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50 Strips Antigen Rapid Test Device Saliva Detection Kit ISO13485

Hangzhou Aichek Medical Technology Co.,Ltd
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Address: 3rd Floor, Building 9, Hexiang Technology Center, Xiasha Street, Qiantang District, 310018 Hangzhou, Zhejiang, P.R. China

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Hangzhou Aichek Medical Technology Co.,Ltd

50 Strips Antigen Rapid Test Device Saliva Detection Kit ISO13485

Country/Region china
City & Province hangzhou zhejiang
Categories Dyestuff Intermediates
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Product Details

Rapid Antigen Detection kit for healthcare professionals and home use

Product NameCOVID-19 antigen rapid test device
FormatsStrip(3mm)Device(4mm) Multi panel
Place of OrigenChina
SpecimenSaliva
Read Time15 minutes
Shelf life2 years
Package25 device/box or 50 strip/Box
Storage2℃-30℃

 

Q&A

What is a rapid diagnostic test?

The key difference between rapid tests and standard tests is how long they take to process results.

As the name suggests, rapid tests can produce fast results. Standard coronavirus tests typically use more complex, time-consuming methods and bulky equipment. Rapid tests are often simpler, allowing them to process samples faster.

The COVID-19 Antigen Rapid Test device is a lateral flow chromatographic immunoassay for the qualitative

detection of the nucleocapsid(N) protein antigen from SARS-CoV-2 in nasopharyngeal swab, oropharyngeal

swab. It provides an aid in the diagnosis of infection with 2019-nCOV.

 

Components Quantity

1

test/kit

25

test/kit

50

test/kit

Test Cassette12550
Extraction tube with extraction buffer12550
Disposable sterile Swab12550
Packing insert111

 

 

 

 

[WARNINGS AND PRECAUTIONS]
l For in vitro diagnostic use only.
l For healthcare professionals and professionals at point of care sites.
l Do not use after the expiration date.
l Please read all the information in this manual before performing the test.
l The test device should remain in the sealed pouch until use.
l All specimens should be considered potentially hazardous and handled in the same manner as an infectious agent. Wear gloves

ifneed, don’t touch the membrane.
l The used test device should be discarded according to federal, state and local regulations.
l The test is intended to be read at 15 minutes. If the test is read before 15 minutes or after 20 minutes, false negative or false positive

results may occur, and the test should be repeated with a new test cassette.
l The test device is a disposable product. Please dispose properly after use.

 

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