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Rapid infectious disease test Sabervet CCV Ag

Rapid infectious disease test Sabervet CCV Ag

Product catalog summary
Intended Use: The Canine Coronavirus Antigen Rapid Test is a lateral flow immunoassay designed for the qualitative detection of Canine Coronavirus (CCV) antigens in fresh feces or rectal swab samples from dogs. It aids in determining CCV infection.
Reagents and Materials Provided: The kit includes test devices, swabs, buffer tubes, a package insert, and a workstation.
Materials Required but not Provided: A timer is needed for the test procedure.
Storage and Stability: Store the test device at room temperature (4-30℃) away from light. Do not freeze. Use before the expiration date on the package.
Warnings, Precautions, and Safety Information: Handle all samples as potentially infectious. Wear protective gloves and wash hands thoroughly. Dispose of all samples and used kits according to regulations.
Test Procedure: Check kit contents before use. Ensure the test is conducted at room temperature (15–30℃). Read results at 5-10 minutes; results are invalid after 15 minutes.
Interpretation of Test Results: A negative result shows only a clear C line. A positive result shows both C and T lines. An invalid result shows no colored line in the C region.
Limitations: Although the test is accurate, false results may occur. Additional clinical or laboratory tests may be required for confirmation.
Performance Characteristics: The diagnostic sensitivity is 98.50%, specificity is 97.33%, and total agreement is 98.00%.
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Catalog excerpts

Rapid infectious disease test Sabervet CCV Ag-1

Canine Coronavirus Antigen Rapid Test(CCV Ag) Canine Coronavirus Antigen Rapid Test is a lateral flow immunoassay intended for the qualitative detection of specific antigen from Canine Coronavirus (CCV) in fresh feces or rectal swab sample. The test is useful for determination of CCV infection. Reagent and Materials Provided • Test devices • Swabs • Buffer tubes • Package insert Materials Required but not Provided The test device is sealed and should be stored away from light at a room temperature (4-30C). Do not freeze. The test device should be used before the expiration date marked on the package label. Warnings, Precautions and Safety Information 1. The test device is used for canine only. 2. The results may be influenced by humidity and temperature. 3. Make sure that the foil pouch containing the test is not damaged before open. Perform the test immediately when the pouch package is opened. 4. Do not reuse the test components. 5. Do not use after the expiry date. 6. Do not mix product components in different lot numbers. 7. As all samples are potentially infectious. Operators should wear protective gloves while handling samples and wash hands thoroughly afterwards. 8. Decontaminate and dispose of all samples, used kits and potentially contaminated materials safely in accordance with national and local regulations. STEP 1 CHECK THE KIT CONTENTS BEFORE USE Test device Swab Buffer tube Take the test device out of the aluminum foil bag and place it on a clean and flat table. Add three drops (about 90 mL) of specimen (mixed sample) vertically into the specimen well (S) of the test device. STEP 3 INTERPRETATION OF TEST RESULT Check the product contents and make sure the test operation is under the room temperature (15—30°C) before testing. STEP 2 TEST PROCEDURE Read the result at 5-10 minutes. The result is invalid after 15 minutes. Positive (+): The presence of both C line and T line, regardless of T line being strong or faint. Negative (-): Only clear C line appears. Unseal the extraction tube containing the buffer. Use the swab to collect some fresh canine feces or fecal sample from its rectum. And then put the swab into the buffer. Invalid: No colored line appears in C region, regardless of T line’s appearance. Rotate the swab more than 10 times. Close the cap of the buffer tube. Although the Canine Coronavirus Antigen Rapid Test is very accurate in detecting Canine Coronavirus Antigen, a low incidence of false results may be occurred. Other clinically or laboratory tests might be required if questionable results are obtained. As other diagnostic tests, a definitive clinical diagnosis should not be based on the result of a single test, but should be diagnosed by the veterinarian after all clinical and laboratory findings have been evaluated. Performance Characteristics batch code in vitro diagnotic medical device contains sufficient for <n> tests temperature limitation

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