Hangzhou Aichek Medical Technology Co.,Ltd

Hangzhou Aichek Medical Technology Co.,Ltd

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

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Hangzhou Aichek Medical Technology Co.,Ltd
City:hangzhou
Province/State:zhejiang
Country/Region:china
Contact Person:MrEdward YU
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CE 99.05% Rapid Antigen Self Test 1pc Lateral Flow Antigen Test Kit

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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

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

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