PEI/Bfarm listed COVID 19 Self Test Antigen Test Kit

Short Description:

Used For COVID 19 Antigen Self Test Kit
Specimen Nasal Swab or Saliva
Certification CE/ISO13485/White List/PEI certified
MOQ 1000 test kits
Delivery time 1 week after Get payment
Packing 1 test kits/Packing box5 test kits/packig box20 test kits/packing box
Test Data Over 95% Sensitivity and Specificity
Shelf Life 2 years
Production Capacity 1 Million/Week
Payment T/T, Western Union, Paypal


Product Detail

Product Tags

PEI/Bfarm listed COVID 19 Self Test Antigen Test Kit

Used For COVID 19 Antigen Self Test Kit
Specimen Nasal Swab or Saliva
Certification CE/ISO13485/White List/PEI certified
MOQ 1000 test kits
Delivery time 1 week after Get payment
Packing 1 test kits/Packing box5 test kits/packig box20 test kits/packing box
Test Data Over 95% Sensitivity and Specificity
Shelf Life 2 years
Production Capacity 1 Million/Week
Payment T/T, Western Union, Paypal

Antigen self test

SHORT INTRODUCTION

Rapid detection of SARS-CoV-2 antigen is a method of detecting SARS-CoV-2 antigen. The anti-SARS-CoV-2 monoclonal antibody package was placed on the test line and bound to colloidal gold. During the test process, the sample reacted with the anti-SARS-CoV-2 antibody binding in the test paper. The mixture then moves upward on the membrane through capillary action and reacts with another anti-SARS-CoV-2 monoclonal antibody in the test area. The complex is captured and forms a color line in the test line area. The SARS-CoV-2 antigen rapid detection contains anti-SARS-CoV-2 monoclonal antibody binding particles, and another anti-SARS-CoV-2 monoclonal antibody packet is placed in the detection line region. 

Features

A. High Sensitivity and Specificity

B. Available for professional and self test

C. PEI/ Befarm listed

D. Fast delivery 

Antigen self test 5pcs packing

Authorized certifications

1.CE/ISO13485

2.White List

3.PEI/Bfarm Listed

4.ANMAT Authorization 

 dfs

PRECAUTIONS FOR USE

- For in vitro diagnostic use only. Do not use after expiration date.

- The Test strip should remain in the sealed pouch until use.

- Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout the procedure and follow the standard procedures for proper disposal of specimens.

- The used Test Strip should be discarded according to national, state and local regulations.

- Humidity and temperature can adversely affect results.

SPECIMEN COLLECTION

covid self test

Test Method 

COVID SELF TEST KIT

INTERPRETATION OF RESULTS

- Positive (+): Two coloured lines appear. One coloured line should always appear in the control line region (C) and another line should be in the T line region.

*NOTE: The intensity of the colour in the test line regions may vary depending on the

concentration of SARS-CoV-2 present in the specimen. Therefore, any shade of

colour in the test line region should be considered positiveand recorded as such.

- Negative (-): One coloured line appears in the control line region (C). No line appears

in the T line region.

- Invalid: Control line fails to appear. Insufficient specimen volume or incorrect proce

dural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test.

If the problem persists, discontinue using the test kit immediately and contact your local distributor.

COVID Antigen self test

This self-test is a one-time in-vitro test for laypersons in a private environment. A POSITIVE result must be confirmed by a laboratory test. To do so, please contact your doctor or go to a screening centre.


  • Previous:
  • Next:

  • Write your message here and send it to us