Joinstar Antigen Rapid Test Cassette Swab Testing Kit with CE Certificate

• Type: Test Strips & Test Tube
• Material: Plastic
• Ethylene Oxide Sterilization: Ethylene Oxide Sterilization
• Group: Adult
• Logo Printing: Without Logo Printing
• Transport: Air
• Delivery Time: 2-5 Days
• Accuracy: 96%
• Quantity: 25 Test/Kit
• Transport Package: Carton
• Specification: 16x12x10cm
• Trademark: Joinstar
• Origin: China
• HS Code: 3002150090

Product Description

Joinstar AntigenTest Cassette  Rapid Test Kit

2021 new model  with CE certificate



General information

Brand: Joinstar

type: Antigen test kit
package: 25 tests per box, 800 tests per carton
Certificate:  CE
Payment:  100% T/T before shipment
Shipment by:  Air freight or express carrier.
Lead time: 3-7 days
MOQ: 1 carton



Test Procedure          
                                                               
Please read the instruction for use carefully before performing the test.
1.    Allow the device, buffer and specimen to equilibrate to room temperature (10ºC~30ºC) prior to testing.
2.    Remove a test cassette from the foil pouch by tearing at the notch and place it on a level surface.
3.    Transfer 10 μL of serum or plasma specimen with pipette or 1 drop (about 20 μL) of whole blood specimen with disposable dropper to the sample well (small well) and then add 2~3 drops (80 μL) of buffer solution to the buffer well (large well).
4.    As the test begins to work, you will see purple color move across the result window in the center of the test device.
5.    Wait for 15 minutes and read the results. Do not read results after 20 minutes.



RESULT INTERPRETATION    

Positive Result
Colored bands appear at both test line (T) and control line (C). It indicates a positive result for the  antibodies in the specimen.

Negative Result
Colored band appear at control line (C) only. It indicates that the
oncentration of the  antibodies is zero or below the detection limit of the test.

Invalid Result
No visible colored band appear at control line after performing the test. The directions may not have been followed correctly or the test may have deteriorated. It is recommended that the specime