Hangzhou Aichek Medical Technology Co.,Ltd

Hangzhou Aichek Medical Technology Co.,Ltd

Manufacturer from China
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25 Packs Home Rapid Antigen Test 99.05% Nucleic Acid Detection Test

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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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25 Packs Home Rapid Antigen Test 99.05% Nucleic Acid Detection Test

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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 :SARS-CoV-2 Antigen Rapid Test Kit 25 Tests Kit Simple Operate Professional Use
OEM :OEM customized packing avaliable
Formats :25T/box 1T/box
Sample :Swab
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Rapid Antigen Test Kit CoV-19 Antigen Rapid Test Kit 25 Tests Kit Simple Operate Professional Use

Product Name

Rapid Antigen Test Kit CoV-19 Antigen Rapid Test Kit 25 Tests Kit Simple Operate Professional Use

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.

PRECAUTIONS

  • For in vitro diagnostic use.
  • Use appropriate precautions in the collection, handling, storage, and disposal of patient samples and used test contents.
  • Use of Nitrile, Latex (or equivalent) gloves is recommended when handling patient samples.
  • Do not reuse the used Test Card or saliva swab.
  • Should never open the foil pouch of the Test Card exposing it to the ambient environment until the Test Card is ready for immediate use.
  • Discard and do not use any damaged or dropped Test Card or material.
  • Inadequate or inappropriate sample collection, storage, and transport may yield false test results.
  • Sample collection and handling procedures require specific training and guidance.
  • To obtain accurate results, do not use visually bloody or overly viscous samples.
  • To obtain accurate results, an opened and exposed Test Card should not be used.
  • Testing should be performed in an area with adequate ventilation.
  • Wear suitable protective clothing, gloves, and eye/face protection when handling the contents of this test.
  • Wash hands thoroughly after handling

25 Packs Home Rapid Antigen Test 99.05% Nucleic Acid Detection Test

25 Packs Home Rapid Antigen Test 99.05% Nucleic Acid Detection Test

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