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Rapid herpes test SaberVet FHV Ag

Rapid herpes test SaberVet FHV Ag

Product catalog summary
Intended Use: The Feline Herpesvirus Antigen Rapid Test is a lateral flow immunoassay designed for the qualitative detection of Feline Herpesvirus (FHV) antigens in feline eye, nasal fluid, or saliva samples. It aids in determining FHV infection.
Reagent 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 necessary for the 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: Ensure the kit contents are complete and the test is conducted at room temperature (15–30 ℃). Collect the specimen using a swab, mix with buffer, and add three drops to the test device. 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: The test is for feline use only. Results may be affected by humidity and temperature. Do not reuse components or mix components from different lots.
Performance Characteristics: The test has a diagnostic sensitivity of 96.00% and a specificity of 98.33%, with a total agreement of 97.40%.
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Catalog excerpts

Rapid herpes test SaberVet FHV Ag-1

Feline Herpesvirus Antigen Rapid Test(FHV Ag) Intended Use Feline Herpesvirus Antigen Rapid Test is a lateral flow immunoassay intended for the qualitative detection of specific antigen from Feline Herpesvirus (FHV) in eye, nasal fluid or saliva sample. The test is useful for determination of FHV 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 (4-30°C). 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 feline 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 Check the product contents and make sure the test operation is under the room temperature (15—30 C) before testing. STEP 2 TEST PROCEDURE Unseal the extraction tube containing the buffer. Use the swab to collect secretions specimen from feline eye, nose or mouth. Take the test device out of the aluminum foil bag and place it on a clean and flat table. Add three drops (about 90 pi) of specimen (mixed sample) vertically into the specimen well (S) of the test device. STEP 3 INTERPRETATION OF TEST RESULT 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. 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 Feline Herpesvirus Antigen Rapid Test is very accurate in detecting Feline Herpesvirus 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 in vitro diagnotic medical device contains sufficient for <n> tests temperature limitation

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