Shop Print Media, No drawers, 92% Polyester / 8% Spandex, Burton Medical®, 50 Foot Length, Size 4 / Size D, 0.12 mm Diameter
- Application
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For Use With
- For Real Time PCR Instruments (22)
- For Real-Time PCR Detection Systems (15)
- For BioFire SpotFire System (8)
- For Vitros ECi / ECiQ / Vitros 3600 / 5600 / XT7600 (6)
- For Evaluating Performance of Molecular Tests (4)
- For Evaluating the Performance of Nucleic Acid Tests for Determination of the Presence of SARS-CoV-2 RNA (4)
- For Real Time PCR Instrument (4)
- For Thermocycler (4)
- For Alinity i System (3)
- For Cobas Liat System (3)
- For Evaluation of the Performance of Molecular Tests (3)
- For GeneXpert Systems (3)
- For ID NOW™ Instrument US (3)
- For Qualitative Molecular Assays (3)
- For RT PCR Instrument with FAM / HEX Fluorescence Channels (3)
- For Vitros ECi / ECiQ / 3600 Immunodiagnostic Systems and the Vitros 5600 / XT 7600 Integrated Systems (3)
- For Access Immunoassay Systems (2)
- For Architect i Systems (2)
- For BD MAX System (2)
- For Cobas Liat Automated PCR Analyzer (2)
- For Cobas Liat® Instrument (2)
- For Evaluating the Performance of Molecular Tests (2)
- For Evaluation of the Performance of Nucleic Acid Tests for Determination of the Presence of SARS-CoV-2 RNA (2)
- For Nucleic Acid Tests (2)
- For QIAstat-Dx Analyzer 1.0 (2)
- For Qualitative Detection by Molecular Assays (2)
- For Quality Control of Clinical Assays and Training of Laboratory Personnel (2)
- For Quality Control of Clinical Assays and Training of Laboratory Personnel, Clinical Specimen (2)
- For Real-time PCR System with FAM / HEX Fluorescence Channels (2)
- For VITROS ECi/ECiQ, 3600 Immunodiagnostic Systems, and VITROS 5600, XT 7600 Integrated Systems (2)
- For Verification of Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (2)
- For use an External, Non-Viable Control Material to Evaluate the Performance of Nucleic Acid Tests that Detect SARS-CoV-2 Virus (2)
- For use as External Controls for Qualitative Detection by Molecular Assays (2)
- For use with Solana SARS-CoV-2 Assay on the Solana Instrument (2)
- Advia, Dimension, Chloridometer, Sweat-Chek, Advanced Osmometers, Vapor Pressure Osmometer (1)
- For AmpliVue Bordetella Assay (1)
- For Anti-SARS-CoV-2 IgG Test on VITROS ECi/ECiQ (Available End of May 2020), VITROS 3600, 5600, XT7600 (1)
- For Applied Biosystems 7500 Fast Dx Real-Time PCR Instrument / QuantStudio Dx Real-Time PCR Instrument / Cepheid SmartCycler II (1)
- For Atellica IM Analyzer (1)
- For Automated Instrument Systems (1)
- For BD Veritor™ Group A Step Test (1)
- For BD Veritor™ System (1)
- For BinaxNOW COVID-10 / Flu A&B Test (1)
- For BinaxNOW™ Influenza A & B Test Kit (1)
- For BinaxNOW™ RSV Test Kit (1)
- For BinaxNOW™ Strep A Test (1)
- For Determination of Presence of Group B Streptococci (GBS) DNA, Validation of Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (1)
- For Determination of the Presence of Respiratory Virus Nucleic Acids (1)
- For ELISA Microtiterplate Reader (1)
- For Estimation of Test Precision and the Detection of Systematic Analytical Deviations of the Alinity i System when used for the Qualitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum and Plasma (1)
- For Estimation of Test Precision and the Detection of Systematic Analytical Deviations of the Architect i System when used for the Qualitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum and Plasma (1)
- For Evaluating Performace of Molecular Tests (1)
- For Evaluating Performance of Nucleic Acid Tests for Determination of Presence of Bacterial Nucleic Acids (1)
- For Evaluating and Comparing Intra and Inter Laboratory Performance of Influenza Rapid Test Systems (1)
- For Evaluating the Performance of NAAT Procedures that Detect SARS-CoV-2 in Direct Specimens (1)
- For Evaluating the Performance of Nucleic Acid Tests for Determination of the Presence of Respiratory Virus Nucleic Acids (1)
- For Evaluating the Performance of Nucleic Acid Tests for Determination of the Presence of Viral and Bacterial Nucleic Acid (1)
- For Evaluating the Performance of Nucleic Acid Tests for Determination of the Presence of Viral and Bacterial Nucleic Acids (1)
- For FREND System (1)
- For GeneXpert System with Touchscreen running Cepheid OS (1)
- For Illumigene Group A Streptococcus DNA Amplification Assay (1)
- For Molecular Applications (1)
- For Monitoring Performance of Molecular Assys (1)
- For Monitoring Precision and Accuracy of the Atellica® IM SARS-CoV-2 IgG (sCOVG) Assay using the Atellica® IM Analyzer (1)
- For Monitoring System Performance of the Access SARS-CoV-2 IgG II Assay using the Access Immunoassay Systems only (1)
- For Monitoring the Extraction, Amplification and Detection Process of Molecular Testing Assays of Respiratory Pathogens (1)
- For Monitoring the Extraction, Amplification and Detection of SARS-CoV-2 Molecular Applications (1)
- For OSOM Flu SARS-CoV-2 Combo Test Kit (1)
- For Quality Control of COVID-19 2.0 Assay on ID NOW Instrument (1)
- For Quality Control of LifeSign COVID-19 / Flu A and B Antigen Detection Test (1)
- For QuickVue Dipstick Strep A, QuickVue+ Strep A or QuickVue In-Line Strep A Kits (1)
- For QuickVue In-Line Strep A Test (1)
- For Quidel's Solana Instrument and Quality Control Testing (1)
- For Quidel® Molecula GAS Assays (1)
- For Quidel® Molecular Influenza A+B Assays (1)
- For Real Time PCR System with FAM / HEX Fluorescence Channels (1)
- For Real-time PCR System with FAM / HEX / ROX / CY5 Fluorescence Channels (1)
- For Solana™ Solana Influenza A + B Assay (1)
- For Tyfast Flu A+B / COVID-19 Multiplex Rapid Test (1)
- For VITROS SARS-CoV-2 Antigen Test, For use on the VITROS 3600 Immunodiagnostic Systems and the VITROS 5600, XT 7600 Integrated Systems (1)
- For Validating and Monitoring the Performance of Molecular Diagnostic Tests for Detecting COVID-19, Flu A/B and RSV A/B (1)
- For Verification on SARS-COV-2 Nucleic Acid Tests (1)
- For Visby Medical Respiratory Health Test (1)
- For Vitros 3600 Immunodiagnostic System and Vitros 5600 / XT 7600 Integrated Systems (1)
- For Xpect® Flu A&B Test (1)
- For cobas SARS-CoV-2 and Influenza Nucleic Acid Test on cobas Liat System (1)
- For illumipro-10 Workstation (1)
- For the Calibration of the ARCHITECT i Systems when used for the Qualitative and Semi-Quantitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum (1)
- For the Calibration of the Alinity i Systems when used for the Qualitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum and Plasma (1)
- For the Calibration of the Alinity i Systems when used for the Qualitative Detection of IgM Antibodies to SARS-CoV-2 (1)
- For the Calibration of the Alinity i Systems when used for the Qualitative and Semi-Quantitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum (1)
- For the Calibration of the Architect i Systems when used for the Qualitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum and Plasma (1)
- For the Estimation of Test Precision and the Detection of Systematic Analytical Deviations of the ARCHITECT i System when used for the Qualitative and Semi-Quantitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum (1)
- For the Estimation of Test Precision and the Detection of Systematic Analytical Deviations of the Alinity i System when used for the Qualitative Detection of IgM Antibodies to SARS-CoV-2 (1)
- For the Estimation of Test Precision and the Detection of Systematic Analytical Deviations of the Alinity i System when used for the Qualitative and Semi-Quantitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum (1)
- For the Qualitative Determination of Total IgG / IgM and IgG Antibodies to SARS-CoV-2 (1)
- For use as a Positive Qualitative Quality Control Serum to Monitor the Precision of Laboratory Testing Procedures for the Determination of Immunoglobulin G (IgG) Antibodies to SARS-CoV-2 on Abbott i Systems (1)
- For use as a Quality Control Serum to Monitor the Precision of Laboratory Testing Procedures for the Determination of Immunoglobulin G (IgG) Antibodies to SARS-CoV-2 on Abbott i Systems (1)
- For use as an External Positive and Negative Quality Control to Monitor the Performance of in vitro Laboratory Nucleic Acid Testing Procedures for the Detection of Influenza A, Influenza B, Respiratory Syncytial Virus and SARS-CoV-2 Virus (1)
- For use in Conjunction with the LumiraDx SARS-CoV-2 Ag Test Strip System on the LumiraDx Instrument (1)
- For use in Monitoring the Performance of Vitros ECi / ECiQ (Available End of May 2020) / Vitros 3600 / 5600 / XT7600 when used for the Determination of Antibodies to SARS-CoV-2 (1)
- For use in Monitoring the Performance of the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems for the Qualitative Detection of the SARS-CoV-2 Nucleocapsid Antigen (1)
- For use in Monitoring the Performance of the VITROS ECi / ECiQ / 3600 Immunodiagnostic Systems and the VITROS 5600 / XT 7600 Integrated Systems when used for the Determination of IgG Antibodies to SARS-CoV-2 (1)
- For use in Monitoring the Performance of the Vitros Immunodiagnostic and Integrated Systems when used for the Determination of IgG Antibodies to SARS-CoV-2 (1)
- For use with BD Veritor System / SARS-CoV-2 and Flu A+B (1)
- For use with BinaxNOW™ COVID-19 Ag Card (1)
- For use with Cepheid Xpert Respiratory Control Panel (1)
- For use with IntelliSwab COVID-19 Rapid Test Kit (1)
- For use with Lyra® Direct SARS-CoV-2 Assay (1)
- For use with OSOM® Ultra Plus Flu A+B Test (1)
- For use with Xpert® Flu and Xpert® Flu/RSV XC Assays (1)
- For use with the BD Veritor™ System for Rapid Detection of SARS-CoV-2 Assay as External Quality Control Materials (1)
- For use with the LumiraDx Instrument and the LumiraDx SARS-CoV-2 Ag Test (1)
- Test Category
- Test Type
- Sample Type
- CLIA Classified
- Specialty
- Test Format
- Number of Tests
- Time to Results
- Country of Origin
- Trade Agreement Act (TAA) Compliant
- Buy American Act (BAA) Compliant
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- #1190348
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- #1238208
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