Boditech AFIAS Carcinoembryonic antigen (CEA)

Boditech AFIAS Carcinoembryonic antigen (CEA)

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Product Details:

Storage Instructions Store reagents at 28C
Measurement Range 1.01,000 ng/mL
Accuracy Correlation coefficient >0.98 with reference method
Usage Type Clinical, Laboratory
Features Rapid, automated, easy-to-use, minimal sample volume, high sensitivity, built-in printer
Frequency 50/60 Hz
Function Detects and quantitates CEA (Carcinoembryonic Antigen)
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Boditech AFIAS Carcinoembryonic antigen (CEA) Price And Quantity

Boditech AFIAS Carcinoembryonic antigen (CEA) Product Specifications

Features Rapid, automated, easy-to-use, minimal sample volume, high sensitivity, built-in printer
Color White/Grey
Use Quantitative measurement of CEA in human serum, plasma, or whole blood
Voltage AC 100240V, 50/60Hz
Usage Type Clinical, Laboratory
Accuracy Correlation coefficient >0.98 with reference method
Technology Fluorescence Immunoassay (FIA)
Wall Mounted No
Equipment Type Immunoassay Analyzer (Carcinoembryonic Antigen Test)
Power Source AC Adapter
Storage Instructions Store reagents at 28C
Measurement Range 1.01,000 ng/mL
Real-Time Operation Yes
Weight 3.7 kg
Power Consumption Approx. 60 VA
Shelf Life 12 months (for reagent kit)
Dimension (L*W*H) 195 mm x 385 mm x 162 mm
Operating Type Fully Automated
Material Plastic, electronics, reagent cartridge
Noise Level Low
Condition New
Display Type LCD Display (with touchscreen)
Portable Yes
Instruments Type Clinical Chemistry Analyzer
Function Detects and quantitates CEA (Carcinoembryonic Antigen)
Frequency 50/60 Hz

Product Description

Brand Boditech

Sample Type Serum/ Plasma/ WB

Pack Size 24T

CAT No SMFP-21

Biomarker Cancer

A high level of CEA in adults can be a sign of certain types of cancers in organs like the colon and rectum, prostate, ovary, lung, thyroid, or liver. The CEA test measures the level of CEA in the patient blood including treatment response and recurrence of cancer patients.

Quantitative & Fast CEA Analysis

The AFIAS CEA Analyzer is specifically engineered for extremely rapid and precise quantitation of carcinoembryonic antigen in serum, plasma, or whole blood. The device provides results in less than 12 minutes with high sensitivity, making it ideal for timely clinical decisions in hospitals and laboratories. Its compact, portable design and versatile sample compatibility deliver reliable performance without compromise.

Advanced Automation & Connectivity

Fully automated operation ensures minimal user intervention, from sample loading to result printing. The system features automatic calibration with each test cartridge and an internal QC system for consistent accuracy. Built-in data storage for 5,000 results, USB, and RS-232 interfaces, plus LIS compatibility make integration and record keeping straightforward for any clinical workflow.

Safe, Reliable, and User-Friendly

Engineered with user comfort and safety in mind, the AFIAS CEA Analyzer operates quietly at low noise levels and has a simple, intuitive touchscreen display for guided operation. Automatic QC, minimal sample requirements, and an easy reagent kit replacement system enhance workflow efficiency while reducing the risk of user error.

FAQ's of Boditech AFIAS Carcinoembryonic antigen (CEA):

Q: How does the AFIAS CEA Analyzer determine carcinoembryonic antigen (CEA) levels?

A: The AFIAS CEA Analyzer uses fluorescence immunoassay (FIA) technology to quantitatively detect CEA in human serum, plasma, or whole blood. The device automatically processes the specimen using a dedicated reagent cartridge, measuring fluorescence intensity that correlates with the CEA concentration.

Q: What types of samples can I use with this analyzer, and how much is required?

A: You can use serum, plasma, or whole blood samples with the AFIAS CEA Analyzer. Only a minimal volume of 30 L per test is required, making it suitable for pediatric and routine adult testing alike.

Q: When should I perform calibration or quality control checks?

A: The analyzer automatically calibrates itself with each new test cartridge, and its internal automatic QC system monitors performance every time you run a sample. No manual intervention for calibration or quality control is needed.

Q: Where can this immunoassay analyzer be installed in a laboratory setting?

A: The AFIAS CEA Analyzer is compact and portable, making it suitable for benchtop use in a variety of environments such as clinical, hospital, or research laboratories. Wall mounting is not required or supported.

Q: What is the process for running a CEA test?

A: To conduct a CEA test, collect 30 L of your sample (serum, plasma, or whole blood). Load the sample into the test cartridge and insert it into the analyzer. The device automates the testing process, displays results on the LCD touchscreen, and prints a hard copy results report within 12 minutes.

Q: How does the AFIAS CEA Analyzer benefit clinical practice?

A: With rapid turnaround time, minimal sample volume, built-in QC, and high sensitivity, the analyzer enables timely and reliable monitoring of CEA levels, supporting cancer diagnosis and patient management with ease.

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