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FDA Approved Medical Antibody Fast Detection Kit Immunoassay

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FDA Approved Medical Antibody Fast Detection Kit Immunoassay

FDA Approved Medical Antibody Fast Detection Kit Immunoassay
FDA Approved Medical Antibody Fast Detection Kit Immunoassay FDA Approved Medical Antibody Fast Detection Kit Immunoassay FDA Approved Medical Antibody Fast Detection Kit Immunoassay FDA Approved Medical Antibody Fast Detection Kit Immunoassay

Large Image :  FDA Approved Medical Antibody Fast Detection Kit Immunoassay

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

FDA Approved Medical Antibody Fast Detection Kit Immunoassay

Description
Technology: Colloidal Gold Usage: Infections Disease Rapid Test Kit
Reaction Time: 15 Minutes Leadtime: 2-7 Working Days
Warranty: 24 Monthes Service: OEM Or ODM
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Product description:Medical Rapid Antigen Test Kit Colloidal Gold FDA approved

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

 

Intended use:

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

 

Main components:

The kit consists of test cards, sample buffer, and SWAB.
Test card: composed of aluminum foil bag, desiccant, test strip and plastic card. Test sheet consists of absorbent paper, nitrocellulose film, test pad, adhesive pad and rubber sheet. t line covering nitrocellulose film with 2019 nvvab (test line), c with goat-mouse polyclonal ab (quality management line) and 2019 nvvab. on the pad
Sample buffer: phosphate, sodium nitride, etc.

 

Test steps:

  • 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:

 

FDA Approved Medical Antibody Fast Detection Kit Immunoassay 0

 

 

 

 

Contact Details
Shenzhen Poweray Biotechnology Co., Ltd.

Contact Person: Ms. Carina

Fax: 86-755-89366646

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