Standard F RSV Ag FIA

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Product Details:

Shelf Life 18 Months
Function Respiratory Syncytial Virus Antigen Detection
Storage Instructions Store at 230C
Instruments Type Fluorescence Immunoassay Analyzer Required
Accuracy High
Display Type Requires Analyzer Instrument for Result
Measurement Range Qualitative
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Standard F RSV Ag FIA Price And Quantity

Minimum Order Quantity 1000 Box

Specificity Up to 98%
Test Principle Lateral Flow Immunochromatography
Test Time Within 15 Minutes
Sensitivity Up to 95%
Sample Type Nasopharyngeal Swab
Packaging Unit 25 Tests/Kit
Intended Use In Vitro Diagnostic

Standard F RSV Ag FIA Product Specifications

Weight Approx. 120 g (Per Kit)
Shelf Life 18 Months
Use Hospital
Real-Time Operation Yes
Color White
Function Respiratory Syncytial Virus Antigen Detection
Storage Instructions Store at 230C
Measurement Range Qualitative
Display Type Requires Analyzer Instrument for Result
Power Consumption Low
Wall Mounted No
Usage Type Diagnostic
Features Rapid, Accurate, Easy to Use, Detects RSV Antigen from Nasopharyngeal Swab
Power Source Battery Operated
Material Plastic, Paper, Reagents
Noise Level Silent
Dimension (L*W*H) 14.5 x 9.6 x 2.5 cm (Box Packaging)
Operating Type Manual
Instruments Type Fluorescence Immunoassay Analyzer Required
Portable Yes
Accuracy High
Technology Fluorescence Immunoassay
Condition New
Equipment Type RSV Antigen FIA Test Device

Specificity Up to 98%
Test Principle Lateral Flow Immunochromatography
Test Time Within 15 Minutes
Sensitivity Up to 95%
Sample Type Nasopharyngeal Swab
Packaging Unit 25 Tests/Kit
Intended Use In Vitro Diagnostic

Product Description

Product detail

Brand	SD Biosensor
Cat No	10RSVC10D
Size	25 T
Specimen	Nasopharyngeal swab / Nasopharyngeal aspirate / Nasopharyngeal wash / Transport media
Specimen volume	4 drops
Test time	15 minutes (Strong positive can be read after 5 minutes.)

Fast and Accurate RSV Detection

Detect RSV antigens swiftly in clinical settings using the Standard F RSV Ag FIA. This device combines efficiency with scientific rigor, enabling healthcare professionals to achieve high sensitivity and specificity in as little as 15 minutes. Its rapid turnaround supports timely patient management.

User-Friendly Hospital Diagnostics

With a minimal learning curve and manual operation, the Standard F RSV Ag FIA test delivers consistent results using nasopharyngeal swabs. Its low power consumption and portable design allow seamless integration into hospital workflows without disruption or excessive maintenance.

Built for Convenience and Reliability

Packaged in sets of 25, the kit features robust plastic and paper materials, as well as stable reagents with an 18-month shelf life. Designed for easy storage (2-30C), the test is silent in operation, helping maintain a calm clinical environment.

FAQ's of Standard F RSV Ag FIA:

Q: How does the Standard F RSV Ag FIA test work?

A: The Standard F RSV Ag FIA test employs lateral flow immunochromatography combined with fluorescence detection to identify RSV antigens in nasopharyngeal swab samples. After manual processing, results are read using a fluorescence immunoassay analyzer within 15 minutes.

Q: What samples are required for this RSV antigen test?

A: This test is specifically designed for use with nasopharyngeal swab specimens, ensuring optimal sensitivity and specificity for detecting respiratory syncytial virus antigens in clinical settings.

Q: When should I use the Standard F RSV Ag FIA?

A: The test should be used when rapid, accurate detection of RSV is needed, such as during peak respiratory infection seasons in hospitals, or when timely diagnosis is critical for patient care decisions.

Q: Where can this test be applied and by whom?

A: The Standard F RSV Ag FIA is intended for use in hospital laboratories by trained healthcare professionals. It is suitable for dealer, distributor, exporter, manufacturer, supplier, trader, and wholesaler channels in India.

Q: What is the process for running the test and obtaining results?

A: First, a nasopharyngeal swab specimen is collected. The sample is processed manually with the kit's reagents, then the test cassette is inserted into a compatible fluorescence immunoassay analyzer, which displays a qualitative result within 15 minutes.

Q: What are the key benefits of using this RSV antigen test?

A: Key benefits include rapid operation (less than 15 minutes), high accuracy, user-friendly manual setup, portability, and minimal power consumption. The silent operation and reliable results support efficient patient management in busy healthcare environments.

Q: How should the kit be stored and what is its shelf life?

A: The kit should be stored at temperatures between 2 and 30C, away from direct sunlight. Each kit maintains its efficacy for 18 months, ensuring sustained performance over time.

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