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15 Minutes Whole Blood Ncp Atrips IGG IGM Virus Test Kits

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Address: No 57, Sicence Avenue, Zhengzhou, China

Contact name:Cara

Zhengzhou Linker Medical Equipment Co., Ltd.

15 Minutes Whole Blood Ncp Atrips IGG IGM Virus Test Kits

Country/Region	china
City & Province	zhengzhou henan
Categories	Laser Pointers

Product Details

High Accuracy Ncp Atrips COVID-19 Corona Virus Antibody Rapid Test IGG IGM CE FDA CDC Test

Name	COVID-19 Test Kit
Certification	CDC,CE,ISO,FDA
Storage	Keep in a dry place away from light.
Test Kit	Do not freeze
Expiry date:	24 months.
Stored Temperature	4-30°C

Product Feature:

1. The specimen: serum, plasma, whole blood;
2. Rapid screening for coronavirus infection within 15 minutes;
3. Equipment is not required, suitable for all kinds of field screening;
4. Reduce the risk of sampling infection;
5. Early diagnosis, early treatment, shorten the course of disease;
6. The kit is transported and stored at room temperature;
7. Reduce the workload of epidemic situation designated hospitals;

Intended Use

COVID-19(SARS-CoV-2)IgG/IgM Test is used for qualitative detection of novel coronavirus IgG/IgM antibodies in human serum, plasma and whole blood. After infection with the novel coronavirus, the common signs include respiratory symptoms, fever, cough, wheezing and dyspnea, etc. In more severe cases, the infection can lead to pneumonia, severe acute respiratory syndrome, kidney failure and even death. Coronaviruses can be expelled from the body through respiratory secretions, transmitted by oral fluids, sneezing, contact, and by airborne droplets.

Warnings and precautions

1. For in vitro diagnostic use only. Operation should be carried out in strict accordance with the instructions, do not use expired or damaged products.

2. Only the diluent in the package can be used, and diluent in different batches cannot be mixed.

3. Do not use tap water, purified water and distilled water as negative controls.

4. The test device should be used within 1 hour after unsealing. If the ambient temperature is higher than 30°C or more humid, use immediately after tearing.

5. If there is no liquid migration in the test window within 30 seconds after adding the detection solution, add another 1 drop of detection solution.

6. Pay attention to the possibility of virus infection when collecting specimens, wear disposable gloves, masks, etc., after washing hands.

7. The test device is disposable. The test device and specimen after use shall be regarded as medical waste with biological infection risk and properly disposed of according to relevant national regulations.

Interpretation of Result

Positive:1. Two or three distinct lines appear. One line should always appear in the control line region (C), and

another one or two apparent colored line(s) should appear in the test line region(s) (T1 and T2).

2. If a line appears on the quality control line, a line appears on the test line T1, and no sline appears on the test line

T2, it indicates that IgG antibody is present in the sample and no IgM antibody is present.

3. If a line appears on the quality control line, a line appears on the test line T2, and no sline appears on the test line

T1, it indicates that IgM antibody is present in the sample and no IgG antibody is present.

Negative: One colored line appears in the control region (C). No Apparent colored lines appear in the test lines

regions (T1 and T2).

Invalid: Control line(C) fails to appear. Insufficient specimen volume or incorrect procedural technologies are the

most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the

problem persists, discontinue using the test kit immediately and contact your local distributor.

Note: The red line in the test line (T) can show different shades of color. However, even a very weak line

should be judged as a positive result during the specified observation period, regardless of the color of the

line

Specimen:

COVID-19(SARS-CoV-2) IgM Test can be performed used on Whole Blood/ Serum/ Plasma.
Testing should be performed immediately after specimen collection.
Use only clear non-hemolyzed specimens.