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SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab
SD Biosensor STANDARD Q HIV 1/2 Ab
SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab SD Biosensor STANDARD Q HIV 1/2 Ab

SD Biosensor STANDARD Q HIV 1/2 Ab

Product Details:

  • Display Type Visual (line-based result window)
  • Function Detection of HIV 1/2 antibodies
  • Accuracy >99% for both sensitivity and specificity
  • Measurement Range Qualitative (Reactive/Non-reactive determination)
  • Shelf Life 24 Months
  • Features Fast results, High sensitivity/specificity, Simple procedure, Room temperature storage
  • Storage Instructions Store at 1C to 30C, protect from direct sunlight, moisture, and heat
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SD Biosensor STANDARD Q HIV 1/2 Ab Price And Quantity

SD Biosensor STANDARD Q HIV 1/2 Ab Product Specifications

  • Approx. 10 g per test device
  • Yes
  • Qualitative detection of antibodies to HIV-1 and HIV-2 in human serum, plasma, or whole blood
  • Single Use
  • White with labeling
  • In vitro Diagnostic (IVD) test kit
  • Store at 1C to 30C, protect from direct sunlight, moisture, and heat
  • Single use, as required
  • Manual
  • Plastic, Nitrogen-purged device with desiccant
  • Rapid Diagnostic Test Kit
  • Lateral Flow Immunochromatography
  • Fast results, High sensitivity/specificity, Simple procedure, Room temperature storage
  • New
  • Not required (manual test)
  • No
  • Detection of HIV 1/2 antibodies
  • Individual device size approx. 91 mm 20 mm
  • Visual (line-based result window)
  • Yes
  • 24 Months
  • >99% for both sensitivity and specificity
  • Qualitative (Reactive/Non-reactive determination)
  • >99.8%
  • 10 µL whole blood/serum/plasma
  • >99.9%
  • Single-use only
  • Within 20 minutes
  • Healthcare professionals
  • Test device, dropper, buffer, instructions for use
  • Immunochromatographic assay

SD Biosensor STANDARD Q HIV 1/2 Ab Trade Information

  • 100 Unit Per Day
  • 1-7 Days

Product Description

Brand SD Biosensor
Sample Type Serum/ Plasma/ WB
Pack Size 30T
CAT No RK057-30

Standard Q HIV 1/2 Ab Test is a rapid immunochromatographic 3rd generation test for the detection of antibodies (IgM, IgG & IgA) against HIV-1 & HIV-2 in human serum, plasma & whole blood. The test is for in vitro diagnostic use and is intended as an aid to early diagnosis of HIV infection. This is intended for professional use, only for initial screening test.




Accurate and Rapid HIV Detection

Designed for real-time operation and manual handling, this in vitro diagnostic kit streamlines the process of detecting HIV-1/2 antibodies. With over 99% sensitivity and specificity, healthcare professionals are equipped with the confidence to accurately screen and confirm HIV status efficiently in various clinical settings.


Simple, Room Temperature Operation

The STANDARD Q HIV 1/2 Ab test is ready for use straight out of the package-no equipment or power source required. Simply add the sample, apply the buffer, and read the visual line-based results within 20 minutes. The kit is stable for 24 months when stored at 1-30C, making it ideal for busy healthcare environments.


User-Friendly & Highly Portable

Compact and weighing only about 10 grams, each test is easy to transport for use in diverse healthcare locales. The straightforward procedure, combined with its single-use nature and built-in desiccant, ensures safe, contamination-free testing wherever needed.

FAQ's of SD Biosensor STANDARD Q HIV 1/2 Ab:


Q: How do I perform the SD Biosensor STANDARD Q HIV 1/2 Ab test?

A: Apply 10 L of whole blood, serum, or plasma to the test device, add buffer as per the instructions, and wait for results to appear in the visual result window within 20 minutes. Detailed, step-by-step guidance is included in the kit.

Q: What samples can be used with this rapid diagnostic test?

A: The test is compatible with human whole blood, serum, or plasma. Only a small volume (10 L) is required to process the test effectively.

Q: When can I expect to see the results after running the test?

A: Results will be ready within 20 minutes of adding the sample and buffer, enabling rapid clinical decision-making without the need for specialized equipment.

Q: Where should I store the unused test kits?

A: Store the kits at room temperature (1C to 30C), protected from direct sunlight, excess moisture, and heat to maintain reliability throughout the 24-month shelf life.

Q: What are the benefits of using this HIV 1/2 Ab rapid test kit?

A: This kit offers fast, highly accurate HIV screening with >99% sensitivity and specificity, is easy to use manually, requires no power, and enables immediate results, which is ideal for point-of-care and outreach testing environments.

Q: Is the kit intended for home use or professional use?

A: The SD Biosensor STANDARD Q HIV 1/2 Ab test is intended exclusively for use by trained healthcare professionals in clinical or outreach settings due to its technical requirements and the sensitivities involved.

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