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SARS-CoV-2 Antigen Rapid Test Kits

China Shenzhen Poweray Biotechnology Co., Ltd. certification
China Shenzhen Poweray Biotechnology Co., Ltd. certification
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SARS-CoV-2 Antigen Rapid Test Kits

SARS-CoV-2 Antigen Rapid Test Kits
SARS-CoV-2 Antigen Rapid Test Kits SARS-CoV-2 Antigen Rapid Test Kits SARS-CoV-2 Antigen Rapid Test Kits SARS-CoV-2 Antigen Rapid Test Kits

Large Image :  SARS-CoV-2 Antigen Rapid 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

SARS-CoV-2 Antigen Rapid Test Kits

Technology: Colloidal Gold Usage: Infections Disease Rapid Test Kit
Test Time: 15 Minutes Storage Condition: 2-30℃
Shelf Life: 2 Years Service: OEM Or ODM
High Light:

Antigen Rapid Test Kits Novel Coronavirus


Antigen Rapid Test Kits SARS-CoV-2

Product description:Novel Coronavirus(SARS-CoV-2) Antigen Test

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



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


Storage Conditions and Validity:
Keep it at 2℃~30℃, and the validity period is tentatively set at 24 months.
Aluminum foil bag is svalid for 4 hour
Production lot number:see details label
For more information:see label


Product details:


SARS-CoV-2 Antigen Rapid Test Kits 0

Product performance indicator:
The coronavirus(Covid-19) antigen detection kit was used to detect 60 positive cases with a sensitivity of 95% of 170 negative specimens tested with the Covid-19 antigen detectior kit,168 were negative,with a specificity of 99.1%


Inspection 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:

SARS-CoV-2 Antigen Rapid Test Kits 1

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.


If any query,pls contact Grace by,mobile/wechat:13310839332




Contact Details
Shenzhen Poweray Biotechnology Co., Ltd.

Contact Person: Ms. Carina

Fax: 86-755-89366646

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