Professional Manufacturer of Rapid Test Devices
Place of Origin: | China |
Brand Name: | Newscen |
Certification: | ISO9001, CE, TUV, SFDA |
Minimum Order Quantity: | 10 Boxes or 400 Kits (40 Kits/Box) |
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Price: | USD0.48/Cassette |
Packaging Details: | 40 Kits/Box, 50 Boxes/Carton, 317g/Box, 18kgs/Carton, Box Size: 250x125x65mm, Carton Size: 650x510x330mm |
Delivery Time: | 8 days |
Payment Terms: | T/T, Western Union, MoneyGram |
Supply Ability: | 100,000 Kits Per Day |
Shelf Life: | 2 Years | Format: | Cassette |
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OEM / ODM: | Available | Result Time: | Read In 20 Minutes |
Box Color: | Violet | CE Certificate: | Yes |
High Light: | Serum Plasma AIDS Test Cassette,Fingertip AIDS Rapid Test Cassette,40uL Plasma AIDS Test Cassette |
HIV(1+2) Antibody Rapid Test Kit
For qualitative detection of HIV(1+2) Antibodies in serum/plasma and whole Blood
Main Features
☀ Sensitivity: 100%
☀ Specificity: Higher than 99%
☀ Simple: No Instrument Required
☀ High accurate, early detection of the presence of HIV
☀ Unique 3-line Patented Design
☀ Convenient: Room Temperature Storage, Built-In Control line
☀ Able to differentiate HIV Type I and Type II
☀ Certified by Authoritative Certification
☀ Winner of "the 2008 National HIV Antigen Diagnostic Kit for Clinical Performance Assessment"
Principle
HIV-1/2 RDT is a chromatographic immunoassay (CIA) for the detection of antibodies to HIV-1/2 in human serum/plasma. HIV-1/2 specific antigens are precoated onto membrane as a capture reagent on the test region.
During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HIV-1/2 specific antigens. Antibodies to HIV-1/2, if present, a red colored band will develop on the membrane in proportion to the amount of HIV-1/2 antibodies present in the specimen.
Absence of this red colored band in the test region suggests a negative result. To serve as a procedural control, red colored band in the control region will always appear regardless the presence of antibodies to HIV-1/2.
Intended Use
The HIV-1/2 Rapid Diagnostic Test (RDT) is a qualitative test for the detection of antibodies to Human Immunodeficiency Virus type 1 and 2 (HIV-1/2) in human serum/plasma.
It is considered as an initial screening test for HIV-1/2 antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA.
Reagents and Materials Provided
Each kit contains:
☀ 40 test cassettes(individually pouched)
☀ One bottle of diluent buffer(5ml)
☀ 40 disposable plastic droppers
☀ Each pouch contains one cassette with one desiccant bag
☀ Instruction for use
Materials Required But Not Provided
☀ Timer or stopwatch
☀ Biohazard disposal container
☀ Blood collection devices, for the testing of venous whole blood, serum or plasma
☀ Disposable gloves
For finger stick samples, the following materials are required:
Alcohol pad
Sterile lancet
Sterile gauze or cotton
Warning
For Invitro Diagnostic Use ONLY
Read the package insert completely before use. It is very important that the correct procedure is followed. Fail to add the patient sample may lead to a false negative result (i.e.a missed positive) .
Storage
Newscen HIV(1+2) Antibody Rapid Test can be stored at room temperature(4-30℃, do not freeze) for 24 months from the date of manufacture.
Keep the test cassette in sealed pouch until use.
Once you have taken the test cassette out of the pouch, perform the test as early as possible(within 1hour) to avoid test cassette from becoming moist. Do not use the test beyond the indicated expiration date.
The diluent buffer should be stored at room temperature(4-30℃, do not freeze) .
Contact Person: Mr. Randy.Zhang
Tel: 008618611273771