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Korea's K-Disaster-SD Biosensor COVID-19 Self-diagnosis Kit 1 Set

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Korea's K-Disaster-SD Biosensor COVID-19 Self-diagnosis Kit 1 Set


STANDARD Q COVID-19 Ag, Home Test SD biosensor corona self-diagnosis test STANDARD Q COVID-19

COVID-19 nasal examination | 15 minutes to see the results.

Two COVID-19 self-tests / 15 minutes of reading.

| STEP 1

Prepare for inspection "Please be aware of the instructions before the inspection."

| 1

Wash your hands thoroughly before the examination.

| | | | Wear disposable plastic gloves when using the product.

Make sure to check the components before inspection.

Inspection device.

Solution container & nozzle cap.

Sterilized cotton swab | Instructions for Use

& Quick guide.

Check the validity period printed on the back of the inspection device bag. We do not use expired devices. Open the pouch to check the color label of the inspection device and desiccant.

Open the solution container & nozzle cap envelope, and take off the lid of the solution container.

Place the solution in the container of the package.

Open the sterilized cotton swab and take it out.

Be careful not to touch the head of the cotton swab.

Put a sterile cotton swab up to about 1.5 cm in both nostrils and rub it more than 10 times.

Put the enclosed sample collection tool (cotton swab) in the nasal cavity (nose) | | Do not soak it in sample extract or other liquid until |.

STEP 3 test process.

Put the cotton swab taken out of the nose into the solution container, stir it more than 10 times, squeeze the cotton swab out of the solution container.

1. Do not allow the solution to come into contact with or swallow your eyes. 2. Avoid direct contact with the solution to the wound.

Press the nozzle cap to close it.

Drop 4 drops on the specimen drip area of the test device.

Do not squeeze all the solution in the solution container.

Read the results after 15 minutes.

' Step 4. Interpret the results.

If only the control line (C line) appears,

C

T

This means that no antigen of the COVID-19 virus was found in the sample, but if you have symptoms related to COVID-19 or are epidemiological, visit a medical institution for PCR testing.

ct

When both the control line (C line) and the test line (T line) appear,

|

| ..

CT

The antigen of the COVID-19 virus has been found in the sample, which means you may have been infected with COVID-19, so be sure to visit a medical institution for PCR testing.

ct

If the invalid control line (C line) does not appear in the result window, it is an invalid result. Re-test with new samples and devices.

CT 14 /

* The results of this examination, clinical findings, and other clinical findings by a medical specialist.

It should be diagnosed based on the results. * Even if the line is faint, the line is considered to exist.


After the inspection, put all the components used in the plastic bag and discard them.

Item Name Infected Body Diagnosis Immunization Reagent

Name of the product

Model name.

STANDARDTM Q COVID-19 Ag Home Test STANDARD Q COVID-19 Ag Home Test (Q-NCOV-03G) In vitro No. 21-322

Permission number.

Purpose of use | COVID-19 by immunochromatography in nasal smear samples by individuals with respiratory infection symptoms.

It is an in vitro diagnostic medical device used as an aid in testing the presence of viral antigens. Component 1 Inspection Device X2, Solution Container & Nozzle Cap X2, Sterilized Cotton Rod X2, User Manual & Quick Guide X1

※ If you have respiratory symptoms or suspect infection, the PCR test must be performed first, and this test cannot replace the PCR test.

K-Disaster-SD Biosensor Korea EXCADE-19 Self-diagnosis Kit 1 Set


STANDAR Q EXCADE-19 Ag, Home Test SD biosensor corona self-diagnosis test STANDAR Q EXCADE-19

Pemeriksaan hidung MARKASE-19 15 15 menit untuk melihat hasilnya.

Dua tes mandiri EXCADE-19 15 menit membaca.

step Langkah 1

Bersiaplah untuk pemeriksaan " Harap berhati-hati instruksi sebelum pemeriksaan."

| 1

Cuci tangan Anda secara menyeluruh sebelum pemeriksaan.

| | | wear Kenakan sarung tangan plastik sekali pakai ketika menggunakan produk.

Pastikan untuk memeriksa komponen sebelum pemeriksaan.

Alat pemeriksaan.

Solusi kontainer & tutup nozzle.

Swab kapas yang disterilkan instruct Instruksi Penggunaan

& Panduan cepat.

Periksa masa berlaku yang dicetak di bagian belakang tas perangkat inspeksi. Kami tidak menggunakan perangkat kadaluarsa. Buka kantongnya untuk memeriksa label warna alat pemeriksaan dan pengering.

Buka wadah larutan & nozzle tutup amplop, dan buka tutup wadah larutan.

Tempatkan solusi dalam wadah paket.

Buka kapas sterilisasi dan keluarkan.

Hati-hati untuk tidak menyentuh kepala kapas swab.

Masukkan kapas steril hingga 1,5 cm di kedua lubang hidung dan gosokkan lebih dari 10 kali.

Masukkan alat pengumpulan sampel tertutup (swab kapas) ke dalam rongga hidung (hidung) | do Jangan merendamnya dalam ekstrak sampel atau cairan lain sampai put.

Langkah 3 proses tes.

Masukkan kapas yang diambil dari hidung ke dalam wadah larutan, aduk lebih dari 10 kali, peras kapas keluar dari wadah larutan.

1. Jangan biarkan solusi untuk datang ke kontak dengan atau menelan mata Anda. 2. Hindari kontak langsung dengan solusi untuk luka.

Tekan tutup nozzle untuk menutupnya.

Teteskan 4 tetes pada area tetesan spesimen alat tes.

Jangan memeras semua larutan dalam wadah larutan.

Baca hasilnya setelah 15 menit.

' Langkah 4. Interpretasikan hasilnya.

Jika hanya baris kontrol (garis C) muncul,

( Untuk keterangan lengkap, lihat publikasinya)

{\fnCandara\fs60\b1\4cH000000\4aH80}T-aku...

Ini berarti bahwa tidak ada antigen dari virus EXCADE-19 ditemukan dalam sampel, tetapi jika Anda memiliki gejala yang berhubungan dengan EXCADE-19 atau epidemiologi, kunjungi institusi medis untuk pengujian PCR.

( Untuk keterangan lengkap, lihat publikasinya)

Ketika kedua baris kontrol (garis C) dan baris tes (garis T) muncul,

|

| ..

( Untuk keterangan lengkap, lihat publikasinya)

Antigen dari virus EXCADE-19 telah ditemukan dalam sampel, yang berarti Anda mungkin telah terinfeksi dengan EXCADE-19, jadi pastikan untuk mengunjungi institusi medis untuk pengujian PCR.

( Untuk keterangan lengkap, lihat publikasinya)

Bila baris kontrol (baris C) tidak valid tidak muncul di jendela hasil, ini adalah hasil yang tidak valid. Uji ulang dengan sampel dan perangkat baru.

( Untuk keterangan lengkap, lihat publikasinya)

* Hasil pemeriksaan ini, temuan klinis, dan temuan klinis lainnya oleh seorang spesialis medis.

Ini harus didiagnosis berdasarkan hasil. * Bahkan jika garisnya samar, garis itu dianggap ada.


Setelah pemeriksaan, masukkan semua komponen yang digunakan dalam kantong plastik dan buang.

Nama Barang Diagnosis Tubuh Terinfeksi Reagen Imunisasi

Nama produknya

Nama model.

STANDARTM Q ENGKIRO-19 Ag Home Test STANDAR Q ENGKIRO-19 Ag Home Test (Q-NCOV-03G) In vitro No. 21-322

Nomor izin.

Tujuan penggunaan covid EXCADE-19 oleh imunokromatografi dalam sampel nasal smear oleh individu dengan gejala infeksi pernapasan.

Ini adalah perangkat medis diagnostik in vitro yang digunakan sebagai bantuan dalam menguji adanya antigen virus. Perangkat Inspeksi Komponen 1 X2, Kontainer Solusi & Nozzle Cap X2, Batang Kapas Disterilkan X2, Panduan Pengguna & Panduan Cepat X1

if Jika Anda memiliki gejala pernapasan atau infeksi tersangka, tes PCR harus dilakukan terlebih dahulu, dan tes ini tidak dapat menggantikan tes PCR.

韩国K-Disaster-SD生物传感器COVID-19自我诊断工具1套


Standard Q COVID-19Ag,家庭测试SD生物传感器电晕自诊断测试Standard Q COVID-19

COVID-19鼻腔检查15分钟见结果。

COVID-19自我测试2次/阅读15分钟。

| 步骤1

检查准备:"检查前请注意指示。"

| 1

考试前请彻底洗手。

||||使用产品时请戴上一次性塑料手套。

检查前请务必确认组件。

检查装置。

溶液容器和喷嘴盖。

灭菌棉签| 使用说明书

& 快速指南。

确认检查装置袋背面的有效期限。 不使用过期的设备。 打开化妆包,确认检查装置和干燥剂的颜色标签。

打开溶液容器和喷嘴盖信封,取下溶液容器的盖子。

将溶液放入包装的容器中。

打开灭菌棉签取出。

请注意不要碰棉签头。

在鼻孔两侧放入约1.5cm的无菌棉签,揉搓10次以上。

将附带的样品采集工具(棉签)放入鼻腔(鼻子)|||之前请勿浸渍在样品提取物或其他液体中。

步骤3的测试过程。

将从鼻子里取出的棉签放入溶液容器中,搅拌10次以上,从溶液容器中挤出棉签。

1.不要让溶液接触眼睛或吞咽。2. 避免直接接触伤口的溶液。

按下喷嘴盖关闭。

在试验装置的试样滴下4滴。

请勿挤压溶液容器内的所有溶液。

15分钟后读取结果。

第四步。 解释结果。

仅显示控制线(C线)时,

T恤

也就是说,虽然在样本中未发现COVID-19病毒抗原,但如果出现与COVID-19相关的症状或流行病学症状,请前往医疗机构进行PCR检查。

动作

控制线(C线)和测试线(T线)同时显示时,

|

| ..

CT技术

在样本中检测到COVID-19病毒抗原,因此可能感染了COVID-19,因此请务必到医疗机构进行PCR检查。

动作

如果结果窗口中未显示无效的控制行 (C行 ),则为无效的结果。 使用新的样本和设备重新测试。

CT14/

* 本检查结果、临床所见及其他医学专家的临床所见。

应该根据结果进行诊断。 ※ 即使线路模糊,也视为存在线路。


检查完毕后,将使用的零件全部放入塑料袋中废弃。

品名感染体诊断免疫试剂

产品名称

型号。

StandardTMQCOVID-19AgHomeTestStandardQCOVID-19AgHomeTest(Q-NCOV-03G)体外编号21-322

许可编号。

使用目的 | COVID-19的鼻涂片标本免疫层析法,对呼吸道感染症状患者进行鼻涂片标本免疫层析。

是用于病毒抗原存在检查的辅助体外诊断医疗器械。 组件 1检查装置 X2、溶液容器 X2、喷嘴盖 X2、灭菌棉棒 X2、使用说明书 X1

※ 发生呼吸道症状或怀疑感染时,请先进行PCR检查,无法代替PCR检查。

 

 

 

 

 

 

 

 

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