Search Results for testing and Respiratory
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Manufacturer Name
- McKesson Brand (1)
- Abbott (16)
- Abbott Rapid Dx North America LLC (9)
- Atila BioSystems Inc (11)
- BD (6)
- Beckman Coulter (3)
- Biomerieux Inc (SPOTFIRE) (4)
- Cepheid (7)
- CorDx Inc (1)
- LifeSign (2)
- Meridian Bioscience Corporation (3)
- Microbiologics Inc (4)
- Microgenics (1)
- Molecular Designs LLC (5)
- NanoEnTek USA Inc (1)
- Orasure Technologies (1)
- Ortho Clinical Diagnostics (7)
- Qiagen LLC (2)
- Quidel (7)
- Roche (2)
- Roche Diagnostics (7)
- Sekisui Diagnostics (4)
- Wondfo USA Co Ltd (2)
- Zeptometrix Corp/Antylia Scientific (27)
- Application
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Brand or Series
- Abbott (3)
- Access® (3)
- AdviseDx (8)
- Alinity i (3)
- Atila (4)
- BD MAX™ (2)
- BD Veritor™ (2)
- BD Veritor™ System (1)
- BinaxNOW™ (5)
- Cobas® Liat® (8)
- Frend™ COVID-19 Total Ab (1)
- Helix Elite™ (2)
- Helix Elite™ Inactivated Standard (2)
- iAMP® (7)
- ID NOW™ (4)
- Illumigene (2)
- illumigene® Mycoplasma Direct (1)
- IntelliSwab® (1)
- LumiraDx™ (1)
- Lyra® (3)
- McKesson Consult® (1)
- Multichem® ID-COVID19 G (1)
- Multichem® ID-COVID19Neg (1)
- NATtrol™ (26)
- OSOM® (1)
- OSOM® Ultra Plus (2)
- QIAstat-Dx® (2)
- Quickvue® In-Line® (2)
- QuickVue™ (1)
- RedX™ (1)
- Simplicity Panel™ (5)
- Solana™ (1)
- Spotfire® (4)
- Status™ (1)
- Thermo Scientific™ AcroMetrix™ (1)
- Tyfast (1)
- Veritor™ System (1)
- Vitros® (7)
- WELLlife™ (2)
- Xpert® (1)
- Xpert® Xpress (6)
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For Use With
- For BioFire SpotFire System (4)
- For Cobas Liat System (3)
- For ID NOW™ Instrument US (3)
- For Architect i Systems (2)
- For Cobas Liat Automated PCR Analyzer (2)
- For GeneXpert Systems (2)
- For GeneXpert Xpress System (2)
- For QIAstat-Dx Analyzer 1.0 (2)
- For Thermocycler (2)
- For Cobas Liat® Instrument (2)
- For BD Veritor System for SARS-CoV-2 / BD Veritor Plus Analyzer (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™ RSV Test Kit (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 Performance of Nucleic Acid Tests for Determination of Presence of Bacterial Nucleic Acids (1)
- For Evaluating the Performance of NAAT Procedures that Detect SARS-CoV-2 in Direct Specimens (1)
- For GeneXpert Xpress System (CLIA Waived) / GeneXpert System with Touchscreen running Cepheid OS (Moderate Complexity) (1)
- For McKesson Consult® COVID-19 / Flu A&B Antigen Test (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 QuickVue Influenza+SARS Test (1)
- For Tyfast Flu A+B / COVID-19 Multiplex Rapid Test (1)
- For cobas SARS-CoV-2 and Influenza Nucleic Acid Test on cobas Liat System (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 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 with BD Veritor System / SARS-CoV-2 and Flu A+B (1)
- For use with BinaxNOW™ COVID-19 Ag Card (1)
- For use with IntelliSwab COVID-19 Rapid Test Kit (1)
- For Real-Time PCR Detection Systems (5)
- 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 Evaluation of the Performance of Molecular Tests (3)
- For RT PCR Instrument with FAM / HEX Fluorescence Channels (3)
- For Access Immunoassay Systems (2)
- For Alinity i System (2)
- For BD MAX System (2)
- For Evaluating Test Performance of Molecular Assays which detect Streptococcus Pyogenes Nucleic Acids (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 OSOM® Ultra Plus Flu A+B Test (2)
- For Real-time PCR System with FAM / HEX Fluorescence Channels (2)
- For Verification of Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (2)
- For Vitros ECi / ECiQ / Vitros 3600 / 5600 / XT7600 (2)
- For Applied Biosystems 7500 Fast Dx Real-Time PCR Instrument / QuantStudio Dx Real-Time PCR Instrument / Cepheid SmartCycler II (1)
- For BinaxNOW™ Influenza A & B 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 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 Evaluating Performace of Molecular Tests (1)
- For Evaluating and Comparing Intra and Inter Laboratory Performance of Influenza Rapid Test Systems (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 Illumigene Group A Streptococcus DNA Amplification Assay (1)
- For LumiraDx Instrument and the LumiraDx SARS-CoV-2 Ag Test (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 Nucleic Acid Tests (1)
- For Quidel's Solana Instrument and Quality Control Testing (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 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 Vitros 3600 Immunodiagnostic System and Vitros 5600 / XT 7600 Integrated Systems (1)
- For Vitros ECi / ECiQ / 3600 Immunodiagnostic Systems and the Vitros 5600 / XT 7600 Integrated Systems (1)
- For WELLlife Covid-19 Antigen Test (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 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 use an External, Non-Viable Control Material to Evaluate the Performance of Nucleic Acid Tests that Detect SARS-CoV-2 Virus (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 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)
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Test Type
- Real Time RT-PCR (17)
- Antibody Test (24)
- Antigen Test (4)
- PCR (4)
- External Control (5)
- Molecular Diagnostic (16)
- Real-Time PCR (3)
- Immunology (2)
- Nucleic Acid Test (2)
- Real-time PCR (10)
- Infectious Disease Immunoassay (2)
- Molecular (2)
- Immunochromatographic Assay (1)
- Isothermal DNA Amplification (1)
- Molecular Diagnostic / RT-PCR (1)
- Molecular Diagnostic / Real-Time PCR (1)
- Molecular Testing (1)
- Antigen Detection (1)
- Immunoassay (1)
- Isothermal Nucleic Acid Amplification Assay (1)
- Quality Control (QC) (1)
- Quantitative Antibody Test (1)
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Volume
- 20 Swabs (6)
- 10 Swabs (8)
- 24 Swabs (4)
- 20 Tubes (2)
- 4 X 4 mL (2)
- 12 Swabs (3)
- 2 X 4 mL (2)
- 3 Sets (2)
- 3 X 4 mL (2)
- 6 Swabs (2)
- 10 Pairs (1)
- 2 Swabs (1)
- 2 X 2.5 mL (1)
- 2 X 5 mL (1)
- 24 X 0.1 mL (1)
- 3 X 0.25 mL / 3 X 10 µL / 3 X 0.3 mL (1)
- 50 Tests (1)
- 6 X 0.3 mL (1)
- 6.6 mL Microparticles, 5.9 mL Conjugate, 7.9 mL Diluent (1)
- Lysis Reagent: 1 mL, Binding Reagent: 1 mL, Elution Reagent: 2 mL, Wash Reagent: 0.5 mL (1)
- 6 X 0.5 mL (13)
- 6 X 1 mL (4)
- 6 X 2 mL (3)
- 1 X 2.0 mL (2)
- 12 X 0.25 mL (1)
- 18 Tests (1)
- 2 X 1 mL (1)
- 2 X 4.0 mL (1)
- 2 mL (1)
- 20 µL Sample Volume (1)
- 21 X 0.25 mL (1)
- 21 X 0.5 mL (1)
- 24 X 0.6 mL (1)
- 25 X 0.6 mL, 6 X 1.8 mL (1)
- 3 X 1 mL (1)
- 3 X 1.5 mL (1)
- 3 X 2 mL (1)
- 35 µL Sample Volume (1)
- 4 X 0.5 mL (1)
- 5 X 1.5 mL (1)
- 6 X 0.25 mL (1)
- 6 X 4 mL (1)
- 6.6 mL Microparticles, 6.1 mL Conjugate, 8.3 mL Diluent (1)
- Levels
- Specialty
- Number of Tests
- Form
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Sample Type
- Nasopharyngeal Swab Sample (6)
- Throat Swab Sample (6)
- Anterior Nasal Swab / Nasopharyngeal Swab Sample (5)
- Nasal Swab / Nasopharyngeal Swab Sample (7)
- Serum / Plasma Sample (6)
- Nasal Swab / Nasopharyngeal Swab / Oropharyngeal Swab Sample (2)
- DNA Sample (4)
- Anterior Nasal / Mid-turbinate Nasal / Nasopharyngeal / Oropharyngeal Swab Sample (1)
- Plasma Sample (1)
- Rectal / Vaginal Swab Sample (1)
- Test Format
- CLIA Classified
- Time to Results
- Latex Free Indicator
- Country of Origin
- Trade Agreement Act (TAA) Compliant
- Buy American Act (BAA) Compliant
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