Coronavirus 2019 Rapid Ag Test Kit Neutralizing Rapid Antibody Test Virus

The storage temperature is 2℃ ~ 30℃ and the validity period is 12 months.
The aluminum foil bag is valid for one hour.
Production Lot Number: Refer to the label for details.
Expiry date: Please see the label for details.

Sample Requirements

1. Collect serum, plasma or whole blood samples.
2. Sediment and plankton in the sample will affect the experimental results, so it needs to be removed by centrifugation.
3. Anti-coagulant: loofah anti-coagulant, EDA anti-coagulant, sodium citrate anti-coagulant are not obvious.
4. Blood collection by experts is needed. Serum/serum/plasma tests are recommended. In emergency or special circumstances, a patient's whole blood sample can also be used for rapid testing.
5. Serum and plasma samples should not be stored for more than 8 hours at room temperature.
It can be stored for 5 days at 2-8 ℃ and 6 months below -20℃, but please avoid repeated freezing and melting. Whole blood samples do not freeze and need to be stored at 2℃ to 8℃ for 48 hours.

Test Method

Please read the instructions carefully before testing. All reagents must be returned to room temperature prior to test. Tests must be carried out at room temperature.
1. Take the test card out of the box and use it within 1 hour.
2. Add 20L sample (serum, plasma or whole blood) to the filling hole of the test card, add 2 drops (~ 60L) of sample buffer memory and start timing.
3. After 10 to 15 minutes of reaction at room temperature, read the results. Invalid after 20 minutes.

Interpretation of Test Results

Test card description:
1. Invalid result: Quality management line (Line C) is invalid and needs to be tested again.
2. Negative result: The appearance color of test line (T line) is greater than that of reference line (R line), quality management line (C line) and reference line (R line).
3. Positive results: red watchband test line (T line) or red watchband, test line (T line) for the baseline line (R line) and quality management (C) line and baseline line (R line) color distinction.

Limitation of Test Method

 This kit is used for qualitative analysis, but only for Invitro assisted diagnosis.
2. Please add appropriate test samples. If the sample size is too large or too small, the result may be incorrect.
3. Hemolysis, lipids in the blood, jaundice, sample contamination, etc., may affect the test results, so it must be avoided as far as possible.
4. The test results of the reagent are for clinical reference only, and should not be used as the sole basis for clinical diagnosis and treatment. The final diagnosis of the disease is made by combining all clinical and examination results.

Precautions

1. This product is only used for Invitro diagnosis.
This product is disposable and can't be reused.
3. Please read the instructions carefully before operation, and strictly follow the instructions of reagent for experimental operation.
4. Please avoid conducting the experiment under harsh environmental conditions (84 disinfectants, sodium hypochlorite, acid, alkali, acetaldehyde, other corrosive gases with high concentration, dust, etc.). Laboratory disinfection needs to be carried out after the experiment.
5. All samples and reagents used shall be considered as potentially infectious substances and shall be disposed of in accordance with local regulations.
6. The reagent must be used within the expiry date stated on the package. To prevent moisture, the test card needs to be removed from the aluminum foil bag as soon as possible after removal.

Logo interpretation

	Do not re-use		Store at 2℃～30℃
	Consult instructions for use		In vitro diagnostic medical device
	Batch code		Use-by date
	Keep dry		Keep away from sunlight
	Authorized representative in the European Community		Manufacturer

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