S0003852

OneStep HIV1/2 WB/Serum/Plsm Test,kit/40


apid diagnostic test Wondfo One Step HIV 1/2 Whole Blood/Serum/Plasma Test, kit/40
Indicative Price 27.20 USD

General description:
Wondfo One Step HIV 1/2 Whole Blood/Serum/Plasma is a rapid, in vitro immunochromatographic direct binding test for detection of HIV 1/2 antibodies in human venous whole blood, fingerstick whole blood, serum or plasma, aid to diagnosis of HIV infection. It is intended for use by trained users (in either laboratory or point-of-care settings).

Technical specifications:
Sensitivity: 100.0%
Specificity: 100.0%
Invalid rate: 0%
Time to result: 15 minutes. Do not wait more than 30 minutes.
Specimen type: Serum, plasma, venous whole blood, capillary whole blood
Sample volume: 10μl

Manufacturer product reference: Guangzhou Wondfo Biotech Co., Ltd, W006-C4P2-F

Items supplied with:
·Pouch individually sealed with one test cassette, one dropper and one desiccant, 40
·Sample diluent bottle (5ml), 2
·Instructions for Use (IFU), 1

Items required, but not supplied:
Specimen collection containers, sterile lancets, alcohol pads, centrifuge (for serum/plasma specimen only), capillary tube (for fingerstick whole blood only), timer, protective gloves, specimen and test waste container

Shelf life:
24 months from the date of manufacturing; do not use beyond its expiry date.

Weight and volume:
Estimated weight: 0.40 kg
Estimated volume: 3.21 dm³

Storage and transportation condition:
Between 2 to 30 °C. Protect against humidity and direct sunlight. Do not freeze reagents.

Packaging and labeling:
Primary packaging: One kit with 40 pouches, each individual sealed pouch contains one test cassette, one dropper, and one desiccant.
Secondary packaging: All contents of One Step HIV1/2 Whole Blood/Serum/Plasma Test for 40 tests.

General recommendations:
·Follow strictly manufacturer instructions for use of the test procedure (especially adherence to reading time).
·Do not use any other specimen than those specified.
·Apply standard biosafety precautions when handling and disposing of potentially infectious material.

Useful links:
WHO list of prequalified in vitro diagnostic products:
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