| Customization: | Available |
|---|---|
| Type: | HIV Test Kit |
| Material: | Plastic |
|
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Suppliers with verified business licenses
Audited Supplier Audited by an independent third-party inspection agency
|
Function |
For the qualitative presumptive detection of antibodies to HIV-1/HIV-2 in serum or plasma specimens. |
|
Formats |
cassette |
|
Specifications |
cassette(4mm) |
|
Specimens |
Serum/Plasma |
|
Specificity |
over 99.8% |
|
Reaction Time |
15 minutes |
|
Shelf Life |
24 months at room temperature 2- 30 degrees |
|
Packing Details |
Cassette
1pcs/box, 500boxes/carton, 120,000pcs/20'ft container |
|
Others |
The kits can be made according to the customers' artwork or design |
High Sensitivity Home Use HIV Blood Test Device
KIT COMPONENTS
1.1test cassette
2.Each pouch contains 1 cassette with desiccant
3.1 bottle of diluent buffer
4.1 disposable plastic dropper
5.Instruction of use
6.Sterile lancet
7.Alcohol pad
8.Band-aid
STORAGE AND STABILITY
1.The kit should be stored at 2-30°C until the expiry date printed on the sealed pouch.
2.The test must remain in the sealed pouch until use.
3.Do not freeze.
4.Cares should be taken to protect components in this kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipments, containers or reagents can lead to false results.
SPECIMEN COLLECTION AND STORAGE
1.The HIV 1/2 Rapid Test Device (Serum/Plasma) is intended only for use with human serum, or plasma specimens.
2. Only clear, non-hemolyzed specimens are recommended for use with this test. Serum or plasma should be separated with soonest possible opportunity to avoid hemolysis.
3.Perform the testing immediately after the specimen collection. Do not leave the specimens at room temperature for prolonged periods. Specimens may be stored at 2-8°C for up to 3 days. For long term storage, specimens should be kept below -20°C.
4. Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Avoid repeated freezing and thawing of specimens.
5. Pack the specimens in compliance with applicable regulations for transportation of etiological agents, in case they need to be shipped.
6. Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.
Production Line
Certificate
Company Information
Hangzhou Wehere Medical Technology Co., Ltd. is a company on the medical health products manufacturing and trading in China. We have a professional medical supplies nearly twenty years. We have three plants to produce all kinds of medical products. Our factories are Anji Sunlight Medical Products Co., Ltd; Yangzhou Zhongyi Medical Products Co., Ltd;Zhejiang Yinda Biotechnology Co., Ltd. On the basis of production management MDD and ISO13485 in our owner factories, guided by brand strategy, under the direct participation of American companies, we are committed to becoming an important member of the global medical and healthcare industry.We are here to support your medical & healthcare needs.
Your any question are welcome!
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