FDA Whole blood Helicobacter Pylori Ab Test Cassette

H. Pylori rapid Test Cassette

For the qualitative detection of Antibodies to H. Pylori in serum /plasma and whole Blood

Main Features

☀ High Sensitivity

☀ High Specificity

☀ Reliable: high accurate, early detection of the presence of H.Pylori

☀ Simple: No Instrument Required

☀ Convenient: Room Temperature Storage, Built-In Control line

☀ Fast: Results in 5-30 minutes, strong positive results may be observed promptly within 3 minutes

☀ Certified by Authoritative Certification System and Standards

☀Winner of "the National Rapid Diagnostic Kit for Clinical Performance Assessment"

Intended Use

The infection of Helicobacter pylori (H. pylori) is associated with a variety of gastro-intestinal diseases, such as stomach ulcer, chronic active gastritis and gastric, duodenal and gastric adenocarcinoma. Antibodies to H. pylori are developed in individuals infected with H. pylori as a serological response. Detecting these specific antibodies to H. pylori can be use as a qualitative assay in the diagnosis of H. pylori infection. It may be used either as an adjunction to endoscopy or as an alternative measure in symptomatic patients.

The H. pylori Rapid Test is a chromatographic immunoassay (CIA) for the rapid determination of antibodies to H. pylori in serum/plasma/whole blood specimens. The test is to be used as an aid in the diagnosis of infection due to H. pylori.

Principle

The H. pylori Rapid Test is a lateral flow, immunochromatographic-screening test. H. pylori antigens are precoated onto membrane as a capture reagent on the test band region. During the assay the specimen serum is allowed to react with H. pylori antigens-gold conjugate. The mixture then moves laterally on the membrane chromatographically to the test region with immobilized antigens of H. pylori. If H. pylori antibodies are present in the specimen, two colored bands are formed on the test region. One colored band in the test region indicates a negative result.

Reagents and Materials Provided

1. One pouched cassette with desiccant.

2. One bottle of diluent buffer.

3. Instruction for use.

Materials Required But Not Provided

1. Clock or timer

2. Specimen collection tube

Warning and Precautions

1. For in vitro diagnostic use only.

2. All patient samples should be treated as if capable of transmitting diseases.

3. Do not interchange reagents from different lots or use test kit beyond expiration date.

4. Icteric, lipemic, hemolysis, heat treated and contaminated sera may cause erroneous results.

Storage

Store the test kits at temperature 4-30°C,in the sealed pouch for the duration of the shelf life (24 months).

Assay Procedure

Serum/Plasma
Add 70-100 ul or 2-3 drops serum or plasma into sample well. Observe the result in 10-15 minutes.

Whole blood
Add 1 drop of whole blood into sample well, after all blood completely absorbed, add 1 drop of whole blood diluent. Observe the result in 10-15 minutes. add 1 drop of diluent. Observe the result in 5-15 minutes.

Interpretation of Results

Negative: Only one pink band appears. This indicates that no H. pylori antibodies have been detected.

Positive: Two pink bands appear. This indicates that the specimen contains H. pylori antibodies.

Invalid: If no band appears, this indicates a possible error in performing the test. The test should be repeated using a new device.

Newscen Biopharm Co., Limited is a professional manufacturer of in vitro diagnostic products and related supporting apparatuses, which is jointly founded by Tianjin Pharmaceutical Group, Tianjin Zhongxin Pharmaceuticals Co., Ltd and oversea Chinese entrepreneurs.

Founded in 2003, the company is one national high tech corporation and Tianjin Grade A medical device manufacturer. Over the years, the company has been committed to the research, development, production and sales of in vitro diagnostic products and related supporting apparatuses, and also has provided OEM and ODM and technology transfer and cooperation as well as some other customer market based diversified services to customers at home and abroad.

NewScen is based on independent innovation and relies on the talent sharing at home and abroad, information interaction advantage, antibody preparation and new product R & D technology platform to develop and produce nine series about one hundred kinds of products including tests and instruments and put on the market in succession.

HIV (1 + 2) antibody rapid test Kit and other IVD (In Vitro Diagnostic) devices obtained National Patent and National Class of New Drug Certificate; HCV Antibody Rapid Test is the first double antigen sandwich test HCV patented product; NewScen’s quantitative test broke through the technical difficulty of the colloid gold quantitative detection, opening up a new situation for clinical application of Colloidal Gold test. Rapid immuno assay reader provides an open and common platform for qualitative and quantitative detection of the Colloidal Gold test.

The company has received CFDA medical device certificates of 32 products, 49 independent Intellectual Property Rights, FDA certificates of series of products and European CE certificates of 16 products. Production management is in strict accordance with the regulations of in vitro diagnostic product production as well as international quality management system (ISO 9001, ISO 13485) so as to ensure high product quality. Products are sold throughout the country and in North America, South America, Southeast Asia, Europe, the Middle East, Africa and other international markets.

Currently, the company integrated Colloidal Gold test, immunochromatographic interpretoscope and cloud technology and other technical advantages, and created management integrated POCT system, so as to achieve convenient, accurate and efficient onsite data collection and remote guidance or data sharing of the monitoring center and promote the development of modern testing technique and the improvement of diagnosis and treatment level.

NewScen has obtained the project support from Tianjin or the country for nine times in succession, has been identified as one Hightech Enterprise in Tianjin, has obtained the title of “Top 100 Enterprise in Tianjin” among Tianjin SMEs, and is the rapid diagnostic Hightech demonstration project base and National 863 Project undertaker awarded by the NDRC (National Development and Reform Commission).

Fecal Occult Blood, Serum Ferritin and Hepatitis C rapid test products were named Tianjin independent innovation products; brand “YBT”products have been awarded the title of “Chinese Women and Children Favorite Brand Product” by Chinese Women and Children Development Center; “YBT” trademark was named “Tianjin Famous Trademark”.

“Honesty, Verity, Authenticity, and Innovation", is our persistent commitment.

“Encouraging Our Employees Growing With Company” is the driving force beneath our surging growth.