{"title":"In Vitro Diagnostics Ivd","description":"","products":[{"product_id":"autotest-vih-screening-hiv","title":"HIV SELF-TEST HIV SCREENING CONTAINS 1 SELF-TEST + SOLUTION + SCALPEL + PLASTER + GAUZE + DISINFECTANT WIPE","description":"\u003cb\u003eDescriptive sheet\u003c\/b\u003e\u003cbr\u003e\u003ch1\u003e HIV self-test\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Screening test for HIV (the virus that causes AIDS) performed on a blood sample taken from the fingertip.\u003cbr\u003e This is a reliable self-test for diagnosing HIV infections that occurred at least three months ago.\u003cbr\u003e Autotest VIH is a single-use in vitro diagnostic device.\u003cbr\u003e Self-test VIH can be performed by non-experts in a private setting.\u003cbr\u003e The test takes approximately 5 minutes to complete and the waiting time before reading the result is 15 minutes.\u003cbr\u003e You will need a clock or other time-keeping device.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e 1. Place the test tube holder on a flat surface. Gently pull the cap containing the buffer solution to separate it from the self-test. Slide it with your finger to the bottom of the test tube holder. \u003cbr\u003e2. Wash your hands, preferably with warm water, and dry them. Open the bags containing the disinfectant wipe and sterile gauze. Rub the disinfectant wipe on your fingertip and wait for it to dry. Remove the cap from the safety scalpel. Place the red end of the scalpel on your fingertip and push down firmly to pierce the skin with the needle.\u003cbr\u003e Gently squeeze your finger to form a first large drop of blood. Wipe away the drop with sterile gauze. Without applying too much pressure, gently squeeze your finger again to form another large drop of blood. With the self-test pointing down, touch the tip of the device to the drop of blood until the tip fills with blood. \u003cbr\u003e3. Make sure the test tube holder containing the buffer solution cap is placed on a flat surface. Hold the self-test with the tip pointing down, firmly in the test tube holder so as to pierce the aluminum membrane of the buffer solution cap.\u003cbr\u003e Push down firmly (you will hear a 3-time click). Look for a pink spot that should begin to appear less than a minute after the test device and buffer cap are inserted into each other. Apply the patch to your finger.\u003cbr\u003e 4. Check the time and wait 15 minutes before reading the result.\u003cbr\u003e Non-reactive self-test: one line appears: control line (HIV negative).\u003cbr\u003e Reactive self-test: two lines appear: control line and test line (probably HIV positive).\u003cbr\u003e If positive:\u003cbr\u003e - contact a doctor as soon as possible and inform him that you have just performed a self-test for HIV and that the result was positive; \u003cbr\u003e- the result of the self-test must be confirmed by an examination carried out at an analysis laboratory;\u003cbr\u003e - protect yourself and protect others.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e If you think you may have been exposed to HIV in the past 3 months, a negative test result is not certain at this time. Therefore, avoid any activity that could cause transmission of HIV to others. Use condoms to protect yourself and your partners. You will need to repeat the self-test 3 months after your most recent risk of exposure to HIV.\u003cbr\u003e - The self-test is intended for strictly private use as a self-test for HIV and must not be used for other diagnoses or other purposes under any circumstances.\u003cbr\u003e - The self-test should only be used with a freshly drawn capillary blood sample following the instructions in this document. Do not use for serum or plasma samples.\u003cbr\u003e - The self-test is a single-use device. Do not reuse. \u003cbr\u003e- Do not open the foil pouch containing the self-test until you are ready to perform the test.\u003cbr\u003e - This self-test should not be used in the follow-up of patients on antiretroviral therapy.\u003cbr\u003e - Anyone using this self-test should consult their doctor before making any therapeutic decisions, regardless of whether the result is positive or negative.\u003cbr\u003e - False positive (0.2% in studies on test specificity) or false negative results may be due to the following circumstances: exposure to HIV in the three months prior to using the test (window period), situations of advanced immunodeficiency or infection by a rare variant or testing performed on HIV-positive subjects undergoing antiretroviral therapy.\u003cbr\u003e - The test result may also be incorrect if the product is not stored as directed or if the limitations of use are not respected. \u003cbr\u003e- Do not use the self-test if the package or foil pouch has been opened or damaged.\u003cbr\u003e - Do not use the self-test if the expiry date indicated on the package has passed.\u003cbr\u003e - If you have difficulty understanding the explanations on the packaging or the instructions for use, contact Mylan immediately at: +39 02 61246462.\u003cbr\u003e - Keep the self-test and all contents of the package out of the reach of children. The components of the VIH self-test can be dangerous if swallowed and may cause irritation.\u003cbr\u003e - Autotest VIH offers an additional HIV testing modality that can be used as a complement to other existing options. Autotest VIH can only diagnose HIV infection and cannot be used to test for other sexually transmitted diseases. \u003cbr\u003e- AAZ-LMB expressly declines any responsibility relating to the use or distribution of the VIH self-test or any of its components, which occurs without strict observance of the indications and limits of use specified in the instructions for use.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store the self-test in the original packaging in a cool, dry place at a temperature between 8°C and 30°C. Keep away from sunlight.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e - 1 aluminium sachet containing: 1 self-test, 1 cap containing the buffer solution, 1 safety scalpel, 1 patch;\u003cbr\u003e - 1 test tube holder;\u003cbr\u003e - 1 sterile gauze;\u003cbr\u003e - 1 disinfectant wipe;\u003cbr\u003e - 1 instruction sheet.\u003c\/div\u003e","brand":"COOPER CONSUMER HEALTH IT SRL","offers":[{"title":"Default Title","offer_id":50734357381454,"sku":"971268634","price":25.64,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-143314.jpg?v=1768760378"},{"product_id":"test-antigenico-rapido-covid-19-flowflex-autodiagnostico-determinazione-qualitativa-antigeni-sars-cov-2-in-tamponi-nasali-mediante-immunocromatografia-provetta-tappo-blu","title":"COVID-19 FLOWFLEX RAPID ANTIGEN TEST SELF-DIAGNOSTIC QUALITATIVE DETERMINATION OF SARS-COV-2 ANTIGENS IN NASAL SWABS BY IMMUNOCHROMATOGRAPHY BLUE CAP TEST TUBE","description":"\u003ch1\u003e Flowflex\u003c\/h1\u003e\n\u003ch2\u003e SARS-CoV-2 Antigen Rapid Test\u003cbr\u003e (Self-Testing)\u003c\/h2\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Lateral flow test for the qualitative detection of SARS-CoV-2 nucleocapsid antigen in anterior nasal swab specimens directly from individuals suspected of having COVID-19 within the first seven days of symptom onset.\u003cbr\u003e The test can be used to analyze samples from asymptomatic subjects.\u003cbr\u003e It does not distinguish between SARS-CoV and SARS-CoV-2.\u003cbr\u003e The results involve the identification of the SARS-CoV-2 antigen. This antigen is generally found in samples taken from the upper respiratory tract during the acute phase of infection.\u003cbr\u003e Test results are read visually within the next 15-30 minutes, based on the presence or absence of colored lines. \u003cbr\u003ePositive results indicate the presence of viral antigens, but a patient's medical history and other personal diagnostic data are required to determine the infection status. Positive results do not rule out bacterial infections or simultaneous infection with other viruses. The detected pathogen may not be the exact cause of the condition.\u003cbr\u003e Negative results obtained in subjects with symptoms lasting more than seven days should be treated as probable negative. If necessary, seek confirmation through molecular testing. Negative results do not rule out SARS-CoV-2 infection.\u003cbr\u003e A colored line, serving as a procedural control, will always appear in the control line area, indicating that sufficient sample volume has been added and membrane adsorption has occurred.\u003cbr\u003e The test is intended for use as an aid in the diagnosis of SARS-CoV-2 infection. \u003cbr\u003eThe usability of self-testing by individuals under 18 has not been established. It is recommended that anyone under 18 be tested by an adult.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e 1. \u003cu\u003ePreparation\u003c\/u\u003e :\u003cbr\u003e Wash or disinfect your hands. Make sure they are dry before starting the test.\u003cbr\u003e Before using the test kit, please read the instructions carefully.\u003cbr\u003e Check the expiration date printed on the foil pouch. Open the pouch. Check the result window and sample well on the cassette.\u003cbr\u003e\u003cbr\u003e 2. \u003cu\u003eSample collection\u003c\/u\u003e :\u003cbr\u003e Anyone 18 years of age or older can perform a self-swab test. Children under 18 must be accompanied by a parent or legal guardian. Follow local guidelines for sample collection for children.\u003cbr\u003e\u003cbr\u003e 3. \u003cu\u003eAnalysis procedure\u003c\/u\u003e : \u003cbr\u003eUnscrew the dropper cap from the extraction solution tube without squeezing it. Insert the tube into the hole on the kit box (or place the tube in the tube holder).\u003cbr\u003e Open the swab package at the end of the stick. Do not touch the absorbent tip of the swab with your hands.\u003cbr\u003e Insert the entire absorbent tip of the swab into one nostril. Using a gentle rotation, push the swab within 1 inch of the nostril's edge. Rotate the swab 5 times, gently touching the inside of the nostril. Remove the swab, insert it into the other nostril, and repeat the procedure.\u003cbr\u003e Remove the swab and insert it into the test tube, rotating it in a circular motion for 30 seconds. Rotate the swab 5 times, simultaneously squeezing the sides of the test tube. Remove the swab while squeezing the test tube. \u003cbr\u003eFirmly attach the dropper tip to the extraction buffer tube containing the sample. Mix thoroughly by swirling or tapping the bottom of the tube. Unscrew the small cap from the end of the dropper. Gently squeeze the tube and dispense 4 drops of solution into the sample well.\u003cbr\u003e Read the result when the timer reaches 15-30 minutes. Do not read if 30 minutes have passed.\u003cbr\u003e\u003cbr\u003e 4. \u003cu\u003eInterpretation of results\u003c\/u\u003e :\u003cbr\u003e NEGATIVE: Only the control line (C) appears and no test line (T). This means that no SARS-CoV-2 antigen has been detected.\u003cbr\u003e A negative test result indicates that you are unlikely to have COVID-19 at this time. \u003cbr\u003eContinue to follow all applicable rules and precautions when interacting with others. A current infection is possible even if the test is negative. If you suspect this, repeat the test after 1 or 2 days, as the coronavirus cannot be accurately detected at all stages of infection.\u003cbr\u003e\u003cbr\u003e POSITIVE: Both the control line (C) and the test line (T) appear. This means that the SARS-CoV-2 antigen has been detected (Note: Any line, even a very faint one, present in the test line area should be considered positive).\u003cbr\u003e A positive test result indicates a very high probability that you have COVID-19. Contact your doctor\/primary care provider or local health authority immediately. Follow local guidelines regarding self-isolation. A confirmatory PCR test must be performed.\u003cbr\u003e  \u003cbr\u003eINVALID: The control line (C) does not appear. The most likely reasons for an invalid result are insufficient specimen volume or incorrect procedure. Reread the instructions and repeat the test with a new cassette.\u003cbr\u003e If your test results continue to be invalid, contact your doctor or a COVID-19 testing center.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Before performing the test, read the package insert carefully. Failure to follow the instructions may result in inaccurate test results.\u003cbr\u003e Do not use the test after the expiration date shown on the pouch.\u003cbr\u003e Do not eat, drink or smoke before and during the test.\u003cbr\u003e Do not use the test if the pouch is damaged.\u003cbr\u003e All used tests, specimens, and potentially contaminated material must be disposed of in accordance with local regulations.\u003cbr\u003e Humidity and temperature can negatively affect results. \u003cbr\u003eThe test line for a sample with a high viral load may appear within 15 minutes or even sooner, when the sample exceeds the test line area.\u003cbr\u003e The test line for a sample with a low viral load may appear within 30 minutes.\u003cbr\u003e Do not collect the nasal swab sample if you have a nosebleed.\u003cbr\u003e Wash hands thoroughly after use.\u003cbr\u003e If the extraction swab accidentally comes into contact with skin or eyes, rinse with large amounts of water and consult a doctor if necessary.\u003cbr\u003e The test is for self-testing only: it should only be used for the detection of SARS-CoV-2 nucleocapsid antigen in anterior nasal swab specimens.\u003cbr\u003e The intensity of the test line does not necessarily correlate with the SARS-CoV-2 viral load in the sample. \u003cbr\u003eA false negative test may occur if the antigen concentration in a sample is below the test's detection limit or if the sample was collected incorrectly.\u003cbr\u003e The results of the analysis must be observed in the light of other clinical data available to the physician.\u003cbr\u003e Positive results do not rule out the presence of co-infections caused by other pathogens. Positive results do not rule out SARS-CoV and SARS-CoV-2.\u003cbr\u003e Negative test results do not rule out the presence of other viral or bacterial infections. A negative result obtained in a subject with symptoms lasting more than 7 days should be treated as probable negative and, if necessary, verified by molecular testing.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store at 2°C to 30°C. Do not freeze.\u003cbr\u003e The test is stable until the expiration date printed on the sealed pouch. Do not use after the expiration date. \u003cbr\u003eThe test must remain in the sealed pouch until ready for use.\u003cbr\u003e Shelf life in intact packaging: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e - 1 test cassette\u003cbr\u003e - 1 extraction swab tube\u003cbr\u003e - 1 disposable swab\u003cbr\u003e - 1 waste bag\u003cbr\u003e - package leaflet\u003cbr\u003e\u003cbr\u003e \u003cb\u003eBibliography\u003c\/b\u003e\u003cbr\u003e 1. Shuo Su, Gary Wong, Weifeng Shi, et al. Epidemiology, Genetic recombination, and pathogenesis of coronaviruses. Trends in Microbiology, June 2016, vol. 24, No. 6:490-502\u003cbr\u003e 2. Susan R. Weiss, Julian L. Leibowitz, Coronavirus Pathogenesis, Advances in Virus Research, Volume 81: 85-164\u003c\/div\u003e","brand":"DPI MEDICAL SOLUTION SRL","offers":[{"title":"Default Title","offer_id":50734361674062,"sku":"983307822","price":4.41,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-243802.jpg?v=1768760443"},{"product_id":"amnios-assorbente-test-2pz","title":"AMNIOTIC FLUID LEAK TEST AMNIOS ABSORBENT 2 PIECES","description":"\u003cb\u003eDescriptive sheet\u003c\/b\u003e\u003cbr\u003e\u003ch1\u003e AMNIOS\u003c\/h1\u003e\n\u003ch3\u003e ABSORBENT TEST 2PCS\u003c\/h3\u003e Home-based test for detecting amniotic fluid leaks.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e 2 pieces.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e PL02A","brand":"IDI INTEGRATORI DIETET.IT. SRL","offers":[{"title":"Default Title","offer_id":50734372716878,"sku":"923005995","price":14.25,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-123257.jpg?v=1768760614"},{"product_id":"test-autodiagnostico-rapido-sofarmapiu-per-la-rilevazione-del-sangue-occulto-nelle-feci","title":"SOFARMAPIU' RAPID SELF-DIAGNOSTIC TEST FOR THE DETECTION OF OCCULT BLOOD IN FECES","description":"\u003ch1\u003e SoFarma\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e\n\u003ch3\u003e TEST\u003cbr\u003e OCCULT BLOOD\u003cbr\u003e IN THE FECES (FOB)\u003c\/h3\u003e \u003cb\u003eDescription\u003c\/b\u003e \u003cbr\u003eRapid chromatographic immunoassay for the qualitative detection of human occult blood in stool. For in vitro diagnostic self-testing only.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Allow the test, specimen, and swab to reach room temperature (15-30°C) before testing.\u003cbr\u003e 1. To collect fecal samples: The stool sample must be collected in a stool collector. It is important to use the stool collector in all types of restrooms to avoid contamination of the sample with any type of chemical, thus preventing sample adulteration. \u003cbr\u003e2. To process stool samples: Unscrew the cap of the sample collection tube, then randomly insert the sample collection applicator into the stool sample in at least 3 different locations. Do not collect the stool sample. Screw and tighten the cap on the sample collection tube, then shake the sample collection tube vigorously to mix the sample and extraction buffer.\u003cbr\u003e 3. Bring the pouch to room temperature before opening. Remove the dipstick from the foil pouch and use it as soon as possible. Best results are obtained if the test is performed immediately after opening the foil pouch. \u003cbr\u003e4. Secure the reaction tube, hold the sample collection tube upright, and break the tip of the sample collection tube. Invert the sample collection tube and transfer 8-10 full drops of the extracted sample (approximately 500 mcl) into the reaction tube. Then immerse the dipstick with the arrows pointing toward the extraction buffer and start the timer. Do not immerse the dipstick beyond the maximum line.\u003cbr\u003e 5. Read the results after 5 minutes. Do not read the results after 10 minutes.\u003cbr\u003e Positive: Two colored lines appear. One colored line should be in the control line region (C) and another colored line should be in the test line region (T).\u003cbr\u003e Note: The intensity of the color in the test line region (T) will vary depending on the concentration of fecal occult blood in the specimen. Therefore, any shade of color in the test line region (T) should be considered positive. \u003cbr\u003eNegative: A colored line appears in the control line region (C). No line appears in the test line region (T).\u003cbr\u003e Invalid: The control line does not appear. Insufficient sample volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test. If the problem persists, discontinue use of the test kit immediately and contact your local distributor.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e - For in vitro diagnostic self-analysis only.\u003cbr\u003e - Do not use after the expiration date.\u003cbr\u003e - The test must remain in the sealed pouch until use.\u003cbr\u003e - Do not eat, drink or smoke in the area where specimens or kits are handled.\u003cbr\u003e - Handle all specimens as if they contain infectious agents. Observe established microbiological precautions during all procedures and follow standard procedures for proper specimen disposal. \u003cbr\u003e- The used test must be disposed of according to local regulations.\u003cbr\u003e - Humidity and temperature can negatively affect results.\u003cbr\u003e - Keep out of reach of children.\u003cbr\u003e - Do not freeze.\u003cbr\u003e - Samples should not be collected during or within three days of a menstrual cycle, or if the patient suffers from bleeding hemorrhoids or blood in the urine.\u003cbr\u003e - Alcohol, aspirin, and other medications taken in excess can cause gastrointestinal irritation resulting in occult bleeding. These substances should be discontinued at least 48 hours before the test.\u003cbr\u003e - No dietary restrictions are required before using the FOB test.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store between 2°C and 30°C.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Package containing:\u003cbr\u003e FOB test;\u003cbr\u003e package leaflet;\u003cbr\u003e reaction tube;\u003cbr\u003e sample collection tube with extraction swab;\u003cbr\u003e feces collector.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e SF-018\u003c\/div\u003e","brand":"SO.FARMA.MORRA SPA","offers":[{"title":"Default Title","offer_id":50734492975438,"sku":"987776729","price":6.21,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-304435.jpg?v=1768762236"},{"product_id":"test-antigenico-rapido-covid-19-sofarmapiu-nasale-autodiagnostico-determinazione-qualitativa-antigeni-sars-cov-2-in-tamponi-nasali-mediante-immunocromatografia","title":"COVID-19 RAPID ANTIGEN TEST SOFARMAPIU' NASAL","description":"\u003ch1\u003e ALL\u003cbr\u003e TEST\u003c\/h1\u003e\n\u003ch2\u003e Rapid Swab for SARS-CoV-2 Antigen\u003c\/h2\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Rapid test for the qualitative detection of SARS-CoV-2 nucleocapsid protein antigens in nasal swab specimens. For in vitro self-testing only.\u003cbr\u003e Single-use test kit intended to detect SARS-CoV-2, the virus that causes COVID-19, in self-collected nasal swab specimens. The test is intended for use in symptomatic individuals who meet the COVID-19 case definition, as well as in asymptomatic individuals, limited to contacts of confirmed or probable COVID-19 cases and at-risk healthcare workers. \u003cbr\u003eThe results are for the detection of SARS-CoV-2 nucleocapsid protein antigens. An antigen is generally detectable in upper respiratory tract samples during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with the patient's history and other diagnostic information is required to determine the infection status. Positive results are indicative of the presence of SARS-CoV-2. Individuals who test positive should self-isolate and seek further care from their healthcare provider. Positive results do not rule out bacterial infection or co-infection with other viruses. Negative results do not rule out SARS-CoV-2 infection. Individuals who test negative and continue to experience COVID-like symptoms should contact their healthcare provider.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e \u003cbr\u003eWash your hands with soap and water for at least 20 seconds before and after the test. If soap and water are not available, use a hand sanitizer with at least 60% alcohol.\u003cbr\u003e Remove the lid from the tube with the extraction buffer and place the tube in the tube holder in the box.\u003cbr\u003e Nasal swab sample collection\u003cbr\u003e 1. Remove the sterile swab from the pouch.\u003cbr\u003e 2. Insert the swab into the nostril until you feel slight resistance (about 2 cm up the nose). Slowly rotate the swab, rubbing it along the inside of the nostril 5-10 times against the nasal wall. \u003cbr\u003eNote: This may be uncomfortable. Do not insert the swab further if you feel significant resistance or pain. If the nasal mucosa is damaged or bleeding, collecting a nasal swab is not recommended. If you are collecting swabs from others, please wear a face mask. With children, it may not be necessary to insert the swab so far into the nostril. For very young children, another person may be needed to hold the child's head while collecting the swab.\u003cbr\u003e 3. Gently remove the swab.\u003cbr\u003e 4. Using the same swab, repeat step 2 in the other nostril.\u003cbr\u003e 5. Remove the swab.\u003cbr\u003e Sample preparation\u003cbr\u003e 1. Place the swab in the extraction tube, making sure it touches the bottom, and swirl the swab to mix well. Press the head of the swab against the tube and swirl the swab for 10-15 seconds. \u003cbr\u003e2. Remove the swab by pressing the swab head against the inside of the extraction tube. Place the swab in the biosafety bag.\u003cbr\u003e 3. Close the cap or insert the tip of the tube onto the tube.\u003cbr\u003e Test procedure\u003cbr\u003e 1. Remove the test cassette from the sealed foil pouch and use it within one hour. Best results are obtained if the test is performed immediately after opening the foil pouch. Place the test cassette on a flat surface.\u003cbr\u003e 2. Invert the sample extraction tube and add 3 drops of the extracted sample to the well (S) of the test cassette and start the timer. Do not move the test cassette during test development.\u003cbr\u003e 3. Read the result after 15 minutes. Do not read the result after 20 minutes.\u003cbr\u003e Note: Upon completion of the test, place all components in the plastic biosafety bag and dispose of according to local regulations.\u003cbr\u003e Reading the results \u003cbr\u003ePositive: *Two colored lines appear. One colored line should appear in the control region (C) and another colored line should appear in the test region (T).\u003cbr\u003e *Note: The intensity of the color in the test line region (T) varies depending on the number of SARS-CoV-2 antigens present in the sample. Therefore, the presence of any shade of color in the test region (T) should be interpreted as a positive result. A positive result means that the person is highly likely infected with COVID-19; positive samples must be confirmed. Immediately self-isolate as required by local regulations and contact your healthcare provider or district health care provider as directed by local authorities. The test will be verified by a confirmatory molecular (PCR) test, and instructions on the next steps will be provided. \u003cbr\u003eNegative: Only one colored line appears in the control region (C). No colored line appears in the test line region (T). It is unlikely that you have COVID-19. However, this test may give an incorrect result (a false negative) in some people with COVID-19. This means that you may have COVID-19 even if the test returned a negative result. Additionally, you can repeat the test with a new kit. If you suspect COVID-19, repeat the test after 1-2 days, as the coronavirus cannot be detected at all stages of infection. Even with a negative result, social distancing and hygiene rules must still be observed.  \u003cbr\u003eInvalid: The control line does not appear. Insufficient sample volume or incorrect procedure techniques are the most likely causes of the missing control line. Review the procedure and repeat the test with a new kit or contact your healthcare provider or a COVID-19 testing center.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e - For self-testing purposes only. Do not use after the expiration date.\u003cbr\u003e - Do not eat, drink or smoke in the area where specimens or kits are handled.\u003cbr\u003e - Do not drink the swab liquid contained in the kit.\u003cbr\u003e - Handle the swab with care and avoid contact with skin or eyes. Rinse immediately with plenty of running water in case of contact.\u003cbr\u003e - Please do not use if the foil package is damaged or has been opened.\u003cbr\u003e - This test kit should be used only as a preliminary test and repeatedly abnormal results should be discussed with a doctor or medical professional. \u003cbr\u003e- Strictly follow the indicated time.\u003cbr\u003e - Use the test only once. Do not disassemble or touch the test window of the test cassette.\u003cbr\u003e - The kit must not be frozen or used after the expiration date printed on the package.\u003cbr\u003e - Children should be tested under the guidance of an adult.\u003cbr\u003e - Wash your hands thoroughly before and after handling.\u003cbr\u003e - Please ensure that an adequate amount of sample is used for testing. Too much or too little sample may lead to inaccurate results.\u003cbr\u003e Limitations\u003cbr\u003e 1. Performance was evaluated with nasal swab specimens only, using the procedures provided in this package insert.\u003cbr\u003e 2. The SARS-CoV-2 Rapid Antigen Detection Test (Nasal Swab) will only indicate the presence of SARS-CoV-2 antigens in the specimen. \u003cbr\u003e3. If the test result is negative or non-reactive and clinical symptoms persist, it is because the virus from very early infection may not be detected, it is recommended to retest with a new kit or test with a molecular diagnostic device to exclude infection in these individuals.\u003cbr\u003e 4. Negative results do not rule out SARS-CoV-2 infection, especially in those who have been in contact with the virus. Follow-up testing with molecular diagnostics should be considered to rule out infection in these individuals.\u003cbr\u003e 5. Positive COVID-19 results may be due to infection with non-SARS-CoV-2 coronavirus strains or other interfering factors.\u003cbr\u003e 6. Failure to follow these procedures may affect test performance.\u003cbr\u003e 7. False negative results may occur if a specimen is collected or handled improperly. \u003cbr\u003e8. False negative results may occur if there are insufficient levels of virus in the sample.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store as packaged in the sealed pouch at room temperature or refrigerated (2-30°C). The test is stable until the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use. Do not freeze. Do not use beyond the expiration date.\u003cbr\u003e Shelf life of intact packaging: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Test cassette, sterile swab, biosafety bag, package insert, extraction swab.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e INCP-502H\u003c\/div\u003e","brand":"SO.FARMA.MORRA SPA","offers":[{"title":"Default Title","offer_id":50734502740302,"sku":"989811435","price":8.01,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/989811435.jpg?v=1768762389"},{"product_id":"test-antigenico-rapido-covid-19-sofarmapiu-nasale-rilevazione-qualitativa-antigeni-sars-cov-2-in-tamponi-nasali-20-pezzi-uso-professionale","title":"COVID-19 NASAL RAPID ANTIGEN TEST QUALITATIVE DETECTION OF SARS-COV-2 ANTIGENS IN NASAL SWABS 20 PIECES PROFESSIONAL USE SOFARMAPIU'","description":"\u003ch1\u003e ALL\u003cbr\u003e TEST\u003c\/h1\u003e\n\u003ch2\u003e Rapid Swab for SARS-CoV-2 Antigen\u003c\/h2\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Rapid test for the qualitative detection of SARS-CoV-2 nucleocapsid protein antigens in nasal swab specimens. For in vitro self-testing only. \u003cbr\u003eSingle-use test kit intended to detect SARS-CoV-2, the virus that causes COVID-19, in self-collected nasal swab specimens. The test is intended for use in symptomatic individuals who meet the COVID-19 case definition, as well as in asymptomatic individuals, limited to contacts of confirmed or probable COVID-19 cases and at-risk healthcare workers. \u003cbr\u003eThe results are for the detection of SARS-CoV-2 nucleocapsid protein antigens. An antigen is generally detectable in upper respiratory tract samples during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with the patient's history and other diagnostic information is required to determine the infection status. Positive results are indicative of the presence of SARS-CoV-2. Individuals who test positive should self-isolate and seek further care from their healthcare provider. Positive results do not rule out bacterial infection or co-infection with other viruses. Negative results do not rule out SARS-CoV-2 infection. Individuals who test negative and continue to experience COVID-like symptoms should contact their healthcare provider.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e \u003cbr\u003eWash your hands with soap and water for at least 20 seconds before and after the test. If soap and water are not available, use a hand sanitizer with at least 60% alcohol.\u003cbr\u003e Remove the lid from the tube with the extraction buffer and place the tube in the tube holder in the box.\u003cbr\u003e Nasal swab sample collection\u003cbr\u003e 1. Remove the sterile swab from the pouch.\u003cbr\u003e 2. Insert the swab into the nostril until you feel slight resistance (about 2 cm up the nose). Slowly rotate the swab, rubbing it along the inside of the nostril 5-10 times against the nasal wall. \u003cbr\u003eNote: This may be uncomfortable. Do not insert the swab further if you feel significant resistance or pain. If the nasal mucosa is damaged or bleeding, collecting a nasal swab is not recommended. If you are collecting swabs from others, please wear a face mask. With children, it may not be necessary to insert the swab so far into the nostril. For very young children, another person may be needed to hold the child's head while collecting the swab.\u003cbr\u003e 3. Gently remove the swab.\u003cbr\u003e 4. Using the same swab, repeat step 2 in the other nostril.\u003cbr\u003e 5. Remove the swab.\u003cbr\u003e Sample preparation\u003cbr\u003e 1. Place the swab in the extraction tube, making sure it touches the bottom, and swirl the swab to mix well. Press the head of the swab against the tube and swirl the swab for 10-15 seconds. \u003cbr\u003e2. Remove the swab by pressing the swab head against the inside of the extraction tube. Place the swab in the biosafety bag.\u003cbr\u003e 3. Close the cap or insert the tip of the tube onto the tube.\u003cbr\u003e Test procedure\u003cbr\u003e 1. Remove the test cassette from the sealed foil pouch and use it within one hour. Best results are obtained if the test is performed immediately after opening the foil pouch. Place the test cassette on a flat surface.\u003cbr\u003e 2. Invert the sample extraction tube and add 3 drops of the extracted sample to the well (S) of the test cassette and start the timer. Do not move the test cassette during test development.\u003cbr\u003e 3. Read the result after 15 minutes. Do not read the result after 20 minutes.\u003cbr\u003e Note: Upon completion of the test, place all components in the plastic biosafety bag and dispose of according to local regulations.\u003cbr\u003e Reading the results \u003cbr\u003ePositive: *Two colored lines appear. One colored line should appear in the control region (C) and another colored line should appear in the test region (T).\u003cbr\u003e *Note: The intensity of the color in the test line region (T) varies depending on the number of SARS-CoV-2 antigens present in the sample. Therefore, the presence of any shade of color in the test region (T) should be interpreted as a positive result. A positive result means that the person is highly likely infected with COVID-19; positive samples must be confirmed. Immediately self-isolate as required by local regulations and contact your healthcare provider or district health care provider as directed by local authorities. The test will be verified by a confirmatory molecular (PCR) test, and instructions on the next steps will be provided. \u003cbr\u003eNegative: Only one colored line appears in the control region (C). No colored line appears in the test line region (T). It is unlikely that you have COVID-19. However, this test may give an incorrect result (a false negative) in some people with COVID-19. This means that you may have COVID-19 even if the test returned a negative result. Additionally, you can repeat the test with a new kit. If you suspect COVID-19, repeat the test after 1-2 days, as the coronavirus cannot be detected at all stages of infection. Even with a negative result, social distancing and hygiene rules must still be observed.  \u003cbr\u003eInvalid: The control line does not appear. Insufficient sample volume or incorrect procedure techniques are the most likely causes of the missing control line. Review the procedure and repeat the test with a new kit or contact your healthcare provider or a COVID-19 testing center.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e - For self-testing purposes only. Do not use after the expiration date.\u003cbr\u003e - Do not eat, drink or smoke in the area where specimens or kits are handled.\u003cbr\u003e - Do not drink the swab liquid contained in the kit.\u003cbr\u003e - Handle the swab with care and avoid contact with skin or eyes. Rinse immediately with plenty of running water in case of contact.\u003cbr\u003e - Please do not use if the foil package is damaged or has been opened.\u003cbr\u003e - This test kit should be used only as a preliminary test and repeatedly abnormal results should be discussed with a doctor or medical professional. \u003cbr\u003e- Strictly follow the indicated time.\u003cbr\u003e - Use the test only once. Do not disassemble or touch the test window of the test cassette.\u003cbr\u003e - The kit must not be frozen or used after the expiration date printed on the package.\u003cbr\u003e - Children should be tested under the guidance of an adult.\u003cbr\u003e - Wash your hands thoroughly before and after handling.\u003cbr\u003e - Please ensure that an adequate amount of sample is used for testing. Too much or too little sample may lead to inaccurate results.\u003cbr\u003e Limitations\u003cbr\u003e 1. Performance was evaluated with nasal swab specimens only, using the procedures provided in this package insert.\u003cbr\u003e 2. The SARS-CoV-2 Rapid Antigen Detection Test (Nasal Swab) will only indicate the presence of SARS-CoV-2 antigens in the specimen. \u003cbr\u003e3. If the test result is negative or non-reactive and clinical symptoms persist, it is because the virus from very early infection may not be detected, it is recommended to retest with a new kit or test with a molecular diagnostic device to exclude infection in these individuals.\u003cbr\u003e 4. Negative results do not rule out SARS-CoV-2 infection, especially in those who have been in contact with the virus. Follow-up testing with molecular diagnostics should be considered to rule out infection in these individuals.\u003cbr\u003e 5. Positive COVID-19 results may be due to infection with non-SARS-CoV-2 coronavirus strains or other interfering factors.\u003cbr\u003e 6. Failure to follow these procedures may affect test performance.\u003cbr\u003e 7. False negative results may occur if a specimen is collected or handled improperly. \u003cbr\u003e8. False negative results may occur if there are insufficient levels of virus in the sample.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store as packaged in the sealed pouch at room temperature or refrigerated (2-30°C). The test is stable until the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use. Do not freeze. Do not use beyond the expiration date.\u003cbr\u003e Shelf life of intact packaging: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Test cassette, sterile swab, biosafety bag, package insert, extraction swab.\u003cbr\u003e 20 pieces.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e INCP-502\u003c\/div\u003e","brand":"SO.FARMA.MORRA SPA","offers":[{"title":"Default Title","offer_id":50734502773070,"sku":"950020406","price":270.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-342027.jpg?v=1768762390"},{"product_id":"test-antigenico-rapido-covid-19-sofarmapiu-salivare-autodiagnostico-determinazione-qualitativa-antigeni-sars-cov-2-in-campioni-salivari-mediante-immunocromatografia","title":"COVID-19 SOFARMAPIU' SALIVARY RAPID ANTIGEN TEST","description":"\u003ch2\u003e ALLTEST\u003c\/h2\u003e\n\u003ch1\u003e Rapid Antigen Test\u003cbr\u003e COVID-19 (Oral Fluid)\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Single-use test intended to detect the novel coronavirus SARS-CoV-2 that causes COVID-19 in human oral fluid.\u003cbr\u003e The test is designed for home use with self-collection of oral fluid samples from symptomatic individuals suspected of being infected with the COVID-19 virus. \u003cbr\u003eIt is a qualitative membrane-based immunoassay for the detection of SARS-CoV-2 antigens in human oral fluid samples.\u003cbr\u003e The test provides only a preliminary result; final confirmation must be based on clinical diagnostic results.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eBefore taking the test\u003c\/u\u003e\u003cbr\u003e Do not put anything in your mouth, including food, drinks, chewing gum, or tobacco products, for at least 10 minutes before taking the test.\u003cbr\u003e Wash your hands with soap and water for at least 20 seconds before testing. If soap and water are not available, use a hand sanitizer with at least 60% alcohol.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eStep 1: Sample collection\u003c\/u\u003e\u003cbr\u003e Remove the funnel and plastic tube from the package, insert the funnel onto the tube.\u003cbr\u003e Cough deeply 3-5 times. Wear a face mask or cover your mouth and nose with a cloth while coughing and maintain social distancing. \u003cbr\u003eGently spit the oral fluid into the funnel. The oral fluid (without bubbles) should reach the height indicated by the reference line.\u003cbr\u003e If the collected fluid is not sufficient, repeat the sample collection steps.\u003cbr\u003e Insert the used funnel into the biosafety bag.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eStep 2: Sample preparation\u003c\/u\u003e\u003cbr\u003e Pull to open the buffer solution and pour the entire solution into the tube with the oral fluid. Replace the cap on the tube. Gently squeeze the tube 10-15 times to mix well.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eStep 3: Running the test\u003c\/u\u003e\u003cbr\u003e Remove the test device from the sealed pouch and use it within one hour. Best results are obtained if the test is performed immediately after opening the foil pouch.\u003cbr\u003e Place the test cassette on a flat surface.\u003cbr\u003e Turn the tube upside down and pour 2 drops of solution into the well (S) of the test device and then start the timer.\u003cbr\u003e Do not move the test cassette while performing the test.\u003cbr\u003e  \u003cbr\u003e\u003cu\u003eStep 4:\u003c\/u\u003e\u003cbr\u003e Read the results after 15 minutes. Do not interpret the results after 20 minutes.\u003cbr\u003e After completing the test, place all test kit components in the biosafety bag and dispose of it according to local regulations.\u003cbr\u003e Do not reuse any used kit components.\u003cbr\u003e Wash your hands thoroughly after disposing of the test.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eReading the results\u003c\/u\u003e\u003cbr\u003e Inform your healthcare provider of the results and carefully follow local instructions\/regulations for COVID cases.\u003cbr\u003e  \u003cbr\u003e- POSITIVE: Two colored lines appear. One colored line should appear in the control region (C) and another colored line should appear in the test region (T). The intensity of the color in the test region (T) varies depending on the number of antigens present in the sample. Therefore, the presence of any shade of color in the test region (T) should be interpreted as a positive result. A positive result means that the person is very likely infected with COVID-19.\u003cbr\u003e Positive samples must be confirmed. Immediately self-isolate, as required by local regulations, and contact your doctor or district health care provider as directed by local authorities. The test will be verified by a confirmatory molecular test (PCR), and instructions on the next steps will be provided.\u003cbr\u003e  \u003cbr\u003e- NEGATIVE: Only one colored line appears in the control region (C). No colored line appears in the test region (T). It is unlikely that the person has COVID-19. However, the test may give an incorrect result (false negative) in some people with COVID-19. This means that they may have COVID-19 even if the test results are negative.\u003cbr\u003e If you experience symptoms such as headache, migraine, fever, loss of taste or smell, contact your nearest healthcare provider, according to your local authority's guidelines.\u003cbr\u003e You can repeat the test with a new kit. If you suspect the virus, repeat the test after 1-2 days, as coronavirus cannot be detected at all stages of infection.\u003cbr\u003e Even with a negative result, distancing and hygiene rules must continue to be observed.\u003cbr\u003e  \u003cbr\u003e- INVALID: The control line does not appear. Insufficient sample volume or incorrect procedure are the most likely causes for the control line not appearing. Review the procedure and repeat the test with a new kit or contact your healthcare provider or a COVID-19 testing center.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Read the package leaflet carefully before performing the test.\u003cbr\u003e The test is intended for in vitro self-diagnosis only.\u003cbr\u003e The test is for single use only; do not reuse. Do not use after the expiration date.\u003cbr\u003e Do not eat, drink, or smoke in the area where specimens or kits are handled.\u003cbr\u003e Do not drink the buffer solution provided in the kit. Handle the buffer solution with care and avoid contact with skin and eyes. In case of contact, rinse immediately with plenty of running water.\u003cbr\u003e Do not use the test if the package is damaged.\u003cbr\u003e Wash your hands thoroughly before and after handling. \u003cbr\u003eIf the preliminary result is positive, inform your doctor and carefully follow local instructions\/regulations for COVID cases.\u003cbr\u003e Tests performed on children and adolescents must be carried out in the presence of adults.\u003cbr\u003e The used test must be disposed of according to local regulations.\u003cbr\u003e Failure to follow certain steps in the test procedure may result in incorrect results.\u003cbr\u003e The results obtained with the test should be considered in addition to other clinical results from other tests and laboratory evaluations.\u003cbr\u003e If the test result is negative or nonreactive but clinical symptoms persist, it's because the virus may not be detectable in the early stages of infection. It's recommended to repeat the test with a new test device 1-2 days later or go to the hospital to rule out infection.\u003cbr\u003e Positive COVID-19 results may be due to infection with non-SARS-CoV-2 virus strains or other interfering factors.\u003cbr\u003e  \u003cbr\u003e\u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store at temperatures between 2°C and 30°C. Do not freeze.\u003cbr\u003e Do not open the package until you are ready to perform the test.\u003cbr\u003e Shelf life in intact packaging: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e - Testing device;\u003cbr\u003e - Sample collection device (funnel, tube and tube tip);\u003cbr\u003e - Buffer solution;\u003cbr\u003e - Package leaflet;\u003cbr\u003e - Bio-security bag.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e ICOV-802H\u003c\/div\u003e","brand":"SO.FARMA.MORRA SPA","offers":[{"title":"Default Title","offer_id":50734502871374,"sku":"989811423","price":8.46,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/989811423.jpg?v=1768762391"},{"product_id":"screen-test-covid-19-saliva","title":"SCREEN RAPID SELF-DIAGNOSTIC ANTIGEN TEST COVID-19 SARS-COV-2 SALIVA SAMPLES SELFTEST COVID SALIVA SCREEN","description":"\u003ch1\u003e SCREEN CHECK TEST\u003c\/h1\u003e\n\u003ch2\u003e Covid-19 Saliva Oral Fluid Test\u003c\/h2\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Single-use test intended to detect the novel coronavirus SARS-CoV-2 that causes COVID-19 in human oral fluid.\u003cbr\u003e The test is intended for home use with self-collection of oral fluid samples from symptomatic individuals suspected of being infected with the COVID-19 virus.\u003cbr\u003e It is a qualitative membrane-based immunoassay for the detection of SARS-CoV-2 antigens in human oral fluid samples.\u003cbr\u003e The test provides only a preliminary result; final confirmation must be based on clinical diagnostic results.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Before taking the test, do not put anything in your mouth, including food, drinks, chewing gum, or tobacco products, for at least 10 minutes before taking the test. \u003cbr\u003eWash your hands with soap and water for at least 20 seconds before taking the test. If soap and water are not available, use a hand sanitizer with at least 60% alcohol.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eStep 1: Sample collection\u003c\/u\u003e\u003cbr\u003e Remove the funnel and plastic tube from the package, insert the funnel into the tube, and cough deeply 3-5 times.\u003cbr\u003e Note: Wear a face mask or cover your mouth and nose with a cloth when coughing and maintain social distancing.\u003cbr\u003e Gently spit the oral fluid into the funnel. The oral fluid (without bubbles) should reach the height indicated by the reference line.\u003cbr\u003e Note: If the fluid collected is not sufficient, repeat the sample collection steps.\u003cbr\u003e Insert the used funnel into the biosafety bag.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eStep 2: Sample preparation\u003c\/u\u003e \u003cbr\u003ePlace the tube in the plastic holder. Pull to open the buffer solution and pour the entire solution into the tube with the oral fluid. Replace the cap on the tube. Gently squeeze the tube 10-15 times to mix well.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eStep 3: Running the test\u003c\/u\u003e\u003cbr\u003e Remove the test device from the sealed pouch and use it within one hour. Best results are obtained if the test is performed immediately after opening the foil pouch.\u003cbr\u003e Place the test device on a flat surface. Invert the tube and place 2 drops of solution into the well (S) of the test device, then start the timer. Do not move the device while performing the test.\u003cbr\u003e Read the results after 15 minutes. Do not interpret the results after 20 minutes.\u003cbr\u003e After completing the test, place all test kit components in a biosafety bag and dispose of it according to local regulations. Do not reuse any used kit components. \u003cbr\u003eWash your hands thoroughly after disposing of the test.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eStep 4: Reading the results\u003c\/u\u003e\u003cbr\u003e Please inform your healthcare provider of your results and carefully follow local COVID guidelines\/regulations.\u003cbr\u003e\u003cbr\u003e - POSITIVE: *Two colored lines appear. One colored line should appear in the control region (C) and another colored line should appear in the test region (T). A positive result means that the person is highly likely infected with COVID-19; positive samples must be confirmed. Immediately self-isolate as required by local regulations and contact your healthcare provider or district health care provider as directed by local authorities. The test should be verified with a confirmatory molecular (PCR) test, and instructions on the next steps will be provided. \u003cbr\u003e*NOTE: The intensity of the color in the test line region (T) varies depending on the number of SARS-CoV-2 antigens present in the specimen. Therefore, the presence of any shade of color in the test region (T) should be interpreted as a POSITIVE result.\u003cbr\u003e\u003cbr\u003e - NEGATIVE: Only one colored line appears in the control region (C). No colored line appears in the test region (T). It is unlikely that the person has COVID-19. However, this test may give an incorrect result (a false negative) in some people with COVID-19. This means that you may have COVID-19 even if the test results are negative. \u003cbr\u003eIf you experience symptoms such as headache, migraine, fever, or loss of taste or smell, contact your nearest healthcare provider in accordance with your local health authority's guidelines. You can also repeat the test with a new kit. If you suspect the virus, repeat the test after 1-2 days, as coronavirus cannot be detected at all stages of infection.\u003cbr\u003e Even with a negative result, distancing and hygiene rules must continue to be observed, and mitigation\/travel, event attendance, and so on should follow local COVID guidelines\/requirements.\u003cbr\u003e\u003cbr\u003e - INVALID: The control line does not appear. Insufficient sample volume or incorrect procedure are the most likely causes of the missing control line. Review the procedure and repeat the test with a new kit or contact your healthcare provider or a COVID-19 testing center.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Read the package leaflet carefully before performing the test. \u003cbr\u003eThe test is intended for in vitro self-diagnosis only.\u003cbr\u003e The test is for single use only; do not reuse. Do not use after the expiration date.\u003cbr\u003e Do not eat, drink, or smoke in the area where specimens or kits are handled.\u003cbr\u003e Do not drink the buffer solution provided in the kit. Handle the buffer solution with care and avoid contact with skin and eyes. In case of contact, rinse immediately with plenty of running water.\u003cbr\u003e Do not use the test if the package is damaged.\u003cbr\u003e Wash hands thoroughly before and after handling.\u003cbr\u003e If the preliminary result is positive, inform your doctor and carefully follow local instructions\/regulations for COVID cases.\u003cbr\u003e Tests performed on children and adolescents must be carried out in the presence of adults.\u003cbr\u003e The used test must be disposed of according to local regulations.\u003cbr\u003e Failure to follow certain steps in the test procedure may result in incorrect results. \u003cbr\u003eThe results obtained with the test should be considered in addition to other clinical results from other tests and laboratory evaluations.\u003cbr\u003e If the test result is negative or nonreactive but clinical symptoms persist, it's because the virus may not be detectable in the early stages of infection. It's recommended to repeat the test 1-2 days later or go to the hospital to rule out infection.\u003cbr\u003e Positive COVID-19 results may be due to infection with non-SARS-CoV-2 virus strains or other interfering factors.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store the test at temperatures between 2-30°C. Do not freeze.\u003cbr\u003e Do not open the package until you are ready to perform the test.\u003cbr\u003e Shelf life when packaging is intact: 12 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e • Test device;\u003cbr\u003e • Sample collection device (funnel, tube and tube cap);\u003cbr\u003e • Buffer solution;\u003cbr\u003e • Package leaflet;\u003cbr\u003e • Bio-security bags.\u003cbr\u003e  \u003cbr\u003e\u003cb\u003eCod.\u003c\/b\u003e ICOV-802H\u003c\/div\u003e","brand":"SCREEN ITALIA SRL","offers":[{"title":"Default Title","offer_id":50734593605966,"sku":"982735728","price":4.41,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-242175_e78f8ded-cdf2-4927-aa23-703437a70330.jpg?v=1768763134"},{"product_id":"test-antigenico-rapido-covid-19-clungene-autodiagnostico-determinazione-qualitativa-antgeni-sars-cov-2-in-tamponi-nasalimediante-immunocromatografia","title":"RAPID ANTIGEN TEST COVID-19 CLUNGENE SELF-DIAGNOSTIC QUALITATIVE DETERMINATION OF SARS-COV-2 ANTAGENS IN NASAL SWABS BY IMMUNOCHROMATOGRAPHY","description":"\u003ch2\u003e CLUNGENE\u003c\/h2\u003e\n\u003ch1\u003e COVID-19 Antigen Rapid Test\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e \u003cbr\u003eLateral flow immunoassay method for the qualitative detection of SARS-CoV-2 nucleocapsid antigen in nasal swabs of subjects with symptoms or other epidemiological reasons suggesting COVID-19 infection.\u003cbr\u003e The test is intended for use by lay people aged 15 and older and, as appropriate, by adults testing another person under 15. Persons over 65 should seek assistance in taking the test.\u003cbr\u003e The test provides only a preliminary screening result for the SARS-CoV-2 virus. Positive results must be confirmed by a laboratory-based PCR test.\u003cbr\u003e People with a negative test result who continue to experience COVID-19-like symptoms should seek medical attention.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eTest preparation\u003c\/u\u003e\u003cbr\u003e Make sure all test components are at room temperature (15-30°C).\u003cbr\u003e Keep a clock, timer, or stopwatch handy. \u003cbr\u003eCheck that the package is intact. Do not use the test if the package is visibly damaged.\u003cbr\u003e Open the test cassette package only immediately before use. Use the test cassette within one hour of opening the package.\u003cbr\u003e Wash your hands with soap and water and dry them thoroughly.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eRunning the test\u003c\/u\u003e\u003cbr\u003e Open the tube containing the extraction reagent by carefully removing the film. Insert the tube into the tube holder (hole on the package). \u003cbr\u003eRemove the swab from the pouch: open the package at the end of the stick. Do not touch the swab head. Remove the swab and gently insert the entire swab head into the nostril, about 2.5 cm deep. Rotate the swab against the wall of the nostril at least 5 times. Remove the swab, insert it into the other nostril, and repeat. Perform this step carefully: false-negative results may occur if the nasal swab is not performed correctly.\u003cbr\u003e Insert the swab into the tube containing the extraction reagent. Rotate the swab 5 times inside the reagent, pressing the swab head against the bottom and side of the tube. Leave the swab in the reagent for 1 minute. Remove the swab by pressing the sides of the tube to expel the liquid from the swab. Close the tube tightly with the cap. \u003cbr\u003eOpen the sealed pouch containing the test cassette and remove it. Place the test cassette on a flat surface.\u003cbr\u003e Hold the tube vertically over the sample well and add 3 drops to the well, gently squeezing the sides of the tube. A false negative result may occur if fewer than 3 drops of sample are added to the well. Adding 1-2 more drops of sample will not affect the result, as long as the control line (C) can be read.\u003cbr\u003e Start the clock\/stopwatch or timer. Read the test result after 15-20 minutes; do not read the result after more than 20 minutes. Incorrect results may occur if the test results are read before 15 minutes or after 20 minutes.\u003cbr\u003e Once the test is performed, collect the used kit parts and swab samples in a disposal bag and dispose of them with household waste. Wash your hands thoroughly after handling.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInterpretation of the results\u003c\/u\u003e \u003cbr\u003e- POSITIVE: Two lines appear, the control line (C) and the test line (T). The color intensity of the test line (T) may be very faint, but the result is still positive. A positive test result indicates that you are likely a carrier of COVID-19. You should undergo a laboratory PCR test as soon as possible to confirm your COVID-19 diagnosis and follow local isolation guidelines to avoid spreading the virus to others.\u003cbr\u003e  \u003cbr\u003e- NEGATIVE: Only one colored line, the control line (C), appears. The test line (T) does not appear. A negative test result indicates that you are likely not a carrier of COVID-19. Even if you get a negative result, you should still follow all guidelines to limit the spread of COVID-19. If symptoms develop or persist, undergo a laboratory PCR test. If infection is suspected, it is recommended to repeat the test after 1–2 days, as the virus cannot be accurately detected at all stages of infection.\u003cbr\u003e\u003cbr\u003e - INVALID: The control line (C) does not appear. The test result is invalid regardless of whether the test line (T) appears or not. Repeat the test with a new cassette or contact your doctor.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e For in vitro diagnostics only. \u003cbr\u003eDo not use this test as the sole basis for managing COVID-19 infection. Please consult a healthcare provider at any time if symptoms persist or worsen, or if you are concerned about your health.\u003cbr\u003e Negative results may occur if the test is not performed within the first 7 days of symptom onset.\u003cbr\u003e Testing on a subject under 15 years of age must be performed by an adult.\u003cbr\u003e Keep out of reach of children to reduce the risk of accidentally drinking the reagent or swallowing small parts.\u003cbr\u003e Do not use after the expiration date.\u003cbr\u003e The test is single use and should only be used with the components provided.\u003cbr\u003e Do not perform the test in direct sunlight.\u003cbr\u003e Avoid contact with the extraction reagent. In case of inhalation, ingestion, or skin or eye exposure to the extraction reagent, immediately take first aid measures in accordance with the safety data sheet (SDS). \u003cbr\u003eThe test requires taking a sample from the nasal cavity. When taking the test, pay close attention to the instructions on how to perform the swab. Performing the sample incorrectly may result in an inaccurate result. This is especially important if you are asymptomatic.\u003cbr\u003e The test cassette must remain in the sealed pouch until ready for use.\u003cbr\u003e Wash your hands thoroughly before and after testing.\u003cbr\u003e The test is to be used only for the qualitative detection of SARS-CoV-2 antigens in nasal swab samples.\u003cbr\u003e The intensity of the test line does not necessarily correlate with the SARS-CoV-2 viral titer present in the sample.\u003cbr\u003e Failure to follow the \"Instructions for Use\" may adversely affect test performance and\/or invalidate the test result.\u003cbr\u003e This is a presumptive test only. If the result is positive, you must immediately undergo a laboratory PCR test and undergo clinical follow-up. \u003cbr\u003eNegative results may occur if the antigen level in a sample is below the test's detection limit. It is recommended to repeat the test after 1-2 days if you suspect a current infection, are in a high-risk environment or where there is an occupational hazard, or have a known exposure to COVID-19.\u003cbr\u003e Negative results do not rule out SARS-CoV-2 infection. If you experience symptoms similar to COVID-19, you should immediately undergo a further laboratory PCR test.\u003cbr\u003e Positive test results do not exclude co-infections with other pathogens.\u003cbr\u003e A positive result cannot determine whether a person is contagious.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store in the sealed pouch at a temperature of 4-30°C.\u003cbr\u003e Shelf life in intact packaging: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e - 1 test cassette;\u003cbr\u003e - 1 test tube containing extraction reagent;\u003cbr\u003e - 1 swab;\u003cbr\u003e - 1 disposal bag;\u003cbr\u003e - 1 instructions for use.\u003cbr\u003e  \u003cbr\u003e\u003cb\u003eCod.\u003c\/b\u003e ISCOVU002-B00\u003c\/div\u003e","brand":"BIG START ITALIA SRL","offers":[{"title":"Default Title","offer_id":50734597079374,"sku":"984821900","price":4.68,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-261625.jpg?v=1768763162"},{"product_id":"test-one-step-strep-a-autodiagnostico-determinazione-qualitativa-antigeni-streptococco-a-da-tampone-faringeo","title":"STREP A ANTIGEN HOME TEST QUALITATIVE DETERMINATION OF STREPTOCOCCUS A ANTIGENS FROM THROAT SWAB 1 PIECE","description":"\u003ch2\u003e SCREEN\u003c\/h2\u003e\n\u003ch1\u003e Strep A\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e A lateral flow immunoassay for the qualitative detection of Group A Streptococcal antigen from throat swab specimens to aid in the early diagnosis of Group A Streptococcal infection. \u003cbr\u003eWhen the specimen is added to the specimen well, capillary action causes the specimen to migrate across the membrane. When Strep A antigen levels in the specimen are at or above the cutoff, a visible colored line appears in the test region, indicating a positive result. The absence of this colored line in the test region suggests a negative result. If the test was performed correctly, a colored line will appear in the control region as a procedural control.\u003cbr\u003e For in vitro self-diagnostic use only.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eSample collection and preparation\u003c\/u\u003e\u003cbr\u003e Collect the sample with the sterile throat swab provided in the kit. Hold your tongue down with a tongue depressor. Swab the back of your throat, tonsils, and other inflamed areas. Avoid touching your tongue, cheeks, and teeth with the swab.\u003cbr\u003e The test should ideally be performed immediately after sample collection.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eRunning the test\u003c\/u\u003e \u003cbr\u003eBring the device and extraction reagents to room temperature (10-30°C) before performing the test.\u003cbr\u003e Add 4 drops of Extraction Reagent A and 4 drops of Reagent B to the respective extraction tube and mix thoroughly.\u003cbr\u003e Place the extraction swab in the test tube. Shake the swab ten times. Leave the swab in the test tube for 1 minute. Then remove the swab while pressing the swab head against the sides of the tube to release as much liquid as possible into the tube. Discard the used swab.\u003cbr\u003e Remove the test from the sealed foil pouch by tearing at the notch and place the test on a clean, dry, flat surface.\u003cbr\u003e Add 3 drops of extracted sample to the sample well on the test cassette.\u003cbr\u003e Wait 10 minutes and read the results. Do not read the results after 15 minutes.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInterpretation of the results\u003c\/u\u003e \u003cbr\u003ePOSITIVE: Two colored lines appear, one in the test region (T) and one in the control region (C). You may have a Group A Streptococcus infection; consult your doctor.\u003cbr\u003e\u003cbr\u003e NEGATIVE: Only one colored line appears in the control region (C). No colored line appears in the test region (T). The concentration of Group A Streptococcus antigen is at or below the detection limit of the test.\u003cbr\u003e\u003cbr\u003e INVALID: No colored line appears, or only one colored line appears in the test region (T) and no colored line appears in the control region (C). Failure of the control region (C) to appear indicates an error during the test procedure or deterioration of the test reagent. Repeat the test using a new kit. If the test still gives an invalid result, contact your local distributor.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e For in vitro self-diagnostic use only. \u003cbr\u003eDo not ingest.\u003cbr\u003e Do not interchange caps between reagents.\u003cbr\u003e Do not use the test beyond the expiration date.\u003cbr\u003e Keep out of reach of children.\u003cbr\u003e Do not use the test if the package is punctured or not properly sealed.\u003cbr\u003e The test is single use: discard after use.\u003cbr\u003e Avoid contact of reagents A and B with eyes, sensitive mucous membranes, cuts, abrasions, etc. If reagents come into contact with skin or eyes, rinse thoroughly with water.\u003cbr\u003e Do not eat, drink, or smoke in the area where specimens are handled and the test is performed.\u003cbr\u003e The device used, the swab, and the extraction tube must be treated as contagious waste and therefore disposed of in biohazard waste containers.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store at 4-30°C. Keep away from sunlight, moisture, and heat. Do not freeze.\u003cbr\u003e Shelf life in intact packaging: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e - 1 sealed sachet (containing a test device and a desiccant sachet); \u003cbr\u003e- 1 extraction tube;\u003cbr\u003e - 1 sterile throat swab;\u003cbr\u003e - extraction reagents A and B;\u003cbr\u003e - package leaflet.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e W039P0001\u003c\/div\u003e","brand":"SCREEN ITALIA SRL","offers":[{"title":"Default Title","offer_id":50997444706638,"sku":"987318110","price":12.15,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-301741_03f34ef0-9b6d-4dd6-b1f0-efb1136067f6.jpg?v=1768765794"},{"product_id":"screen-test-rapido-streptococco-tampone-faringeo-2-pezzi","title":"STREP A ANTIGEN HOME TEST QUALITATIVE DETERMINATION OF STREPTOCOCCUS A ANTIGENS FROM THROAT SWAB 2 PIECES","description":"\u003ch1\u003e SCREEN STEP-A\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Rapid immunochromatographic test for the qualitative and presumptive detection of Group A Streptococcal antigens using a swab. The test is an in vitro diagnostic device and is used as an aid in the diagnosis of Group A Streptococcal infection in patients with symptoms. The Strep Screen Test is intended for self-diagnosis. Children under 18 years of age must be supervised or assisted by an adult during the test. The test procedure is not automated. Test results should not be used as the sole basis for diagnosis but are recommended for interpretation by a physician in a clinical setting.\u003cbr\u003e  \u003cbr\u003e\u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e - The test must be used at room temperature (15°C to 30°C). If the test has been stored in a cool place (below 15°C), let it stand at room temperature for 30 minutes before using.\u003cbr\u003e - Make sure the packaging is intact. Do not use the test if the packaging is visibly damaged.\u003cbr\u003e - Do not open the foil pouch until you are ready to perform the test. Use the test within one hour of opening.\u003cbr\u003e - Note: Samples must be analyzed immediately after collection. Follow local regulations for disposal of used tests.\u003cbr\u003e \u003cu\u003eTEST PROCEDURE\u003c\/u\u003e\u003cbr\u003e 1. Wash your hands with soap and water or use hand sanitizer for 20 seconds.\u003cbr\u003e 2. Add 4 drops of reagent 1 to the tube provided.\u003cbr\u003e 3. Add 4 drops of reagent 2 to the test tube. Mix the solution by gently shaking the test tube.\u003cbr\u003e 4. Insert the test tube into the test tube holder on the front of the package or test tube holder. \u003cbr\u003e5. Open the swab package by pulling the free ends of the package. Remove the swab from the stem. Do not touch the tip of the swab.\u003cbr\u003e 6. Hold the tongue still with a tongue depressor.\u003cbr\u003e 7. Insert the swab into the test tube.\u003cbr\u003e 8. Rotate the swab by squeezing the bottom of the tube 10-15 times to exert light pressure on the tip of the swab.\u003cbr\u003e 9. Remove the swab. Squeeze the tube to expel as much liquid as possible from the swab.\u003cbr\u003e 10. Insert the nozzle back into the extraction tube.\u003cbr\u003e 11. Invert the tube and add 3 drops of solution to the sample well, gently squeezing the tube.\u003cbr\u003e 12. Read the result after 5 minutes. After more than 10 minutes, the result is no longer valid.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReading the results\u003c\/b\u003e\u003cbr\u003e Positive: Two colored lines appear on the membrane. One line appears in the control region (C) and another in the test region (T). \u003cbr\u003eNegative: Only one colored stripe appears in the control area (C). No stripe appears in the control area.\u003cbr\u003e Invalid: The control line does not appear. Any test that does not produce a control line at the specified time should be discarded. Review the procedure and repeat the test with a new test. If the problem persists, discontinue use of the kit immediately and contact the distributor.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e 1. For in vitro diagnostic use only.\u003cbr\u003e 2. Read the instructions for use before use. The instructions for use must be read carefully and followed.\u003cbr\u003e 3. Do not test or use components after the expiration date.\u003cbr\u003e 4. Do not use if the case is damaged or open.\u003cbr\u003e 5. Do not use the extraction buffer if it becomes discolored or cloudy. Discoloration or turbidity may indicate microbial contamination. \u003cbr\u003e6. Avoid cross-contamination of samples by using a new extraction tube for each sample obtained.\u003cbr\u003e 7. Do not mix or interchange reagents from different lots. Do not interchange solution bottle caps.\u003cbr\u003e 8. Avoid contact with eyes, skin, and mucous membranes with the swab. If the swab comes into contact with the skin, rinse thoroughly with water.\u003cbr\u003e 9. Keep out of reach of children.\u003cbr\u003e 10. Use only the test components provided.\u003cbr\u003e 11. Keep the swab clean. Do not touch the swab tip and ensure it does not touch any surface before use. Place the swab in the swab immediately after collecting the sample.\u003cbr\u003e 12. This is a single-use test. Do not reuse the tests.\u003cbr\u003e 13. This test is for human use only.\u003cbr\u003e 14. Dispose of kit components and used swab samples in household waste. \u003cbr\u003e15. Since the test device contains a toxic composition and the highest morbidity rate of upper respiratory tract infection was found in children, for children under 18 years of age the test should be performed by parents or other adult family members.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e 1. As with all diagnostic tests, the definitive clinical diagnosis should not be based on the results of a single test, but should be made by the physician only after evaluating all clinical and laboratory findings.\u003cbr\u003e 2. Failure to follow the TEST PROCEDURE and INTERPRETATION OF RESULTS may negatively influence and\/or distort the test result.\u003cbr\u003e 3. The test does not distinguish asymptomatic carriers of Group A Streptococcus from those with symptomatic infection.\u003cbr\u003e 4. Respiratory infections, including pharyngitis, can be caused by streptococci of serogroups other than group A and by other pathogens. \u003cbr\u003e5. The accuracy of the test depends on the quality of the swab sample. False negatives may result from improper sample collection or storage.\u003cbr\u003e 6. A negative result can also be obtained from patients at the onset of the disease due to the low antigen concentration.\u003cbr\u003e 7. The device has not been tested on children under 4 years of age.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e 1. Store at 2-30°C in the sealed pouch until the expiry date.\u003cbr\u003e 2. Keep away from sunlight, moisture and heat.\u003cbr\u003e 3. Do not freeze.\u003cbr\u003e 4. Open the pouch preferably just before testing. Use the test kit within 1 hour of opening the pouch.\u003cbr\u003e 5. The contents of the kit are stable until the expiry dates indicated on the outer packaging and containers.\u003cbr\u003e 6. The swabs in the kit are stable until the expiration date indicated on the swab tube.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Materials provided:\u003cbr\u003e - 2 tests;\u003cbr\u003e - reagent 1;\u003cbr\u003e - reagent 2;\u003cbr\u003e - sterile tongue depressor;\u003cbr\u003e - waste bag; \u003cbr\u003e- sterile swab;\u003cbr\u003e - WorkStation;\u003cbr\u003e - extraction tube with nozzle;\u003cbr\u003e - package leaflet.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e ICOV-802H\u003c\/div\u003e","brand":"SCREEN ITALIA SRL","offers":[{"title":"Default Title","offer_id":51073921548622,"sku":"971664533","price":15.21,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/971664533.jpg?v=1768766461"},{"product_id":"test-multidrugs-1-test-profar","title":"MULTIDRUG TEST 1 PROFAR TEST","description":"\u003cfont face=\"Arial\" size=\"4\"\u003e\u003cb\u003eSelf-diagnosis test\u003c\/b\u003e\u003c\/font\u003e\u003cbr\u003e \u003cfont face=\"Arial\" size=\"6\"\u003e\u003cb\u003eMultidrugs\u003c\/b\u003e\u003c\/font\u003e\u003cbr\u003e\u003cbr\u003e\u003cdiv align=\"justify\"\u003e\n\n \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Rapid self-test for the immediate and quantitative detection of various drugs and drug metabolites in human urine samples. Also suitable for professional use for point-of-care measurements.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Package containing 1 test.\u003c\/div\u003e","brand":"FEDERFARMA.CO SPA","offers":[{"title":"Default Title","offer_id":51114541744462,"sku":"974849337","price":17.55,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-167314.jpg?v=1768767264"},{"product_id":"screen-test-rapido-screen-test-candida-autodiagnostico-1-pezzo","title":"SCREEN TEST RAPID SCREEN TEST CANDIDA SELF-DIAGNOSTIC 1 PIECE","description":"\u003ch2\u003e SCREEN CHECK TEST\u003c\/h2\u003e\n\u003ch1\u003e Candida Screen Test\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e A rapid, qualitative self-test capable of detecting the presence of Candida antigens in vaginal swab samples. \u003cbr\u003eThe test is based on the immunochromatographic method. The sample collected by swab is added to the sample pad through the cap containing the dilution buffer. From there, the sample migrates to the conjugate pad, releasing anti-Candida antibodies conjugated to blue-colored latex particles. The resulting Candida antigen-antibody conjugate complex continues to migrate to the nitrocellulose membrane strip. The complex is then captured on the support membrane by immobilized anti-Candida antibodies, generating a signal line.\u003cbr\u003e If Candida antigens are present in the swab sample, a biological reaction will occur and the result will be positive. A blue line will appear in the test line region (T) on the membrane.\u003cbr\u003e The test includes a built-in control system, represented by the control line (C). The control line confirms that the test was performed correctly.\u003cbr\u003e  \u003cbr\u003e\u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Leave the test cassette at room temperature (between 15°C and 27°C) before performing the procedure.\u003cbr\u003e Open the test kit only when you are ready to perform the procedure. Do not use the test if the pouch is damaged. Keep a watch\/stopwatch handy.\u003cbr\u003e Make sure the surface on which the procedure will be performed is clean. Wash your hands. The test can be performed at any time of day.\u003cbr\u003e Remove the device from the sealed bag and place it horizontally on a flat surface. Hold the device steady with one hand. With the other hand, gently remove the foil seal from the purple cap. The purple cap contains a liquid.\u003cbr\u003e Remove the swab from the wrapper. Insert the swab about 2 cm into the vagina and rotate for 20 seconds. Gently remove the swab. \u003cbr\u003eRotate the swab in the liquid in the purple cap for 20 seconds. Gently remove the swab, pressing it against the inside wall of the purple cap. Discard the swab.\u003cbr\u003e Hold the device steady with one hand. Rotate the purple cap counterclockwise until it reaches the end position, then rotate it counterclockwise until it reaches the starting position. Repeat this step two more times. At the end position, the notches on the purple cap should align with the indentation on the white base.\u003cbr\u003e Read the results after 10 minutes.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInterpretation of the results\u003c\/u\u003e\u003cbr\u003e POSITIVE: a blue line appears at the control line (C) and a further blue line appears at the test line (T).\u003cbr\u003e The test result indicates that Candida antigens are present in your vaginal discharge. Contact your doctor to confirm the result and initiate treatment.\u003cbr\u003e  \u003cbr\u003eNEGATIVE: Only one blue line appears at the control line (C) and no blue line appears at the test line (T).\u003cbr\u003e The test result indicates that Candida antigens are not present in vaginal secretions. If symptoms or complaints persist, it is advisable to consult a doctor.\u003cbr\u003e\u003cbr\u003e INVALID: If neither line appears or only the test line (T) appears, the test result cannot be interpreted. You must perform a new test, carefully following the instructions.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e For in vitro diagnostic use only.\u003cbr\u003e Do not introduce inside the body.\u003cbr\u003e The test is not reusable.\u003cbr\u003e The test only works if the instructions are followed carefully.\u003cbr\u003e A negative test result doesn't rule out other infections. Contact your doctor.\u003cbr\u003e The test should not be used during menstruation.\u003cbr\u003e Suitable only for women aged 18 years and over.\u003cbr\u003e Do not use during pregnancy. \u003cbr\u003eDo not use the test within 7 days of taking any medicines for vaginal infections.\u003cbr\u003e Do not use the test within 24 hours of using creams, gels, foams, douches or other intimate hygiene products.\u003cbr\u003e Do not use after the expiration date printed on the foil pouch.\u003cbr\u003e Keep out of reach of children.\u003cbr\u003e Dispose of the device and the swab with normal household waste.\u003cbr\u003e Do not use the stick if it falls to the ground.\u003cbr\u003e Do not use test components if they are broken.\u003cbr\u003e Do not use if liquid leaks from the cap. The amount of liquid inside the cap is crucial to ensuring proper functioning of the test.\u003cbr\u003e Do not twist the cap before removing the seal or inserting the test stick. Twisting the top of the device is irreversible and will invalidate the test.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store in a dry place at room temperature (between 2°C and 30°C). \u003cbr\u003eShelf life in intact packaging: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e - 1 test cassette;\u003cbr\u003e - 1 sterile swab;\u003cbr\u003e - 1 instruction sheet for use;\u003cbr\u003e - 1 translated information sheet.\u003c\/div\u003e","brand":"SCREEN ITALIA SRL","offers":[{"title":"Default Title","offer_id":51114552230222,"sku":"987315811","price":20.61,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-306631.jpg?v=1768767320"},{"product_id":"screen-test-sierologico-rapido-autodiagnostico-covid-19-anticorpi-igg-sars-cov-2-nel-sangue-screen","title":"SCREEN RAPID SELF-DIAGNOSTIC SEROLOGICAL TEST COVID-19 IGG SARS-COV-2 ANTIBODIES IN BLOOD SCREEN","description":"\u003ch1\u003e SCREEN\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e\n\u003ch2\u003e CHECK TEST\u003cbr\u003e Covid-19 RBD Test\u003c\/h2\u003e \u003cb\u003eDescription\u003c\/b\u003e \u003cbr\u003eA rapid immunochromatographic test for the qualitative detection of IgG antibodies to the SARS-CoV-2 spike (S) protein receptor-binding domain (RBD) in human fingerstick whole blood approximately 10 days after vaccination. It is designed to aid in the identification of individuals with an adaptive immune response to SARS-CoV-2. Results are for the detection of SARS-CoV-2 IgG S-RBD antibodies. Positive results indicate the presence of IgG antibodies to SARS-CoV-2.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Before the test:\u003cbr\u003e Bring the test and buffer to room temperature (15-30°C) before use.\u003cbr\u003e Wash your hands thoroughly with warm water and dry them.\u003cbr\u003e Remove the test cassette from the sealed pouch and use it within 1 hour.\u003cbr\u003e Do not touch the test area (the strip next to the letters C, T, and S) of the test strip. Best results are obtained if the test is performed immediately after opening. Place the test on a flat, clean surface. \u003cbr\u003e1. Use the alcohol swab to clean the tip of your middle or ring finger where you want to prick your finger. Let it dry for 10 seconds.\u003cbr\u003e 2. Gently twist and remove the lancet cap. Open the lancet only just before testing.\u003cbr\u003e 3. Press the sterile lancet firmly against the tip of your middle or ring finger.\u003cbr\u003e 4. To increase blood flow, use your thumb and forefinger to apply gentle pressure around the puncture site.\u003cbr\u003e 5. Without squeezing the dropper, apply it to the blood. The blood should reach the line indicated on the dropper. You can massage your finger again to obtain more blood if the line is not reached. Avoid air bubbles; if air bubbles appear, discard the blood in a plastic bag (e.g., a biosafety bag), then repeat the previous collection steps. \u003cbr\u003e6. Place the tip of the dropper in contact with the center of the sample well(s) and release all the blood immediately after collection.\u003cbr\u003e 7. Add 2 drops of buffer to the sample well (S) and start the timer. Do not move the test during development.\u003cbr\u003e 8. Read the results after 10 minutes. Do not interpret results after 20 minutes.\u003cbr\u003e Positive: *Two colored lines appear. One colored line in the control region (C) and another in the test region (T). A positive result in the test region indicates the detection of SARS-CoV-2 S-RBD IgG in the specimen.\u003cbr\u003e *Note: The intensity of the color in the test line (T) varies depending on the amount of S-RBD SARS-CoV-2 IgG present in the specimen. Therefore, any shade of color in the test region (T) should be considered positive. \u003cbr\u003eNegative: A colored line appears in the control region (C). No colored line appears in the test region (T). A negative result indicates that the SARS-CoV-2 IgG S-RBD antibody was not detected in the specimen.\u003cbr\u003e Invalid: The control line does not appear. Insufficient sample volume or improper procedural techniques are the most common reasons for the control line not appearing. Review the procedure and repeat the test with a new device. If the problem persists, discontinue use of the test immediately and contact your supplier.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e 1. This package insert must be read in its entirety before performing the test. Failure to follow the instructions in the package insert may result in inaccurate test results.\u003cbr\u003e 2. For in vitro self-test diagnostic use only.\u003cbr\u003e 3. Keep out of reach of children. Testing on children and young people should be performed by an adult. \u003cbr\u003e4. Do not eat, drink, or smoke in the specimen or kit handling area.\u003cbr\u003e 5. Do not use if the test package is damaged.\u003cbr\u003e 6. Wash your hands thoroughly before performing the test.\u003cbr\u003e 7. Make sure you use an adequate amount of sample during the test. Too little or too much sample may cause inconsistent results.\u003cbr\u003e 8. Do not touch the test reaction area on the device strip.\u003cbr\u003e 9. The used test must be disposed of according to local regulations. Do not reuse any component of the kit.\u003cbr\u003e 10. Do not drink the buffer contained in the kit. Handle the buffer carefully to avoid contact with skin or eyes; if this occurs, rinse immediately with running water.\u003cbr\u003e 11. The SARS-CoV-2 S-RBD IgG Antibody Rapid Test (Fingerstick Whole Blood) should only be used on individuals vaccinated against COVID-19. \u003cbr\u003eDo not use the kit beyond the expiration date printed on the sealed package. Do not open the sealed package until you are ready to perform the test.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store in the sealed container at room temperature or refrigerated (2-30°C). Do not freeze.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Package containing:\u003cbr\u003e - test cassette (each cassette is in a sealed package with desiccant);\u003cbr\u003e - package leaflet;\u003cbr\u003e - buffer;\u003cbr\u003e - alcohol swab;\u003cbr\u003e - sterile lancet;\u003cbr\u003e - dropper;\u003cbr\u003e - biosafety bag.\u003c\/div\u003e","brand":"SCREEN ITALIA SRL","offers":[{"title":"Default Title","offer_id":51759605711182,"sku":"983834096","price":7.23,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-258229.jpg?v=1768770174"},{"product_id":"screen-test-autodiagnostico-antigenico-rapido-covid-19-sars-cov-2-tamponi-nasali-selftest-covid-test-antigene-screen","title":"SCREEN RAPID ANTIGEN SELF-DIAGNOSTIC TEST COVID-19 SARS-COV-2 NASAL SWABS SELFTEST COVID ANTIGEN TEST SCREEN","description":"\u003cb\u003eDescriptive sheet\u003c\/b\u003e\u003cbr\u003e\u003ch1\u003e SCREEN CHECK TEST\u003c\/h1\u003e\n\u003ch2\u003e SARS-CoV-2 Antigen Rapid Test\u003c\/h2\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e \u003cbr\u003eSingle-use test intended to detect SARS-CoV-2 that causes COVID-19 with self-collected nasal swab specimens from symptomatic individuals suspected of being infected with COVID-19.\u003cbr\u003e The results are for the detection of SARS-CoV-2 nucleocapsid protein antigens. An antigen is usually detectable in upper respiratory tract samples during the acute phase of infection.\u003cbr\u003e Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is needed to determine infection status. Positive results are indicative of the presence of SARS-CoV-2. Individuals who test positive should self-isolate and seek further care from their healthcare provider. Positive results do not rule out bacterial infection or co-infection with other viruses. \u003cbr\u003eNegative results do not rule out SARS-CoV-2 infection. Individuals who test negative and continue to experience COVID-like symptoms should contact their healthcare provider.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Wash your hands with soap and water for at least 20 seconds before and after testing. If soap and water are not available, use a hand sanitizer with at least 60% alcohol. Remove the cap from the extraction swab tube and place the tube in the tube holder in the box.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eNasal swab sample collection\u003c\/u\u003e :\u003cbr\u003e Remove the sterile swab from the pouch. Insert the swab into the nostril until you feel a slight resistance (about 2 cm up the nose). Slowly rotate the swab, rubbing it along the inside of the nostril 5-10 times against the nasal wall. \u003cbr\u003eNote: This may be uncomfortable. Do not insert the swab further if you feel strong resistance or pain. When the nasal mucosa is damaged or bleeding, collecting a nasal swab is not recommended. If you are collecting swabs from others, please wear a face mask. With children, it may not be necessary to insert the swab so far into the nostril. For very young children, another person may be needed to hold the child's head while collecting the swab.\u003cbr\u003e Gently remove the swab.\u003cbr\u003e Using the same swab, repeat steps two in the other nostril.\u003cbr\u003e Remove the sterile swab.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eSample preparation\u003c\/u\u003e :\u003cbr\u003e Place the swab in the extraction tube, make sure it touches the bottom and shake the swab to mix well. Press the head of the swab against the tube and rotate the swab for 10-15 seconds. \u003cbr\u003eRemove the swab by pressing the swab head against the inside of the extraction tube. Place the swab in the biosafety bag.\u003cbr\u003e Close the cap of the extraction tube.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eTest\u003c\/u\u003e :\u003cbr\u003e Remove the test cassette from the sealed foil pouch and use it within one hour. Best results are obtained if the test is performed immediately after opening the foil pouch.\u003cbr\u003e Place the test cassette on a flat surface.\u003cbr\u003e Open the small cap and invert the sample extraction tube and add 3 drops of the extracted sample to the sample well (S) of the test cassette and start the (timer).\u003cbr\u003e Do not move the test cassette during test development.\u003cbr\u003e Read the result at 15 minutes. Do not read the result after 20 minutes.\u003cbr\u003e At the end of the test, place all components in a plastic biosafety bag and dispose of according to local regulations.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eReading the results\u003c\/u\u003e : \u003cbr\u003ePOSITIVE: Two distinct colored lines appear. One colored line should appear in the control region (C) and another colored line should appear in the test region (T). The intensity of the color in the test line region (T) varies depending on the number of SARS-CoV-2 antigens present in the sample. Therefore, any shade of color in the test region (T) should be interpreted as a POSITIVE result. A positive result means that the person is very likely to have COVID-19, positive samples should be confirmed. Immediately self-isolate as per local regulations and contact your healthcare provider or district health care provider as instructed by local authorities. The test will be verified by a confirmatory molecular (PCR) test and instructions on the next steps will be provided.\u003cbr\u003e  \u003cbr\u003eNEGATIVE: Only one colored line appears in the control region (C). No colored lines appear in the test line region (T). It is unlikely that the person has COVID-19. However, this test may give an incorrect result (a false negative) in some people with COVID-19. This means that you may have COVID-19 even if the test gave a negative result. If you experience symptoms such as headache, migraine, fever, loss of taste and smell, contact your nearest healthcare provider according to the rules of your local authority. You can also repeat the test with a new kit. If you suspect coronavirus, repeat the test after 1-2 days, as coronavirus cannot be detected at all stages of infection. Even with a negative result, distancing and hygiene rules must still be observed.\u003cbr\u003e  \u003cbr\u003eINVALID: The control line does not appear. Insufficient sample volume or incorrect procedure techniques are the most likely causes of the missing control line. Review the procedure and repeat the test with a new kit or contact your healthcare provider or a COVID-19 testing center.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Please read all information in the package leaflet before performing the test.\u003cbr\u003e For self-testing in vitro self-diagnostic use only. Do not use after the expiration date.\u003cbr\u003e Do not eat, drink, or smoke in the area where specimens or kits are handled.\u003cbr\u003e Do not drink the swab liquid contained in the kit. Handle the swab with care and avoid contact with skin or eyes, rinse immediately with plenty of running water in case of contact.\u003cbr\u003e Please do not use if the foil package is damaged or has been opened. \u003cbr\u003eThis test kit should be used only as a preliminary test and repeatedly abnormal results should be discussed with a doctor or medical professional.\u003cbr\u003e Strictly follow the indicated time.\u003cbr\u003e Use the test only once. Do not disassemble and touch the test window of the test cassette.\u003cbr\u003e The kit must not be frozen or used after the expiration date printed on the package.\u003cbr\u003e Keep out of reach of children.\u003cbr\u003e Testing for children and adolescents should be done in the presence of an adult.\u003cbr\u003e Do not use the test on children under 2 years of age.\u003cbr\u003e Young children should be swabbed with the help of a second adult.\u003cbr\u003e Wash hands thoroughly before and after handling.\u003cbr\u003e Please ensure that adequate amount of sample is used for testing. Too much or too little sample may lead to deviation of results. \u003cbr\u003ePerformance was evaluated with nasal swab samples only, using the procedures provided in the package insert.\u003cbr\u003e The test only indicates the presence of SARS-CoV-2 antigens in the sample.\u003cbr\u003e If the test result is negative or non-reactive and clinical symptoms persist, it is because the virus from very early infection may not be detected. It is recommended to retest with a new kit or test with a molecular diagnostic device to rule out infection in these individuals. Negative results do not rule out SARS-CoV-2 infection, especially in those who have been in contact with the virus. Follow-up testing with a molecular diagnostic should be considered to rule out infection in these individuals.\u003cbr\u003e Positive COVID-19 results may be due to infection with non-SARS-CoV-2 coronavirus strains or other interfering factors. \u003cbr\u003eFailure to follow test procedures may impair test performance.\u003cbr\u003e False negative results can occur if a sample is improperly collected or handled. False negative results can occur if there are insufficient levels of virus in the sample.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store as packaged in the sealed pouch at room temperature or refrigerated (2-30° C), avoiding areas of excessive humidity. Do not freeze.\u003cbr\u003e The test is stable until the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use.\u003cbr\u003e Do not use beyond expiration date.\u003cbr\u003e Validity with intact packaging: 12 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e - Test cassette;\u003cbr\u003e - Sterile swab;\u003cbr\u003e - Package leaflet;\u003cbr\u003e - Extraction swab;\u003cbr\u003e - Biosafety bag.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eBibliography\u003c\/b\u003e \u003cbr\u003e1. Diagnosis and Treatment Protocol for Novel Coronavirus Pneumonia (Trial Version 7). National Health Commission \u0026amp; National Administration of Traditional Chinese Medicine.2020.\u003c\/div\u003e","brand":"SCREEN ITALIA SRL","offers":[{"title":"Default Title","offer_id":52605230612814,"sku":"983192143","price":2.69,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-243478.jpg?v=1768772821"},{"product_id":"test-one-step-strep-a-determinazione-qualitativa-antigeni-streptococco-a-in-tampone-faringeo-autodiagnostico-wondfo","title":"ONE STEP SELF-DIAGNOSTIC TEST FOR THE QUALITATIVE DETECTION OF STREPTOCOCCUS A ANTIGEN IN A THROAT SWAB","description":"\u003cb\u003eDescriptive sheet\u003c\/b\u003e\u003cbr\u003e\u003ch1\u003e Wondfo\u003c\/h1\u003e\n\u003ch2\u003e Streptococcus A\u003c\/h2\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e A lateral flow immunoassay for the qualitative detection of Group A Streptococcal antigen from throat swab specimens to aid in the early diagnosis of Group A Streptococcal infection.\u003cbr\u003e For in vitro self-diagnostic use only.\u003cbr\u003e When specimen is added to the specimen well, capillary action causes the specimen to migrate across the membrane. When group A streptococcal antigen levels in specimens are at or above the cutoff, a visible colored line appears in the test region (T), indicating a positive result. The absence of this colored line in the test region (T) suggests a negative result. If the test was performed correctly, a colored line will appear in the control region (C) as a procedural control.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eSample collection and preparation\u003c\/b\u003e\u003cbr\u003e 1. Collect the sample with the sterile throat swab provided in the kit. \u003cbr\u003e2. Hold your tongue down with a tongue depressor. Swab the back of your throat, tonsils, and other inflamed areas. Avoid touching your tongue, cheeks, and teeth with the swab.\u003cbr\u003e 3. The test should ideally be performed immediately after sample collection.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Bring the device and extraction reagents to room temperature (10°C-30°C) before performing the test.\u003cbr\u003e 1. Add 4 drops of Extraction Reagent A and 4 drops of Reagent B to the respective extraction tube and mix thoroughly.\u003cbr\u003e 2. Place the sample extraction swab into the tube.\u003cbr\u003e Shake the swab ten times. Leave the swab in the tube for one minute. Then remove the swab, pressing the swab head against the inside of the tube as you remove it to remove as much liquid as possible from the swab. Discard the swab.\u003cbr\u003e 3. Cap the test tube and mix the contents by shaking gently. \u003cbr\u003eThe sample must be tested immediately.\u003cbr\u003e 4. Remove the test from the sealed foil pouch by tearing at the notch and placing the test on a clean, dry, flat surface. Add 3 drops of mixed liquid sample from the tube to the sample well (represented by an arrow) of the test cassette by inverting and squeezing the tube.\u003cbr\u003e 5. Wait 10 minutes and read the results. Do not read the results after 15 minutes.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eReading the results\u003c\/b\u003e\u003cbr\u003e Positive\u003cbr\u003e If two colored lines are visible in both the test (T) and control (C) regions, the result is positive. This indicates that you may be experiencing a stage A Strep infection and should consult your doctor.\u003cbr\u003e Negative\u003cbr\u003e If only one colored line appears in the control region (C) and no colored line appears in the test region (T), the result is negative.\u003cbr\u003e Indicates that the concentration of group A streptococcal antigen is at or below the limit of detection of the test. \u003cbr\u003eInvalid\u003cbr\u003e No visible line or only one visible line in the test region but not in the control region. This indicates a procedural error and\/or deterioration of the test reagent.\u003cbr\u003e Repeat the test with a new kit. If the test is still invalid, please contact the distributor or the store where you purchased the product, providing the batch number.\u003cbr\u003e\u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e 1. This kit is for in vitro self-diagnostic use only.\u003cbr\u003e Do not ingest.\u003cbr\u003e 2. Do not interchange caps between reagents.\u003cbr\u003e 3. Do not use the test beyond the expiration date.\u003cbr\u003e 4. Keep out of reach of children.\u003cbr\u003e 5. Do not use the test if the pouch is punctured or not properly sealed.\u003cbr\u003e 6. Discard after use. The test is for single use only.\u003cbr\u003e 7. Avoid contact of reagents A and B with eyes, sensitive mucous membranes, cuts, abrasions, etc. If these reagents come into contact with skin or eyes, rinse thoroughly with water. \u003cbr\u003e8. Do not eat, drink or smoke in the area where the samples are and where the test will be performed.\u003cbr\u003e 9. Protective gloves should be worn when handling the sample. Wash your hands thoroughly after the procedure.\u003cbr\u003e 10. The device used, the swab and the extraction tube must be treated as contagious waste and therefore disposed of in biohazard containers.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e 1. The results of this test should not be used to determine pharyngitis infections, since pharyngitis can be caused by organisms other than group A streptococcus. This test does not provide any information about pharyngitis other than that caused by group A streptococcal infection.\u003cbr\u003e 2. A negative result may occur due to an insufficient amount of specimen collected, or the addition of insufficient reagent A and B. If symptoms persist or worsen, always consult your doctor. \u003cbr\u003e3. Excess blood or mucus in the collected sample may interfere with the performance of the test and could lead to a false-positive result. Do not touch your tongue, cheeks, teeth, or any bleeding areas of the mouth with the swab during sample collection.\u003cbr\u003e 4. As with any diagnostic procedure, a diagnosis should be confirmed only by a physician after evaluating all clinical and laboratory findings.\u003cbr\u003e 5. Since the test kit contains a toxic composition and the highest rate of morbidity from upper respiratory tract infections has been found in children, the test should be performed by parents or another adult family member on all minors under 16 years of age.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store at 4°C-30°C in the sealed container until the expiry date.\u003cbr\u003e Keep away from sunlight, moisture, and heat. Do not freeze. \u003cbr\u003ePreferably open the pouch just before performing the test.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Content\u003cbr\u003e 1. 2 individually sealed sachets, each containing:\u003cbr\u003e - testing device;\u003cbr\u003e - desiccant sachet.\u003cbr\u003e The desiccant is for storage purposes only, it is not used during the testing procedure.\u003cbr\u003e 2. 2 extraction tubes.\u003cbr\u003e 3. 2 sterile throat swabs. The swab is used to collect the sample.\u003cbr\u003e 4. Extraction reagents A and B (Caution: Reagent B is toxic if swallowed).\u003cbr\u003e 5. Package leaflet with instructions for use.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e W39-CH\u003c\/div\u003e","brand":"MY BENEFIT SRL","offers":[{"title":"Default Title","offer_id":52605239492942,"sku":"986720504","price":7.14,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-279863.jpg?v=1743133400"},{"product_id":"screen-test-rapido-screen-test-celiachia-per-rilevazione-intolleranza-glutine-1-pezzo","title":"SCREEN TEST RAPID SCREEN TEST CELIAC DISEASE FOR DETECTION OF GLUTEN INTOLERANCE 1 PIECE","description":"\u003cb\u003eDescriptive sheet\u003c\/b\u003e\u003cbr\u003e\u003ch2\u003e SCREEN CHECK TEST\u003c\/h2\u003e\n\u003ch1\u003e Celiac Disease Screen Test\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Rapid immunochromatographic test that can be used as an aid in the diagnosis of gluten intolerance. Detects IgA anti-transglutaminase (tTG) antibodies from a whole blood sample. \u003cbr\u003eIf anti-tTGA IgA antibodies are present, they bind to colloidal gold-labeled anti-IgA antibodies (mouse IgG) and to tTG (derived from lysis of red blood cells by the dilution buffer). tTG binds this complex to the static protein line (test line) and produces a visible reddish line. The test also includes a control system consisting of a reference line.\u003cbr\u003e The test result must be confirmed by a doctor who can discuss with the patient the possibility of a gluten-free diet.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Before starting the test, bring the cassette and the sample dilution buffer to room temperature (15°C to 27°C). Open the container with the sample dilution buffer by removing the lid and place it upright on the table.\u003cbr\u003e  \u003cbr\u003eUnscrew the gray cap of the automatic lancing device by turning it until it loosens. Then turn it at least two more times. Only then can it be removed, otherwise its function is not guaranteed. The lancing device can only be used once. Press the lancing device with the round opening against the side of the clean fingertip and press the trigger.\u003cbr\u003e Open the plastic container and carefully remove the glass capillary tube. Squeeze a drop of blood from your fingertip. Hold the glass capillary tube horizontally in the drop of blood until the capillary tube is completely filled. Use the provided plaster as needed. \u003cbr\u003ePlace the filled glass capillary tube into the container with the sample dilution buffer and close the lid tightly. Shake the container a few times until the blood in the capillary tube is completely mixed with the solution. Wait until the liquid has collected at the bottom of the container before removing the lid from the container. Then open the lid of the container.\u003cbr\u003e Open the foil pouch of the cassette only shortly before use. Remove the test cassette and place it on a flat surface. Use the pipette to take a few drops of the diluted sample. Hold the pipette with the diluted sample vertically over the sample well (S) and add exactly 5 drops. Make sure that no liquid gets on the result window, marked T and C. After applying the drops, do not touch or move the test cassette. \u003cbr\u003eAfter adding the 5 drops, read the result after 10-15 minutes. Low values ​​may not be detected until 10 minutes have passed and false positive results may occur after more than 15 minutes.\u003cbr\u003e\u003cbr\u003e \u003cu\u003eInterpretation of results\u003c\/u\u003e\u003cbr\u003e POSITIVE: A light or dark red line appears at the control line (C) and a light or dark red line appears at the test line (T).\u003cbr\u003e The test shows that IgA antibodies associated with gluten intolerance have been detected in the blood sample. The detection of these antibodies most likely indicates the presence of gluten intolerance. For a definitive diagnosis, consult your doctor.\u003cbr\u003e\u003cbr\u003e NEGATIVE: A light to dark red line appears at the control line (C) and no red line appears at the test line (T). \u003cbr\u003eThe test shows that no IgA antibodies indicating gluten intolerance are detectable in the blood sample. It is therefore possible to almost completely exclude the presence of gluten intolerance. In case of gastrointestinal disorders or other symptoms, further diagnostic investigation by the doctor is necessary.\u003cbr\u003e\u003cbr\u003e INVALID: No red line appears at the control line (C) or only one red line appears at the test line (T).\u003cbr\u003e The test was not performed correctly and is invalid. Make sure you followed all the steps in the instructions for use exactly. Perform a new test with a new blood sample.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e The test is intended for external use only.\u003cbr\u003e Do not ingest test components. Avoid skin and eye contact with specimen diluent pad.\u003cbr\u003e Keep the test out of the reach of children.  \u003cbr\u003eThe product can only be used until the expiry date printed on the product itself.\u003cbr\u003e If the instructions for use are not followed correctly and in detail, the test results may be false. The final diagnosis must be made by a doctor.\u003cbr\u003e Do not use the test if the packaging is damaged. Do not use damaged test components.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Do not expose the test to direct sunlight or frost. Do not freeze. Store in a dry place at temperatures between 10°C and 27°C.\u003cbr\u003e Validity with intact packaging: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e - 1 test cassette;\u003cbr\u003e - 1 pipette;\u003cbr\u003e - 1 glass capillary tube;\u003cbr\u003e - 1 bottle of solution with sample dilution buffer;\u003cbr\u003e - 1 sterile lancet;\u003cbr\u003e - 1 alcohol swab;\u003cbr\u003e - 1 patch;\u003cbr\u003e - 1 leaflet;\u003cbr\u003e - 1 translated information sheet.\u003c\/div\u003e","brand":"SCREEN ITALIA SRL","offers":[{"title":"Default Title","offer_id":52783976841550,"sku":"987315823","price":16.11,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-306655.jpg?v=1768774576"},{"product_id":"test-rapido-faringeo-strepto-a-sofarmapiu-rilevazione-antigene-streptococco-a-su-tampone-faringeo-mediante-immunocromatografia-professionale-10-pezzi","title":"RAPID PHARYNGEAL TEST STREPTO A SOFARMAPIU' DETECTION OF STREPTOCOCCUS A ANTIGEN ON PHARYNGEAL SWAB BY PROFESSIONAL IMMUNOCHROMATOGRAPHY 10 PIECES","description":"\u003cb\u003eDescriptive sheet\u003c\/b\u003e\u003cbr\u003e\u003ch1\u003e TEST\u003cbr\u003e STREPTOCOCCUS\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Rapid test for the detection of group A streptococcus in throat infections.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Sample collection\u003cbr\u003e Use only the sterile reagents and swabs provided in the kit.\u003cbr\u003e Collect the sample with the sterile throat swab provided in the kit. Swab the posterior pharynx, tonsils and other inflamed areas.\u003cbr\u003e Avoid contact of the swab with the tongue, cheeks and teeth. \u003cbr\u003eThe test should preferably be performed immediately after specimen collection. Specimens may be stored in a clean, dry plastic tube at room temperature for up to 8 hours or at 2-8°C for up to 72 hours. Swabs containing modified Stuart or Amies transport medium may also be used with this product.\u003cbr\u003e If culture is desired, gently rotate the swab tip on a group A selective blood plate (GAS) before using the swab with the Strepto A Rapid Test Device (Throat Swab).\u003cbr\u003e Test procedure\u003cbr\u003e Bring the test card, reagents, throat swab and\/or controls to room temperature (15-30°C) before testing.\u003cbr\u003e Remove the card from the sealed pouch and use it immediately. \u003cbr\u003eHolding the Reagent 1 bottle upright, add 4 drops (approximately 240 mcl) to a sample extraction tube. Reagent 1 is red in color. Holding the Reagent 2 bottle upright, add 4 drops (approximately 160 mcl) to the tube. Reagent 2 is colorless. Mix the solution by gently swirling the tube. Adding Reagent 2 to Reagent 1 changes the color of the solution from red to yellow.\u003cbr\u003e Immediately add the throat swab to the yellow solution in the tube. Shake the swab in the tube 15 times. Leave the swab in the tube for 1 minute. Then press the swab into the tube and squeeze the bottom of the tube while removing the swab. Discard the swab.\u003cbr\u003e Insert the dropper tip into the top of the tube. Place the card on a clean flat surface. Add 3 drops of solution (100 mcl) to the sample well (S) and start the timer. \u003cbr\u003eWait for the red band(s) to appear.\u003cbr\u003e Read the result after 5 minutes. Do not interpret the result after 10 minutes.\u003cbr\u003e Interpretation of results\u003cbr\u003e Positive: Two distinct red lines appear, one in the control region (C), the other in the test region (T). A positive result indicates that Streptococcus A has been detected in the sample.\u003cbr\u003e Negative: A red line appears in the control region (C). No red or pink line appears in the test region (T). A negative result indicates that Strep A antigen is not present in the specimen or is present below the detectable threshold of the test. The patient specimen should be cultured to confirm the absence of Strep A infection. If clinical symptoms are inconsistent with the results, another specimen should be collected for culture. \u003cbr\u003eInvalid: No band appears. The most likely reasons for the control band not appearing are insufficient sample volume or incorrect procedure. Review the procedure and repeat the test with a new card. If the problem persists, discontinue use of the kit and contact your local distributor.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e If swallowed: Call a poison control center or doctor if you feel unwell.\u003cbr\u003e In case of eye contact: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If irritation persists, seek medical advice.\u003cbr\u003e Do not freeze. Do not use after expiration date.\u003cbr\u003e For professional in vitro diagnostic use only.\u003cbr\u003e Do not eat, drink or smoke in the area where specimens and kits are handled. \u003cbr\u003eHandle all specimens as if potentially infectious. Observe appropriate precautions against microbiological hazards at all stages of the analysis and follow standard procedures for proper disposal of specimens.\u003cbr\u003e Wear protective clothing when analyzing samples: lab coat, disposable gloves, and eye protection.\u003cbr\u003e Humidity and temperature can negatively affect results.\u003cbr\u003e Do not use the test if the pouch is damaged.\u003cbr\u003e Reagent 2 contains an acidic solution. If the solution comes into contact with skin or eyes, rinse with plenty of water.\u003cbr\u003e Positive and negative controls contain Proclin300 as a preservative.\u003cbr\u003e Do not interchange reagent bottle caps.\u003cbr\u003e Do not interchange the caps of the external control solution bottles. \u003cbr\u003eThe Rapid Test Card Strpto A (Throat Swab) is for in vitro diagnostic use only. The test must be used to determine the antigen of Streptococcus A on throat swab only. It is not able to determine the quantitative value or the percentage of increase in the antigen status of Streptococcus A.\u003cbr\u003e This test only indicates the presence of Strep A antigen in the specimen due to either viable or non-viable Group A Strep bacteria.\u003cbr\u003e A negative result should be confirmed by culture. A negative result may be due to inadequate or less than detectable levels of Strep A antigen in the throat swab.\u003cbr\u003e The sterile swabs provided with this test are to be used for specimen collection. No other swabs have been validated for this test. \u003cbr\u003eExcessive blood or mucus on the swab may interfere with the test results and cause a false positive. Avoid contact of the swab with the tongue, cheeks, teeth, and any oral areas where there are open wounds when the samples are collected.\u003cbr\u003e As with all diagnostic tests, results must be interpreted in light of the patient's overall clinical picture.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e\u003cbr\u003e Store at room temperature or in the refrigerator (2-30°C).\u003cbr\u003e Validity with intact packaging: 16 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Kit contents:\u003cbr\u003e - reagent 1 for Strepto A (2 M sodium nitrite)*;\u003cbr\u003e - reagent 2 for Strepto A (0.027 M citric acid);\u003cbr\u003e - card;\u003cbr\u003e - sterile swabs;\u003cbr\u003e - methodical;\u003cbr\u003e - dropper dispenser;\u003cbr\u003e - test tubes for sample extraction;\u003cbr\u003e - test tube\/reagent support;\u003cbr\u003e - positive control for Strepto A (non-viable Strepto A Proclin 300 0.01%);\u003cbr\u003e - negative control for Strepto A (non-viable Strepto C Proclin 300 0.01%). \u003cbr\u003e*Keep out of reach of children. Wear gloves and eye and face protection.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 70773\u003c\/div\u003e","brand":"SO.FARMA.MORRA SPA","offers":[{"title":"Default Title","offer_id":53091664920910,"sku":"950019416","price":135.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-342028.jpg?v=1768784527"},{"product_id":"test-antigenico-rapido-covid-19-wizbiotech-autodiagnostico-rilevazione-qualitativa-antigene-sars-cov-2-in-tamponi-nasali","title":"WIZBIOTECH COVID-19 RAPID ANTIGEN TEST SELF-DIAGNOSTIC QUALITATIVE DETECTION OF SARS-COV-2 ANTIGEN IN NASAL SWABS","description":"\u003ch1\u003e SARS-CoV-2 Antigen Rapid Test\u003cbr\u003e (Colloidal Gold)\u003c\/h1\u003e\n\u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e \u003cbr\u003eThe SARS-CoV-2 Rapid Antigen Test (Colloidal Gold) is intended for the qualitative detection of SARS-CoV-2 antigen (nucleocapsid protein) in nasal cavity (anterior nasal) swab specimens from individuals suspected of having COVID-19. The test kit is intended for self-testing or at-home testing.\u003cbr\u003e It uses immune lateral chromatography technology. When the test sample contains SARS-CoV-2, the SARS-CoV-2 antigen will react with the antibody coated on the test line (T), causing a red band to appear in the test line (T) region. When the SARS-CoV-2 content in the test sample is too low or nonexistent, a red band will not appear in the test line (T). Regardless of whether the test sample contains SARS-CoV-2, a red band will appear in the quality control line (C) region, which is the basis for judging the effectiveness of the test.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Test procedure \u003cbr\u003eIt takes about 15 minutes to prepare before each test and results can be obtained after 30 minutes.\u003cbr\u003e Preparatory work\u003cbr\u003e 1. Use the test kit at room temperature (15°C-30°C). If the test kit has previously been stored in a cool place (below 15°C), equilibrate to 15-30°C for 30 minutes before testing.\u003cbr\u003e 2. Prepare a timer, tissues, hand sanitizer\/soap, and hot water.\u003cbr\u003e 3. Wash your hands thoroughly (at least 20 seconds) with soap and warm water\/hand sanitizer. This step ensures the kit is not contaminated, then dry your hands.\u003cbr\u003e\u003cbr\u003e Sample collection\u003cbr\u003e 1. Take out the sample extraction tube, unscrew the extraction tube cap.\u003cbr\u003e 2. Place the extraction tube on the bracket (fixed to the box) to prevent liquid leakage.\u003cbr\u003e 3. Tear the swab packaging from the end of the stick and remove the swab.\u003cbr\u003e 4. Clean the nostrils with a swab: \u003cbr\u003e- insert the soft head of the swab into the nostril less than 1 inch (normally about 0.5-0.75 inches);\u003cbr\u003e - gently rotate the swab against the nasal wall with moderate force at least five times;\u003cbr\u003e - use the same swab to repeat the collection procedure in the other nostril.\u003cbr\u003e Warning: False negative results may occur if the antigen sample is not collected correctly. Anyone under 18 should be tested with the assistance of a legal guardian or an authorized person.\u003cbr\u003e\u003cbr\u003e Sample processing\u003cbr\u003e 1. Remove the extraction tube, dip the soft swab head into the extraction solution and immerse it in the liquid.\u003cbr\u003e 2. Press the soft head of the swab firmly against the inside wall of the extraction tube and rotate the swab clockwise or counterclockwise approximately 10 times. \u003cbr\u003e3. Push the head of the swab along the inside wall of the sample extraction tube under the liquid in the tube as far as possible, withdraw the swab.\u003cbr\u003e 4. Tighten the standby tube.\u003cbr\u003e\u003cbr\u003e Sample test\u003cbr\u003e 1. Tear off the foil bag, take out the test card and place it horizontally on the test bench.\u003cbr\u003e Warning: The platform must be in a horizontal and stable state, and tilting and swinging are strictly prohibited.\u003cbr\u003e 2. Disconnect the sample addition hole cover of the extraction tube.\u003cbr\u003e 3. Gently squeeze the extraction tube and drop 2 drops of liquid vertically into the sample well of the test card.\u003cbr\u003e Warning: Bubbles in the extraction tube may result in incorrect sample volume and inaccurate test results. If bubbles are present in the extraction tube, gently shake the extraction tube to squeeze out some of the liquid and remove the bubbles. \u003cbr\u003e4. Start timing. Read the results after 15 minutes. Do not read before 15 minutes or after 30 minutes.\u003cbr\u003e 5. Upon completion of the test, place all test kit materials into the biohazard waste bag and dispose of it according to your local biohazard waste disposal policy.\u003cbr\u003e 6. Rinse your hands thoroughly (at least 20 seconds) with soap and warm water\/hand sanitizer.\u003cbr\u003e\u003cbr\u003e Interpretation of the results\u003cbr\u003e Negative: The quality control line (C line) appears in the red band, while the test line (T line) does not appear in the red band.\u003cbr\u003e - It is necessary to continue to adopt measures regarding contact with others and self-protection.\u003cbr\u003e - It is possible that there is an infection, even if the result is negative.\u003cbr\u003e - If you still suspect the infection, repeat the test after 1-2 days. Due to the coronavirus, it cannot be accurately detected at every stage of infection. \u003cbr\u003ePositive: Both the quality control line (C line) and the test line (T line) appear as red bands.\u003cbr\u003e Caution: Regardless of the color shades, within the specified detection time, the result must be considered positive.\u003cbr\u003e - COVID-19 infection is present.\u003cbr\u003e - Contact your doctor or local health department.\u003cbr\u003e - Follow self-quarantine requirements and protection guidelines in your area.\u003cbr\u003e - Perform PCR test for confirmation.\u003cbr\u003e Invalid: Once the red line in the control line region (C line) does not appear, it will be considered invalid.\u003cbr\u003e Warning: Invalid results may indicate that you did not strictly follow the steps in the instructions for use.\u003cbr\u003e -It may be caused by incorrect operation in the detection process.\u003cbr\u003e - Please repeat the test.\u003cbr\u003e - If your test result is still invalid, contact your doctor or the COVID-19 testing center.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e \u003cbr\u003e1. For in vitro diagnostic use only.\u003cbr\u003e 2. For use with swab specimens from the nasal cavity (anterior nasal).\u003cbr\u003e 3. For the detection of SARS-CoV-2 proteins only, not for the detection of other viruses or pathogens.\u003cbr\u003e 4. Persons under 18 years of age must be tested with the assistance of a legal guardian or an authorized person.\u003cbr\u003e 5. Keep the test kit or kit components out of the reach of children and pets before and after use.\u003cbr\u003e 6. The test paper package contains a desiccant, do not eat.\u003cbr\u003e 7. The sample extraction solution in the extraction tube contains chemicals. Direct contact should be avoided, and eating is prohibited. If the solution comes into contact with skin, mucous membranes, or eyes, rinse with water. Please contact your GP or healthcare professional and seek medical advice if necessary. \u003cbr\u003e8. The use of gloves or other protective devices is recommended when performing the tests.\u003cbr\u003e 9. It is prohibited to use the test kit that has not been stored as required.\u003cbr\u003e 10. Do not use the test kit beyond the expiration date.\u003cbr\u003e 11. Do not use kit components that have been opened or modified.\u003cbr\u003e 12. Leave the test card sealed in its foil pouch until immediately before use. Do not use if the pouch is damaged or opened.\u003cbr\u003e 13. Disposable swabs are sterile products. Do not use if the swab package is damaged or opened.\u003cbr\u003e 14. Use of the swab must strictly follow the instructions for use; otherwise, it may cause nasal bleeding, breakage and retention of the swab, or other risks.\u003cbr\u003e 15. Do not immerse the swab in the extraction solution or other liquid before collecting the specimen with disposable swabs.\u003cbr\u003e 16. Do not touch the soft tip of the swab when handling the swab sample. \u003cbr\u003e17. Correct sample collection and handling are essential for accurate results.\u003cbr\u003e 18. Do not mix components from different kit lots.\u003cbr\u003e 19. All kit components are single-use items. Do not use with multiple specimens. Do not reuse the test kit or used kit components.\u003cbr\u003e 20. Before making any significant therapeutic or management decisions, it is recommended to consult with your family doctor or other professionals. Avoid taking medications in private or engaging in any action that could endanger yourself or others.\u003cbr\u003e 21. Used test kit components and samples can be placed in plastic bags with normal household waste. If the test result is positive, carefully dispose of the waste components and relevant samples and thoroughly clean and disinfect the work surface to ensure hygiene.\u003cbr\u003e 22. Do not eat, drink, or smoke in the area where samples or test kits are handled.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eConservation\u003c\/b\u003e \u003cbr\u003eThe test kit should be stored at 2°C-30°C, in a dry place and away from direct sunlight (do not freeze the kit or its components).\u003cbr\u003e The test card must be used within 60 minutes of opening the foil pouch.\u003cbr\u003e Shelf life of intact packaging: 24 months.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Materials provided:\u003cbr\u003e - 1 test;\u003cbr\u003e - test device;\u003cbr\u003e - extraction pipe;\u003cbr\u003e - disposable swab;\u003cbr\u003e - biohazard waste bag;\u003cbr\u003e - instructions for use.\u003c\/div\u003e","brand":"DPI MEDICAL SOLUTION SRL","offers":[{"title":"Default Title","offer_id":53959223640398,"sku":"987761335","price":10.5,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-303601.jpg?v=1768787028"},{"product_id":"test-antigenico-rapido-covid-19-deepblue-determinazione-qualitativa-antigeni-sars-cov-2-in-tamponi-nasofaringei-orofaringei-mediante-immunocromatografia-25-pezzi-uso-professionale","title":"TEST ANTIGENICO RAPIDO COVID-19 DEEPBLUE DETERMINAZIONE QUALITATIVA ANTIGENI SARS-COV-2 IN TAMPONI NASOFARINGEI\/OROFARINGEI MEDIANTE IMMUNOCROMATOGRAFIA 25 PEZZI USO PROFESSIONALE","description":"\u003ch1\u003eDEEPBLUE COVID-19\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescrizione\u003c\/b\u003e\u003cbr\u003e Kit per il test dell'antigene (oro colloidale).\u003cbr\u003e Utilizzato per la rilevazione qualitativa in vitro dell'antigene del SARS-CoV-2 in tamponi nasali anteriori umani, tamponi nasofaringei (NP), tamponi orofaringei o saliva.\u003cbr\u003e Questo kit utilizza il metodo del doppio sandwich di anticorpi per rilevare gli antigeni SARS-CoV-2. Quando una quantità appropriata di campione viene aggiunta al pozzetto del dispositivo di analisi, il campione avanza lungo il dispositivo di analisi. Se il campione contiene un antigene, l'antigene si lega all'anticorpo monoclonale della proteina N del topo anti-SARS-CoV-2 etichettato con oro colloidale sul cuscinetto legante, e il complesso immunitario forma un complesso a sandwich con un altro anticorpo monoclonale della proteina N del topo anti-SARS-CoV-2 rivestito che è stato rivestito sulla linea del test, apparirà una linea colorata visibile, che indica che l'antigene SARS-CoV-2 è positivo. Il dispositivo di test contiene anche una linea di controllo della qualità, indipendentemente dalla presenza di una linea di test, la linea rossa di controllo della qualità dovrebbe apparire. Se la linea di controllo della qualità non appare, indica che il risultato del test non è valido e che è necessario rifare il test.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eModalità d'uso\u003c\/b\u003e\u003cbr\u003e COLLEZIONE DI CAMPIONI\u003cbr\u003e \u003cu\u003eCampione di tampone nasale anteriore\u003c\/u\u003e\u003cbr\u003e 1. Lasciare che la testa del paziente si rilassi naturalmente, estrarre il tampone, tenere il tampone a non più di 8 cm dalla punta.\u003cbr\u003e 2. Inserire con attenzione il tampone nella narice del paziente, la punta del tampone deve essere inserita fino a 2-3 cm fino a quando non si incontra resistenza.\u003cbr\u003e 3. Far rotolare il tampone 5 volte lungo la mucosa all'interno della narice per assicurarsi che il muco e le cellule siano raccolte. Usando lo stesso tampone, ripetere questo processo per l'altra narice per assicurarsi che venga raccolto un campione adeguato.\u003cbr\u003e \u003cu\u003eCampione di tampone nasofaringeo\u003c\/u\u003e\u003cbr\u003e Lasciare che la testa del paziente si rilassi naturalmente, inserire con attenzione il tampone nella narice del paziente. Tamponare la superficie del rinofaringe posteriore e ruotare il tampone più volte; usare lo stesso tampone e prelevare campioni dall'altra narice nello stesso modo.\u003cbr\u003e \u003cu\u003eCampione di tampone orofaringeo\u003c\/u\u003e\u003cbr\u003e Far inclinare la testa del paziente, aprire la bocca ed emettere suoni \"ah\", esponendo le tonsille faringee su entrambi i lati. Tenere il tampone e pulire delicatamente entrambi i lati delle tonsille faringee del paziente avanti e indietro almeno tre volte.\u003cbr\u003e \u003cu\u003eCampione di tampone saliva\u003c\/u\u003e\u003cbr\u003e Tossire delicatamente prima della raccolta, concentrare la saliva nella bocca (se c'è dello sputo quando si tossisce, tenere lo sputo in bocca), inserire la punta morbida del tampone in bocca e farla assorbire fin quando il tampone non sia pieno di saliva.\u003cbr\u003e \u003cu\u003ePreparazione del campione\u003c\/u\u003e\u003cbr\u003e 1. Spelare gentilmente il sigillo in foglio di alluminio.\u003cbr\u003e 2. Mettere il campione del tempone nella provetta di estrazione, ruotare il tampone per circa 10 secondi e premere la testa del tampone contro la parete della provetta 3 volte per rilasciare l'antigene nel tampone.\u003cbr\u003e 3. Rimuovere il tampone schiacciando i lati del tubo per estrarre il liquido dal tampone, in modo da rimuovere tanto liquido possibile dal tampone. Smaltire i tamponi secondo il metodo di smaltimento dei rifiuti biopericolosi.\u003cbr\u003e 4. Premere fermamente sul tappo dell'ugello sul tubo di estrazione.\u003cbr\u003e \u003cu\u003eProcedura di test\u003c\/u\u003e\u003cbr\u003e 1. Aprire il pacchetto e tirare fuori il dispositivo di test.\u003cbr\u003e 2. Tenere la provetta di estrazione verticalmente e aggiungere due gocce di campione nel pozzetto del campione. Avvitare il timer.\u003cbr\u003e 3. Leggere i risultati a 15 minuti. I risultati dopo 30 minuti non sono più validi.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInterpretazione dei risultati\u003c\/b\u003e\u003cbr\u003e Risultato negativo: se c'è solo una linea di controllo di qualità C, la linea di rilevazione T è incolore, indicando che l'antigene SARS-CoV-2 non è stato rilevato e il risultato è negativo.\u003cbr\u003e Risultato positivo: se appaiono sia la linea di controllo qualità C che la linea di rilevazione T, indicando che l'antigene SARS-CoV-2 è stato rilevato e il risultato è positivo.\u003cbr\u003e Risultato non valido: se la linea di controllo qualità C non viene osservata, non sarà valida indipendentemente dalla presenza della linea di rilevamento T e il test dovrà essere condotto nuovamente.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAvvertenze\u003c\/b\u003e\u003cbr\u003e 1. Leggere attentamente le istruzioni prima di usare il kit e controllare rigorosamente il tempo di reazione. Se non si seguono le istruzioni, si otterranno risultati imprecisi.\u003cbr\u003e 2. Il campione deve essere testato in un laboratorio con determinate condizioni. Tutti i campioni e i materiali durate il test devono essere manipolati in conformità con la pratica di laboratorio per le malattie infettive.\u003cbr\u003e 3. Non mangiare, bere, masticare la gomma, fumare la sigaretta né la vape nei 30 minuti prima del campionamento della saliva.\u003cbr\u003e 4. Proteggere dall'umidità, non aprire il sacchetto di platino di alluminio prima che sia pronto il test. Non usarlo se il sacchetto di alluminio è danneggiato o se il dispositivo di test è umido.\u003cbr\u003e 5. Si prega di utilizzarlo entro il periodo di validità.\u003cbr\u003e 6. Bilanciare tutti i reagenti e i campioni a temperatura ambiente (15-30 °C) prima dell'uso.\u003cbr\u003e 7. Non sostituire i componenti di questo kit con quelli di altri kit.\u003cbr\u003e 8. Non diluire il campione durante il test, altrimenti si possono ottenere risultati imprecisi.\u003cbr\u003e 9. Il kit deve essere conservato in stressa conformità con le condizioni specificate in questo manuale. Si prega di non conservare il kit in condizioni di congelamento.\u003cbr\u003e 10. I metodi di test e i risultati devono essere interpretati in stretta conformità con questa specifica.\u003cbr\u003e 11. Possono verificarsi risultati negativi se il titolo dell'antigene SARS-CoV-2 nel campione è inferiore al limite minimo di rilevamento di questo kit.\u003cbr\u003e 12. Se il reagente di estrazione è imballaggio individuale e un pezzo per un dispositivo di test, il numero di lotto, la data di scadenza e altre informazioni non possono essere contrassegnati separatamente a causa dello spazio è limitato, ma quelle informazioni saranno coerenti con il kit di test corrispondente.\u003cbr\u003e 13. Sia le infezioni sintomatiche che quelle asintomatiche possono essere testate.\u003cbr\u003e Non c'è riduzione della sensibilità del test Deepblue Antigen contro la variante britannica, la variante brasiliana, la variante delta indiana o la variante sudafricana.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimitazioni\u003c\/b\u003e\u003cbr\u003e 1. Questo kit di test viene utilizzato solo per la diagnosi in vitro.\u003cbr\u003e 2. Questo lit di test è usato solo per rilevare estratti di tamponi nasali anteriori, nasofaringei, orofaringei o saliva umani. I risultati di altri campioni possono essere errati.\u003cbr\u003e 3. Questo kit è usato solo per la rilevazione qualitativa e non può indicare il livello di antigene SARS-CoV-2 nel campione.\u003cbr\u003e 4. Questo kit di test è solo uno strumento diagnostico ausiliario clinico. Se il risultato è positivo, si raccomanda di utilizzare altri metodi per ulteriori esami in tempo e la diagnosi del medico prevarrà.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eConservazione\u003c\/b\u003e\u003cbr\u003e Trasporto e stoccaggio del campione.\u003cbr\u003e Dopo la raccolta dei campioni, il tampone può essere conservato nel reagente di estrazione fornito con il kit. I campioni appena raccolti dovrebbero essere trattati il prima possibile, ma non più tardi di un'ora dopo la raccolta del campione. I campioni raccolti possono essere conservati a 2-8 °C per non più di 24 ore.\u003cbr\u003e Conservare a -70 °C per lungo tempo, ma evitare ripetuti cicli di congelamento-disgelo.\u003cbr\u003e Conservare a 4 °C-30 °C.\u003cbr\u003e Validità confezionamento integro: 24 mesi.\u003cbr\u003e Dopo che il sacchetto di foglio di alluminio è stato aperto, il dispositivo di test dovrebbe essere usato il più presto possibile ed entro un'ora.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormato\u003c\/b\u003e\u003cbr\u003e Materiali forniti:\u003cbr\u003e - tampone sterilizzato;\u003cbr\u003e - tubo di estrazione dell'antigene con reagente di estrazione;\u003cbr\u003e - dispositivo di test;\u003cbr\u003e - istruzione;\u003cbr\u003e - portaprovette (solo per 25 pezzi\/scatola).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e COVAG1NS-25\u003c\/div\u003e","brand":"LEADING MED SRL","offers":[{"title":"Default Title","offer_id":55204803346766,"sku":"951606957","price":28.18,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-382044.jpg?v=1768796880"},{"product_id":"screen-test-sars-cov-2-influenza-a-b-rsv-20-pezzi","title":"SCREEN TEST SARS-COV-2\/INFLUENZA A+B\/RSV 20 PEZZI","description":"\u003ch1\u003eSCREEN\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescrizione\u003c\/b\u003e\u003cbr\u003e Il test rapido Antigene Combo SARS-CoV-2\/Influenza A+B\/RSV è un test immunocromatografico rapido per l’individuazione qualitativa degli antigeni della proteina Nucleocapside SARS-CoV-2, Influenza A, Influenza B e Virus Respiratorio Sinciziale (RSV) presenti nel tratto nasofaringeo umano.\u003cbr\u003e Solo per uso diagnostico professionale in vitro.\u003cbr\u003e Il test rapido Antigene Combo SARS-CoV-2\/Influenza A+B\/RSV (Tampone Nasofaringeo) è un test immunocromatografico rapido per l’individuazione qualitativa degli antigeni della proteina Nucleocapside SARS-CoV-2, Influenza A, Influenza B e Virus Respiratorio Sinciziale (RSV) presenti nel tratto nasofaringeo di individui con sospetta infezione da SARS-CoV-2\/Influenza\/RSV unitamente a valutazione clinica e altri test di laboratorio.\u003cbr\u003e I risultati individuano gli antigeni della proteina Nucleocapside SARS-CoV-2, Influenza A+B e RSV. Un antigene generalmente è individuabile nei campioni delle vie respiratorie superiori durante la fase acuta di un’infezione. Risultati positivi indicano la presenza di antigeni virali, ma è necessario un confronto clinico anamnestico del paziente e altre informazioni diagnostiche per determinare lo stato infettivo. Risultati positivi non escludono l’infezione batterica o virale. L’agente individuato potrebbe non essere la causa certa della patologia. I risultati negativi non escludono l’infezione da SARS-CoV-2 e\/o Influenza A+B\/RSV e non dovrebbero essere usati come unica base per terapia o decisioni circa il paziente. I risultati negativi dovrebbero sempre essere considerati presunti e confermati da un test molecolare, se necessario per la gestione del paziente. I risultati negativi dovrebbero essere valutati contestualmente alla recente esposizione del paziente, alla sua storia clinica e alla presenza di sintomi e segni clinici compatibili con SARS-CoV-2, Influenza A+B e RSV.\u003cbr\u003e Il test rapido Antigene SARS-CoV-2 (Tampone Nasofaringeo) è un test immunologico qualitativo basato su membrana per l’individuazione della proteina Nucleocapside SARS-CoV-2 nei campioni da tampone nasofaringeo. L’anticorpo del SARS-CoV-2 riveste l’area della linea del test. Durante il test il campione reagisce con le particelle di anticorpo SARSCoV-2 che ricoprono la membrana. Il composto poi migra verso l’alto sulla membrana per azione capillare e reagisce con l’anticorpo SARS-CoV-2 nell’area della linea del test. Se il campione contiene proteina Nucleocapside SARS-CoV-2, appare una linea colorata nella zona della linea del test come risultato. Se il campione non contiene antigeni del SARSCoV-2 non compare nessuna linea colorata nella zona della linea del test, indice di un risultato negativo. Come controllo procedurale, comparirà sempre una linea colorata nell’area della linea di controllo, indice che è stato utilizzato un volume adeguato di campione e la membrana è stata imbevuta correttamente.\u003cbr\u003e Il test rapido Influenza A+B (Tampone Nasofaringeo) è un test immunologico qualitativo a scorrimento laterale per l’individuazione delle nucleoproteine dell’Influenza A e B in campioni da tampone nasofaringeo. In questo test, le nucleoproteine specifiche all’anticorpo dell’Influenza A e B ricoprono separatamente le zone delle linee del test. Durante il test, il campion estratto reagisce all’anticorpo dell’Influenza A e\/o B che ricoprono le particelle. Il composto migra poi verso l’alto sulla membrana per reagire all’anticorpo dell’Influenza A e\/o B sulla stessa e produrre una o due linee colorate nell’area del test. La presenza di queste linee colorate in una o entrambe le aree del test indica un risultato positivo. Come controllo procedurale, comparirà sempre una linea nell’area di controllo se il test è stato eseguito correttamente.\u003cbr\u003e Il Test Rapido RSV (Tampone Nasofaringeo) è un test immunologico qualitativo a scorrimento laterale per l’individuazione di nucleoproteine del Virus Respiratorio Sinciziale nei campioni da tampone nasofaringeo. In questo test, l’anticorpo specifico delle nucleoproteine del Virus Respiratorio Sinciziale ricopre la zona della linea del test. Durante il test, il campione estratto reagisce con l’anticorpo del Virus Respiratorio Sinciziale che ricopre le particelle. Il composto poi migra verso l’alto sulla membrana per reagire con l’anticorpo del Virus Respiratorio Sinciziale sulla stessa e produrre una linea colorata nella zona del test. La presenza di questa linea colorata nella zona del test indica un risultato positivo. Come controllo procedurale, comparirà sempre una linea nella zona di controllo se il test è stato eseguito correttamente.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eModalità d'uso\u003c\/b\u003e\u003cbr\u003e \u003cu\u003ePrelievo, trasporto e conservazione campione\u003c\/u\u003e\u003cbr\u003e Prelievo del campione\u003cbr\u003e 1. Inserire un tampone sterile nella narice del paziente, fino a raggiungere la superficie nasofaringea posteriore.\u003cbr\u003e 2. Strofinare sulla superficie nasofaringea posteriore.\u003cbr\u003e 3. Estrarre il tampone sterile dalla cavità nasale.\u003cbr\u003e Attenzione: se il tampone si rompe durante il prelievo del campione, ripetere l’operazione con un nuovo tampone.\u003cbr\u003e Trasporto e conservazione del campione\u003cbr\u003e I campioni dovrebbero essere testati il prima possibile dopo il prelievo.\u003cbr\u003e Se i tamponi non vengono analizzati immediatamente, si raccomanda di conservarli in una provetta asciutta, sterile e ben chiusa. Il campione da tampone, se conservato in un ambiente asciutto e sterile, è stabile fino a 24 ore a 2-8 °C.\u003cbr\u003e \u003cu\u003ePreparazione campione\u003c\/u\u003e\u003cbr\u003e Per la preparazione del campione è possibile usare solo il buffer di estrazione e le provette fornite nel presente kit.\u003cbr\u003e Si prega di fare riferimento alla card Procedurale per le informazioni dettagliate sull’Estrazione del Campione.\u003cbr\u003e 1. Posizionare il campione del tampone nella provetta di Estrazione con il Buffer di Estrazione. Ruotare il tampone per circa 10 secondi premendone l’estremità contro le pareti della provetta per rilasciare l’antigene in esso contenuto.\u003cbr\u003e 2. Estrarre il tampone, sempre premendo l’estremità sulla parete della provetta di Estrazione, per espellere più liquido possibile. Gettare il tampone secondo il protocollo per lo smaltimento di rifiuti a rischio biologico.\u003cbr\u003e *NOTA: Il campione dopo l’estrazione è stabile per 2 ore a temperature ambiente o 24 ore a 2-8 °C.\u003cbr\u003e \u003cu\u003eIstruzioni per l'uso\u003cbr\u003e Portare il test e il campione estratto a temperatura ambiente stabile (15-30 °C) prima del test.\u003cbr\u003e 1. Estrarre il test dalla confezione sigillata e usarlo entro un’ora. Si ottengono risultati migliori se il test viene eseguito immediatamente dopo l’apertura della confezione sigillata.\u003cbr\u003e 2. Rovesciare la provetta di raccolta campione e versare 3 gocce di campione estratto in ogni pozzetto per campioni, poi avviare il timer.\u003cbr\u003e 3. Attendere la comparsa della\/e linea\/e colorata\/e. Leggere i risultati a 15 minuti. Non interpretare i risultati dopo 20 minuti.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInterpretazione dei risultati\u003c\/b\u003e\u003cbr\u003e SARS-CoV-2\/RSV POSITIVO:* compaiono due linee colorate nella finestra SARSCoV-2\/RSV. Una dovrebbe essere nella zona di controllo (C) e l’altra in quella di test (T).\u003cbr\u003e Un risultato positivo nella zona del test indica la presenza di antigeni di SARS-CoV-2\/RSV nel campione.\u003cbr\u003e Influenza A POSITIVO:* compaiono due linee colorate nella finestra FLU. Una dovrebbe essere nella zona di controllo (C) e un'altra linea colorata dovrebbe comparire nella regione di test influenza A (A). Un risultato positivo nella zona del test indica la presenza di antigeni di Influenza A nel campione.\u003cbr\u003e Influenza B POSITIVO:* compaiono due linee colorate nella finestra FLU. Una dovrebbe essere nella zona di controllo (C) e l’altra in un'altra linea colorata dovrebbe comparire nella regione di test influenza B (B). Un risultato positivo nella zona del test indica la presenza di antigeni di Influenza B nel campione.\u003cbr\u003e Influenza A e Influenza B POSITIVO:* compaiono tre linee colorate nella finestra FLU.\u003cbr\u003e Una dovrebbe essere nella zona di controllo (C) e due linee colorate dovrebbero comparire nella regione di test influenza A (A) e nella regione di test influenza B (B). Un risultato positivo nella zona del test indica la presenza di antigeni di Influenza A e B nel campione.\u003cbr\u003e *NOTA: l’intensità di colore nella zona del test (T) varia a seconda della quantità di antigene di SARS-CoV-2, Influenza A e\/o B, RSV presente nel campione. Pertanto qualsiasi intensità di colore in quest’area (T\/B\/A) dovrebbe essere classificata come positiva.\u003cbr\u003e NEGATIVO: compare solo una linea colorata nella zona di controllo (C). Non è visibile alcuna linea colorata nella zona del test (T\/B\/A).\u003cbr\u003e NULLO: non compare la linea di controllo. Una quantità di volume insufficiente o tecniche procedurali scorrette sono le ragioni più probabili della mancata comparsa della linea di controllo. Rivedere la procedura e ripetere il test con un nuovo dispositivo. Se il problema persiste interrompere l’uso del kit e contattare immediatamente il distributore locale.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAvvertenze\u003c\/b\u003e\u003cbr\u003e 1. Leggere questo foglietto illustrativo nella sua interezza prima di eseguire il test. La mancata esecuzione delle istruzioni in questo foglietto illustrativo può condurre a risultati del test inaccurati.\u003cbr\u003e 2. Test diagnostico in vitro solo per uso professionale. Non usare oltre la data di scadenza.\u003cbr\u003e 3. Non mangiare, bere o fumare nell’area di manipolazione di campioni o kit.\u003cbr\u003e 4. Non usare il test se la confezione risulta danneggiata.\u003cbr\u003e 5. Manipolare tutti i campioni come potenzialmente infetti. Osservare le precauzioni stabilite per limitare il rischio microbiologico durante tutte le fasi di prelievo, manipolazione, conservazione e smaltimento dei campioni dei pazienti e delle parti dei kit usati. 6. Indossare abbigliamento protettivo quali camici da laboratorio, guanti usa e getta e protezione per gli occhi durante l’analisi dei campioni.\u003cbr\u003e 7. Il Mezzo di Trasporto Virale (VTM) può influenzare il risultato del test, non conservare i campioni in mezzi di trasporto virale; i campioni estratti per i test PCR non possono essere usati per il test.\u003cbr\u003e 8. Lavare accuratamente le mani dopo la manipolazione.\u003cbr\u003e 9. Si prega di assicurarsi che venga usato un quantitativo adeguato di campione per il test.\u003cbr\u003e Una quantità eccessiva o ridotta può causare risultati deviati.\u003cbr\u003e 10. I test usati dovranno essere smaltiti secondo i regolamenti locali.\u003cbr\u003e 11. Umidità e temperatura possono influenzare negativamente i risultati.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimiti\u003c\/b\u003e\u003cbr\u003e 1. Le istruzioni di procedimento del test e interpretazione dei risultati devono essere seguite attentamente nell’analisi degli antigeni SARS-CoV-2\/Influenza A\/Influenza B\/RSV su campioni da tampone nasofaringeo su individui sospetti. Per una prestazione ottimale del test, il corretto prelievo dei campioni è fondamentale. La mancata esecuzione della corretta procedura può portare a risultati inaccurati.\u003cbr\u003e 2. Le prestazioni del Test rapido Combo Antigene SARS-CoV-2\/Influenza A\/Influenza B\/RSV (Tampone Nasofaringeo) sono state valutate solo usando le procedure previste in questo foglietto illustrativo. La modifica di tali procedure può alterare le prestazioni del test.\u003cbr\u003e 3. Il Test rapido Combo Antigene SARS-CoV-2\/Influenza A\/Influenza B\/RSV (Tampone Nasofaringeo) è solo per uso diagnostico in vitro. Questo test dovrebbe essere impiegato per l’individuazione di antigeni SARS-CoV-2\/Influenza A\/Influenza B\/RSV su campioni da tampone nasofaringeo e per coadiuvare la diagnosi in pazienti con sospetta infezione da SARS-CoV-2, Influenza A, Influenza B o RSV unitamente a valutazione clinica e altri esami di laboratorio. Questo test qualitativo non è in grado di fornire né un valore quantitativo né il tasso di crescita nella concentrazione degli antigeni di SARS-CoV-2, Influenza A, Influenza B\/RSV.\u003cbr\u003e 4. Il Test rapido Combo Antigene SARS-CoV-2\/Influenza A\/Influenza B\/RSV (Tampone Nasofaringeo) indica solo la presenza di antigeni SARS-CoV-2, Influenza A, Influenza B o RSV nel campione e non dovrebbe essere usato come unico criterio per la diagnosi di infezioni da SARS-CoV-2, Influenza A\/B\/RSV.\u003cbr\u003e 5. I risultati ottenuti con il presente test dovrebbero essere valutati unitamente ad altri risultati clinici da altri test di laboratorio e analisi.\u003cbr\u003e 6. Se il risultato del test è negativo o non-reattivo e permangono sintomi clinici, si consiglia di ripetere il test a distanza di qualche giorno con un nuovo kit o con strumentazione diagnostica molecolare per escludere l’infezione in questi individui.\u003cbr\u003e 7. Il test mostrerà risultati negativi nelle seguenti condizioni:\u003cbr\u003e a) la concentrazione degli antigeni di nuovo Coronavirus, Influenza A, Influenza B o virus RSV nel campione è inferiore al limite di individuazione minimo del test;\u003cbr\u003e b) Il tempo ottimale di valutazione (picco della concentrazione del virus) dopo l’infezione non è stato verificato, quindi prelevare campioni in momenti diversi sullo stesso paziente può aiutare ad evitare falsi negativi;\u003cbr\u003e c) prelievo e conservazione del campione non adeguati.\u003cbr\u003e 8. I risultati negativi non escludono un’infezione da SARS-CoV-2, in particolare in quegli individui entrati in contatto con il virus. Si consiglia ulteriore analisi con mezzi diagnostici molecolari per escludere l’infezione in tali individui.\u003cbr\u003e 9. Un risultato negativo per Influenza A, B o RSV ottenuto con il presente kit dovrà essere confermato da coltura RT-PCR.\u003cbr\u003e 10. I risultati positivi per SARS-CoV-2 possono essere dovuti ad infezione con ceppi di coronavirus non- SARS-CoV-2 o altri fattori interferenti. Un risultato positivo per Influenza A e\/o B e RSV non esclude un’infezione concomitante con altri agenti patogeni e, quindi, va valutata la possibilità di un’infezione batterica preesistente.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eConservazione\u003c\/b\u003e\u003cbr\u003e Conservare nella confezione sigillata a temperatura ambiente o refrigerata (2-30 °C). Il test è stabile fino alla data di scadenza stampata sulla confezione sigillata. Il test deve rimanere nella confezione sigillata fino all’uso. Non congelare. Non usare oltre la data di scadenza.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormato\u003c\/b\u003e\u003cbr\u003e Cassette di test, buffer di estrazione, card procedura, foglietto illustrativo, provette e puntali di estrazione, tamponi sterili, base di lavoro.\u003c\/u\u003e\n\u003c\/div\u003e","brand":"SCREEN ITALIA SRL","offers":[{"title":"Default Title","offer_id":55204812587342,"sku":"988656753","price":107.02,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-315378.jpg?v=1768797034"},{"product_id":"test-antigenico-rapido-covid-19-alltest-autodiagnostico-determinazione-qualitativa-antigeni-sars-cov-2-e-influenza-a-b-in-tamponi-nasali-mediante-immunocromatografia-1","title":"TEST ANTIGENICO RAPIDO COVID-19 ALLTEST AUTODIAGNOSTICO DETERMINAZIONE QUALITATIVA ANTIGENI SARS-COV-2 E INFLUENZA A+B IN TAMPONI NASALI MEDIANTE IMMUNOCROMATOGRAFIA","description":"\u003ch2\u003eJusChek\u003c\/h2\u003e \u003ch1\u003eTest antigenico rapido combinato\u003cbr\u003e per SARS-CoV-2 e influenza A\/B (tampone nasale)\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescrizione\u003c\/b\u003e\u003cbr\u003e Test rapido per la rilevazione qualitativa di antigeni della proteina nucleocapside di SARS-CoV-2 e delle nucleoproteine dell'influenza A e dell'influenza B nei campioni di tampone nasale.\u003cbr\u003e Il test è destinato all'uso in soggetti sintomatici\/asintomatici con sospetta infezione da COVID-19 e\/o influenza A\/B.\u003cbr\u003e I risultati indicano la rilevazione di antigeni della proteina nucleocapside di SARS-CoV-2 e delle nucleoproteine dell'influenza A e B. Un antigene è generalmente rilevabile nei campioni delle vie respiratori superiori durante la fase acuta dell'infezione.\u003cbr\u003e I risultati positivi indicano la presenza di antigeni virali, ma è necessaria una correlazione clinica con l'anamnesi del paziente e altre informazioni diagnostiche per determinare lo stato dell'infezione. I risultati positivi sono indicativi della presenza di SARS-CoV-2 e\/o dell'influenza A\/B. I soggetti che risultano positivi devono autoisolarsi e rivolgersi al proprio operatore sanitario per assistenza aggiuntiva. Un risultato positivo non esclude la presenza di infezione batterica o di co-infezione da altri virus. Un risultato negativo non esclude la presenza dell'infezione da SARS-CoV-2 e\/o dall'influenza A\/B.\u003cbr\u003e I soggetti che risultano negativi e continuano a manifestare i sintomi del COVID-19 o dell'influenza devono rivolgersi al proprio operatore sanitario per assistenza aggiuntiva.\u003cbr\u003e Per uso autodiagnostico in vitro.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eModalità d'uso\u003c\/b\u003e\u003cbr\u003e \u003cu\u003ePrelievo del campione\u003c\/u\u003e\u003cbr\u003e Lavarsi le mani con acqua e sapone per almeno 20 secondi prima e dopo il test. Se non sono disponibili acqua e sapone, utilizzare un disinfettante per le mani con almeno il 60% di alcool.\u003cbr\u003e Rimuovere il tampone sterile dalla custodia. Non toccare l'estremità morbida del tampone. Inserire il tampone nella narice fino a quando non si avverte una leggera resistenza (circa 2 cm di profondità nella cavità nasale). Ruotare lentamente il tampone, strofinandolo lungo la parte interna della narice per 5-10 volte. Quest'operazione potrebbe risultare fastidiosa. Se si avverte una forte resistenza o dolore, non inserire il tampone più in profondità.\u003cbr\u003e Quando la mucosa nasale è danneggiata o sanguina, il prelievo con tampone nasale non è raccomandato.\u003cbr\u003e Se si esegue il prelievo ad altre persone, indossare la mascherina.\u003cbr\u003e Con i bambini, potrebbe non essere necessario inserire il tampone così a fondo nella narice. Per i bambini molto piccoli, potrebbe essere necessaria un'altra persona che mantenga la testa del bambino durante il prelievo.\u003cbr\u003e Rimuovere delicatamente il tampone. Utilizzando lo stesso tampone, ripetere il procedimento nell'altra narice.\u003cbr\u003e Estrarre il tampone.\u003cbr\u003e \u003cbr\u003e \u003cu\u003ePreparazione del campione\u003c\/u\u003e\u003cbr\u003e Rimuovere il coperchio della provetta con la soluzione tampone di estrazione e posizionare la provetta nel portaprovette nella scatola.\u003cbr\u003e Posizionare il tampone nella provetta di estrazione, assicurandosi che tocchi il fondo, e agitare il tampone per mescolare bene. Premere la punta del tampone contro la provetta e ruotare il tampone per 10-15 secondi. Rimuovere il tampone premendo la punta del tampone contro la parete interna della provetta di estrazione.\u003cbr\u003e Collocare il tampone in un sacchetto di plastica. Chiudere la provetta di estrazione.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eEsecuzione del test\u003c\/u\u003e\u003cbr\u003e Rimuovere la cassetta per test dalla busta di alluminio sigillata e utilizzarla entro un'ora. I risultati più affidabili si ottengono se il test viene eseguito immediatamente dopo l'apertura della busta.\u003cbr\u003e Posizionare la cassetta per test su una superficie piana e uniforme. Capovolgere la provetta di estrazione del campione e aggiungere 3 gocce di campione estratto in ciascun pozzetto (S) della cassetta per test, quindi avviare il timer. Durante il test, non spostare la cassetta.\u003cbr\u003e Leggere il risultato dopo 10 minuti. Non interpretare il risultato dopo 20 minuti.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInterpretazione dei risultati\u003c\/u\u003e\u003cbr\u003e Comunicare i risultati del test al proprio operatore sanitario e seguire attentamente le linee guida\/i requisiti locali di contrasto alla diffusione del COVID-19.\u003cbr\u003e \u003cbr\u003e POSITIVO al SARS-CoV-2: una linea colorata deve trovarsi nell'area di controllo (C) e l'altra nell'area di test (T). L'intensità del colore nell'area di test (T) varierà in base alla quantità di antigene di SARS-CoV-2 presente nel campione. Pertanto, qualsiasi sfumatura di colore nell'area di test (T) deve essere considerata come un risultato positivo.\u003cbr\u003e Un risultato positivo indica con molta probabilità la presenza di un'infezione da COVID-19, ma tale esito deve essere confermato da ulteriori test. Mettersi immediatamente in auto-isolamento in conformità alle linee guida locali e contattare subito il medico di base o il servizio sanitario locale seguendo le istruzioni fornite dalle autorità locali. Il risultato del test verrà convalidato con un test PCR di conferma e verranno illustrati i passaggi successivi da seguire.\u003cbr\u003e \u003cbr\u003e POSITIVO all'influenza A: nella finestra FLU A+B vengono visualizzate due linee colorate. Una linea colorata deve trovarsi nell'area di controllo (C) e l'altra nell'area dell'influenza A (A). L'intensità del colore nell'area di test (A) varierà in base alla quantità di antigene dell'influenza A presente nel campione. Pertanto, qualsiasi sfumatura di colore nell'area di test (A) deve essere considerata come un risultato positivo.\u003cbr\u003e Un risultato positivo indica con molta probabilità la presenza di un'infezione da influenza A, ma tale esito deve essere confermato da ulteriori test. Mettersi immediatamente in auto-isolamento in conformità alle linee guida locali e contattare subito il medico di base o il servizio sanitario locale seguendo le istruzioni fornite dalle autorità locali. Il risultato del test verrà convalidato con un test PCR di conferma e verranno illustrati i passaggi successivi da seguire.\u003cbr\u003e \u003cbr\u003e POSITIVO all'influenza B: nella finestra FLU A+B vengono visualizzate due linee colorate. Una linea colorata deve trovarsi nell'area di controllo (C) e l'altra nell'area dell'influenza B (B). L'intensità del colore nell'area di test (B) varierà in base alla quantità di antigene dell'influenza B presente nel campione. Pertanto, qualsiasi sfumatura di colore nell'area di test (B) deve essere considerata come un risultato positivo.\u003cbr\u003e Un risultato positivo indica con molta probabilità la presenza di un'infezione da influenza B, ma tale esito deve essere confermato da ulteriori test. Mettersi immediatamente in auto-isolamento in conformità alle linee guida locali e contattare subito il medico di base o il servizio sanitario locale seguendo le istruzioni fornite dalle autorità locali. Il risultato del test verrà convalidato con un test PCR di conferma e verranno illustrati i passaggi successivi da seguire.\u003cbr\u003e \u003cbr\u003e POSITIVO all'influenza A e all'influenza B: nella finestra FLU A+B vengono visualizzate tre linee colorate. Una linea colorata deve trovarsi nell'area di controllo (C) e le altre due nell'area dell'influenza A (A) e dell'influenza B (B). L'intensità del colore nell'area di test (A\/B) varierà in base alla quantità di antigene dell'influenza A\/B presente nel campione. Pertanto, qualsiasi sfumatura di colore nell'area di test (A\/B) deve essere considerata come un risultato positivo.\u003cbr\u003e Un risultato positivo indica con molta probabilità la presenza di un'infezione da influenza A e da influenza B, ma tale esito deve essere confermato da ulteriori test. Mettersi immediatamente in auto-isolamento in conformità alle linee guida locali e contattare subito il medico di base o il servizio sanitario locale seguendo le istruzioni fornite dalle autorità locali. Il risultato del test verrà convalidato con un test PCR di conferma e verranno illustrati i passaggi successivi da seguire.\u003cbr\u003e \u003cbr\u003e NEGATIVO: nell'area di controllo (C) compare una linea colorata. Non viene visualizzata alcuna linea colorata evidente nell'area di test (T\/B\/A).\u003cbr\u003e È improbabile che sia presente un'infezione da COVID-19 e\/o da influenza A\/influenza B. Tuttavia, è possibile che questo test fornisca un risultato negativo errato (falso negativo) in alcuni soggetti con COVID-19 e\/o influenza A\/influenza B. Ciò significa che il soggetto potrebbe presentare un'infezione da COVID-19 e\/o da influenza A\/influenza B anche in caso di risultato negativo del test. Inoltre, è possibile ripetere il test con un nuovo kit.\u003cbr\u003e In caso di sospetta infezione, ripetere il test dopo 1-2 giorni, poiché non è possibile rilevare con precisione il coronavirus\/il virus dell'influenza in tutte le fasi dell'infezione.\u003cbr\u003e Anche se il risultato del test è negativo, è necessario rispettare le norme relative al distanziamento e all'igiene, a spostamenti e viaggi, alla partecipazione ad eventi e così via, secondo le linee guida\/i requisiti locali relativi al COVID-19\/all'influenza.\u003cbr\u003e \u003cbr\u003e NON VALIDO: non compare la linea di controllo. Le cause più probabili della mancata comparsa della linea di controllo sono volume insufficiente del campione o tecniche procedurali non corrette.\u003cbr\u003e Leggere nuovamente le istruzioni e ripetere il test, impiegando un nuovo kit, oppure contattare un centro per tamponi COVID-19\/per l'influenza.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAvvertenze\u003c\/b\u003e\u003cbr\u003e Solo per l'autotest in vitro. Non utilizzare oltre la data di scadenza.\u003cbr\u003e Prima di eseguire il test, leggere tutte le informazioni contenute nel foglio illustrativo.\u003cbr\u003e Non mangiare, bere o fumare nell'area in cui vengono manipolati i campioni o i kit.\u003cbr\u003e Non bere la soluzione di estrazione contenuta nel kit. Maneggiare con cura la soluzione di estrazione ed evitare che entri in contatto con la pelle o gli occhi; in caso di contatto, sciacquare immediatamente con abbondante acqua corrente.\u003cbr\u003e Se la confezione in alluminio è danneggiata o è stata aperta, non utilizzare il prodotto.\u003cbr\u003e Questo kit di test deve essere utilizzato solo come test preliminare e risultati ripetutamente anomali devono essere analizzati con il medico o un operatore sanitario.\u003cbr\u003e Rispettare rigorosamente i tempi indicati.\u003cbr\u003e Utilizzare il test una sola volta. Non smontare e toccare la finestra della cassetta per test.\u003cbr\u003e Il kit non deve essere congelato o utilizzato dopo la data di scadenza stampata sulla confezione.\u003cbr\u003e Nei bambini, il test deve essere eseguito con l'aiuto di un adulto.\u003cbr\u003e Lavarsi accuratamente le mani prima e dopo la manipolazione.\u003cbr\u003e Assicurarsi di utilizzare una quantità appropriata di campione per il test. Una quantità eccessiva o insufficiente di campione potrebbe causare una deviazione dei risultati.\u003cbr\u003e Le prestazioni sono state valutate solo con campioni da tampone nasale, impiegando le procedure descritte nel foglio illustrativo.\u003cbr\u003e Il test indica solo la presenza di antigeni di SARS-CoV-2 e\/o dell'influenza A\/influenza B nel campione.\u003cbr\u003e Se il risultato del test è negativo o non reattivo e i sintomi clinici persistono, è possibile che il virus non venga rilevato nelle primissime fasi dell'infezione. Si consiglia di ripetere il test con un nuovo dispositivo o con uno strumento diagnostico molecolare per escludere l'infezione in questi soggetti. I risultati negativi non escludono l'infezione da SARS-CoV-2, in particolare in coloro che sono stati a contatto con il virus. Per escludere l'infezione in questi soggetti, si dovrebbe considerare l'esecuzione di un test molecolare di conferma.\u003cbr\u003e Un risultato negativo per influenza A o influenza B ottenuto da questo kit deve essere confermato da coltura\/RT-PCR.\u003cbr\u003e I risultati positivi al COVID-19 possono essere dovuti a infezione da ceppi di coronavirus non SARS-CoV-2 o ad altri fattori di interferenza. Un risultato positivo per l'influenza A e\/o B non esclude la co-infezione da altro patogeno, pertanto andrebbe considerata la possibilità di un'infezione batterica soggiacente.\u003cbr\u003e La mancata osservanza delle procedure di test potrebbe alterare le prestazioni del test.\u003cbr\u003e Se un campione viene prelevato o manipolato in modo improprio, il test potrebbe dare risultati falsi negativi.\u003cbr\u003e Se nel campione sono presenti livelli di virus inferiore al limite di rilevamento del test, il test potrebbe restituire risultati falsi negativi.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eConservazione\u003c\/b\u003e\u003cbr\u003e Conservare nella confezione sigillata a temperatura ambiente o in frigorifero (2-30 °C). Il test è stabile fino alla data di scadenza stampata sulla busta sigillata. Il test deve rimanere nella busta sigillata fino all'uso.\u003cbr\u003e Validità a confezionamento integro: 24 mesi.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormato\u003c\/b\u003e\u003cbr\u003e Il kit contiene:\u003cbr\u003e - cassetta di test;\u003cbr\u003e - tampone sterile;\u003cbr\u003e - foglio illustrativo;\u003cbr\u003e - soluzione di estrazione.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e SARS-CV2-ALTC\u003c\/div\u003e","brand":"T TEX SRL","offers":[{"title":"Default Title","offer_id":55228239872334,"sku":"985593324","price":3.28,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-271757.jpg?v=1768798907"},{"product_id":"test-rapido-antigeni-h-pylori-ihp-602h","title":"TEST RAPIDO ANTIGENI H PYLORI\/IHP-602H","description":"\u003ch1\u003eALLTEST\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescrizione\u003c\/b\u003e\u003cbr\u003e Il Test rapido su card antigene H.pylori (Feci) è un test immunologico cromatografico rapido per la rilevazione qualitativa degli antigeni H.pylori in campioni di feci umane, che fornisce risultati in 10 minuti. Il test utilizza anticorpi specifici per gli antigeni H.pylori per rilevare selettivamente gli antigeni H.pylori nei campioni di feci umane.\u003cbr\u003e Il Test rapido su card antigene H.pylori (Feci) è un test immunologico qualitativo a flusso laterale per la rilevazione degli antigeni di H.pylori in campioni di feci umane. In questo test, la membrana viene prerivestita con anti-H.pylori sulla zona della linea del test. Durante il test, il campione reagisce con la particella rivestita di anti-H. anticorpi pylori. La miscela migra verso l'alto sulla membrana per azione capillare per reagire con l'anti-H.pylori sulla membrana e generano una linea colorata. La presenza di questa linea colorata nella zona del test indica un risultato positivo, mentre la sua assenza indica un risultato negativo. Per fungere da controllo procedurale, una linea colorata apparirà sempre nella regione della linea di controllo indicando che è stato aggiunto un volume adeguato di campione e che si è verificata la traspirazione della membrana.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eModalità d'uso\u003c\/b\u003e\u003cbr\u003e 1. Lavarsi le mani con sapone e risciacquare con acqua.\u003cbr\u003e 2. Per raccogliere i campioni fecali\u003cbr\u003e Il campione di feci deve essere raccolto nella carta per la raccolta delle feci o in contenitori di raccolta puliti. Utilizzare la carta per la raccolta delle feci, evitando la contaminazione del campione prendendo precauzioni affinché il campione o il lato della carta contenente il campione non venga a contatto con oggetti contaminanti, compresi i detergenti per WC.\u003cbr\u003e 3. Per processare i campioni fecali\u003cbr\u003e Svitare il tappo della provetta di raccolta del campione,quindi infilare in modo casuale l'applicatore di raccolta del campione nel campione fecale in almeno 3 diversi siti. Non raccogliere il campione fecale.\u003cbr\u003e Avvitare e serrare il tappo sulla provetta di raccolta del campione, quindi agitare vigorosamente la provetta di raccolta del campione per miscelare il campione e il tampone di estrazione per 2 minuti.\u003cbr\u003e 4. Portare la busta a temperatura ambiente prima di aprirla. Rimuovere H.pylori test dalla busta di alluminio e utilizzarla il prima possibile. I migliori risultati si ottengono se il test viene eseguito immediatamente dopo aver aperto la busta di alluminio.\u003cbr\u003e 5. Aprire il tappo della provetta di raccolta del campione e rompere la punta. Capovolgere la provetta di raccolta del campione e trasferire 2 gocce piene del campione estratto nel pozzetto del campione (S) della card del test, quindi avviare il timer. Evitare di intrappolare bolle d'aria nel pozzetto del campione (S).\u003cbr\u003e 6. Leggere i risultati a 10 minuti. Non leggere i risultati dopo 20 minuti.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLettura dei risultati\u003c\/b\u003e\u003cbr\u003e POSITIVO: * Vengono visualizzate due linee. Vengono visualizzate sia la linea del T (test) che la linea C (controllo). Questo risultato significa che c'è la presenza dell'antigene H.pylori nelle feci e che dovresti consultare un medico. *NOTA: L'intensità del colore nella regione della linea del test (T) varierà a seconda della concentrazione dell'antigene H.pylori presente nel campione. Pertanto, qualsiasi sfumatura di colore nella zona della linea del test (T) dovrebbe essere considerata positiva.\u003cbr\u003e NEGATIVO: Viene visualizzata una linea colorata nell'area della linea di controllo (C). Nessuna linea appare nella zona della linea del test (T).\u003cbr\u003e Questo risultato significa che la presenza dell'antigene H.pylori nelle feci non è rilevabile.\u003cbr\u003e NON VALIDO: La linea di controllo non viene visualizzata. Un volume di campione insufficiente o tecniche procedurali errate sono le ragioni più probabili del guasto della linea di controllo. Rivedere la procedura e ripetere il test con un nuovo test. Se il problema persiste, interrompere immediatamente l'utilizzo del kit di test e contattare il distributore locale.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAvvertenze\u003c\/b\u003e\u003cbr\u003e - Solo per autoanalisi diagnostica in vitro. Non utilizzare dopo la data di scadenza.\u003cbr\u003e - Non mangiare, bere o fumare nell'area in cui vengono manipolati i campioni o i kit.\u003cbr\u003e - Un contenitore pulito per raccogliere il campione fecale.\u003cbr\u003e - Seguire rigorosamente il tempo indicato.\u003cbr\u003e - Usare il test una sola volta. Non smontare e toccare la finestra del test H.pylori.\u003cbr\u003e - Il kit non deve essere congelato o utilizzato dopo la data di scadenza stampata sulla confezione.\u003cbr\u003e - Il test utilizzato deve essere smaltito secondo le normative locali.\u003cbr\u003e - Tenere fuori dalla portata dei bambini.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimitazioni\u003c\/b\u003e\u003cbr\u003e 1. Il Test rapido su card antigene H.pylori (Feci) è solo per autoanalisi diagnostica in vitro. Il test deve essere utilizzato per la rilevazione degli antigeni H.pylori solo nei campioni di feci. Né il valore quantitativo né il tasso di aumento della concentrazione di antigeni H.pylori possono essere determinati da questo test qualitativo.\u003cbr\u003e 2. Il Test rapido su card antigene H.pylori (Feci) indicherà solo la presenza di H.pylori nel campione e non deve essere utilizzata come unico criterio diagnostico affinché H.pylori sia un agente eziologico per l'ulcera peptica o duodenale.\u003cbr\u003e 3. Come per tutti i test diagnostici, tutti i risultati devono essere interpretati insieme ad altre informazioni cliniche a disposizione del medico.\u003cbr\u003e 4. Se il risultato del test è negativo e i sintomi clinici persistono, si consigliano ulteriori test utilizzando altri metodi clinici. Un risultato negativo non preclude mai la possibilità di infezione da H.pylori.\u003cbr\u003e 5. A seguito di alcuni trattamenti antibiotici, la concentrazione di antigeni H.pylori può diminuire fino a una concentrazione inferiore al livello minimo di rilevamento del test. Pertanto, la diagnosi deve essere fatta con cautela durante il trattamento antibiotico.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eConservazione\u003c\/b\u003e\u003cbr\u003e Il kit può essere conservato a temperatura ambiente o refrigerato (2-30 °C). La card del test è stabile fino alla data di scadenza stampata sulla confezione sigillata. La card del test deve rimanere nella busta sigillata fino all'uso. Non congelare. Non utilizzare oltre la data di scadenza.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormato\u003c\/b\u003e\u003cbr\u003e H.pylori test, provetta di raccolta del campione con tampone di estrazione, foglietto illustrativo, carta per la raccolta delle feci.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e IHP-602H\u003c\/div\u003e","brand":"NOI TEST SRL","offers":[{"title":"Default Title","offer_id":55414464643406,"sku":"951992193","price":9.43,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-389410.jpg?v=1772589115"},{"product_id":"test-antigenico-rapido-covid-19-clungene-autodiagnostico-determinazione-qualitativa-antgeni-sars-cov-2-in-tamponi-nasali-mediante-immunocromatografia","title":"TEST ANTIGENICO RAPIDO COVID-19 CLUNGENE AUTODIAGNOSTICO DETERMINAZIONE QUALITATIVA ANTGENI SARS-COV-2 IN TAMPONI NASALI MEDIANTE IMMUNOCROMATOGRAFIA","description":"\u003ch2\u003eCLUNGENE\u003c\/h2\u003e \u003ch1\u003eCOVID-19 Antigen Rapid Test\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescrizione\u003c\/b\u003e\u003cbr\u003e Metodo di immunodosaggio a flusso laterale per la rilevazione qualitativa dell’antigene nucleocapside di SARS-CoV-2 nel tampone nasale di soggetti con sintomi o altre ragioni epidemiologiche che facciano sospettare di infezione da COVID-19.\u003cbr\u003e Il test è destinato all’uso da parte di soggetti non professionisti a partire dai 15 anni e, a seconda del caso, da adulti per testare un altro soggetto minore di 15 anni. I soggetti sopra i 65 anni devono richiedere assistenza nell’esecuzione del test.\u003cbr\u003e Il test fornisce solo un risultato preliminare di screening per il virus SARS-CoV-2. I risultati positivi devono essere confermati tramite un test PCR eseguito in laboratorio.\u003cbr\u003e Le persone con un risultato di test negativo che continuano a manifestare sintomi simili a quelli da COVID-19 devono rivolgersi al medico.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eModalità d'uso\u003c\/b\u003e\u003cbr\u003e \u003cu\u003ePreparazione del test\u003c\/u\u003e\u003cbr\u003e Assicurarsi che tutti i componenti per il test siano a temperatura ambiente (15-30 °C).\u003cbr\u003e Tenere a portata di mano un orologio, un timer o un cronometro.\u003cbr\u003e Verificare che la confezione sia integra. Non usare il test se la confezione risulta danneggiata in modo visibile.\u003cbr\u003e Aprire la confezione della cassetta per il test solo al momento dell'utilizzo. Utilizzare la cassetta per il test entro un'ora dall'apertura della confezione.\u003cbr\u003e Lavarsi le mani con acqua e sapone e asciugarle accuratamente.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eEsecuzione del test\u003c\/u\u003e\u003cbr\u003e Aprire la provetta contenente il reagente di estrazione rimuovendo con attenzione la pellicola. Inserire la provetta nel porta-provetta (foro presente sulla confezione).\u003cbr\u003e Rimuovere il tampone dalla busta: aprire la confezione dall'estremità del bastoncino. Non toccare la testina del tampone. Estrarre il tampone ed inserire delicatamente l'intera testina del tampone nella narice, ad una profondità di circa 2,5 cm. Ruotare il tampone contro la parete della narice per almeno 5 volte. Rimuovere il tampone, inserirlo nell'altra narice e ripetere la medesima operazione. Eseguire attentamente questa operazione: possono verificarsi risultati falsi negativi se il tampone nasale non viene eseguito correttamente.\u003cbr\u003e Inserire il tampone nella provetta contenente il reagente di estrazione. Ruotare il tampone 5 volte all'interno del reagente, premendo la testina del tampone contro il fondo e il lato della provetta. lasciare il tampone nel reagente per 1 minuto. Rimuovere il tampone premendo i lati della provetta in modo da far uscire il liquido dal tampone. Chiudere bene la provetta con il tappo.\u003cbr\u003e Aprire la busta sigillata contenente la cassetta di test ed estrarla. Posare la cassetta di test su una superficie piana.\u003cbr\u003e Tenere la provetta verticalmente sopra il pozzetto del campione e aggiungere 3 gocce nel pozzetto, premendo delicatamente i lati della provetta. Può verificarsi un risultato falso negativo se si aggiungono meno di 3 gocce di campione nel pozzetto. Il risultato non sarà influenzato se si aggiungono 1-2 gocce di campione in più, a condizione che si possa leggere la linea di controllo (C).\u003cbr\u003e Avvia l’orologio\/cronometro o timer. Leggere il risultato del test dopo 15-20 minuti, non leggere il risultato se sono trascorsi più di 20 minuti. Possono verificarsi risultati errati se i risultati del test vengono letti prima di 15 minuti o dopo 20 minuti.\u003cbr\u003e Una volta eseguito il test, raccogliere le parti del kit usate e i campioni del tampone in un sacchetto di smaltimento e smaltirli con i rifiuti domestici. Lavarsi accuratamente le mani dopo la manipolazione.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInterpretazione dei risultati\u003c\/u\u003e\u003cbr\u003e - POSITIVO: appaiono due linee, la linea di controllo (C) e la linea di test (T). L'intensità di colore della linea di test (T) può essere molto debole, il risultato è comunque da interpretarsi positivo. Un risultato positivo del test indica che probabilmente si è portatori della malattia COVID-19. È necessario sottoporsi a un test PCR di laboratorio il prima possibile per confermare la diagnosi di COVID-19 e seguire le linee guida locali per l’isolamento al fine di evitare la trasmissione del virus ad altri.\u003cbr\u003e \u003cbr\u003e - NEGATIVO: appare solo una linea colorata, la linea di controllo (C). Non appare la linea di test (T). Un risultato negativo del test indica che probabilmente non si è portatori della malattia COVID-19. Anche se si ottiene un risultato negativo, si devono comunque seguire tutte le linee guida per limitare la diffusione del COVID-19. Se si sviluppano dei sintomi o se i sintomi persistono, sottoporsi a un test PCR di laboratorio. Se si sospetta un’infezione, si raccomanda di ripetere il test dopo 1–2 giorni, poiché il virus non può essere rilevato con precisione in tutte le fasi dell’infezione.\u003cbr\u003e \u003cbr\u003e - NON VALIDO: la linea di controllo (C) non appare. Il risultato del test non è valido indipendentemente dalla comparsa o meno della linea di test (T). Ripetere il test con una nuova cassetta o contattare il medico.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAvvertenze\u003c\/b\u003e\u003cbr\u003e Solo per la diagnostica in vitro.\u003cbr\u003e Non utilizzare questo test come unica base per gestione dell'infezione da COVID-19. Si prega di consultare in qualsiasi momento un operatore sanitario se i sintomi persistono o peggiorano, o se si teme per la propria salute.\u003cbr\u003e Possono verificarsi risultati negativi se il test non viene eseguito entro i primi 7 giorni dalla manifestazione dei sintomi.\u003cbr\u003e Il test su un soggetto di età inferiore ai 15 anni deve essere eseguito da un adulto.\u003cbr\u003e Tenere fuori dalla portata dei bambini per ridurre il rischio di bere accidentalmente il reagente o di ingerire piccole parti.\u003cbr\u003e Non utilizzare dopo la data di scadenza.\u003cbr\u003e Il test è monouso e da utilizzare solo con i componenti forniti.\u003cbr\u003e Non eseguire il test alla luce diretta del sole.\u003cbr\u003e Evitare il contatto con il reagente di estrazione. In casi di inalazione, ingestione o esposizione della pelle o degli occhi al reagente di estrazione, adottare immediatamente le misure di primo soccorso in conformità con la scheda di sicurezza (SDS).\u003cbr\u003e Il test richiede il prelievo di un campione dalla cavità nasale. Durante l'esecuzione del test prestare particolare attenzione alle istruzioni su come eseguire il tampone. L'esecuzione errata del campionamento può comportare un risultato errato. Questo è particolarmente importante in caso di assenza di sintomi.\u003cbr\u003e La cassetta per il test deve rimanere nella busta sigillata fino al momento dell'utilizzo.\u003cbr\u003e Lavare le mani accuratamente prima e dopo il test.\u003cbr\u003e Il test deve essere usato solo per la rilevazione qualitativa degli antigeni SARS-CoV-2 in campioni prelevati con tampone nasale.\u003cbr\u003e L'intensità della linea di test non è necessariamente correlata al titolo virale di SARS-CoV-2 presente nel campione.\u003cbr\u003e L'inosservanza delle \"Istruzioni per l'uso\" può influire negativamente sulla prestazione del test e\/o invalidare il risultato del test.\u003cbr\u003e Si tratta di un test esclusivamente presuntivo. In caso di risultato positivo, è necessario sottoporsi immediatamente a un test PCR di laboratorio e a un follow-up clinico.\u003cbr\u003e Si possono verificare risultati negativi se il livello di antigene in un campione è inferiore al limite di rilevamento del test. Si raccomanda di ripetere il test dopo 1-2 giorni se si sospetta un'infezione in corso, se ci si trova in un ambiente ad alto rischio o dove c'è un rischio professionale, o si ha un'esposizione nota a COVID-19.\u003cbr\u003e I risultati negativi non escludono l'infezione da SARS-CoV-2. Se si manifestano sintomi simili a quelli da COVID-19, è necessario sottoporsi immediatamente a un ulteriore test PCR di laboratorio.\u003cbr\u003e I risultati positivi del test non escludono co-infezioni con altri agenti patogeni.\u003cbr\u003e Un risultato positivo non può determinare se una persona è contagiosa.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eConservazione\u003c\/b\u003e\u003cbr\u003e Conservare nella busta sigillata a una temperatura di 4-30 °C.\u003cbr\u003e Validità a confezionamento integro: 24 mesi.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormato\u003c\/b\u003e\u003cbr\u003e Il kit contiene:\u003cbr\u003e - 1 cassetta di test;\u003cbr\u003e - 1 provetta contenente reagente di estrazione;\u003cbr\u003e - 1 tampone;\u003cbr\u003e - 1 sacchetto di smaltimento;\u003cbr\u003e - 1 istruzioni per l'uso.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e 101126\u003c\/div\u003e","brand":"GAMMADIS FARMACEUTICI SRL","offers":[{"title":"Default Title","offer_id":59770517848398,"sku":"989375757","price":1.73,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0845\/6214\/9710\/files\/TE009-329588.jpg?v=1780188334"}],"url":"https:\/\/farmaspeed.it\/en\/collections\/diagnostici-in-vitro-ivd.oembed","provider":"Farmaspeed","version":"1.0","type":"link"}