SD Biosensor STANDARD i-Q COVID/Flu Ag Combo Test

SD Biosensor STANDARD i-Q COVID/Flu Ag Combo Test

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Product Details:

Measurement Range Qualitative detection
Display Type Digital (via compatible reader)
Storage Instructions 2-30C; Avoid direct sunlight and freezing
Instruments Type Fluorescent Immunoassay Analyzer (requires STANDARD i-Q reader)
Function Detection of Viral Antigens
Features Simultaneous detection of COVID-19 and Influenza A/B; Rapid results; High sensitivity; Easy operation; Minimal sample required
Shelf Life 12 Months
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SD Biosensor STANDARD i-Q COVID/Flu Ag Combo Test Price And Quantity

SD Biosensor STANDARD i-Q COVID/Flu Ag Combo Test Product Specifications

Usage Type Point of Care; Professional Use
Noise Level Silent Operation
Power Source Battery or Adapter (as per reader)
Voltage DC (as per reader)
Operating Type Automatic (Reader-based)
Features Simultaneous detection of COVID-19 and Influenza A/B; Rapid results; High sensitivity; Easy operation; Minimal sample required
Condition New
Shelf Life 12 Months
Accuracy High Sensitivity and Specificity (Refer IFU)
Frequency Single-Use Test
Real-Time Operation Yes
Wall Mounted No
Display Type Digital (via compatible reader)
Equipment Type Diagnostic Rapid Test Kit
Color White with Color-coded Indications
Storage Instructions 2-30C; Avoid direct sunlight and freezing
Technology Lateral Flow Immunoassay (LFA), Fluorescent Immunoassay (FIA)
Portable Yes
Use Detection of SARS-CoV-2, Influenza A & B Antigens
Measurement Range Qualitative detection
Weight Portable Lightweight
Power Consumption Low
Dimension (L*W*H) Depending on Reader/Cartridge size
Material Plastic and Electronic Components
Instruments Type Fluorescent Immunoassay Analyzer (requires STANDARD i-Q reader)
Function Detection of Viral Antigens

Specificity (Influenza) Refer IFU for clinical performance
Intended Users Healthcare Professionals
Sample Type Nasopharyngeal Swab
Kit Contents Test Cartridges, Extraction Buffer, Swabs, Instruction Manual
Test Time Approx. 10-15 minutes
Sensitivity (SARS-CoV-2) Refer IFU for clinical performance

SD Biosensor STANDARD i-Q COVID/Flu Ag Combo Test Trade Information

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

Product Description

BrandSD Biosensor
Sample TypeNaopharyngeal
Pack Size25T
CAT No09COV280D

The STANDARD i-Q COVID/Flu Ag Combo Test is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 and Influenza A and Influenza B present in human naopharyngeal specimens. The STANDARD i-Q COVID/Flu Ag Combo Test for rapid detection of SARS-CoV-2, Influenza A and Influenza B is a differentiated test, such that SARS-CoV-2 viral antigens can be distingushed from Influenza A or Influenza B viral antigens from a single specimen using a single test strip.

Advanced Dual Pathogen Detection

This innovative combo test kit offers simultaneous screening for both COVID-19 and Influenza A/B using a single nasopharyngeal sample. Its dual detection capability reduces workload and enables rapid isolation decisions, minimizing the risk of transmission in healthcare facilities. The high specificity and sensitivity ensure confidence in ruling out or confirming infections quickly.

User-Friendly and Rapid Results

With a straightforward procedure and digital interpretation via the STANDARD i-Q reader, results are obtainable in just 10-15 minutes. The kit's minimal sample requirement and easy-to-follow instructions enhance efficiency, making it a preferred choice at the point of care for busy professionals needing rapid antigen detection without complexity.

Flexible and Reliable Performance

Designed for portability and silent operation, this diagnostic kit is robust across a range of storage and environmental conditions (2-30C). Its lightweight build enables use in fixed and mobile settings, while the low power consumption and long shelf life (12 months) add practicality for hospitals, clinics, and urgent care environments.

FAQ's of SD Biosensor STANDARD i-Q COVID/Flu Ag Combo Test:

Q: How does the SD Biosensor STANDARD i-Q COVID/Flu Ag Combo Test work?

A: This diagnostic rapid test kit uses lateral flow and fluorescent immunoassay technology to detect SARS-CoV-2, Influenza A, and Influenza B antigens from a nasopharyngeal swab. The sample is processed with the supplied extraction buffer and applied to the test cartridge, which is then analyzed by the STANDARD i-Q reader for digital result interpretation.

Q: What types of samples are required for this test kit?

A: The test requires a nasopharyngeal swab specimen, ensuring accurate detection of viral antigens. Swabs and all necessary reagents are included in the kit for convenient sample collection and handling.

Q: When should this combo test be used?

A: This test is intended for use when rapid and simultaneous detection of COVID-19 and Influenza A/B is needed in symptomatic patients. It is designed for professional use, particularly in point-of-care settings such as clinics, hospitals, or emergency facilities.

Q: Where can healthcare professionals use this diagnostic kit?

A: The kit's portable and compact design makes it suitable for use in various healthcare settings, including hospitals, clinics, mobile test centers, and outpatient departments. It requires a compatible STANDARD i-Q reader for result interpretation.

Q: What is the process for using the test kit?

A: Healthcare professionals collect a nasopharyngeal swab sample, process it with the extraction buffer, and apply it to the test cartridge. The cartridge is inserted into the STANDARD i-Q reader, which delivers digital results within approximately 10-15 minutes.

Q: What benefits does this combo test offer?

A: Key benefits include rapid turnaround time, simultaneous detection of multiple respiratory viruses, high sensitivity and specificity, easy operation, and minimal sample requirement. This enables prompt clinical decisions and effective infection control.

Q: Is the SD Biosensor STANDARD i-Q COVID/Flu Ag Combo Test reusable?

A: No, each test cartridge is single-use and intended for one patient only. Proper disposal should be followed according to medical waste guidelines after use.

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