STANDARD F iFOB FIA

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Product Details:

Frequency 50/60 Hz
Measurement Range 10 - 1000 ng/mL
Accuracy High as per clinical standards for IVD analyzers
Features Compact, easy operation, rapid result, accurate, high throughput
Instruments Type POC Diagnostic Analyzer
Storage Instructions Store at room temperature; avoid direct sunlight
Display Type Digital LCD display
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STANDARD F iFOB FIA Price And Quantity

STANDARD F iFOB FIA Product Specifications

Wall Mounted No
Display Type Digital LCD display
Power Consumption 20 W
Material Plastic, Metal
Instruments Type POC Diagnostic Analyzer
Storage Instructions Store at room temperature; avoid direct sunlight
Weight Approx. 2.2 kg
Condition New
Features Compact, easy operation, rapid result, accurate, high throughput
Power Source Electric
Real-Time Operation Yes
Accuracy High as per clinical standards for IVD analyzers
Measurement Range 10 - 1000 ng/mL
Frequency 50/60 Hz
Use In-vitro Diagnostic use, Quantitative measurement of Fecal Occult Blood (FOB)
Noise Level Low
Shelf Life Refer to kit and package instructions
Dimension (L*W*H) Approx. 280 x 216 x 130 mm
Technology Fluorescence Immunoassay (FIA)
Color White and Green
Equipment Type iFOB FIA Analyzer
Portable Yes
Usage Type Professional Diagnostic
Voltage 100-240 V AC, 50/60 Hz
Operating Type Semi-Automatic
Function Quantitative detection of human occult blood in feces

Connection Ports USB, RS232
Operating Environment Temperature 10-30C, Humidity 10-70% RH
Data Storage Capacity Up to 10,000 results
Test Throughput Up to 60 tests/hour
Calibration Automatic/Manual options
Sample Type Fecal sample (stool)
Printer Support Built-in thermal printer
Maintenance Low and easy maintenance
Result Time Approx. 5 - 10 minutes per sample
Sample Volume 10-50 L

Product Description

Brand	SD Biosensor
Sample Type	Fecal
Pack Size	50T
CAT No	10IFO10C
Biomarker	Cancer Marker

STANDARD F iFOB FIA is a fluorescent immunoassay for the quantitative measurement of hemoglobin in fecal sample. This test is offered as a screening test for the early detection of bowel cancer in patients without symptoms.

Fast and Accurate Results

The STANDARD F iFOB FIA Analyzer delivers rapid results for fecal occult blood detection, typically within 5 to 10 minutes per sample. Its advanced fluorescence immunoassay technology ensures precise and reliable outcomes, contributing to effective patient screening and timely decision-making in clinical practice.

User-Friendly Operation

Intuitive controls, a digital LCD display, and semi-automatic features simplify operation, even for high-throughput environments. Automatic and manual calibration options, along with low maintenance requirements, make the analyzer a practical choice for busy healthcare professionals seeking efficient workflows.

Compact and Portable Design

Weighing approximately 2.2 kg and measuring just 280 x 216 x 130 mm, this analyzer is highly portable and space-saving. Its robust construction and electric power efficiency (20 W) ensure dependable performance, whether used in hospital laboratories or point-of-care diagnostic facilities.

FAQ's of STANDARD F iFOB FIA:

Q: How does the STANDARD F iFOB FIA Analyzer detect fecal occult blood?

A: The analyzer uses fluorescence immunoassay (FIA) technology to quantitatively measure human occult blood in fecal (stool) samples, offering precise detection within a measurement range of 10-1000 ng/mL.

Q: What is the throughput and result time for this analyzer?

A: The device can process up to 60 tests per hour, with each result available in approximately 5 to 10 minutes, enabling efficient handling of high patient volume.

Q: When and where should I use this analyzer?

A: This analyzer is designed for professional diagnostic use in clinical laboratories, hospitals, and point-of-care settings. It operates effectively in environments with temperatures between 10-30C and humidity from 10-70% RH.

Q: What is the sample volume required and how do I prepare a sample?

A: A fecal sample of 10-50 L is required. Samples should be collected following clinical guidelines and stored at room temperature, avoiding direct sunlight until testing.

Q: How is calibration performed on this device?

A: The STANDARD F iFOB FIA offers both automatic and manual calibration options, ensuring accuracy and compliance with clinical standards for in-vitro diagnostics.

Q: What are the main benefits of using this equipment?

A: Key benefits include compact and portable design, high accuracy, fast results, built-in data storage for up to 10,000 results, low maintenance, and user-friendly operation with a built-in thermal printer for immediate documentation.

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