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Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits

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China Shenzhen Poweray Biotechnology Co., Ltd. certification
China Shenzhen Poweray Biotechnology Co., Ltd. certification
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Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits

Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits
Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits

Large Image :  Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits

Product Details:
Place of Origin: Shenzhen,China
Brand Name: POWERAY
Certification: CE,ISO 13485, SGS ,FDA certs
Model Number: PW-001
Payment & Shipping Terms:
Minimum Order Quantity: 1000tests
Price: US$0.5-US$0.9/test
Packaging Details: 1/5/25/50 test/box 50boxes/carton
Delivery Time: 2-7 days
Payment Terms: T/T, Western Union, MoneyGram
Supply Ability: 5000000kits/week

Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits

Description
Power Source: Manual Validity Period: 24 Monthes
Test Time: 15 Minutes Storage Condition: 2-30℃
Usage: Infections Disease Rapid Test Product Feature: High Accuracy,Results In 15 Minutes,easy To Use,no Equipment Required
High Light:

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FDA Non Invasive Covid 19 Test Kits

Product description:Non Invasive Colloidal Gold Antigen Rapid Test Kit CE Certification

Antigen Rapid Test Kit is faster and less intrusive than a Polymerase Chain Reaction(PCR)test.This makess it easy for the public to use to test themselves if needed.In general,Antigen Rapid Test Kid has a sensitivity(ability of a test to identify patients with the disease)of about 95% for cases with higher viral loads and a specificity(ability of a test to identify patients without the disease)range of 99.1%.As the sensitivity and specificity of Antigen Rapid Test Kit are lower as compared to PCR tests,if you test Antigen Rapid test Kit positive or invalid twice,you will need to follow up with a confirmatory PCR test.You should not repeat the Antigen Rapid Test Kit.Even if you do test negative in the repeated test,it may be a false negative result and hence you need to go for a confirmatory PCR test.Poweray Antigen Rapid Test Kits has good performance and with high sensitivity to detect the antigen at the early stage of infection.High performance rapid test enable immediate treatment or isolation measures to minimize transmission

 

Product usage:

This kit is used for vitro qualitative detection of coronavirus(Covid-19) in human pharyngeal or nasal secretions,sailva samples.

Used as a supplementary test indicator for suspected cases of new coronavirus nucleic acid test negative or used in conjunction with nucleic acid testing in the diagnosis of suspected cases

 

Test procedure:

  • Remove the foil from the top of the extraction buffer tube
  • Open the swab package at the stick end
  • Gently insert the swab into the nostril and the tip of the swab should be inserted 1/2-3/4 inch away from the edge of the nostril
  • Roll the swab along the mucous membrane inside the nostril 5 times,taking about 15 seconds to collect the speciman
  • Insert the sampling swab into the sample buffer
  • Swirl the tube for 30 seconds
  • Rotate the swab 5 times while squeezing the tube
  • Remove the swab while squeezing the tube
  • Cover the emitter
  • Add 2 drops to extract the treated sample to the loading well of the test card and then start the timer
  • Leave at room temperature for 15 minutes before reading the results.The result will be invalid after 20 minutes

Detailed explanation of test results:

 

Non Invasive Immunoassay Colloidal Gold Antigen Test Covid 19 Test Kits 0

Limitation of test method:
1. This product is used for qualitative testing and only for in vitro assisted diagnosis.
2.This product applies for nose samples. Other sample type results may be inaccurate or invalid.
3. appropriately adds samples for testing. Too large or too small sample size may lead to inaccurate results.
4.It should not be the sole basis for clinical trials and treatment. The final diagnosis can be made after a comprehensive evaluation of all clinical

and experimental results.

 

Company profile:

shenzhen Poweray Biotechnology CO.,LTD. is a new high-tech enterprise, professionalcomitted to the field of biomedicine in vitro diagnostic reagent industry POCT product perservation solution,sample diluent,and the virus nucleic acid extract of research and development,production and sales of the national high-tech enterprises,production managment in strict accordance with the international quality maanagement system operation,ensure the high quality of product.Adhering to the enterprise spirit of precision,excellence,integrity and serving the people,and aiming at serving human health with science and technology,the company bases itself on advanced technologies and transformation of research achievements,especially POCT in the fields of hBA1c detection and specific protein detection,and cooperates with domestic universities in research and development ,thus breaking a number of international monopoly technologies.

 

 

 

 

Contact Details
Shenzhen Poweray Biotechnology Co., Ltd.

Contact Person: Ms. Carina

Fax: 86-755-89366646

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