Boditech AFIAS Alpha-Fetoprotein (AFP)

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Product Details:

Usage Type Single Use Disposable, Diagnostic Laboratory Use
Frequency Single Test per Cartridge
Display Type Instrument-Dependent (results displayed on AFIAS Analyzer)
Measurement Range Varies by Analyzer (typically 01000 ng/mL or as per analyzer specification)
Shelf Life 18 Months from Manufacture
Instruments Type Immunoassay Analyzer Reagent (for use with AFIAS platform)
Features High Sensitivity, Rapid Test, Minimal Sample Volume
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Boditech AFIAS Alpha-Fetoprotein (AFP) Price And Quantity

Boditech AFIAS Alpha-Fetoprotein (AFP) Product Specifications

Measurement Range Varies by Analyzer (typically 01000 ng/mL or as per analyzer specification)
Shelf Life 18 Months from Manufacture
Condition New
Instruments Type Immunoassay Analyzer Reagent (for use with AFIAS platform)
Features High Sensitivity, Rapid Test, Minimal Sample Volume
Portable Yes (Cartridge design)
Usage Type Single Use Disposable, Diagnostic Laboratory Use
Equipment Type Immunoassay Analyzer Reagent (AFP Detection)
Material Plastic Cartridge
Use Alpha-Fetoprotein (AFP) Detection in human serum, plasma or whole blood
Technology Fluorescence Immunoassay (FIA)
Frequency Single Test per Cartridge
Dimension (L*W*H) Individual Cartridge Size: Compact, Standard (precise dimensions not listed)
Display Type Instrument-Dependent (results displayed on AFIAS Analyzer)
Color White/Labelled
Noise Level Silent Operation
Storage Instructions 28C, Protect from Light
Function Quantitative Measurement of Alpha-Fetoprotein (AFP)
Accuracy High, CE-IVD Certified
Wall Mounted No
Real-Time Operation Yes
Power Consumption Not Applicable (Reagent Kit)
Weight Lightweight (Single Use Cartridge)
Power Source Instrument Based (Powered by Analyzer)
Operating Type Automatic

Lot Traceability Yes, with barcode
Pack Size 24 Tests per Kit
Regulatory Status For in vitro diagnostic use only
Intended Use Tumor Marker Screening for HCC, Germ Cell Tumors, Other Clinical Diagnostics
Sample Volume 50 L
Analytical Sensitivity Meets clinical diagnostic requirements as per IFU
Calibration Analyzer Calibrated
User Interface Analyzer-Based, Barcode Recognition
Test Time Within 12 minutes
Sample Type Serum, Plasma, Whole Blood

Product Description

Brand Boditech

Sample Type Serum/ Plasma/ WB

Pack Size 24T

CAT No SMFP-27

Biomarker Cancer

High levels of AFP in adults may indicate the possibility of the liver, the ovaries, or the testicles, as well as noncancerous liver diseases such as cirrhosis and hepatitis. The AFP plus measures the level of AFP to help diagnose or rule out related abnormalities.

Rapid and Accurate AFP Quantification

Boditech AFIAS Alpha-Fetoprotein (AFP) test enables timely diagnosis, offering a swift turnaround time of under 12 minutes. By employing advanced fluorescence immunoassay (FIA) technology, it ensures high analytical sensitivity and reliable quantitative results. This efficiency delivers confidence for clinicians screening for hepatocellular carcinoma, germ cell tumors, and conducting other clinical investigations.

Effortless Testing with Minimal Sample Volume

Requiring only 50 L of serum, plasma, or whole blood, the single-use disposable cartridges are easy to handle and allow for fast sample processing. The analyzer-based design automates calibration and result interpretation, reducing manual intervention and streamlining laboratory workflows. All results are instantly displayed on the AFIAS analyzer, supporting real-time decision-making.

Secure, Traceable, and Compliant

Each test cartridge is barcoded for accurate lot traceability, supporting regulatory and clinical compliance. The product bears CE-IVD certification, suitable for use in diagnostic laboratories. Designed for safety and reliability, the kit's storage and handling specifications preserve accuracy throughout its 18-month shelf life. Its compact and lightweight format ensures portability and easy integration into a variety of laboratory settings.

FAQ's of Boditech AFIAS Alpha-Fetoprotein (AFP):

Q: How does the AFIAS Alpha-Fetoprotein (AFP) test operate within the laboratory setting?

A: The test uses fluorescence immunoassay (FIA) technology and is performed using an AFIAS Analyzer. After placing a 50 L serum, plasma, or whole blood sample into the plastic cartridge and scanning the barcode, the cartridge is inserted into the analyzer, which automatically calibrates and processes the sample to provide results within 12 minutes.

Q: What are the sample requirements and benefits of the Boditech AFIAS AFP test?

A: Only 50 L of sample (serum, plasma, or whole blood) is needed for each test. This minimal sample volume is beneficial in situations where sample availability is limited or rapid processing is required, making it ideal for routine tumor marker screening and other diagnostic applications.

Q: When should the Boditech AFIAS AFP test be used in clinical diagnostics?

A: This test is intended for screening and diagnosing conditions associated with elevated alpha-fetoprotein levels, such as hepatocellular carcinoma (HCC), germ cell tumors, and for other relevant clinical investigations. It is suitable for use in hospital laboratories and diagnostic centers requiring rapid and reliable tumor marker analysis.

Q: Where can the Boditech AFIAS AFP test be implemented and by whom?

A: The test kit is designed for use in diagnostic laboratories equipped with AFIAS Analyzers by qualified laboratory professionals. In India, it is accessible through dealers, distributors, exporters, manufacturers, suppliers, traders, and wholesalers.

Q: What is the process to obtain accurate results with this test kit?

A: Begin by collecting a serum, plasma, or whole blood sample. Apply 50 L to the cartridge, scan the barcode for lot traceability, and insert it into the AFIAS Analyzer. The analyzer handles calibration and measurement, displaying precise, quantitative AFP results on its interface in real-time.

Q: What advantages does the AFIAS Alpha-Fetoprotein (AFP) reagent offer diagnostic laboratories?

A: The kit delivers high sensitivity and rapid results, supports single-use convenience, ensures secure lot traceability, and aligns with CE-IVD regulatory standards. Its compact, lightweight design and automated operation streamline laboratory workflows and minimize manual errors, bolstering both efficiency and result accuracy.

Q: How should the AFIAS AFP cartridges be stored for optimal performance?

A: Store the cartridges at 2-8C and protect them from light. Proper storage conditions are essential to maintain the 18-month shelf life and ensure test accuracy throughout the kit's use period.

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