Specifications

Function Progesterone Level Quantification
Use For Quantitative Detection of Progesterone in Human Serum, Plasma or Whole Blood
Real-Time Operation Yes
Storage Instructions Store at 2-30C, Keep Away from Direct Sunlight
Weight Approx. 100 grams per kit
Portable Yes
Operating Type Automatic (Requires Finecare Analyzer)
Voltage Depends on Analyzer (Test Kit Itself: Not Applicable)
Shelf Life 18 Months
Power Consumption Depends on Analyzer (Test Kit Itself: Not Applicable)
Condition New
Equipment Type Rapid Quantitative Test Kit
Wall Mounted No
Usage Type Clinical Laboratory, Point of Care
Power Source Compatible Analyzer Powered (Typically Electric)
Display Type Digital (With Finecare FIA Meter)
Color White Cassette with Labels
Features Quick Results, High Sensitivity and Accuracy, Quantitative Measurement, Easy to Use, Requires Finecare FIA Meter
Accuracy 95%
Material Plastic Cassette, Reagent Solution
Instruments Type Diagnostic Test Kit
Dimension (L*W*H) Kit: Approx. 135 x 75 x 25 mm (box size)
Frequency Single Use/Test
Technology Fluorescence Immunoassay (FIA)
Noise Level Silent Operation
Measurement Range 0.5~60 ng/mL

Test Time Within 15 Minutes
Specimen Types Serum, Plasma, or Whole Blood
Sample Volume Required 75 L Serum/Plasma/Whole Blood
Sensitivity <0.5 ng/mL (varies as per lot)
Packing 25 Tests per Kit
Lot Traceability Each Cassette Individually Marked
Result Type Numerical Value on Digital Display
Analyzer Compatibility Finecare FIA Meter (Model Specified by Manufacturer)
Intended Users Professional Use Only
Expiry Date Marking Available on Individual Kit
Internal Quality Control Built-In Control Line on Each Test Cassette

Finecare Progesterone Rapid Quantitative Test Trade Information

FOB Port JAIPUR
Payment Terms Cash Advance (CA), Cash in Advance (CID), Cheque, Telegraphic Transfer (T/T)
Delivery Time 10 Days
Packaging Details Standard
Main Export Market(s) South America, Australia, Central America, North America, Asia, Eastern Europe, Western Europe, Middle East, Africa
Main Domestic Market All India

Product Description

The Finecare Progesterone Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare FIA System for quantitative determination of progesterone in human serum, plasma or whole blood. The test is used as an aid to the track ovulation.
STORAGE AND STABILITY1. 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

Quick and Accurate Progesterone Testing

This rapid quantitative test kit provides clinicians with reliable progesterone measurements in under 15 minutes. Designed for professional environments, the Finecare kit leverages fluorescence immunoassay technology for superior sensitivity (<0.5 ng/mL), presenting results digitally via compatible Finecare analyzers. Its accuracy and speedy operation make it ideal for urgent diagnostic settings.

User-Friendly and Reliable Design

Each test cassette is equipped with a built-in control line for internal quality assurance. Clearly labeled cassettes and easy-to-follow instructions streamline the testing process for laboratory professionals. With 25 tests per kit and individual lot and expiry markings, consistent quality and traceability are guaranteed throughout use.

Versatile Applications and Storage

This kit supports multiple specimen types, including serum, plasma, and whole blood. Its compact box design promotes portability for point-of-care use, while robust construction allows for safe storage between 2-30C. Maintaining accuracy (95%), the Finecare test delivers consistent results within a broad measurement range (0.5~60 ng/mL), meeting various clinical needs.

FAQ's of Finecare Progesterone Rapid Quantitative Test:

Q: How does the Finecare Progesterone Rapid Quantitative Test work?

A: The test utilizes fluorescence immunoassay technology to quantitatively detect and measure progesterone in human serum, plasma, or whole blood. After applying the specimen to the cassette, results are produced within 15 minutes via the Finecare FIA Meter as a digital value.

Q: What types of specimens can be used with this test kit?

A: This kit accepts serum, plasma, or whole blood samples, requiring just 75 L per test, which enables flexible usage in clinical laboratories or point-of-care settings.

Q: When can I interpret the results, and how are they displayed?

A: Results are available within 15 minutes after specimen application. They are displayed as numerical values on the Finecare FIA Meter's digital screen, ensuring instant and clear interpretation by professionals.

Q: Where should I store the test kit, and what is its shelf life?

A: Kits should be stored at 2-30C, away from direct sunlight, to maintain integrity. Each kit has a shelf life of 18 months from the manufacturing date, indicated clearly on individual boxes.

Q: What is the process for running a test?

A: Professionals should first collect a serum, plasma, or whole blood sample, apply 75 L to the cassette, and insert it into the Finecare FIA Meter. The analyzer automatically processes the test and provides a digitized result in less than 15 minutes.

Q: What benefits does this test offer in clinical practice?

A: Clinicians benefit from rapid results, high sensitivity (<0.5 ng/mL), quantitative output, reliable internal controls, and ease of use. Its portability, accuracy (95%), and compatibility with Finecare analyzers enhance diagnostic workflows and patient care.

Q: Is the test kit portable and easy to use outside traditional laboratories?

A: Yes, the lightweight kit with individually packed cassettes is portable, supporting both clinical laboratory and point-of-care usage when paired with the Finecare FIA Meter. Instructions are simple, ensuring efficient operation in various clinical environments.

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