Sample Requirements
1. Serum, plasma or whole blood samples are collected.
2. The precipitates and suspended solids in the sample will affect
the experimental results and should be removed by centrifugation.
3. Anticoagulation: heparin anticoagulation, EDTA anticoagulation,
sodium citrate anticoagulant effect is not obvious.
4. Blood collection should be carried out by a professional.
Serum/serum/plasma tests are recommended. In urgent or exceptional
circumstances, a patient's whole blood sample can also be used for
rapid testing.
5. The storage time of serum and plasma samples at room temperature
shall not exceed 8 hours.
It can be stored at 2-8 °C for 5 days and below -20 °C for 6
months, but repeated freeze-thaw should be avoided. Whole blood
samples should not be frozen and should be stored at 2 °C to 8 °C
for no more than 48 hours.
Test Method
Read the operating instructions carefully before testing. All
reagents should be returned to room temperature prior to testing,
and testing should be performed at room temperature.
1. Remove the test card from the box and use it within 1 hour.
2. Add 20 L of sample (serum, plasma, or whole blood) to the filled
well of the test card, add 2 drops (~60 L) of sample buffer, and
then start timing.
3. React at room temperature for 10-15 min and then read the
results. Invalid after 20 minutes.
Interpretation of Test Results
Test Card Description:
1. Invalid result: The quality control line (c line) is invalid and
needs to be retested.
2. Negative result: The appearance color of the detection line (T
line) is higher than or equal to the reference line (R line), the
quality control line (C line) and the reference line (R line).
3. Positive results: The red band can not see the test line (t
line) or red band, the test line (t line) is lower than the
reference line (R line), the quality control (c) line and the
reference line (R line) are colored.
Limitation of Test Method
This kit is for qualitative analysis and is intended for in vitro
diagnostics only.
2. Make sure to add an appropriate amount of sample for testing.
Too much or too little sample size can lead to inaccurate results.
3. Hemolysis, blood lipids, jaundice, sample contamination, etc.
may affect the test results and should be avoided as much as
possible.
4. The test results of this reagent are for clinical reference only
and shall not be used as the sole basis for clinical diagnosis and
treatment. All clinical and laboratory results are combined to make
a final diagnosis of the disease.
Precautions
1. This product is only used for in vitro diagnostics.
2. This product is a disposable product and cannot be recycled.
3. Carefully read the instructions before operation, and carry out
experimental operations in strict accordance with the reagent
instructions.
4. Avoid experiments under harsh environmental conditions
(including 84 disinfectants, sodium hypochlorite, acid, alkali,
acetaldehyde and other high concentration corrosive gases, dust,
etc.). Laboratory disinfection should be performed after the end of
the experiment.
5. All samples and reagents used should be considered potentially
infectious substances and disposed of in accordance with local
regulations.
6. Reagents should be used within the validity period indicated on
the outer packaging. The test card should be removed from the
aluminum foil bag as soon as possible after removal to prevent
moisture.
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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