Customization: | Available |
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Type: | IVD Reagent |
Format: | Cassette |
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Typhoid fever Rapid Test is an immunochromatographic assay designed for the qualitative detection of specific IgG and IgM andodies against a specific Salmonella typhi antigen in human serum, plasma or whole blood. It is intended to be used as in vitro diagnostic of typhoid fever. The results obtained should not be the sole determinant for clinical decision.
MAINCONTENTS
• Rapid test cassette with desiccant.
• Disposable pipettes
• Buffer
• Package insert
STORAGEANDSTABILITY
• Store at 2 ~ 30 º C in the sealed pouch for 24 months.
• Keep away from direct sunlight, moisture and heat.
• DONOTFREEZE.
DIRECTIONOFUSE
Bring tests, specimens, buffer and/or controls to room temperature (15-30°C) before use.
1. Remove the test from its sealed pouch, and place it on a clean, level surface. Label the device with patient or control identification. For best results, the assay should be performed within one hour.
2. Using the provided disposable pipette, transfer 1 drop of whole blood, serum or plasma to the specimen well (S) of the cassette and add 1 drop of buffer to the sample well, then start the timer. Avoid trapping air bubbles in the specimen well (S), and do not add any solution to the result area. As the test begins to work, color will migrate across the membrane.
3. The result should be read in 15 minutes. Do not interpret the result after 20 minutes.
SAMPLECOLLECTION
• Typhoid fever Rapid Test (Whole Blood/Serum/Plasma) is intended for use with human whole blood, serum or plasma specimens only.
• Only clear, non-hemolyzed specimens are recommended for use with this test. Serum or plasma should be separated as soon as possible to avoid hemolysis.
• Perform testing immediately after specimen collection. Do not leave specimens at room temperature for 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.
• Containers containing anticoagulants such as EDTA, citrate, or heparin should be used for whole blood storage.
• 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.
• If specimens are to be shipped, pack them in compliance with all applicable regulations for transportation of etiological agents.
• Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.
LIMITATIONS
• This product is designed for use with human serum, plasma and whole blood only.
• The test is a qualitative assay and is not for quantitative determination of antibodies concentration levels. The intensity of the band does not have linear correlation with the antibody titer of the specimen.
• The results obtained should only be interpreted in conjunction with other diagnostic results and clinical information.
1.Are you a Manufacturer?
Yes,we are manufacturer based in Foshan,China with 100 workers,more than 5000 square meter non-dust workshop,advanced automate machines and professional R&D team ensure the high quality,speedy delivery and large production capacity.
2.Can we put our logo/text om the product or package?
Yes,we can do OEM or even ODM.All of our products can be customized.
3.Can you provide free samples?
Yes, free sample are available.
4.How long is your production time?
Our production time is usually two weeks after receiving the deposit and four weeks for one contaoner order quantity.
5.How to make the payment?
By T/T,L/C,Paypal,Western union and made in China is also acceptable.