Standard F Covid-19 Ag FIA

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Product Details:

Measurement Range Qualitative detection of SARS-CoV-2 Nucleocapsid Protein
Accuracy High (Manufacturer-rated 98% sensitivity, 100% specificity)
Features Rapid test, High sensitivity and specificity, Easy to operate, Quantitative results
Shelf Life 12 months
Usage Type Professional
Function Detection of COVID-19 antigen
Instruments Type Diagnostic analyzer
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Standard F Covid-19 Ag FIA Price And Quantity

Minimum Order Quantity 1000 Box

Standard F Covid-19 Ag FIA Product Specifications

Measurement Range Qualitative detection of SARS-CoV-2 Nucleocapsid Protein
Noise Level Low
Accuracy High (Manufacturer-rated 98% sensitivity, 100% specificity)
Power Source Electric
Operating Type Automatic
Use Hospital
Function Detection of COVID-19 antigen
Usage Type Professional
Shelf Life 12 months
Features Rapid test, High sensitivity and specificity, Easy to operate, Quantitative results
Real-Time Operation Yes
Technology Fluorescent Immunoassay (FIA)
Equipment Type Covid-19 Antigen FIA (Fluorescent Immunoassay)
Material Plastic, Electronic Components
Frequency 50/60 Hz
Portable Yes
Power Consumption 30 W
Storage Instructions Store at 2C to 30C, avoid direct sunlight
Dimension (L*W*H) 270 x 240 x 120 mm
Wall Mounted No
Voltage 100-240 V
Instruments Type Diagnostic analyzer
Weight 2.1 kg
Display Type LCD Display
Color White
Condition New

Test Principle Sandwich immunodetection
Sample Type Nasopharyngeal swab
Sample Volume 100 L
Time to Result Within 30 minutes
Operating Temperature 15C to 30C
Result Interpretation Automatic via instrument
Data Output Digital/USB export

Product Description

Jump on the opportunity to elevate your diagnostic capabilities with the Standard F Covid-19 Ag FIA, a top-rated and imposing solution for rapid COVID-19 detection. This top-tier, professional-use instrument harnesses breathtaking sandwich immunodetection technology to deliver real-time, quantitative results in less than 30 minutes. Engineered for value, its digital/USB data output and automatic result interpretation optimize workflow in clinical settings. Compact, portable, and low-noise, it offers high sensitivity (98%) and specificity (100%), ensuring accuracy. Designed for hospitals, its robust build supports rigorous use while maximizing efficiency.

Professional Application & Operational Superiority

Standard F Covid-19 Ag FIA is tailored for professional use in hospitals, ensuring stringent reliability for critical diagnostics. Direction of use involves collecting a nasopharyngeal swab, introducing the sample into the device, and letting the automatic system process and display results. Competitive advantages include rapid, highly sensitive antigen detection, user-friendly LCD interface, and seamless digital export. Its cutting-edge technology and ease of operation make it the gold standard for fast and accurate COVID-19 testing.

Certifications, Delivery, and Packaging Details

The Standard F Covid-19 Ag FIA stands distinguished with internationally recognized certifications, reflecting its significant market value. Goods are securely transported across India, with an estimated delivery time dependent on location and dealer arrangements. Packaging is expertly designed to minimize expenditure on damages and maintain integrity during transit. Each package contains user-friendly components, guaranteeing hassle-free setup upon arrival, ensuring quality is sustained from manufacturer to end-user, and supporting broad distribution networks.

FAQ's of Standard F Covid-19 Ag FIA:

Q: How is the Standard F Covid-19 Ag FIA used in hospital settings?

A: In hospitals, trained professionals collect a nasopharyngeal swab, deposit 100 L of the sample, and use the automated analyzer to obtain results in under 30 minutes. The process is streamlined for minimal operator intervention.

Q: What distinguishes this Covid-19 antigen analyzer from traditional testing methods?

A: This analyzer utilizes sandwich immunodetection with fluorescence, offering automatic quantification, high sensitivity, and specificity. Unlike manual tests, results are interpreted automatically and can be exported digitally for superior workflow integration.

Q: When can results be expected after sample collection?

A: Results are available within 30 minutes following the application of the sample to the device, supporting rapid clinical response and efficient patient management.

Q: Where should the Standard F Covid-19 Ag FIA be stored for optimal performance?

A: Store the device and consumables at temperatures from 2C to 30C while avoiding direct sunlight to maintain the product's top performance and shelf life.

Q: What are the benefits of using this diagnostic analyzer in professional healthcare environments?

A: Key benefits include high accuracy, rapid turnaround, digital data handling, portability, and automated operation, contributing to precise diagnosis and enhanced operational workflow in healthcare facilities.

Q: What safety certifications does the Standard F Covid-19 Ag FIA carry?

A: The device holds recognized international certifications, affirming adherence to stringent quality and safety standards expected in medical diagnostics.

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