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CE 99.05% Rapid Antigen Self Test 1pc Lateral Flow Antigen Test Kit

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COVID19 Rapid Test Kit [30]
Antigen Rapid Test Kit [26]
Antibody Rapid Test Kit [40]
Infectious Disease Rapid Test Kits [22]
Neutralizing Antibody Rapid Test [20]
Rapid Antigen Self Test [24]
Saliva Antigen Rapid Test [16]
Swab Antigen Rapid Test [26]
Home Rapid Antigen Test [24]
HCG Pregnancy Rapid Test [8]
Fertility Rapid Test [6]
DOA Rapid Test [43]
LFT Lateral Flow Test [24]
Uncut Sheet Rapid Test [101]
IVD In Vitro Diagnostic [8]

Hangzhou Aichek Medical Technology Co.,Ltd

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CE 99.05% Rapid Antigen Self Test 1pc Lateral Flow Antigen Test Kit

Name: CE 9905 Rapid Antigen Self Test 1pc Lateral Flow Antigen Test Kit
Brand: Aichek
Price: 1 USD

Brand Name : Aichek

Model Number : COVID-19-G02001A

Certification : CE

Place of Origin : China

MOQ : 5000 Test

Price : negotiable

Payment Terms : T/T

Supply Ability : negotiable

Packaging Details : 40box/carton

Storage : 2℃-30℃

User : Professional

Accuracy : 99.05% (95% CI: 97.58%~99.63%)

Certificate : CE ISO 13485

Key words : Selftest COV-19 Rapid Lateral Flow Antigen Test Kit , Ce Approval Rapid Antigen Kit Test

OEM : OEM customized packing avaliable

Formats : 25T/box 1T/box

Sample : Swab

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Selftest COV-19 Rapid Lateral Flow Antigen Test Kit ,

Ce Approval Rapid Antigen Kit Test

Product Name	Selftest COV-19 Rapid Lateral Flow Antigen Test Kit
Formats	Device(4mm)
Place of Origen	China
Specimen	Swab
Read Time	15 minutes
Shelf life	2 years
Package	25 device/box or 1Test/Box
Storage	2℃-30℃

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.

[QUALITY CONTROL]

A procedural control is included in the test. A colored line appearing in the control region (C) is considered an internal procedural control. It confirms sufficient specimen volume, adequate membrane wicking and correct procedural technique.Control standards are not supplied with this kit. However, it is recommended that positive and negative controls be tested as good laboratory practice to confirm the test procedure and to verify propertest performance.

[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.

CE 99.05% Rapid Antigen Self Test 1pc Lateral Flow Antigen Test Kit

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