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CoV-19 Antigen Detection Kit 25PCS One Step Rapid Test Kit High Sensitivity

Categories	Rapid Antigen Self Test
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:	CoV-19 Antigen Rapid Test Kit Safe Reliable 15 Min Antigen Self Test Kit 5PCS Self Testing
OEM:	OEM customized packing avaliable
Formats:	25T/box 1T/box
Sample:	Swab

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Hangzhou Aichek Medical Technology Co.,Ltd

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CoV-19 Antigen Detection Kit 25PCS One Step Rapid Test Kit High Sensitivity

High Sensitivity CoV-19 Antigen Detection Kit 25PCS One Step Rapid Test Kit

Product Name	High Sensitivity CoV-19 Antigen Detection Kit 25PCS One Step Rapid 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.

[INTERPRETATION OF RESULTS]

POSITIVE RESULT: Two colored bands appear on the membrane. One bland appears in the control region (C) and another band appears in the

test region (T).

NEGATIVE RESULT: Only one colored band appears in the control region (C). No apparent colored band appears in the test region (T).

INVALID RESULT: Control band fails to appear. Results from any test which has not produced a control band at the specified reading time

must be discarded. Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and

contact your local distributor.

[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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