Testsea Disease Test TB Tuberculosis Rapid Test Kit

Short Description:

Brand Name:

testsea

Product name:

TB Tuberculosis Test

Place of Origin:

Zhejiang, China

Type:

Pathological Analysis Equipments

Certificate:

ISO9001/13485

Instrument classification

Class II

Accuracy:

99.6%

Specimen:

Whole Blood/Serum/Plasma

Format:

Cassete/Strip

Specification:

3.00mm/4.00mm

MOQ:

1000 Pcs

Shelf life:

2 years


Product Detail

Product Tags

Quick Details

Brand Name:

testsea

Product name:

TB Tuberculosis Test

Place of Origin:

Zhejiang, China

Type:

Pathological Analysis Equipments

Certificate:

ISO9001/13485

Instrument classification

Class II

Accuracy:

99.6%

Specimen:

Whole Blood/Serum/Plasma

Format:

Cassete/Strip

Specification:

3.00mm/4.00mm

MOQ:

1000 Pcs

Shelf life:

2 years

HIV 382

Intended Use

The Tuberculosis Rapid Test Strip (Serum/plasma) is a rapid chromatographic immunoassay for the qualitative detection of anti-TB (M. tuberculosis, M. bovis and M. africanum) antibodies (all isotypes: IgG, IgM, IgA, etc.) in Serum or plasma.

HIV 382

HIV 382

Summary

Tuberculosis (TB) is spread primarily via airborne transmission of aerosolized droplets developed by coughing, sneezing and talking. Areas of poor ventilation pose the greatest risk of exposure to infection. TB is a major cause of morbidity and mortality worldwide, resulting in the greatest number of deaths due to a single infectious agent. The World Health Organization reports that more than 8 million new cases of active tuberculosis are diagnosed annually. Almost 3 million deaths are attributed to TB as well. Timely diagnosis is crucial to TB control, as it provides early initiation of therapy and limits further spread of infection. Several diagnostic methods for detecting TB have been used over the years including skin test, sputum smear, and sputum culture and chest x-ray. But these have severe limitations. Newer tests, such as PCR-DNA amplification or interferon-gamma assay, have been recently introduced. However, the turn-around time for these tests is long, they require laboratory equipment and skilled personnel, and some are neither cost effective nor easy to use. 

Test Procedure

Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing.

1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
2. Place the test device on a clean and level surface.
3. For serum or plasma specimen: Hold the dropper vertically and transfer 3 drops of serum or plasma (approximately 100μl) to the specimen well(S) of the test device, then start the timer. See illustration below.
4. For whole blood specimens: Hold the dropper vertically and transfer 1 drop of whole blood(approximately 35μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl) and start the timer. See illustration below.  
5. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.  

Applying sufficient amount of specimen is essential for a valid test result. If migration (the wetting of membrane) is not observed in the test window after one minute, add one more drop of buffer (for whole blood) or specimen (for serum or plasma) to the specimen well.

Interpretation of Results

Positive: Two lines appear. One line should always appear in the control line region(C), and another one apparent colored line should appear in the test line region.

Negative: One colored line appears in the control region(C).No apparent colored line appear in the test line region.

Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure.

★ Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

Exhibition Information

Exhibition Information (6)

Exhibition Information (6)

Exhibition Information (6)

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Exhibition Information (6)

Exhibition Information (6)

Honorary Certificate

1-1

Company Profile

We, Hangzhou Testsea Biotechnology Co., Ltd is a fast-growing professional biotechnology company specialized in researching, developing, manufacturing and distributing of advanced in-vitro diagnostic(IVD) test kits and medical instruments.
Our facility is GMP, ISO9001, and ISO13458 certified and we have CE FDA approval. Now we are looking forward to cooperating with more overseas companies for mutual development.
We produce fertility test, infectious diseases tests, drugs abuse tests, cardiac marker tests, tumor marker tests, food and safety tests and animal disease tests, in addition, our brand TESTSEALABS have been well known in both domestic and overseas markets. Best quality and favorable prices enable us to take over 50% the domestic shares.

Product Process

1.Prepare

1.Prepare

1.Prepare

2.Cover

1.Prepare

3.Cross membrane

1.Prepare

4.Cut strip

1.Prepare

5.Assembly

1.Prepare

6.Pack the pouches

1.Prepare

7.Seal the pouches

1.Prepare

8.Pack the box

1.Prepare

9.Encasement

Exhibition Information (6)

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