Bottled rapid test kit results in interpretation package

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  • COVID-19 Antigen Rapid Test Results - How do I

    The COVID-19 Antigen Rapid Test is a rapid membrane-based lateral flow immunoassay for the qualitative detection of SARS-CoV-2 antigens in human nasopharyngeal swab specimens. The use of a COVID-19 Antigen Rapid Test allows you to detect the presence of SARS-CoV-2 virus antigens in our body and to take initial precautionary isolation measures in order to reduce further spread of the virus.

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  • COVID-19 Antibody Rapid Test Result Interpretation ...

    The COVID-19 IgM/IgG Rapid Antibody Test is a fast and effective method for screening IgM and IgG antibodies against SARS-CoV-2. This test can also suggest information on the stage of infection. The below articles describes how to interpret and understand an antibody rapid test result. The antibodies IgG and IgM are the most used markers of ...

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  • COVID-19 IgG/IgM Rapid Test Cassette (Whole

    2020-5-30 · False positive results for COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) may occur due to cross-reactivity from pre-existing antibodies or …

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  • COVID-19 Antigen Rapid Test Cassette

    2021-3-9 · COVID-19 Antigen Rapid Test Cassette English For in vitro diagnostic use only. ... Store as packaged in the sealed pouch at temperature (4 30℃or 40 86℉). The kit is Once open the pouch, the test should be used within one hour. Prolonged exposure ... [INTERPRETATION OF RESULTS] Positive Two lines appear.

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  • SARS-CoV-2 Antigen Rapid Test Kit Use only swabs

    2021-1-12 · SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) antibodies conjugated to colloi Instructions for Use (IFU) 【PRODUCT NAME】 date and the validity is tentatively 24 months. SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 2. The test cassette should be used within 1 hour after taking 【PACKAGE AND SPECIFICATION】

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  • Panbio COVID-19 Ag Rapid Test Device - Abbott

    2021-3-8 · Panbio™ COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapid ... The shelf life of the kit is as indicated on the outer package. 6. Do not use the test kit if the pouch is damaged or the seal is broken. ... Failure to follow the instructions for test procedure and interpretation of test results may adversely affect test performance ...

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  • Step-by-Step Instructions For OraQuick HCV Rapid

    2017-1-16 · OraQuick® HCV Rapid Antibody Test Kit Controls are available separately for use only with OraQuick ... perform and test and interpret the results. Refer to the Kit Control Package Insert for complete instructions. ... † Refer to the Test Result and Interpretation section in these instructions. B8 B10 B9 B11 B12 B13 B14 B15 Absorbent Packet

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  • PSA Rapid Test Cassette LIMITATIONS (Whole Blood

    2017-9-28 · Package Insert A rapid test for the qualitative detection of Prostate Specific Antigen (PSA) in whole blood, ... dispense the whole blood to the specimen area of the test cassette. discontinue using the test kit immediately and contact your local distributor. ... 【INTERPRETATION OF RESULTS】 (Please refer to the illustration above)

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  • RAPIDʹL.mono Agar - Bio-Rad

    2021-4-21 · RAPIDʹL.mono Agar. User Guide. Selective chromogenic medium for detection and enumeration of Listeria monocytogenes and other species of Listeria in food products for human consumption and in environmental samples . Catalog #3563694, Prepared plates, 90 mm x 20 dishes

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  • Rapid HIV Testing - a Testing and Interpretation Guide

    2016-6-23 · 5. Rapid HIV test results will be reported electronically or by hardcopy to the healthcare provider requesting the test. Rapid HIV Testing – a Testing and Interpretation Guide . Laboratory Report . Volume 2, Number 3, October 2012

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  • RaPID Assay PCB Test Kit - Duke University

    2000-4-4 · RaPID Assay PCB Test Kit A00133/A00134 Intended Use The RaPID Assay PCB Test Kit can be used as a ... time to read the package inserts in their entirety and review ... accounted for when interpreting results. See “Results Interpretation”, Section 3a for further details. Use

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  • COVID-19 Antigen Rapid Test (Swab) - Safecare

    2021-6-7 · The Safecare COVID-19 Antigen Rapid Test is a lateral flow immunoassay intended for qualitative detection of nucleocapsid protein antigen in direct nasal swabs or nasopharyngeal swab specimens from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset.. Results are for the identification of SARS-CoV-2 nucleocapsid protein antigen.

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  • BTNX | Products

    The Rapid Response TM Single Drug Test Strip is a rapid, qualitative test for the detection of a selected drug in human urine. It is intended for in vitro diagnostic use only. Interpretation of test results are: positive (one line), negative (two lines), invalid (no lines or no Control line). For the alcohol strip results can be interpreted by ...

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  • OraQuick HCV Rapid Antibody Test Customer Letter

    2014-6-19 · The package insert for the OraQuick ® HCV Rapid Antibody Test contains warnings and precautions, restrictions on the sale, distribution, and use of the device, and information about how the device works, how to use the device, interpretation of the results, and limitations of the OraQuick ® HCV Rapid Antibody Test and the meaning of a reactive

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  • Coronavirus COVID-19 IgG/IgM Rapid Test Kit (25

    2021-3-9 · The shelf life of the kit is as indicated on the outer package. 6. Do not use the test kit if the pouch is damaged or the seal is broken. ... interpretation of test results may adversely affect test performance and/or produce invalid results. ... Ag Rapid Test Device Results. COVID-19 Ag Rapid Test Device. Panbio™ COVID-19 Ag Rapid Test .

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  • Panbio COVID-19 Ag Rapid Test Device - Abbott

    2021-2-15 · SARS-CoV-2 Antigen Rapid Test Package Insert REF L031-11815 English A rapid test for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in nasal swab specimens. For professional in vitro diagnostic use only. INTENDED USE The SARS-CoV-2 Antigen Rapid Test is a lateral flow chromatographic immunoassay for the qualitative

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  • COVID-19 Antigen Rapid Test (Swab) - Safecare

    2021-6-7 · The Safecare COVID-19 Antigen Rapid Test is a lateral flow immunoassay intended for qualitative detection of nucleocapsid protein antigen in direct nasal swabs or nasopharyngeal swab specimens from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset.. Results are for the identification of SARS-CoV-2 nucleocapsid protein antigen.

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  • SARS-CoV-2 Antigen Rapid Test Kit Use only swabs

    2021-1-12 · SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) antibodies conjugated to colloi Instructions for Use (IFU) 【PRODUCT NAME】 date and the validity is tentatively 24 months. SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 2. The test cassette should be used within 1 hour after taking 【PACKAGE AND SPECIFICATION】

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  • SARS-CoV-2 Antigen Rapid Test

    2020-12-1 · SARS-CoV-2 An gen Rapid Test (Immunochromatography) Packing Specifica on The combina on form of the product is single casse e. Intended Use The SARS-CoV-2 An gen Rapid Test is intended for in vitro qualita ve detec on to SARS-CoV-2 an gen in human nasopharyngeal swab or oropharyngeal swab samples. Test Principle

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  • Rapid Disease Tests & Rapid Test Kits You Can Trust |

    The COVID-19 IgM/IgG Rapid Test by BioMedomics, Inc. demonstrates a combined sensitivity and specificity of 100% and ~99% respectively, making it one of the most accurate and reliable tests in the world. There is a critical, global need for serology assays that can complement nucleic acid (PCR) tests for diagnosing COVID-19 infection.

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  • COVID-19 IgM/IgG Rapid Test – BioMedomics Inc.

    Coronavirus (COVID-19) Antigen Rapid Test Cassette (Swab) COVID-19 is an infectious disease caused by a new coronavirus that can spread from person to person. COVID-19 symptoms can range from mild (or no symptoms) to severe illness. The Coronavirus (COVID-19) Antigen Rapid Test Cassette (Swab) is an in vitro immunochromatographic assay for the ...

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  • Coronavirus Antigen Rapid Test Cassette | COVID-19

    RELIABLE – Good sensitivity and perfect specificity compared to PCR test results. Test Procedure Test Result Interpretation Great Performance 386 clinical samples confirmed by PCR test were compared by Genrui SARS-Cov-2 Antigen lest Kit (Collaidal Gold), The results are shown as below.

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  • Lateral Flow Rapid Test - Genrui Bio

    2017-9-28 · Package Insert A rapid test for the qualitative detection of Prostate Specific Antigen (PSA) in whole blood, ... dispense the whole blood to the specimen area of the test cassette. discontinue using the test kit immediately and contact your local distributor. ... 【INTERPRETATION OF RESULTS】 (Please refer to the illustration above)

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  • PSA Rapid Test Cassette LIMITATIONS (Whole Blood

    2021-6-19 · Test results must NOT be read visually. The BD Veritor Plus System Analyzer (purchased separately) must be used for interpretation of all test results. Refer to table above. Positive Test Results:SARS-CoV-2 antigen present; does not rule out coinfection with other pathogens. Negative Test Results: Negative results are presumptive.

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  • Quick reference guide BD Veritor™ System for rapid

    2021-6-14 · Antigen Rapid Diagnostic Test (RDT) training package; ... precautions and interpretation of test results must be followed strictly. Failure to accurately follow the test procedure and inter- ... 63 Reagent kit size (number of tests) 25–50 individual test devices/cassettes.

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  • COVID-19 Rapid Antibody Test Kit: Frequently Asked ...

    2020-3-16 · The COVID-19 Rapid Test Kit is an professional medical testing kit that can detect the presence of IgG and IgM antibodies in human blood. These two antibodies indicate if a person is infected with 2019-nCoV novel coronavirus (COVID-19) with results available after 15 minutes.

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  • CoVid-19 Rapid Test - Rethink My Healthcare

    The results show that the product is based on the serum plasma test results, and the consistency rate of the whole blood test results is 96.85% (95% CI: 95.87% to 97.60%). After preliminary evaluation, it is basically confirmed that the clinical performance of COVID-19 Rapid Test Kit IgG + IgM (Colloidal Gold) can meet the emergency use ...

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  • COVID-19 Rapid Test Kit IgG + IgM (Colloidal Gold)

    2021-3-12 · Antigen Combo Rapid Test Cassette English monoclonal antibody For professional use only. ... Only the swab provided in the kit is to be used for specimen collection. 1. Remove the swab from the package. 2. Tilt patient's head back about 70°. ... [INTERPRETATION OF RESULTS] infection and should not be used as the sole basis for treatment or ...

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  • COVID-19/Influenza A+B Antigen Combo Rapid Test

    2020-11-20 · 5. Test results must be evaluated in conjunction with other clinical data available to the physician. 6. Reading the test results earlier than 15 minutes or later than 20 minutes may give incorrect results. 7. Panbio™ COVID-19 Ag Rapid Test Device is not intended to detect from defective (non-infectious) virus during

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  • COVID-19 Ag Rapid Test Device - World Health

    2000-4-4 · RaPID Assay PCB Test Kit A00133/A00134 Intended Use The RaPID Assay PCB Test Kit can be used as a ... time to read the package inserts in their entirety and review ... accounted for when interpreting results. See “Results Interpretation”, Section 3a for further details. Use

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  • RaPID Assay PCB Test Kit - Duke University

    2021-6-19 · Test results must NOT be read visually. The BD Veritor Plus System Analyzer (purchased separately) must be used for interpretation of all test results. Refer to table above. Positive Test Results:SARS-CoV-2 antigen present; does not rule out coinfection with other pathogens. Negative Test Results: Negative results are presumptive.

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  • Quick reference guide BD Veritor™ System for rapid

    2020-12-9 · 3. The results obtained should only be interpreted in conjunction with other diagnostic results and clinical information. 4. Due to the limitations of the test, for cases where interpretation of result seems difficult, we strongly recommend repeating the test using TYPHIDOT 1 hour or TYPHIDOT 3 hours.

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  • TYPHIDOT Rapid IgG/IgM (Combo) (A rapid test for

    2020-11-16 · HIV rapid test training package: trainer materials. Geneva: World Health Organization ... (these may be sold separately and must be compatible with the test kit, or they will be included in the standard test kit contents); ... Provide the participant with the SARS-CoV-2 Antigen RDT Reading Sheet and record their interpretation of the test results.

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  • SARS-CoV-2 Antigen Rapid Diagnostic Test Training

    1. Open the foil pouch and take out the test cassette. 2. Add 100ul or 2-3 drops of serum sample into the sample well and then keep it at room temperature (10 ℃ -30 ℃) for 15 minutes. - Results Interpretation. 1. Time for reading results: results should be read within 20 minutes after addition of test ample. 2.

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  • Rapid COVID-19 Testing Kit | Coronavirus Test Kits ...

    2020-8-24 · ANNEX 4c : GUIDELINE ON COVID-19 TESTING USING ANTIGEN RAPID TEST KIT (RTK-Ag) FOR THE HEALTH FACILITIES, MINISTRY OF MALAYSIA VERSION 4.0 1. OBJECTIVE This revised guideline is aimed to replace the previous Guideline on “Guideline on COVID-19 Testing Using Antigen Rapid Test Kit (RTK-Ag) for The Health

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  • ANNEX 4c : GUIDELINE ON COVID-19 TESTING USING

    2021-3-1 · Rapid™ Response COVID-19 Antigen Rapid Test HEALTH CANADA APPROVED RESULTS AFTER 15 MINS SAMPLE TYPE: NASAL SWAB SPECIFICITY 100% Background Performance Target Customers Fact Sheet COVID-19 Antigen Rapid Test Device engineered and designed in canada 270 Jameson Drive Peterborough, ON K9J 6X6, CANADA [email protected] 1.888.226.2775

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  • Rapid Response COVID-19 Antigen Rapid Test

    2020-12-4 · The COVID-19 Antigen Rapid Test (Nasopharyngeal Swab) is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 antigens in nasopharyngeal swab specimens from individuals with suspected SARS-CoV-2 infection in conjunction with clinical presentation and the results of other laboratory tests.

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  • COVID-19 Antigen Rapid Test STORAGE AND STABILITY ...

    2021-3-12 · SARS-CoV-2 Rapid Antigen Test 1 2 3 LIMITATIONS 1. The test procedure, precautions and interpretation of results of this test must be followed strictly. 2. Failure to follow the test procedure may adversely affect test performance and/or invalidate the test result. 3. The test should be used for the detection of SARS-CoV-2 antigen from human

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  • SARS-CoV-2 Rapid Antigen Test - Roche Canada

    2018-6-28 · the test isolate by comparison of test results to reactivity patterns stored in an Electronic RapID Compendium (ERIC™) database or by use of the ... RapID ANA II Reagent (provided with kit) (15 ml/Btl) ... esculetin complex that may be formed can interfere with test interpretation.

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  • Evaluation of Abbott BinaxNOW Rapid Antigen Test

    Product Description The Rapid Response TM Fecal Immunochemical Test (FIT) Cassette is a rapid, qualitative test for the determination of human occult blood in feces, to aid in the early detection of gastrointestinal problems such as colorectal cancer. Traditional guaiac-based methods to detect fecal occult blood lack sensitivity and specificity, and also have diet restrictions prior to testing.

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  • RapID ANA II System - Thermo Fisher Scientific

    Determine™ HIV-1/2 Ag/Ab Combo. Introducing the first FDA approved rapid point-of-care test that detects both HIV-1/2 antibodies and free HIV-1 p24 antigen. This 4th generation test has the ability to identify HIV earlier than 2nd and 3rd generation antibody-only tests.1 It enables health care providers to diagnose HIV infection earlier ...

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  • BTNX | Products

    2009-1-27 · The COBAS AmpliPrep/COBAS TaqMan HCV Test is an in vitro nucleic acid amplification test for the quantitation of hepatitis C viral (HCV) RNA in human plasma or serum of HCV-infected individuals using the COBAS AmpliPrep Instrument for automated specimen processing and the

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