HIV 1+2 Test Device Whole Blood C10-22 (Cassette)
This test is a single use, rapid device intended for qualitative detection of antibodies to Human Immunodeficiency Virus 1/2 in whole blood, serum or plasma specimens. It is intended for use in medical institution as an aid for the diagnosis and management of patients related to infection with HIV and for screening of blood donors, or blood products as well.
Chasing buffer, sterile lancet, alcohol pre pad, pipette, bandage
Principle of Test:
|Product Name||Specimen||Format||Catalog No.||Sensitivity||Package Size||Strip Width|
|HIV 1+2 Test||Serum/
|Cassette||C10-20||99.40%||25 Tests||4.0 mm|
|Strip||C10-11||50 Tests||3.5 mm|
|Cassette||C10-21||25 Tests||4.0 mm|
|C10-22||1 Test||4.0 mm|
|Strip||C10-21||50 Tests||3.5 mm|
INTENDED USE: This test is a single use, rapid device intended for qualitative detection of antibodies to Human Immunodeficiency Virus 1/2 in whole blood, serum or plasma specimens. It is intended for use in medical institution as an aid for the diagnosis and management of patients related to infection with HIV and for screening of blood donors, or blood products as well.
1. Bring the pouched test device to room temperature(15-30℃) prior to testing. Do not open the pouch until ready to perform the assay.
2. Remove the test device from the sealed pouch. Lay it on a flat, clean and dry surface.
3. Use the pipette to draw and slowly add 1 drop of whole blood/serum/plasma to the sample well.
4. Hold the buffer bottle vertically and add 1-2 drops to the sample well./ If using a pipette, change a new one to avoid cross-contamination. Draw and transfer 2-3 drops of buffer to the sample well.
5. Interpret test results within 10-15 minutes. Do not interpret after 20 minutes.
CAUTION: The above interpreting time is based on room temperature range of 15 – 30℃. If your room temperature is significantly lower than 15℃, then the interpreting time should be properly increased to 30 minutes.
INTERPRETATION OF RESULTS
NEGATIVE: The presence of only one line in the control region indicates a negative result (Figure 1).
HIV-1 Positive: The control line and HIV-1 line (T1) are visible in the result window. The test is positive for HIV-1.
HIV-2 Positive: The control line and HIV-2 line (T2) are visible in the result window. The test is positive for HIV-2.
HIV-1 and HIV-2 Positive: The control line, HIV-1 (T1) and HIV-2 (T2) lines are visible in the result window. The test is positive for HIV-1and HIV-2.
Regarding the positive results for both HIV-1 and HIV-2 in one patient, it is possible for reasons as follows：
1. There is the homology in the amino acid sequence of HIV type-1 and type-2. So, it is possible that the test results show the positive results for HIV-1 and HIV-2 in one patient, simultaneously.
2. Provisionally, you can conclude virus type according to the line density. If the line density of type-1 is darker than that of type-2 in the result window, you can read as HIV-1 positive. If the line density of type-2 is darker than that of type-1 in the result window, you can read as HIV-2 positive. If you want to determine virus type or co-infection exactly, you should perform the confirmatory assay (e.g Western blot etc.).
INVALID: If the pink color line in C region is not visible, the result is considered invalid (Figure 3)
regardless of the presence or absence of the test line(s).
NOTE: Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for the control line failure. Review the procedure and repeat the test with a new device. If problem persists, please contact your local distributor.