Buy Green Spring SARS-CoV-2 Antigen Rapid Test Kit - Green Spring Rapid Test 4 in 1! Detect COVID-19 infections quickly and accurately with our Green Spring SARS-CoV-2 Antigen Rapid Test Kit. The high sensitivity of 96.77% and 100% specificity ensure high-quality performance.The 4 sampling options (nasopharyngeal, oropharyngeal, nasal, and saliva) allow for flexible and individual sample collection. Features of the Green Spring SARS-CoV-2 Antigen Rapid Test Kit ✓ Listed on the Common RAT List of the HSC✓ Test result after 15 minutes✓ Can be performed flexibly and independently of location✓ Only for medical professionals✓ Listed on the positive list of the Paul-Ehrlich-Institut✓ BfArM listed, Test-ID: AT417/20 All of our tests are CE certified and suitable for use in the European market. What's included in the Green Spring SARS-CoV-2 Antigen Rapid Test Kit 4 in 1 25 sterile swabs25 test cassettes25 extraction tubes1 tube stand1 user manual Order now and detect COVID-19 quickly, reliably, and easily with the Green Spring SARS-CoV-2 Antigen Rapid Test Kit - Green Spring Rapid Test! Why Buy the Green Spring SARS-CoV-2 Antigen Rapid Test Kit - Green Spring Rapid Test? ✓ MONEY-BACK GUARANTEE Our goal is your satisfaction with your purchase. If the purchased goods do not meet your expectations, you can return them within the 14-day cancellation period and you will be refunded the purchase price. Comparison - Professional COVID-19 Antigen Rapid Tests Manufactured by Hecin Testsealabs Bioteke Longsee Green Spring Roche Siemens Sensitivity 97.09% 92.10% 96.49% 95.51% 96.77% 96.52% 97.25% Specificity 99.78% 98.10% 99.28% 99.72% 100% 99.60% 100% Manufactured in China China China China China South Korea China Listed for the"EU common list" Yes, in category A Yes Yes Yes, in category A Yes Yes Yes Frequently Asked Questions Before Buying the Green Spring SARS-CoV-2 Antigen Rapid Test Kit What is the Green Spring SARS-CoV-2 Antigen Rapid Test Kit? The Green Spring SARS-CoV-2 Antigen Rapid Test Kit is a rapid COVID-19 antigen test with high specificity and sensitivity. It has been evaluated by the Paul Ehrlich Institute and differs from other rapid tests by offering 4 options for sample collection (nasal, nasopharyngeal, oropharyngeal, or saliva swab). Does the Green Spring Rapid Test for SARS-CoV-2 Antigen have the capability to detect mutations? Yes, the Green Spring 4-in-1 COVID-19 antigen rapid test can detect, among other variants, the Delta and Omicron variants. Is the Green Spring Rapid Test safe? The Green Spring SARS-CoV-2 Antigen Rapid Test Kit - Green Spring Rapid Test has been evaluated by the PEI and has an overall sensitivity of 100%. The test's sensitivity is 95.51% and specificity is 99.72%. Since the test is on the "Common List" (European Commission list), it can be assumed to be safe. How long does it take to get the results of the Green Spring SARS-CoV-2 Antigen Rapid Test Kit? You can read the results of the Green Spring test in just 15 minutes. Is the Green Spring test suitable for children? Yes, the Green Spring SARS-CoV-2 Antigen Rapid Test is more suitable for children than other tests, especially because it can be done with lollipops. How is the professional Green Spring Rapid Test packaged? There are 25 tests in one box, and 1000 in one whole carton. How long is the Green Spring SARS-CoV-2 Antigen Rapid Test Kit - Green Spring Rapid Test storable? The Green Spring SARS-CoV-2 Antigen Rapid Test can be stored at room temperature or between 4 and 35 degrees for up to 12 months. Does the Green Spring Rapid Test detect the Omicron variant? Yes, the tests have been evaluated by the Paul-Ehrlich-Institut. The Omicron variant is detected in full. Which tests are on the Paul-Ehrlich-Institut's checklist? The list includes tests that meet the sensitivity criteria and are in the top 20% of the list. You can read the exact details here. Who is allowed to use the Green Spring Rapid Test? These tests are exclusively intended for professional use. Home antigen tests can be found here. Technical Data Packing 25 packages Cardboard 40 boxes - 1000 pieces Standards and market conformity Professional use (only available for professional users) Quick test 4 in 1 Approved in Germany EN ISO 13485:2016 B Company number: AT417/20 Listed for EU-wide recognition in the "EU Common List" of the European Commission - Directorate General Health and Food Safety. CE-certified and reimbursable test, listed at the Federal Institute for Drugs and Medical Devices according to the Coronavirus Test Regulation (TestV) 96.77% sensitivity 100% specificity With an integrated buffer solution Green Spring SARS-CoV-2 Antigen Rapid Test Kit Test Instructions Rapid test for the qualitative detection of SARS-CoV-2 nucleocapsid antigens. For professional use. PURPOSE The Green Spring® SARS-CoV-2 Antigen Rapid Test is for the rapid qualitative detection of SARS-CoV-2 nucleocapsid protein antigen in human saliva, nasal, nasopharyngeal or throat swab specimens. The results are used for the detection of SARS-CoV-2 antigen. The antigen is generally detectable in upper respiratory tract specimens during the acute phase of infections. Positive results do not rule out bacterial infection or co-infection with other viruses. The pathogen detected may not be the sole cause of the disease. Negative results should be treated as suspected cases and confirmed with a molecular assay. Negative results should be considered in the context of a patient's recent exposures, history and presence of clinical signs and symptoms consistent with COVID-19. These tests should only be used by professionals or trained individuals. SUMMARY The novel coronaviruses belong to a ß-genus. COVID-19 is an acute respiratory infectious disease. Humans are generally susceptible to it. Currently, patients infected with the novel coronavirus are the main source of infection; asymptomatically infected people may also be a source of infection. The main manifestations include fever, fatigue and a dry cough. A stuffy or runny nose, sore throat, muscle aches and diarrhoea occur in a few cases. TEST PRINCIPLE The Green Spring® SARS-CoV-2 Antigen Rapid Test is a qualitative, membrane-based immunoassay for the detection of SARS-CoV-2 nucleocapsid protein antigens. The test line region is coated with SARS-CoV-2 antibody. The sample reacts with the SARS-CoV-2 antibody in the test line region. If the sample contains SARS-CoV-2 antigens, a coloured line appears in the test line area (T) as a relevant result. As a procedural control, a coloured line appears in the control line area (C), indicating that the correct volume of sample has been added and membrane wetting has occurred correctly STORAGE AND STABILITY Store the tests in the sealed foil pouch at room temperature or refrigerated (2 - 30 °C). The test is stable until the expiry date printed on it. The test cassettes must be stored in the sealed foil pouch until use. Do not freeze. Do not use after the expiry date. Protect from sun, moisture and heat. MATERIALS SUPPLIED • Test cassette with one pack of desiccant: 25 pieces • Sterile swab: 25 pieces • Extraction tubes with buffer: 25 disposable extraction tubes with 0.5 ml extraction buffer each and 25 nozzle caps. • Workstation: 1 piece • Package insert: 1 instruction leaflet Precautionary Measures 1. The package leaflet must be read carefully before performing the test. Failure to follow the instructions in the package leaflet may lead to inaccurate test results. 2. For professional use in in vitro diagnostics only. Do not use after the expiry date. 3. Do not eat, drink or smoke for 10 minutes before and during sample collection. 4. Do not use the test if the packaging or test components are damaged. 5. All specimens must be considered potentially infectious. Observe established precautions against microbiological hazards throughout the collection, handling, storage and disposal of patient specimens and used test components. 6. Wear protective clothing such as lab coats, disposable gloves and eye protection while samples are being examined 7. Wash your hands thoroughly after performing the test. 8. Samples stored in viral transport media (VTM) may influence test results. 9. All used test components should be disposed of according to local regulations. 10. Humidity and temperature can adversely affect the results PREPARATION Only use the materials supplied with the respective set. Test the samples immediately Use the test kit only at room temperature (15 to 30 °C). The test kit is intended only for swab specimens that are collected and tested directly (i.e. swabs that have NOT been placed in transport media). This kit is NOT intended for testing liquid specimens such as wash or aspirate specimens or swabs in transport media, as results may be affected by dilution. 1. Tear off the foil pouch, remove the test cassette and place it on a clean and flat surface. 2. Freshly collected samples should be processed within 1 hour. 3. Label the respective test cassette for each test or control. 4. Place the labelled extraction tubes in a rack in the designated area of the workspace. SAMPLING The correct sample collection is the most important step. Choose one of the four methods and then proceed with the test procedure. 1) Salvia (Lolli-Test) Be aware that false results may occur if saliva is not collected properly. 1. Place an extraction tube in the cardboard workstation. 2. Press the tip of the tongue against the lower root of the jaw. Cough deeply. Make the sound of "kuuua" to concentrate the saliva. 3. Place the swab on the tongue for at least 10 seconds, turning it 3 times or more to fully absorb the saliva. 2) Anterio-nasal swab (nose in front) Make sure to collect enough nasal secretions with the swab. It is advisable to blow your nose first. 1. Place an extraction tube in the cardboard workstation. 2. Carefully insert the swab into the patient's nostril. The tip of the swab should be inserted up to 2.5 cm deep from the edge of the nostril. 3. Dab along the mucous membrane in the nostril to ensure that both mucus and cells are collected. 4. Remove the swab from the nostril while gently rotating it between your fingers. 3) Nasopharyngeal swab (nose and throat) 1. Place an extraction tube in the cardboard workstation. 2. Tilt the patient's head slightly backwards. Hold the swab like a pen and insert it through the nostril parallel to the palate. 3. While inserting, gently rub and roll the swab. As soon as you feel the throat resistance, stop and let the swab absorb secretion. 4. Slowly and gently remove the swab outwards while gently rotating it between your fingers. 4) Oropharyngeal swab (throat) 1. Place an extraction tube in the cardboard workstation. 2. Have the patient open his/her mouth wide and make "Ah" sounds, exposing the pharyngeal tonsils on both sides. 3. Hold the swab firmly and wipe back and forth on the pharyngeal tonsils on both sides at least three times per side with moderate force. Do not touch the palate, tongue, teeth or gums. 4. Remove the swab while gently rotating it between your fingers. For best results, the nasopharyngeal (nose to throat) method is recommended. TESTING After taking the sample, perform the test as follows: 1. Tear off the seal of the extraction buffer tube. 2. Insert the swab into the tube and dip it up and down into the liquid for at least 10 seconds. Then hold the swab against the bottom of the tube and turn it 3 times, making sure that no contents splash out of the tube. 3. Remove the swab while squeezing the sides of the tube to extract the liquid from the swab. 4. Place the dropper tip firmly on the extraction buffer tube and mix the liquid thoroughly. 5. Add 3 drops (approx. 100μL) via the dropper tip into the sample well of the test cassette. 6. Evaluate the test results after 15 minutes. Do not evaluate the results after 20 minutes. INTERPRETATION OF THE TEST RESULT POSITIVE: Two lines appear. One coloured line appears in the control line region (C) and another coloured line appears in the test line region (T). A positive result in the test region indicates the detection of SARS-CoV-2 antigens in the sample. A positive result does not exclude infection with other pathogens NEGATIVE: A coloured line appears in the control area (C). No visible coloured line appears in the test line area (T). A negative result does not rule out viral infection with SARS-CoV-2 and should be confirmed by molecular diagnostic methods if COVID-19 is suspected. INVALID: The control line does not appear. Insufficient sample volume or incorrect handling are the most likely reasons for the control line not appearing. Check the procedure and repeat the test with a new test cassette. If the problem persists, stop using the test kit immediately and contact your dealer. QUALITY CONTROL The control area (C) serves as an internal procedure control. A coloured line appears when the procedure or sample volume has been applied correctly. Control standards are not supplied with this test. As good laboratory practice, it is recommended that positive and negative controls be performed regularly to verify test performance. RESTRICTIONS • This test is intended for the qualitative detection of SARS-CoV-2 viral antigens only. The exact concentration of SARS-CoV-2 virus antigens cannot be determined in this test. • Test results are for clinical reference only and should not be the sole basis for clinical diagnosis and treatment. Clinical management of patients should be considered in combination with their symptoms, physical signs, patient history, other laboratory tests, therapeutic responses and epidemiological information. • Proper sample collection is crucial. Failure to follow the procedure can lead to inaccurate test results. Improper collection, storage or even freezing and thawing of the sample can lead to inaccurate test results. • A false-negative test result may occur if the viral antigen level in a sample is below the detection limit of the test or if the sample was not collected or transported properly; therefore, a negative test result does not rule out the possibility of SARSCoV-2 infection. • A positive result does not exclude co-infection with other pathogens. • Monoclonal antibodies may not recognise SARS-CoV-2 viruses with slightly altered amino acid levels in the region of the target epitope, or may recognise them with less sensitivity. • The amount of antigen in a sample may decrease with increasing disease duration. Samples taken after the 5th day of illness are more likely to be negative compared to an RTPCR test. • The tests target the nucleocapsid proteins. Performance is not affected by mutations in the spike protein. Mutations in the nucleocapsid protein are not excluded in the future. You can download these instructions here download General FAQ How does Odem ensure high quality at such a fair price? The Better AG, founded in 2006 in Switzerland, has become the main supplier for thousands of companies in recent years. The strategy: • Bulk purchasing • Close quality control of the goods • Passing on the purchasing advantages to our customers • By offering the possibility to receive free samples, our customers are not taking any risks. What is the money-back guarantee? If you are not satisfied with your goods, you can return them within 14 days of purchase and receive a full refund. What payment options are available? We offer a convenient payment by invoice after receipt of the goods to a German bank account. Has the goods already been cleared through customs? Yes, the goods have already been cleared through customs and will be delivered to you from our German warehouse. You will not incur any additional costs. Product Sheet Download

Buy Antigen Test Kit - Bioteke Antigen Test for Professional Use Buy Antigen Test Kit - Antigen Rapid Test from Bioteke The Bioteke COVID Test - Antigen Rapid Test is a quick and reliable way to detect a possible infection with the SARS-CoV-2 virus. As an important part of pandemic control, it is of utmost importance for us to offer our customers a fast and reliable testing option. Read on to learn more about the Bioteke Antigen Test kit. Buy Antigen Test Kit: What is the Bioteke Antigen Rapid Test? The Bioteke COVID Test is an Antigen Rapid Test for the detection of Covid-19. It uses a lateral flow technology to detect antibodies against SARS-CoV-2 in human blood. This test is CE certified and meets the sensitivity and specificity requirements of the European Union. The Bioteke COVID Test is suitable for professional use in medical facilities such as doctor's offices, clinics, and laboratories. However, the test should be performed by trained personnel to ensure accurate results. Performance and Accuracy of the Bioteke Antigen Rapid Test One of the most important features of a COVID Test is its performance and accuracy. The Bioteke Antigen Rapid Test has been clinically tested and has a sensitivity of 96.49% and a specificity of 99.28%. This means that the test result is correct in most cases and there are rarely false positive or false negative results.Additionally, the test is easy and quick to perform. No preparation or training is required and the result is available within 15 minutes. How the Bioteke COVID Test - Antigen Rapid Test Works In this test procedure, an anti-SARS-CoV-2-N antibody is immobilized in the test zone of the membrane. After a swab sample is placed in the sample window, it reacts with anti-SARS-CoV-2-N antibody-coated particles located on the sample pad.The COVID Tests are individually packaged, making them ideal for rapid and hygienic use. The special features are easy sample collection, easy readability, and clearly displayed results. The result is available even after 15-20 minutes. Tested and approved by the Federal Institute for Drugs and Medical Devices (BfArM). No additional equipment is required. Intended and released for professional use. Before You Buy Antigen Test Kit: Comparison with Other COVID Tests When comparing the Bioteke Antigen Rapid Test with other COVID Tests, there are some important differences to consider.Compared to PCR tests performed in labs, Antigen Rapid Tests like the Bioteke COVID Test are faster and easier to use. However, they require higher sensitivity to ensure the same accuracy.Compared to other antigen rapid tests on the market, the Bioteke Antigen Rapid Test can offer a better value for money as it contains 25 tests per pack. Additionally, it has high accuracy, making it an excellent choice for use in medical facilities and similar settings. Conclusion The Bioteke COVID-19 Antigen Rapid Test is a reliable and easy-to-use solution for detecting a possible infection with the SARS-CoV-2 virus. If you need to buy an antigen test kit, the Bioteke Antigen Rapid Test is a great option to consider. The test is CE certified and meets the sensitivity and specificity requirements of the European Union. It is suitable for professional use in medical facilities such as doctor's offices, clinics, and laboratories, and is designed for easy and quick testing. When compared to other COVID-19 tests, such as PCR tests, the Bioteke Antigen Rapid Test is faster and easier to use. It does require a higher level of sensitivity to ensure accuracy, but it provides excellent performance and is a cost-effective option, with 25 tests included in each package. The test is based on lateral flow technology, and the results are available in just 15 minutes. It has been clinically tested and has a sensitivity of over 95% and a specificity of over 99%, making it a highly accurate option. The Bioteke Antigen Rapid Test is also approved by the Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM). In conclusion, if you need to buy an antigen test kit, the Bioteke COVID-19 Antigen Rapid Test is a great choice. It is reliable, easy to use, and provides accurate results in just 15 minutes. With its high sensitivity and specificity, it is a great option for regular COVID-19 testing in medical facilities and other settings. Comparison - Professional COVID-19 Antigen Rapid Tests Manufactured by Hecin Testsealabs Bioteke Longsee Green Spring Roche Siemens Sensitivity 97.09% 92.10% 96.49% 95.51% 96.77% 96.52% 97.25% Specificity 99.78% 98.10% 99.28% 99.72% 100% 99.60% 100% Manufactured in China China China China China South Korea China Listed for the"EU common list" Yes, in category A Yes Yes Yes, in category A Yes Yes Yes FAQ's on Buying Antigen Test Kit - Bioteke Antigen Rapid Test for Professional Use Are Bioteke Rapid Tests suitable for home use? No, the Bioteke COVID tests are designed for professional use in medical facilities such as doctor's offices, clinics, and laboratories, and should only be performed by trained personnel. How does the Bioteke Rapid Test work? The Bioteke Rapid Test is an antigen rapid test based on lateral flow technology. It detects specific proteins of the SARS-CoV-2 virus and displays a result within 15 minutes. How reliable are the Bioteke COVID tests? The Bioteke Rapid Tests are considered very reliable and offer high sensitivity and specificity. This means that they also work reliably with low virus loads and have a low error rate. Therefore, you can buy the COVID antigen test kit here at OdemShop with a clear conscience. Can the Bioteke Rapid Test also be used on children? Yes, the Bioteke Rapid Test can also be used on children. However, the test should always be performed by trained personnel. How long does it take to get the result of the Bioteke Rapid Test? The Bioteke Rapid Test provides a result within 15 minutes. This means that you can quickly and easily determine whether or not you are infected with the SARS-CoV-2 virus. Why should I buy the Bioteke COVID Rapid Test at OdemShop? You can purchase the Bioteke Rapid Test for COVID-19 at various online shops and pharmacies. But why should you choose OdemShop? OdemShop not only offers fast and reliable shipping but also excellent customer service and expert advice. Our customer reviews speak for themselves and show that we strive for customer satisfaction. Technical Data MaskPacks of 25 Carton1000 pieces Certificate, standard & protection classProfessional use (supplied to professional users only)Quick test 3 in 1Approved in GermanyBFarm number: AT 349/21CE-certified and reimbursable test listed at the Federal Institute for Drugs and Medical Devices according to the Coronavirus Test Regulation (TestV)96.49% sensitivity - 99.28% specificityWith integrated buffer solution Hecin COVID-19 Professional Antigen Rapid Test Mask Instructions General FAQ How does Odem ensure high quality at such a fair price? The Better AG, founded in 2006 in Switzerland, has become the main supplier for thousands of companies in recent years. The strategy: • Bulk purchasing • Close quality control of the goods • Passing on the purchasing advantages to our customers • By offering the possibility to receive free samples, our customers are not taking any risks. What is the money-back guarantee? If you are not satisfied with your goods, you can return them within 14 days of purchase and receive a full refund. What payment options are available? We offer a convenient payment by invoice after receipt of the goods to a German bank account. Has the goods already been cleared through customs? Yes, the goods have already been cleared through customs and will be delivered to you from our German warehouse. You will not incur any additional costs. Product sheet Download

Buy Testsealabs COVID Test Kit With our Testsealabs Rapid Test Kit, you can quickly and reliably detect COVID-19 infections. Thanks to a high sensitivity of 92.10% and a specificity of 98.10%, the test offers excellent accuracy. The three possible sampling methods (anterior nasal, nasopharyngeal, oropharyngeal) offer flexible and individually tailored sampling. Testsealabs COVID Test Kit 3-in-1 Rapid Tests ✓ BfArM listed, test ID: AT082/20✓ Evaluated by the Paul-Ehrlich-Institut✓ Listed on the Common RAT List of the HSC, Device ID: 1392✓ Can detect Delta and Omicron variants✓ Test results readable after 15 minutes✓ All materials included in delivery✓ Flexible and location-independent✓ For medical personnel only Our tests are all CE-certified and suitable for use in the European market. Delivery Contents of the Testsealabs COVID Test Kit 25 sterile swabs25 test cassettes25 extraction tubes1 tube stand1 user manual Order now and quickly, reliably and easily detect COVID-19 with the Testsealabs antigen test set! Why Buy the Testsealabs COVID Test Kit? ✓ MONEY-BACK GUARANTEE Our goal is your satisfaction with your purchase. If the purchased product does not meet your expectations, you can return it within the 14-day cancellation period and receive a refund of the purchase price. Comparison - Professional COVID-19 Antigen Rapid Tests Manufactured by Hecin Testsealabs Bioteke Longsee Green Spring Roche Siemens Sensitivity 97.09% 92.10% 96.49% 95.51% 96.77% 96.52% 97.25% Specificity 99.78% 98.10% 99.28% 99.72% 100% 99.60% 100% Manufactured in China China China China China South Korea China Listed for the"EU common list" Yes, in category A Yes Yes Yes, in category A Yes Yes Yes Frequently Asked Questions about Testsealabs COVID Test Kit What is a Testsealabs COVID Test Kit Antigen Test? A Testsealabs SARS-CoV-2 Antigen Rapid Test is a professional, on-site antigen test for COVID-19 that directly detects the pathogen and its antigens. The test consists of a swab from the back of the nose or throat and a test cassette that works according to the lateral flow principle. In a time frame of 10-15 minutes, it is possible to determine the presence of COVID-19 antigens in the sample. The test consists of 25 test cassettes, swabs, extraction tubes, and buffer doses. It is intended for professional use and must be brought to room temperature before use. Can the Testsealabs Rapid Test Kit detect mutations? Yes, the Testsealabs SARS-CoV-2 Antigen Rapid Test Kit can detect, among others, the Delta and Omicron variants. Is the Testsealabs Antigen Test Kit safe? Yes, the sensitivity of the test is 92.10% and the specificity is 98.10%. As the test is on the "Common List" (list of the European Commission), the test is considered safe throughout Europe.In addition, the Testsealabs SARS-CoV-2 Ag Rapid Test Kit has been evaluated by the PEI. How does the Testsealabs Antigen Test Kit work? Through nasopharyngeal or oropharyngeal sample collection. How long does it take to get the result of the Testsealabs Antigen Rapid Test? 15 minutes. How is the professional Testsealabs SARS-CoV-2 Ag Rapid Test packaged? There are 25 tests in one box, and 750 in a whole carton. How long is the professional Testsealabs Covid-19 Antigen Rapid Test shelf life? Stable at room temperature or between 4 and 35 degrees for up to 12 months. Does the Testsealabs SARS-CoV-2 Antigen Rapid Test Kit detect the Omicron variant? Yes, the Testsealabs COVID-19 Ag tests have been tested by the Paul-Ehrlich-Institut. The Omicron variant is fully detected. How did the tests perform on the Paul-Ehrlich-Institut's control list? The tests are on the list that meets the sensitivity criteria. You can read the details here. Who is allowed to use the tests? These tests are exclusively for professional use. Lay antigen tests can be found here. How did the tests perform on the Paul-Ehrlich-Institut's checklist? The list contains tests that meet the sensitivity criteria and are in the top 20% of the list. You can read the exact details here. Where can I find more information about antigen tests? For extensive information on antigen tests, you can consult our information center. Where can I find the instructions for the Testsealabs Rapid Test Kit antigen test? You can find the instructions here. Specifications Testsealabs PackPacks of 25 Carton30 boxes - Total: 750 tests Standards and market conformity Professional use (distribution to professional users only) Rapid test 3 in 1 Approved in Germany TÜV South EN ISO 13485:2016 BFarm number: AT082 / 20 This test is included in the Federal Institute for Drugs and Medical Devices list under the regulation on coronavirus testing (TestV). It has been certified with a CE mark and is eligible for cost reimbursement. 92.10% sensitivity - 98.10% specificity With integrated buffer solution A guide for using the Testsealabs Professional Antigen Rapid Test Instructions for the Testsealabs Professional Rapid Antigen Tests Testsealabs Covid-19 Antigen (SARS-CoV-2) Rapid Test Cassette (Swab)

Purchase Longsee Rapid Detection Kit for Quick Testing of 2019-nCOV Ag Detect 2019-Ncov infections quickly and reliably with our Longsee rapid detection kit. Within 15 minutes, the kit provides reliable results. All necessary materials are included in the kit and no further equipment or laboratories are necessary. Thanks to a sensitivity of 95.51% and a specificity of 99.72%, professional application is guaranteed. Features of Longsee Rapid Detection Kit for 2019-nCOV Ag ✓ Listed on the "Common List" - Device-ID: 1216 at the European Commission ✓ 95.51% sensitivity , 99.72% specificity ✓ Overall sensitivity (Paul Ehrlich Institute evaluation): 100%. ✓ Detects virus variants such as delta and omicron ✓ Only given to authorised groups of people (professional test) ✓ Results in 15 minutes ✓ Only for in vitro diagnostics ✓ No equipment required ✓ CE certified and suitable for use in the German market Our tests are all CE certified and suitable for use in the European market. Contents of Longsee Rapid Detection Kit for COVID-19 Antigen Testing 25 sterile swabs 25 test cassettes 25 extraction tubes 1 instruction manual  Order now and detect COVID-19 quickly, reliably and easily with the Longsee Antigen Test Kit! Why Order Longsee Rapid Detection Kit for 2019-nCOV Ag from OdemShop? ✓ MONEY-BACK GUARANTEE Our goal is your satisfaction with your purchase. If the purchased goods do not meet your expectations, you can return them within the 14-day cancellation period and you will be refunded the purchase price. Comparison - Professional COVID 19 Antigen Rapid Test Made by Hecin Testsealabs Bioteke Longsee Greenspring Roche Siemens Sensitivity 97.09% 92.10% 96.49% 95.51% 96.77% 96.52% 97.25% Specificity 99.78% 98.10% 99.28% 99.72% 100% 99.60% 100% Made in China China China China China South Korea China Listed for the"EU common list" Yes, in category A Yes Yes Yes, in category A Yes Yes Yes Frequently asked questions before you buy the Longsee Rapid Detection Kit for COVID-19 What is Guangdong Longsee Biomedical Co Inc? Guangdong Longsee Biomedical Co. Inc. is a leading biomedical engineering company. With a strong research and development department and an extensive product range, the company offers solutions for a wide range of healthcare applications, e.g., manufacturing the Longsee Rapid Detection Kit for COVID-19 mentioned here. What is a Longsee Rapid Detection Kit for COVID-19? The Longsee SARS-CoV-2 test is a rapid test method for the rapid detection of infection with Covid-19. It is based on immunochromatography technology, requires only a few test steps and provides a result within 15 minutes. Can the Longsee rapid test detect mutations? Yes, mutations such as the Omikron mutation can be detected with the COVID-19 antigen rapid test from Longsee. This is also confirmed by the Common RAT List of the HSC (List of COVID-19 Antigen Rapid Tests of the European Commission). Is the Longsee rapid test safe? The Longsee COVID-19 Antigen Rapid Test has been evaluated by the PEI and has an overall sensitivity of 100%. The sensitivity of the test is 95.51% and the specificity is 99.72%. As the test is on the "Common List" (list of the European Commission), it can be assumed that it is classified as safe. How does the Longsee Rapid Detection Kit for COVID-19 work? By nasal, nasopharyngeal or oropharyngeal sampling How long does the test result of the Longsee Rapid Detection Kit for COVID-19 take? 15 Minutes. How is the Longsee Rapid Detection Kit for COVID-19 packaged? There are 25 tests per pack / box , in a whole box 700 pieces. How long can professional Longsee Rapid Detection Kit for COVID-19 be stored? Can be stored at room temperature or from 4 to 35 degrees for up to 12 months.Does the Longsee test recognise the Omikron variant? Yes, the tests have been checked by the Paul Ehrlich Institute. The Omikron variant is fully proven.How did the tests perform in the Paul Ehrlich Institute's control list? The tests are on the list that meet the sensitivity criterion. You can read the exact details here.Who may use the tests? These tests are intended for professional use only. You can find layman antigen tests hereWhere can I find more information on antigen testing? For comprehensive information on antigen testing, you can consult our Blog Where can I find the instructions for the Longsee quick test? You can find the instructions here Technical data Longsee Pack 25er Packs Carton 25 Cartons - 1050 Piece Standards - and market conformity Professional use (for professional use only) Quick test 3 in 1 Approved in Deutschland BFarm-Number: AT731 / 21 Listed for EU-wide recognition in the "Common List of EU" of the European Commission - Directorate General Health and Food Safety CE-certified and reimbursable test listed at the Federal Institute for Drugs and Medical Devices according to the Coronavirus Test Ordinance (TestV) 95.51% sensitivity - 99.72% specificity With integrated buffer solution Guide to the Longsee Professional Rapid Antigen Tests 2019-nCoV Ag Rapid Test Kit (Immuno-chromatography) Instructions for use [INTENDED USE] The rapid test in this kit is based on immuno-chromatography and is designed for the rapid qualitative determination of SARS-CoV-2 nucleocapsid antigen in nasal or throat swab specimens from individuals with suspected COVID-19 infection. The kit is intended for the rapid diagnosis of SARS-CoV-2 infections.  For in vitro diagnostic use only. For professional use only [SUMMARY] The novel coronaviruses belong to the genus β. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, patients infected with the novel coronavirus are the main source of infection; asymptomatic infected persons can also be a source of infection. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations are fever, fatigue, and dry cough. In some cases, nasal congestion, runny nose, sore throat, myalgia, and diarrhea can also be observed. [PRINCIPLE OF THE TEST] This kit uses immuno-chromatography technology to detect the presence or absence of 2019-nCoV nucleocapsid proteins in swab specimens from patients with signs and symptoms of infection, where there is suspicion of 2019-nCoV by the double antibody sandwich method. When the concentration of 2019-nCoV antigens in specimens is higher or equal to the minimum detection limit, these antigens react separately with corresponding antibodies to form complexes, and the 2019-nCoV antibodies are coated in the detection area (T). These antigens are captured and a red reaction line is formed. The result is considered positive. Otherwise, the result formed in T without a red line is considered negative. Under normal test conditions, the quality control area (C) should be colored to indicate that the test is valid.  [COMPONENTS] [RESULT EVALUATION] To read the test results, you just need to look at the observation window. 1. Positive: If two color bands are visible at the position of the quality control line (C-line) and the test line (T-line) in the result window, the test result is positive. The test result indicates the presence of 2019-nCoV antigens in the sample. 2. Negative: If a color band appears at the position of the quality control line (C-line) and no color band appears at the detection line (T-line) in the observation window, the test result is negative. The test result indicates that the sample is negative for 2019-nCoV antigens or the concentration is below the detection limit of the set. 3. Invalid: If no band appears at the position of the quality control line (C-line) and the test line (T-line) in the observation window, the test result is INVALID. The sample should be re-taken and the test repeated. [LIMITATIONS] 1. This reagent is intended for in vitro diagnostics and professional use only. 2. This reagent is used for the qualitative detection of 2019-nCoV antigens in saliva and sputum samples, but cannot accurately determine the content of antigens in samples. 3. This kit has good analytical performance, but improper sample collection and storage can affect the accuracy of the results. 4. Test results are for reference only and not for final diagnosis, and should not be used as the sole basis for clinical diagnosis and treatment. The clinical management of patients should be combined with their symptoms, signs, medical history, and other tests. A comprehensive consideration of laboratory examination and treatment response should be taken into account. 5. Due to the limitations of the methodology, experimenters should pay more attention to negative results, which must be combined with other test results to make a comprehensive assessment. It is recommended to use nucleic acid tests or methods for virus culture identification for verification and confirmation. 6. Analysis of the possibility of false-negative results: 1) Improper sample collection, transport and processing, as well as low virus titers in the sample, can lead to false-negative results. 2) Viral gene mutations can cause changes in antigenic determinants, resulting in false-negative results. You can download this guide here. General FAQs How does Odem ensure high-quality at such a fair price? The Better AG, founded in 2006 in Switzerland, has become the main supplier to thousands of companies in recent years. The strategy: Purchasing in large volumes Tight quality control of goods Passing on the purchasing advantages to our customers By offering the possibility to receive free samples, there are no risks to the customers. What is the money-back guarantee? If you are not satisfied with your purchase, you can return it within 14 days of receipt for a full refund. What payment options are available? We offer a convenient payment via invoice after receipt of goods to a German bank account. Has the goods already been cleared by customs? Yes, the goods have already been cleared by customs and will be delivered to you from our German warehouse. You will not incur any additional costs. Product Sheet Download

Covid, Influenza A & Influenza B Professional Test The Covid, Influenza A & Influenza B Professional Test for professional use has developed the Covid, Influenza A & Influenza B Test Cassette 3in1 for rapid detection. Our Sejoy 3in1 - Influenza A/B + Covid-19 Combo Ag Test for anterior nasopharyngeal and oropharyngeal swabbing offers the opportunity to get certainty quickly and easily within 15 minutes.   ✓Rapid diagnostics  ✓ Interruption of infection chains  ✓ Risk assessment of respiratory diseases for a potentially severe course✓ RResource-efficient way to promote the health of employees  Mitarbeitern  Rapid tests are individually packaged and thus best suited for quick and hygienic use. The special features are easy sample collection, easily readable and clearly displayed results and the result is even available after 15 minutes. Tested and approved by the Federal Institute for Drugs and Medical Devices. *No additional equipment is required. Intended and approved for professional use. 25 Tests/KitPositiveSARS-CoV-2 positive: Two clear colour lines appear in the left window. One colour line should be in the control region (C) and another colour line in the test region (T). A positive result in the test region indicates the detection of SARS-CoV-2 antigens in the sample. Influenza B (Grip B) positive: Two distinct colour lines appear in the right window. One colour line should be in the control region (C) and another colour line in the influenza B region (B). A positive result in the influenza B region means that influenza B antigen was detected in the sample.Influenza A : Two distinct colour lines appear in the right window. One colour line should be in the control region (C) and another colour line in the influenza A region (A). A positive result in the influenza A region means that influenza A antigen was detected in the sample. Hinweis: The intensity of the colour in the test line region (T) depends on the amount of SARS-CoV-2 antigen, Flu A and/or B antigen present in the sample. Any colour shading in the test region (T/A/B) should therefore be considered positive. NegativeA coloured line appears in the control region (C). No visible coloured line appears in the test line region (T/A/B).  InvalidThe control line is not displayed. Insufficient sample volume or incorrect procedure techniques are the most likely reasons for control line failure. Check the procedure and repeat the test with a new test cassette. If the problem persists, stop using the test kit immediately and contact your local distributor. ✓ According to the Paul Ehrlich Institute, the Omicron variant detects ✓ Easy to read result after 15 minutes How a quick test should be: simple and clear. ✓ 3 in 1 Combi test ✓ Sars-Cov-2 97.40% sensitivity and 99.10% specificity ✓ Influenza A 99% sensitivity and 98.90% specificity ✓ Influenza A 99% sensitivity and 98.90% specificity ✓ NO EQUIPMENT REQUIRED Apply the tests simply and easily. ✓ CE CERTIFICATION Our tests are all CE certified and suitable for use in the European market. ✓ MONEY-BACK GUARANTEE Our goal is your satisfaction with your purchase. If the purchased goods do not meet your expectations, you can return them within the 14-day cancellation period and you will be refunded the purchase price. Application of Covid, Influenza A & Influenza B Professional Technical Data Pack 25er Packs Carton 800 Piece Standards - and Market Conformity Professional use (dispensing to professional users only) Rapid Test 3 in 1 - SARS-CoV-2 | InfluenzaA | InfluenzaB  Approved in Germany Product-specific FAQ  In which languages are the instructions for the Sejoy 3 in 1 Combi Antigen Test available? Available in 6 different languages: English, German, French, Italian, Croatian, Dutch   How long can the Sejoy antigen test be stored? Can be stored at room temperature or from 2 to 30 degrees for up to 18 months.   How is Sejoy packaged? There are 25 tests in a box, 800 in a whole box   Do these rapid antigen tests detect the omicron variant? Yes, the tests have been checked by the Paul Ehrlich Institute. The Omikron variant is fully proven.   Who may use the tests? These tests are intended for professional use only. You can find layman antigen tests here   Where can I find more information on antigen testing? For comprehensive information on antigen testing, you can consult our  Blog.   How did the tests perform in the control list of the Paul ehrlich Institute? The tests are on the list that meet the sensitivity criterion. You can read the exact details here. General FAQs How does Odem ensure high-quality at such a fair price? The Better AG, founded in 2006 in Switzerland, has become the main supplier to thousands of companies in recent years. The strategy: Purchasing in large volumes Tight quality control of goods Passing on the purchasing advantages to our customers By offering the possibility to receive free samples, there are no risks to the customers. What is the money-back guarantee? If you are not satisfied with your purchase, you can return it within 14 days of receipt for a full refund. What payment options are available? We offer a convenient payment via invoice after receipt of goods to a German bank account. Has the goods already been cleared by customs? Yes, the goods have already been cleared by customs and will be delivered to you from our German warehouse. You will not incur any additional costs. Product sheet Download

Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test We all want to stay healthy and safe, and in a world where COVID-19 is affecting our daily lives, it's more important than ever to take care of our health and protect ourselves from possible infection. An easy and effective way to quickly and easily test for a possible infection is the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test. In this article, we'll introduce you to this rapid test in more detail and show you how to use it to protect yourself and your loved ones. What is the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test? The Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test is a reliable and easy-to-use test that allows for quick and accurate diagnosis of COVID-19. The test is based on the colloidal gold immunochromatography method, which was specifically developed for the detection of SARS-CoV-2 antigens. The test provides high sensitivity and specificity and can deliver results within 15-20 minutes. How does the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test work? The Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test is an immunochromatographic rapid test that detects the presence of SARS-CoV-2 antigens in the nasopharyngeal cavity. The test is performed with a sterile swab that is inserted through the nostril into the back of the throat. The swab is then dipped into an extraction buffer and placed on the test cassette holder. After 15-20 minutes, you can read the result: a red line in the control window indicates that the test has worked, while a second red line in the test window indicates a positive result, indicating the presence of SARS-CoV-2 antigens. Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test - is it reliable? The Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test is a reliable test that has high sensitivity and specificity. A clinical study has shown that the test has a sensitivity of 97.09% and a specificity of 99.78%. This means that the test produces very few false positive and false negative results, and therefore has high accuracy. Where can I buy the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test? The Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test is approved for professional use and should not be sold to the general public. Who can use the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test? The Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Rapid Test is intended for professional use and should not be provided to individuals. The test is intended for use by medical professionals or public health authorities to quickly and effectively identify and control COVID-19 infections. Comparison - Professional COVID-19 Antigen Rapid Tests Manufactured by Hecin Testsealabs Bioteke Longsee Green Spring Roche Siemens Sensitivity 97.09% 92.10% 96.49% 95.51% 96.77% 96.52% 97.25% Specificity 99.78% 98.10% 99.28% 99.72% 100% 99.60% 100% Manufactured in China China China China China South Korea China Listed for the"EU common list" Yes, in category A Yes Yes Yes, in category A Yes Yes Yes Frequently Asked Questions about Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method Can I use the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method at home? No, the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method is only intended for professional use and cannot be provided to individuals. The test should only be conducted by medical personnel or health authorities to ensure proper application and interpretation of results. How long does it take to get the result of the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method? The Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method delivers results in just 15 minutes after sample collection. This makes the test a fast and effective method for identifying COVID-19 infections. Where can I buy the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method? The Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method is only approved for professional use and is obtained by medical institutions, authorities, and the like. Private individuals cannot directly purchase the test. How does the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method work? The Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method is a rapid test based on the colloidal gold method. The test uses special antibodies to identify specific proteins present on the surface of the coronavirus. If the coronavirus is present in a sample, the antibodies will bind to the virus and indicate this through a visible color change. How is the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method performed? The test is performed by inserting a swab into the nasopharynx. The sample is then applied to a test strip coated with special antibodies. After 15 minutes, the result can be read based on a color change. Who is the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method suitable for? The Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method is intended for professional use by medical personnel. The test can help identify asymptomatic cases and slow the spread of COVID-19. How does the Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method differ from other COVID-19 tests? The Hecin 2019 nCOV Antigen Test Kit Colloidal Gold Method is a rapid test that is capable of delivering results within 15 minutes and is on the Category-A list of the European Commission. This is a quality feature that only few tests have. Technical Data Box 20 pack Carton 800 pack Certificate, Standard & Protection class Professional use (only for professional users) Approved in Germany Listed for EU-wide recognition in the "EU common list", ID number: 1747 CE-certified and reimbursable test listed with the Federal Institute for Drugs and Medical Devices according to the Coronavirus Test Ordinance (TestV) 97.09% sensitivity · 99.78% specificity Instructions for FFP2NR mask General FAQ How does Odem ensure high quality at such a fair price? The Better AG, founded in 2006 in Switzerland, has become the main supplier for thousands of companies in recent years. The strategy: • Bulk purchasing • Close quality control of the goods • Passing on the purchasing advantages to our customers • By offering the possibility to receive free samples, our customers are not taking any risks. What is the money-back guarantee? If you are not satisfied with your goods, you can return them within 14 days of purchase and receive a full refund. What payment options are available? We offer a convenient payment by invoice after receipt of the goods to a German bank account. Has the goods already been cleared through customs? Yes, the goods have already been cleared through customs and will be delivered to you from our German warehouse. You will not incur any additional costs. Product sheet Download