SD Biosensor STANDARD Q Influenza A/B

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Product Details:

Instruments Type Lateral Flow Immunoassay
Storage Instructions Store at 230C, protect from sunlight and moisture
Accuracy High accuracy with sensitivities and specificities above 90%
Function Detection of Influenza A and B antigens
Features Quick results, easy to use, no additional instruments needed
Measurement Range Qualitative: Positive/Negative results
Usage Type Single Use
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SD Biosensor STANDARD Q Influenza A/B Price And Quantity

Disposability Disposable after single use
Sample Type Nasopharyngeal Swab
Limit of Detection As per manufacturers data sheet (contact supplier for precise value)
Reading Window Dual (for Influenza A and B)
Package Contents Test devices, extraction buffer, swabs, instruction manual
Model Name STANDARD Q Influenza A/B
Kit Storage Temperature 230C
Intended User Healthcare professional
Result Time 1015 minutes

SD Biosensor STANDARD Q Influenza A/B Product Specifications

Noise Level Silent/None
Portable Yes
Features Quick results, easy to use, no additional instruments needed
Weight Approx. 10 g per kit
Function Detection of Influenza A and B antigens
Accuracy High accuracy with sensitivities and specificities above 90%
Wall Mounted No
Condition New
Storage Instructions Store at 230C, protect from sunlight and moisture
Instruments Type Lateral Flow Immunoassay
Material Plastic and paper components
Operating Type Manual
Display Type Visual (Line Indication)
Shelf Life 24 months from manufacturing date
Technology Immunochromatographic Assay
Usage Type Single Use
Real-Time Operation Yes
Equipment Type Rapid Diagnostic Test Kit
Color White
Measurement Range Qualitative: Positive/Negative results
Dimension (L*W*H) Approx. 90 mm x 20 mm x 5 mm (per cassette)
Use Detection and differentiation of Influenza A and B virus antigens in human respiratory specimens

Disposability Disposable after single use
Sample Type Nasopharyngeal Swab
Limit of Detection As per manufacturers data sheet (contact supplier for precise value)
Reading Window Dual (for Influenza A and B)
Package Contents Test devices, extraction buffer, swabs, instruction manual
Model Name STANDARD Q Influenza A/B
Kit Storage Temperature 230C
Intended User Healthcare professional
Result Time 1015 minutes

SD Biosensor STANDARD Q Influenza A/B Trade Information

Supply Ability 100 Unit Per Day
Delivery Time 1-7 Days

Product Description

Brand	SD Biosensor
Sample Type	Nasopharyngeal
Pack Size	25T
CAT No	09INF40D

STANDARD Q Influenza A&B Test performs qualitative analysis by detecting influenza virus A type and B type antigens in human nasopharynx.

Fast and Accurate Influenza Detection

Experience rapid and precise identification of Influenza A and B antigens with STANDARD Q Influenza A/B. Within just 10-15 minutes, healthcare professionals can differentiate between both virus types, allowing for quicker clinical decisions and improved patient management. Its sensitivity and specificity rates of over 90% ensure dependable results, making it indispensable during flu season.

Convenient, Reliable, and Easy-to-Use Kit

This rapid test kit contains all essentials: test devices, extraction buffer, swabs, and instructions. The sample collection and testing processes are straightforward, enabling user-friendly operation without the need for electronic instruments. Visual line indicators offer immediate results, simplifying workflow and limiting waiting times in busy clinical settings.

Ideal for Healthcare Environments

Engineered for convenience and portability, the STANDARD Q Influenza A/B Kit is suitable for hospitals, clinics, and on-site diagnostic facilities. Its compact dimensions and silent operation suit any work area, while single-use design and safe disposability reduce contamination risk and support hygiene protocols.

FAQ's of SD Biosensor STANDARD Q Influenza A/B:

Q: How does the STANDARD Q Influenza A/B test kit work?

A: This kit uses immunochromatographic technology to qualitatively detect and differentiate Influenza A and B antigens in a nasopharyngeal swab sample. Once the sample is applied and processed with the extraction buffer, the presence or absence of visible lines in the dual reading window indicates a positive or negative result for each virus type within 10-15 minutes.

Q: What is the recommended process for sample collection and testing?

A: Collect a nasopharyngeal swab specimen from the patient, mix it thoroughly with the provided extraction buffer, and then apply the processed sample onto the designated area of the test device. Follow the instructions in the manual for precise procedural steps, and interpret results visually after 10-15 minutes.

Q: When should the test be used?

A: The STANDARD Q Influenza A/B test is intended for use when patients exhibit symptoms consistent with influenza. Early testing can facilitate timely diagnosis and appropriate clinical management, particularly during seasonal outbreaks or when rapid differentiation between Influenza A and B is necessary.

Q: Where can this rapid test kit be utilized?

A: This kit is designed for use in healthcare settings such as hospitals, clinics, emergency departments, and outreach medical camps across India. Its portability and silent operation also make it suitable for point-of-care situations where rapid diagnosis is essential.

Q: What are the benefits of using this test kit?

A: Benefits include rapid results within 10-15 minutes, high sensitivity and specificity (typically above 90%), ease of use without additional instruments, dual detection for distinguishing A and B virus types, single-use safety, and hassle-free disposal, ensuring high standards of infection control.

Q: How should the kit be stored and disposed of after use?

A: Store the kit at a temperature between 2-30C, away from direct sunlight and moisture. After single use, the entire test device and other components should be disposed of as biohazardous waste according to local regulations and institutional protocols.

Q: What kind of result display does this test kit use?

A: Results are displayed visually on the test device using dedicated lines for Influenza A and B, clearly indicating positive or negative outcomes for each on the dual reading window. No electronic reader is required, making interpretation straightforward for healthcare professionals.

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