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Biovantion Inc.

  • China,Beijing ,Beijing
  • Verified Supplier

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China One Step Test DENGUE NS1-IgM/IgG Whole Rapid Test For medical use
China One Step Test DENGUE NS1-IgM/IgG Whole Rapid Test For medical use

  1. China One Step Test DENGUE NS1-IgM/IgG Whole Rapid Test For medical use
  2. China One Step Test DENGUE NS1-IgM/IgG Whole Rapid Test For medical use

One Step Test DENGUE NS1-IgM/IgG Whole Rapid Test For medical use

  1. MOQ: 1500 Box
  2. Price: Discussible
  3. Get Latest Price
Payment Terms L/C, D/A, D/P, T/T, Western Union, MoneyGram
Supply Ability 1000000 Box/carton
Delivery Time 4-7 days
Packaging Details carton/box
Test Time 5-20 miuntes
Packaging Specifications 25 Test/Kit
Brand BIOVANTION
Exp two years
Storage Normal temperature(2℃-30℃)
Specimen Whole blood, serum, plasma,
Assification class1
Test Method Colloidal Gold
Brand Name BIOVANTION
Model Number TY0023
Certification ISO 13485
Place of Origin CHINA

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  1. Product Details
  2. Company Details

Product Specification

Payment Terms L/C, D/A, D/P, T/T, Western Union, MoneyGram Supply Ability 1000000 Box/carton
Delivery Time 4-7 days Packaging Details carton/box
Test Time 5-20 miuntes Packaging Specifications 25 Test/Kit
Brand BIOVANTION Exp two years
Storage Normal temperature(2℃-30℃) Specimen Whole blood, serum, plasma,
Assification class1 Test Method Colloidal Gold
Brand Name BIOVANTION Model Number TY0023
Certification ISO 13485 Place of Origin CHINA
High Light Colloidal Gold TestColloidal Gold Antigen TestAntigen Test Kit Colloidal Gold

                                                   One Step H. Pylori Test Device (Serum/Plasma)

INTENDED USE

  The Dengue Ag NS1-IgM/ IgG rapid test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG anti– dengue virus, IgM anti-dengue virus and dengue antigen (Dengue Ag) in human serum, plasma or whole blood. It is intended to be used by professionals as a screening test and as an aid in the diagnosis of infection with dengue virus. Any reactive specimen with the Dengue Ag NS1-IgM/ IgG rapid test must be confirmed with alternative testing method(s).

 

Product details Description
Test Time 5-20 miuntes
Packaging Specifications 25 Test/Kit
Exp two years
Manufacturer BIOVANTION
Preservation method Normal temperature
Assification Class1
Package carton/box
Sample Type Pharyngeal

Features of H. Pylori Ag Reply test

1. Sensitive
2. Accurate

3. High quality
4. Economic price

5. Reliable and Easy to Use

 

PRECAUTIONS

1) For in vitro diagnostic use and professional use only.

2) Read the package insert instruction before use the kit.

3) Do not use beyond the expiration date which appears on the package label.

4) Do not open the sealed pouch, unless ready to conduct the assay.

5) Bring all reagents to room temperature (15°C-30°C) before use.

6) Do not use the components in any other type of test kit as a substitute for the components in this kit.

7) Haemolized blood may be used for the testing, but do not take precipitants.

8) Wear protective clothing and disposable gloves while assaying samples. Wash hands thoroughly after performing the test.

9) Handle all specimens as if they contain infectious agents. When the assay procedure is completed, dispose of specimens carefully after autoclaving them for at least one hour. Alternatively, they can be treated with 0.5 to 1% solution of sodium hypochlorite for one hour before disposal.

10) Do not smoke, drink, or eat in areas where specimens or kit reagents are being handled.

 

11) Wear protective clothing and disposable gloves while assaying samples. Wash hands thoroughly after performing the test.

12) Handle all specimens as if they contain infectious agents. When the assay procedure is completed, dispose of specimens carefully after autoclaving them for at least one hour. Alternatively, they can be treated with 0.5 to 1% solution of sodium hypochlorite for one hour before disposal.

13) Do not smoke, drink, or eat in areas where specimens or kit reagents are being handled.

11) Read result after 30 minutes may give erroneous results.

12) Do not perform the test in a room with strong air flow, ie. an electric fan or strong air- conditioning.

13) As with all diagnostic tests, a definitive clinical diagnosis should not be based on the results of a single test, but should only be made by the physician after all clinical and laboratory findings have been evaluated.

14) Excess sample volume (>5µL) can give false positives.

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Biovantion Inc is independent from international department of Bioneovan Co., Ltd., which established in 2 0 0 5, is an in vitro diagnostic reagents manufacturer engaged in the research, development, production, and focus on clinical testing for infectious diseases, such as Hepatitis virus, Noro vir... Biovantion Inc is independent from international department of Bioneovan Co., Ltd., which established in 2 0 0 5, is an in vitro diagnostic reagents manufacturer engaged in the research, development, production, and focus on clinical testing for infectious diseases, such as Hepatitis virus, Noro vir...

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  • Biovantion Inc.
  • Room230/232, Building 1, No.538 YongfengTun, Haidian District, Beijing
  • https://www.biovantion.com/

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