7. As all samples are potentially infectious. Operators should wear protective gloves while handling samples Feline Pancreatic Lipase Rapid TestFPL 8. Decontaminate and dispose of all samples, used kits and accordance with national and local regulations. Feline Pancreatic Lipase Rapid Test is a lateral ow 1.Serum or plasma should be used with this test. immunoassay intended for the determination of Feline Serum: Collect the whole blood into the collection tube Pancreas-Specic Lipase Levels in feline serum or (NOT containing anticoagulants such as heparin, EDTA and sodium citrate), and then centrifuge whole blood to get serum. Plasma: Collect the whole blood into the collection Reagent and Materials Provided · Test devices · Quantitative droppers · Buer tubes · Package insert Materials Required but not Provided tube (containing anticoagulants such as heparin, EDTA and sodium citrate) and then centrifuge whole blood to get plasma. Unseal the extraction tube containing the buer. Place the extraction tube in the workstation. Normal level (-): If the color intensity of the T1 line is lighter than the color intensity of the reference T2 line, FPL levels are normal. C T2 T1 Invalid: No colored line appears in C region, regardless of T line’s appearance. C T2 T1 Squeeze the upper air bag to absorb the sample (serum or plasma) . Please make sure some sample getting into the lower air bag and there is no bubbles in the lower tube. Then press the upper air bag to transfer the sample (about 75 μL) left in the lower tube into the buer. 2.Samples should be stored at 2~8°C. Please freeze Although the Feline Pancreatic Lipase Rapid Test is very the samples at ‐20°C or below for longer storage and accurate in detecting Feline Pancreas-Specic Lipase levels, a avoid repeated freezing and thawing. low incidence of false results may be occurred. Other clinically 3.Samples containing precipitate may yield inconsis or laboratory tests might be required if questionable results are tent test results. They must be claried prior to obtained. As other diagnostic tests, a denitive clinical diagnosis should not be based on the result of a single test, but 4.Hemolyzed or contaminated samples may lead to Timer Abnormal level (+): If the color intensity of the T1 line is equal to or darker than the color intensity of the reference T2 line, FPL levels are abnormal. TEST PROCEDURE and wash hands thoroughly afterwards. Specimen Collection, Handling, and Transport erroneous results. Cover the tube, Jiggle the extraction tube until the specimen and the buer are mixed completely. should be diagnosed by the veterinarian after all clinical and laboratory ndings have been evaluated. Storage and Stability The test device is sealed and should be stored away batch code contains sucient for tests in vitro diagnotic medical device temperature limitation from light at a room temperature (4-30℃). Do not freeze. The test device should be used before the expiration CHECK THE KIT CONTENTS BEFORE USE date marked on the package label. 1. The test device is used for feline only. Take the test device out of the aluminum foil bag, and place it on a clean, at table. Add three drops (about 90 μL) of the mix sample vertically into the specimen well (S) of the test device. Warnings, Precautions and Safety Information 2. The results may be inuenced by humidity and damaged before open. Perform the test immediately STEP 3 Test device Quantitative Package insert 4. Do not reuse the test components. 6. Do not mix product components in dierent lot numbers. INTERPRETATION OF TEST RESULT when the pouch package is opened. 5. Do not use after the expiry date. AddressBlock A, Building 3, No. 8, Xiyuan 9th Road, Xihu District, Hangzhou, Zhejiang, 310030 P.R. China temperature. 3. Make sure that the foil pouch containing the test is not Hangzhou Antigenne Technology Co., Ltd Check the product contents and make sure the test operation is under the room temperature (15–30℃) before testing.