Unveiling QL Biotech's highly efficient HBsAg/HCV/HIV/Syphilis Combo Rapid Test Device. This product provides a qualitative membrane-based immunoassay designed for the identification of antibodies pertaining to HIV 1&2. The test strip can be utilized with whole blood, serum, or plasma samples, ensuring its adaptability in different clinical settings. The versatile nature of our HBsAg/HCV/HIV/Syphilis Combo Rapid Test Device makes it an invaluable tool in the diagnosis and monitoring of these infectious diseases. The accurate detection it provides reduces the uncertainty and anxiety often associated with waiting for laboratory results. Time being of the essence, this device delivers prompt results, aiding in early diagnosis and timely intervention. The tool is designed with user convenience and reliability in mind, crafted to operate efficiently with whole blood, serum, or plasma. The qualitative, membrane-based immunoassay of the device offers trustworthy results, aiding healthcare professionals to confidently address HBsAg/HCV/HIV/Syphilis Combo related health concerns.

• HIV 1/2 Rapid Test Strip(Whole Blood/Serum/Plasma)
  Allow the test strip, specimen, buffer, and/or controls to equilibrate to room temperature (15‐30°C) prior to testing. 
  1. Remove the test strip from the foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed within one hour. 
  2. Peel off the tape from the test card, and stick the test strip in the middle of test card with arrows pointing down on the test card. 
  For Serum, Plasma or Venipuncture Whole Blood specimen: Hold the dropper vertically and transfer 2 drops of serum, plasma or venipuncture whole blood (approximately 80 L) to the 
  “Specimen Pad” of the test strip, then add 1 drop of buffer (approximately 40L) and start the timer. 
  For Fingerstick Whole Blood specimen: 
  To use a capillary tube: Fill the capillary tube and transfer approximately 80L of fingerstick whole blood specimen to the “Specimen Pad” of the test strip, then add 1 drop of buffer (approximately 40L) and start the timer. 
  To use hanging drop: Allow 2 hanging drops of fingerstick whole blood specimen to fall into the center of the “Specimen Pad” on the test strip, then add 1 drop of buffer (approximately 
  40L) and start the timer. 
  3. Wait for the colored line(s) to appear. The result should be read at 15 minutes. Do not interpret results after 20 minutes.
  HIV 1/2 Rapid Test Strip（Serum/Plasma）
  HIV 1/2 Rapid Test Device (Whole Blood/Serum/Plasma)
  Allow the test device, specimen, buffer, and/or controls to equilibrate to room temperature 
  (15‐30°C) prior to testing. 
  1. Remove the test device from the foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed within one hour. 
  2. Place the test device on a clean and level surface. Hold the dropper vertically and transfer 2 drops of serum, plasma (approximately 80L) to the specimen well (S) of the sample pad then add 1 drop of buffer (approximately 40L) and start thetimer. 
  3. Wait for the colored line(s) to appear. The result should be read at 10 minutes. Do not interpret results after 20 minutes. 
  HIV 1/2 Rapid Test Device（Serum/Plasma）
  Allow the test device, specimen, buffer, and/or controls to equilibrate to room temperature (15‐30°C) prior to testing. 
  1. Remove the test device from the foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed within one hour. 
  2. Place the test device on a clean and level surface. 
  For Serum, Plasma specimen: Hold the dropper vertically and transfer 2 drops of serum, plasma (approximately 80L) to the specimen well (S) of the test device, then add 1 drop of buffer (approximately 40L) and start the timer. 
  3. Wait for the colored line(s) to appear. The result should be read at 10 minutes. Do not interpret results after 20 minutes.

INVALIDRESULT:

Control line (C) falls to appear. Insufficient buffer volume or incorrect procedural techniques are the most likely reasons for control line failure.

Review the procedure and repeat the procedure with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

*NOTE: The intensity of the color in the test line region (T) will vary depending on the concentration of HIV antibodies present in the specimen. Therefore, any shade of colored in the test region (T) should be considered positive.

Furthermore, QL Biotech is committed to ensuring the highest quality standards in our product line. Our HBsAg/HCV/HIV/Syphilis Combo Rapid Test Device is a testament to this commitment, designed to provide accurate, efficient, and reliable results in the detection of HIV 1&2 antibodies. This tool stands as a beacon of assurance in aiding the combat against these infectious diseases, accelerating diagnosis, and treatment. In conclusion, the HBsAg/HCV/HIV/Syphilis Combo Rapid Test Device from QL Biotech is a dependable addition to any healthcare provider's toolkit. Its user-friendly design, versatile application, and rapid, reliable results make it a valuable asset in the diagnosis and intervention of these infectious diseases. Be assured of precision and timeliness with QL Biotech's HBsAg/HCV/HIV/Syphilis Combo Rapid Test Device.