Product Details:
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Power Source: | Manual | Validity Period: | 24 Monthes |
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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: | immunoassay colloidal gold antigen test,FDA Non Invasive colloidal gold antigen test,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:
Detailed explanation of test results:
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 Person: Ms. Carina
Fax: 86-755-89366646