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Finecare PSA (Prostate Specific Antigen) Rapid Quantitative Test

92 INR/Kit

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Product Details:

Shelf Life 24 Months
Accuracy >99% (analytical sensitivity and specificity)
Display Type Digital (with Finecare Analyzer)
Storage Instructions Store at 2C 30C, Avoid direct sunlight
Measurement Range 0.5 to 100 ng/mL
Instruments Type Rapid Test Cassette
Function Quantitative detection of PSA
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Finecare PSA (Prostate Specific Antigen) Rapid Quantitative Test Price And Quantity

Minimum Order Quantity 2 Box
Price 92 INR/Kit

Sensitivity 0.2 ng/mL
Result Interpretation Compatible with Finecare FIA Meter
Compatibility Finecare FIA System
Intended Use Professional in vitro diagnostic use
Storage Temperature 2°C to 30°C
CE Marked Yes
Clinical Application Prostate cancer screening, monitoring PSA levels
Minimum Sample Volume 10 µL
Expiry Date Printed on kit packaging
Test Time Within 15 minutes
Quality Control Built-in control line
Sample Type Human Serum/Plasma
Package 25 tests/kit

Finecare PSA (Prostate Specific Antigen) Rapid Quantitative Test Product Specifications

Operating Type Manual/Automatic via Analyzer
Use Detection and Quantification of Prostate Specific Antigen (PSA) in Human Serum/Plasma
Power Consumption Low
Color White with marking
Frequency Single-use, not frequency-based
Function Quantitative detection of PSA
Features Rapid Quantitative Result, High Sensitivity, CE marked, Simple operation, Minimal sample volume
Usage Type Clinical, Laboratory
Equipment Type Immunofluorescence Analyzer Test
Dimension (L*W*H) Standard cassette size; approximately 90 mm 25 mm 6 mm (Test device)
Storage Instructions Store at 2C 30C, Avoid direct sunlight
Noise Level Silent Operation
Weight Lightweight; <50 g per cassette
Portable Yes
Measurement Range 0.5 to 100 ng/mL
Condition New
Instruments Type Rapid Test Cassette
Material Lateral Flow Test Strip, Plastic Cassette
Voltage 100-240V (Analyzer) (Applicable for analyzer device)
Technology Immunofluorescence Chromatographic Assay
Wall Mounted No
Shelf Life 24 Months
Real-Time Operation Yes
Accuracy >99% (analytical sensitivity and specificity)
Power Source Analyzer powered by AC supply or batteries
Display Type Digital (with Finecare Analyzer)

Sensitivity 0.2 ng/mL
Result Interpretation Compatible with Finecare FIA Meter
Compatibility Finecare FIA System
Intended Use Professional in vitro diagnostic use
Storage Temperature 2°C to 30°C
CE Marked Yes
Clinical Application Prostate cancer screening, monitoring PSA levels
Minimum Sample Volume 10 µL
Expiry Date Printed on kit packaging
Test Time Within 15 minutes
Quality Control Built-in control line
Sample Type Human Serum/Plasma
Package 25 tests/kit

Finecare PSA (Prostate Specific Antigen) 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
Sample Policy Contact us for information regarding our sample policy
Main Export Market(s) Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
Main Domestic Market All India

Product Description

PSA (Prostate Specific Antigen) Rapid Quantitative Test: -
The Finecare PSA Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare FIA System for quantitative determination of Prostate Specific Antigen (PSA) in human whole blood, serum or plasma. The test is used as an aid in diagnosis of prostatic cancer.

Technical Details

Fast, Accurate PSA Quantification

Designed for rapid and reliable PSA detection, Finecare PSA Rapid Quantitative Test uses lateral flow immunofluorescence technology to provide precise results in under 15 minutes. Ideal for prostate cancer screening and monitoring, its analytical sensitivity reaches 0.2 ng/mL, supporting early detection and patient management.

Seamless Compatibility and Operation

Each test cassette pairs perfectly with the Finecare FIA Meter, enabling digital interpretation and simple workflow. The device operates quietly, and can be powered by AC supply or batteries, making it portable and versatile for clinical or laboratory settings. Both manual and automatic operation modes are supported.

Built-in Quality Control and Long Shelf Life

The kit features an internal control line for reliable, real-time operation. With a shelf life of 24 months and storage temperature range of 2C to 30C, Finecare PSA tests can be stored conveniently and securely, ensuring performance consistency across multiple applications.

FAQ's of Finecare PSA (Prostate Specific Antigen) Rapid Quantitative Test:

Q: How does the Finecare PSA Rapid Quantitative Test work for detecting PSA levels?

A: The test utilizes immunofluorescence chromatographic assay technology to quantitatively measure PSA in human serum or plasma. Results are interpreted digitally when the test cassette is placed in the compatible Finecare FIA Analyzer, delivering precise and rapid readings within 15 minutes.

Q: What is the minimum sample volume required for the test, and what specimen types are accepted?

A: Only 10 L of human serum or plasma is needed per test, making it minimally invasive and suitable for both clinical and laboratory use.

Q: When should Finecare PSA Rapid Quantitative Test be used?

A: It is recommended for prostate cancer screening, monitoring PSA levels in diagnosed patients, and assessing therapeutic response. The rapid turnaround time makes it ideal for applications requiring timely, quantitative results.

Q: Where can the Finecare PSA test be stored, and what are the recommended storage conditions?

A: Store the kit at temperatures between 2C and 30C, away from direct sunlight. Ensure packaging is intact and unopened until use. The shelf life for each kit is 24 months, with the expiry date indicated on the packaging.

Q: What process should be followed to perform the test and interpret the results?

A: Begin by collecting a serum or plasma sample, add it to the test cassette, and insert into the Finecare FIA Analyzer. The built-in control line verifies the test's validity, and the digital display provides quantitative PSA results, ranging from 0.5 to 100 ng/mL.

Q: What are the key benefits of using Finecare PSA Rapid Quantitative Test?

A: This test offers high sensitivity (0.2 ng/mL), rapid results (within 15 minutes), minimal sample use, and precise quantification (>99% accuracy). Its CE marking and built-in controls ensure reliable performance in both hospital and reference laboratory environments.

Q: Is this test suitable for point-of-care use and how portable is it?

A: Yes, the test cassettes are lightweight and portable, requiring only the Finecare FIA Analyzer-which operates on AC or battery power. This makes the system ideal for point-of-care settings, outreach programs, and facilities needing mobile diagnostic solutions.

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