Runbio David Medial Detection H. Pylori Antigen/Antibody Test with Wholesale Price
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Product Highlights
- Shelf Life: 2 Years
- Format Options: Available in Strip and Cassette formats
- Specimen Compatibility: Supports Serum, Plasma, and Whole Blood
- OEM Service: OEM Service Available
- ODM Service: ODM Service Available
- Certification: ISO9001:2015 Certified
- Customization Flexibility: Offers Full, Minor, and Flexible Customization
- Lead Time: Within 15 workdays off-peak, one month peak season
Product Attributes
- Customization
- Available
- Type
- IVD Instrument
- Shelf Life
- 2 Years
- Model NO.
- RH-HP
- Format
- Strip and Cassette
- Specimen
- Serum/Plasma/Whole Blood
- Transport Package
- Carton
- Specification
- 3mm/4.2mm
- Trademark
- Neutral
- Origin
- China
Product Images of Runbio David Medial Detection H. Pylori Antigen/Antibody Test with Wholesale Price
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Product Description
The test is to be used as an aid in the diagnosis of infection due to H. pylori, formely known as Campylobacter pylori, in patients with gastrointestinal symptoms
SPECIMEN COLLECTION AND PREPARATION
Whole blood
Collection using a lancet:Finger prick whole blood sample could be collected by first using an alcohol swab to clean the finger of the person being tested, then puncturing the center of the finger pad skin with a disposable sterile blood lancet, holding the finger downward, dripping the blood into the test cassette's sample well, or collect blood from the puncture site with a disposable plastic dropper and dispense one full drops (about 25µl) of fresh blood into the sample well
Collection by venipuncture: Collect whole blood in a collection tube (containing anticoagulants such as heparin, EDTA and sodium citrate) by venipuncture.
-If blood specimens are not immediately tested, they should be stored refrigerated at 2-8°C. When stored at 2-8°C, the blood specimens must be used within 3 days.
Whole Blood can not be frozen.
Plasma or Serum
1.Separate the serum or plasma from blood as soon as possible to avoid hemolysis. Only clear, non-hemolyzed samples can be used. Avoid grossly lipemic or turbid samples.Whole Blood can not be frozen.
2.If serum or plasma samples are not tested immediately, they should be refrigerated at 2‐8ºC. For storage period longer than 7 days, freezing is recommended. Avoid frequent (more than 3 times) thaw-and-freeze of specimens. Prior to testing, bring frozen specimens and refrigerated specimens to room temperature slowly and mix gently.
6.Do not use heat-inactivated samples.
TEST PROCEDURE
If stored refrigerated, ensure that the pouched device ,Sample diluents and specimen is brought to room temperature(about 20 minutes) before use.
1.Remove the Test Device from the sealed pouch . Use it as soon as possible within 1 hour after removal from pouch.
2.Place the test device on a clean, flat surface.
3.Fill the plastic dropper with the specimen.
Holding the dropper vertically, dispense One drop (about 25μL) of specimen into the sample well.
4.Then holding the bottle in a vertical position,add One drop (about 50μL) of the Sample Diluent from the dropper bottle to the sample well.Set up timer.
5.Read the test results within 10-20 minutes. Do not read the results after 20 minutes. To avoid confusion, discard the test device after interpreting the result.
For the interpretation of the test result the line(s) that has(ve) appeared in the test result window are visually interpreted.
1. Positive Result: If both C and T bands are developed, the test indicates for the presence of antibodies to H. Pylori in the specimen. The result is positive.
2. Negative Result: If only the C band is developed, the test indicates that no detectable antibodies to H. Pylori are present in the specimen. The result is negative.
3. Invalid Result: No visible band at all or no colored band appears on the control (C) region. 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 distributors.




About the Supplier
This supplier has been audited by BV. Verify the report on the official BV website with ID "MIC-ASR241285". Items marked "" are certified.
Company Profile
Founded in 2001, Equinox Biotech Co., Ltd. is located in the China and Israel Science and Technology Innovation Cooperation Zone (Shantou) covering an area of 20, 000 m2.
We have gotten CE and ISO 13485 certificates. Our production management is strictly in accordance with the international quality management system to ensure product quality.
Relying on the advantages of talents and technology, we have established a perfect industrialization system of R&D, production and marketing in the field of bio diagnosis, which provides a powerful driving force to the company's sustainable development.
We have world-leading production lines and experienced staffs with a daily production capacity of 2 million test kits.
Our main products are rapid diagnostic kits covering areas like fertility diagnosis, drug of abuse detection, rapid diagnosis of infectious diseases and tumor detection. At present, we have obtained 510 (K) approval, Health Canada approval and CE certification for some of the products. Because of excellent quality, such as good reproducibility and specificity, high sensitivity and easy operation, and competitive price, they are favored by customers from the United States, Europe, Africa, Middle East, Asia, South America, South Asia and other international markets.
We are committed to providing people with products and services of outstanding quality, thus making their lives easier and more convenient.
About Our Factory & Business Background
-
Business Type
- Manufacturer/Factory & Trading Company
- Address
- Rongsheng Technological Zone, University Road, Shantou, Guangdong, China
-
Plant Area
- 16245 square meters
-
Number of Employees
- 543
-
Registered Capital
- 60,000,000 RMB
-
Terms of Payment
- T/T, Small-amount payment
-
International Commercial Terms(Incoterms)
- FOB, CIF, CFR, EXW
-
Average Lead Time
- Peak Season Lead Time, one month, Off Season Lead Time, within 15 workdays
-
Nearest Port
- Shantou Port, Shenzhen Port
-
Minimum Order Quantity
- 1000 PCS
-
Supply Chain Partners
- 20
Our Production Capability & Technical Expertise
-
Main Products
- HCG Pregnancy Test, Lh Ovulation Test, Fsh Test, Male Sperm Test, Drug Test, HIV Test, HCV Test, HBV Test
-
Production Lines
- 3
-
Production Machines
- Automatic Packaging Facility
-
Inspection Type for Finished Products
- Random inspection Visual inspection Function inspection
-
Inspection Method for Finished Products
- Have instructions and uniformly followed
-
Customization Options
- Customization from Samples,Customization from Designs,Full Customization,Minor Customization,Flexible customization
-
ODM Service Available
- Yes
-
OEM Service Available
- Yes
-
R&D Engineers
- 22 people
-
Traceability of Raw Materials
- Yes
-
Own Brand
- Yes
Our Industry Experience & Global Business Record
-
Year of Establishment
- 2001-04-30
-
Export Year
- 20 years
-
Main Markets
- Southeast Asia/ Mideast
-
Repeat Buyers Choice
- 50%~80%
-
Number of Foreign Trading Staff
- 8
-
Overseas Agent/Branch
- No
Our Certifications, Standards & Industry Recognition
-
Management System Certification
- ISO9001:2015
-
Cooperated with Fortune 500
- No
FAQ
- What types of specimens can be tested?
- The test supports Serum, Plasma, and Whole Blood specimens.
- How long is the shelf life of the test?
- The shelf life is 2 Years.
- What formats are available for this test?
- The test is available in Strip and Cassette formats.
- Can the product be customized?
- Yes, we offer Full Customization, Minor Customization, and Flexible customization based on samples or designs.
- What is the lead time for orders?
- Off-peak lead time is within 15 workdays, while peak season lead time is one month.
- Is the manufacturer certified?
- Yes, the company holds ISO9001:2015 certification.
- What payment terms are accepted?
- We accept T/T and Small-amount payment.
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