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Quick Details

  • Type: Pathological Analysis Equipments
  • Brand Name: Encode
  • Place of Origin: Guangdong, China (Mainland)
  • Model Number: SHI-401
  • Accuracy: 99.98%
  • delivery time: 7-10days
  • OEM: Available
  • Specimen: Whole blood, plasma, serum
  • Manufacture: 22 years
  • Read time: 10-15mins
  • expiration: 24 months
  • format: strip
  • Size: 3mm/4mm
  • shipment: by sea/air is available

Packaging & Delivery

Packaging Details Diagnostic test HIV Rapid test strip
1. Individual foil test cassette ;
2. 25 tests in one box ;
3. Encode brand or OEM package ;
Delivery Time Shipped in 7 days after payment

Product Description

Diagnostic test HIV Rapid test strip                                


Advantage  Diagnostic test HIV Rapid test strip

  • 21 years experience
  • Simple operation, reliable result
  • High sensitivity and specificity,precision
  • Sexually Transmitted Disease test kits.


IntroductionDiagnostic test HIV Rapid test strip



HIV 1/2 rapid test kit


Whole blood,plasma,serum


Individually packed test card with desiccant,Disposable pipette,Buffer,Single-use Lancet,Alcohol Swab,Package insert






24 Months




HIV is the etiologic agent of Acquired Immune Deficiency Syndrome (AIDS). The virion is surrounded by a lipid envelope that is derived from host cell membrane. Several viral glycoproteins are on the envelope. Each virus contains two copies of positive-sense genomic RNAs. HIV-1 has been isolated from patients with AIDS and AIDS-related complex, and from healthy people with high potential risk for developing AIDS. HIV-2 has been isolated from West African AIDS patients and from seropositive asymptomatic individuals. Both HIV-1 and HIV-2 elicit immune response. Detection of HIV antibodies in serum, plasma or whole blood is the most efficient and common way to determine whether an individual has been exposed to HIV and to screen blood and blood products for HIV. Despite of the differences in their biological characters, serological activities and genome sequences, HIV-1 and HIV-2 show strong antigenic cross-reactivity. Most HIV-2 positive sera can be identified by using HIV-1 based serological tests.


Intend to useDiagnostic test HIV Rapid test strip


The HIV 1/2 Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid visual immunoassay for the qualitative presumptive detection of antibodies to HIV-1/HIV-2 in human whole blood, serum, or plasma specimens. This kit is intended to be used as an aid in the diagnosis of HIV infection.



Specimen and storageDiagnostic test HIV Rapid test strip


  • The HIV 1/2 Human Immunodeficiency Virus Rapid Test Device (Whole Blood/Serum/Plasma) can be performed using whole blood (from venipuncture or fingerstick), serum, or plasma.
  • To collect Fingerstick Whole Blood specimens:

1. Wash the patient’s hand with soap and warm water or clean with an alcohol swab. Allow to
2. Puncture the skin with a sterile lancet. Wipe away the first sign of blood.
3. Gently rub the hand from wrist to palm to finger to form a rounded drop of blood over the
puncture site.
 4. Add the Fingersitck Whole Blood specimen to the test device by using a capillary tube or hanging drop.

  • Separate serum or plasma from blood as soon as possible to avoid hemolysis. Use only clear, nonhemolyzed specimens.
  • Testing should be performed immediately after specimen collection. Do not leave th specimens at room temperature f prolonged periods. Serum and plasma specimens may be stored at 2-8°C for up to 3 days. For long term storage, specimens should be kept below -20°C. Whole blood collected by venipuncture should be stored at 2-8°C if the test is to be run within 2 days of collection. Do not freeze whole blood specimens. Whole blood collected by fingerstick should be tested immediately.
  • Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly.
  •  If specimens are to be shipped, they should be packed in com

Operating  Steps   Diagnostic test HIV Rapid test strip


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. Placee test device on a clean and level surface. Hold the dropper vertically and transfer 2 drops of specimen (approximately 80 uL) to the specn well (S) of the test device, then add 1 drop of buffer (approximately 40 uL) 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.



 Performance CharacteristicsDiagnostic test HIV Rapid test strip


The HIV 1/2 Human Immunodeficiency Virus Rapid Test Device (Whole Blood/Serum/Plasma) has
been compared with a leading commercial HIV EIA test. The correlation between these two systems is 99.8%
The HIV 1/2 Human Immunodeficiency Virus Rapid Test Device (Whole Blood/Serum/Plasma) has been tested by anti-HIV 1 low titer performance panel, anti-HIV 2 performance panel and antiHIV 1 seroconversion panel (Boston Biomedica, Inc.)And it has also been compared with leading commercial EIA HIV test on clinical specimens. The results show that HIV 1/2 Human Immunodeficiency Virus Rapid Test Device (Whole Blood/Serum/Plasma) is very sensitive to HIV 1 and/or HIV 2 antibodies.
The specificity of the test is comparable to a leading commercial HIV EIA test. The HIV 1/2 Human Immunodeficiency Virus Rapid Test Device (Whole Blood/Serum/Plasma) is highly specific for anti-HIV 1 and/or HIV 2 compared to a leading commercial HIV EIA test.




Packaging & Shipping


 Storage and stability 

The kit can be stored at room temperature or refrigerated (2-30°C). The test device is stable
through the expiration date printed on the aled pouch. The test device must remain in the sealed  pouch until use. DO NOT FREEZE. Do not use beyond the expiration date.

Product List


Sexually Transmitted disease Tests


Item NO.



Neisseria           Gonorrhea


Detect N.G infection by Enzyme Reaction

urine/Cervical secretion/urethral discharge


N.G Ag test cassette

Endocervical or urethral secretion

Chlamydia             Trachomatis


CT Ag test cassette

Endocervical or urethral secretion

Bacterial                    Vaginosis


Detect BV based on four indicator:H2O2 ,SA,LE,PH

vaginal secretion


Detect BV based on polyamine test

vaginal secretion


Detect BV based on  sialidase activity test

vaginal secretion


Detect BV based on Six indicator:H2O2 ,SA,LE,PH,CV,TV)

vaginal secretion



Syphilis  test


HIV 1/2


Human Immunodeficiency Virus (HIV 1/2) test


HIV 1+O/2


Human Immunodeficiency Virus (HIV 1+O/2) test cassette




HSV-2 Rapid Test




Rubella IgG/IgM Rapid Test



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Company Information




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