Other products from "GENMARK DIAGNOSTICS, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00857167005153 eSensor® Cystic Fibrosis (CF) MT002015 eSensor® Cystic Fibrosis (CF) Genotyping Test (24) eSensor® XT-8
2 00857167005238 eSensor® Thrombophilia Risk Test Reagent Test (TRT) MT004008 eSensor® Thrombophilia Risk Test Reagent Test Pack (TRT) (48) eSensor® XT-8
3 00857167005146 eSensor® Cystic Fibrosis (CF) KT020657 eSensor® Cystic Fibrosis Genotyping Test Cartridge Pouch (CF) (8) eSensor® XT-8
4 00857167005139 eSensor® Respiratory Viral Panel (RVP) MT005101 eSensor® Respiratory Viral Panel Reagent (RVP) (48) eSensor® XT-8
5 00857167005221 eSensor® Thrombophilia Risk Test (TRT) MT004008 eSensor® Thrombophilia Risk Test Amplification Reagents (TRT) (48) eSensor® XT-8
6 00857167005184 eSensor® Cystic Fibrosis (CF) MT002014 eSensor® Cystic Fibrosis Genotyping Test Reagent Pack (CF) (24) eSensor® XT-8
7 00857167005214 eSensor® Thrombophilia Risk Test (TRT) MT004008 eSensor® Thrombophilia Risk Test Detection Reagents (TRT) (48) eSensor® XT-8
8 00857167005276 Warfarin Sensitivity Test (WST) MT002001 eSensor® Warfarin Sensitivity Test Reagent Pack (WST) (24) eSensor® XT-8
9 00857167005207 eSensor® Thrombophilia Risk Test (TRT) MT004013 eSensor® Thrombophilia Risk Test (TRT) (48) eSensor® XT-8
10 00857167005177 eSensor® Cystic Fibrosis (CF) MT002014 eSensor® Cystic Fibrosis Genotyping Test Detection Reagents (CF) (24) eSensor® XT-8
11 00857167005160 eSensor® Cystic Fibrosis (CF) MT002014 eSensor® Cystic Fibrosis Genotyping Test Amplification Reagents (CF) (24) eSensor® XT-8
12 00857167005252 Warfarin Sensitivity Test (WST) MT002001 eSensor® Warfarin Sensitivity Test Detection Reagents (WST) (24) eSensor® XT-8
13 00857167005245 Warfarin Sensitivity Test (WST) MT002001 eSensor® Warfarin Sensitivity Test Amplification Reagents (24) eSensor® XT-8
14 00857167005191 eSensor® Thrombophilia Risk Test (TRT) KT021053 eSensor® Thrombophilia Risk Test Cartridge Pouch (TRT) (8) eSensor® XT-8
15 00857167005122 eSensor® Respiratory Viral Panel (RVP) MT005101 eSensor® Respiratory Viral Panel Detection Reagents (RVP) (48) eSensor® XT-8
16 00857167005115 eSensor® Respiratory Viral Panel (RVP) MT005101 eSensor® Respiratory Viral Panel Amplification Reagents (48) eSensor® XT-8
17 00857167005108 eSensor® Respiratory Viral Panel (RVP) MT005100 eSensor® Respiratory Viral Panel Cartridges (RVP) (48) eSensor® XT-8
18 00857167005092 eSensor® Respiratory Viral Panel (RVP) KT021620 eSensor® Respiratory Viral Panel Cartridge Pouch (RVP) (8) eSensor® XT-8
19 00857167005061 Warfarin Sensitivity Test (WST) MT002000 eSensor® Warfarin Sensitivity Test Cartridges (WST) (24) eSensor® XT-8
20 00857167005047 Warfarin Sensitivity Test (WST) KT020591 eSensor® Warfarin Sensitivity Test Cartridge Pouch (WST) (8) eSensor® XT-8
21 00857167005337 BCID-GP Cartridge Pouch KT021791 ePlex Blood Culture Identification Gram Positive (GP) Panel Cartridge Pouch PEO,PEN,PAM Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Resistance Markers,Gram-Positive Bacteria And Their Resistance Markers 2 ePlex
22 00857167005320 BCID-GP 12 Kit Box EA003012 ePlex Blood Culture Identification Gram Positive (GP) Panel 12-Kit Box PEO,PEN,PAM Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Resistance Markers,Gram-Positive Bacteria And Their Resistance Markers 2 ePlex
23 00857167005313 BCID-GN 12 Kit Box EA002012 ePlex Blood Culture Identification Gram Negative (GN) Panel 12-test kit box PEO,PEN,PAM Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Resistance Markers,Gram-Positive Bacteria And Their Resistance Markers 2 ePlex
24 00857167005306 BCID-GN Cartridge Pouch KT021836 ePlex Blood Culture Identification Gram Negative (GN) Cartridge Pouch PEO,PEN,PAM Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Resistance Markers,Gram-Positive Bacteria And Their Resistance Markers 2 ePlex
25 00857167005290 BCID-FP 12 Kit Box EA005012 ePlex Blood Culture Identification Fungal Pathogen (FP) 12-test kit box PEO,PEN,PAM Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Resistance Markers,Gram-Positive Bacteria And Their Resistance Markers 2 ePlex
26 00857167005283 BCID_FP Cartridge Pouch KT022279 ePlex Blood Culture Identification Fungal Pathogen (FP) Cartridge Pouch PEO,PEN,PAM Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Fungal Organisms, Nucleic Acid-Based Assay,Gram-Negative Bacteria And Associated Resistance Markers,Gram-Positive Bacteria And Their Resistance Markers 2 ePlex
27 00857167005009 ePlex System Base NSU Instrumentation For Clinical Multiplex Test Systems 2 ePlex
28 00857167005030 ePlex Respiratory Panel (RP) EA001012 ePlex Respiratory Panel Kit, 12 test, IVD OZY,OZX,OZE,OTG,OQW,OOU,OEP,OEM,OCC Chlamydophila Pneumoniae Dna Assay System,Mycoplasma Pneumoniae Dna Assay System Chlamydophila Pneumoniae Dna Assay System,Mycoplasma Pneumoniae Dna Assay System,Influenza A And Influenza B Multiplex Nucleic Acid Assay,Non-Sars Coronavirus Multiplex Nucleic Acid Assay,2009 H1n1 Influenza Virus (Swine Origin), Nucleic Acid Or Antigen, Detection And Identification,Parainfluenza Multiplex Nucleic Acid Assay,Influenza A Virus Subtype Differentiation Nucleic Acid Assay,Human Metapneumovirus (Hmpv) Rna Assay System,Respiratory Virus Panel Nucleic Acid Assay System 2 ePlex System
29 00857167005023 ePlex Respiratory Panel (RP) KT022006 ePlex Sample Delivery Device RP Panel OZY,OZX,OZE,OTG,OQW,OOU,OEP,OEM,OCC Chlamydophila Pneumoniae Dna Assay System,Mycoplasma Pneumoniae Dna Assay System Chlamydophila Pneumoniae Dna Assay System,Mycoplasma Pneumoniae Dna Assay System,Influenza A And Influenza B Multiplex Nucleic Acid Assay,Non-Sars Coronavirus Multiplex Nucleic Acid Assay,2009 H1n1 Influenza Virus (Swine Origin), Nucleic Acid Or Antigen, Detection And Identification,Parainfluenza Multiplex Nucleic Acid Assay,Influenza A Virus Subtype Differentiation Nucleic Acid Assay,Human Metapneumovirus (Hmpv) Rna Assay System,Respiratory Virus Panel Nucleic Acid Assay System 2 ePlex System
Other products with the same Product Codes "OZY, OZX, OZE, OTG, OQW, OOU, OEP, OEM, OCC"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00840733102189 480250 480250 The Alethia Mycoplasma Direct DNA amplification assay, performed on the Alethia The Alethia Mycoplasma Direct DNA amplification assay, performed on the Alethia Reader, is a qualitative in vitro diagnostic test for the direct detection of DNA from Mycoplasma pneumoniae in human throat swabs obtained from patients suspected of having Mycoplasma pneumoniae infection.The Alethia Mycoplasma Direct assay utilizes loop-mediated isothermal DNA amplification (LAMP) technology to detect Mycoplasma pneumoniae by targeting a segment of the Mycoplasma pneumoniae genome.Results from the Alethia Mycoplasma Direct DNA amplification assay should be used in conjunction with clinical presentation, other laboratory findings, and epidemiological risk factors as an aid in the diagnosis of Mycoplasma infection and should not be used as the sole basis for treatment or other patient management. Positive results do not rule out co-infection with other organisms and negative results in persons with respiratory tract infections may be due to pathogens not detected by this assay. Lower respiratory tract infections due to M. pneumoniae may not be detected by this assay. If lower respiratory tract infection due to M. pneumoniae is suspected, additional laboratory testing using methods other than the Alethia Mycoplasma Direct DNA Amplification Assay may be necessary. Alethia™ Mycoplasma Direct MERIDIAN BIOSCIENCE, INC.
2 00840733102103 479890 479890 The Alethia Mycoplasma Direct External Control Kit contains Positive Control Rea The Alethia Mycoplasma Direct External Control Kit contains Positive Control Reagent for use with the Alethia Mycoplasma Direct test kit. The External Positive Control Reagent is used in conjunction with the Alethia Sample Preparation Apparatus II/Negative Control III reagent provided with the Alethia Mycoplasma Direct Kit as part of routine Quality Control Testing. External controls are used to aid the user in detection of unexpected conditions that may lead to test errors. Alethia™ Mycoplasma Direct External Control Kit MERIDIAN BIOSCIENCE, INC.
3 00840733101281 279890 279890 The illumigene Mycoplasma Direct External Control Kit contains Positive Control The illumigene Mycoplasma Direct External Control Kit contains Positive Control Reagent for use with the illumigene Mycoplasma Direct test kit. The External Positive Control Reagent is used in conjunction with the illumigene Sample Preparation Apparatus II/Negative Control III reagent provided with the illumigene Mycoplasma Direct Kit as part of routine Quality Control Testing. External controls are used as part of a routine quality control program. illumigene Mycoplasma Direct External Control Kit MERIDIAN BIOSCIENCE, INC.
4 00840733101274 280250 280250 The illumigene Mycoplasma Direct DNA amplification assay, performed on the illum The illumigene Mycoplasma Direct DNA amplification assay, performed on the illumipro-10, is a qualitative in vitro diagnostic test for the direct detection of DNA from Mycoplasma pneumoniae in human throat swabs obtained from patients suspected of having Mycoplasma pneumoniae infection. The illumigene Mycoplasma Direct assay utilizes loop-mediated isothermal DNA amplification (LAMP) technology to detect Mycoplasma pneumoniae by targeting a segment of the Mycoplasma pneumoniae genome. Results from the illumigene Mycoplasma Direct DNA amplification assay should be used in conjunction with clinical presentation, other laboratory findings, and epidemiological risk factors as an aid in the diagnosis of Mycoplasma infection and should not be used as the sole basis for treatment or other patient management. illumigene Mycoplasma Direct MERIDIAN BIOSCIENCE, INC.
5 00840733101175 280550 280550 "The illumigene Mycoplasma DNA amplification assay, performed on the illumipro-1 "The illumigene Mycoplasma DNA amplification assay, performed on the illumipro-10, is a qualitative in vitro diagnostic test for the direct detection of DNA from Mycoplasma pneumoniae in human throat and nasopharyngeal swabs obtained from patients suspected of having Mycoplasma pneumoniae infection. The illumigene Mycoplasma assay utilizes loop-mediated isothermal DNA amplification (LAMP) technology to detect Mycoplasma pneumoniae by targeting a segment of the Mycoplasma pneumoniae genome. Results from the illumigene Mycoplasma DNA amplification assay should be used in conjunction with clinical presentation, other laboratory findings, and epidemiological risk factors as an aid in the diagnosis of Mycoplasma infection and should not be used as the sole basis for treatment or other patient management. illumigene Mycoplasma MERIDIAN BIOSCIENCE, INC.
6 00840733101144 279940 279940 The illumigene Mycoplasma External Control Kit contains Positive and Negative Co The illumigene Mycoplasma External Control Kit contains Positive and Negative Control Reagents for use with the illumigene Mycoplasma test kit. External controls are used as part of a routine quality control program. External controls are used as part of a routine quality control program. illumigene Mycoplasma External Control Kit MERIDIAN BIOSCIENCE, INC.
7 00840487101711 20-011-024 20-011-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Amplification Tray LUMINEX CORPORATION
8 00840487101711 20-011-024 20-011-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Amplification Tray LUMINEX CORPORATION
9 00840487101711 20-011-024 20-011-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Amplification Tray LUMINEX CORPORATION
10 00840487101711 20-011-024 20-011-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Amplification Tray LUMINEX CORPORATION
11 00840487101711 20-011-024 20-011-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Amplification Tray LUMINEX CORPORATION
12 00840487101667 20-009-024 20-009-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Extraction Tray LUMINEX CORPORATION
13 00840487101667 20-009-024 20-009-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Extraction Tray LUMINEX CORPORATION
14 00840487101667 20-009-024 20-009-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Extraction Tray LUMINEX CORPORATION
15 00840487101667 20-009-024 20-009-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Extraction Tray LUMINEX CORPORATION
16 00840487101667 20-009-024 20-009-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Extraction Tray LUMINEX CORPORATION
17 00840487101612 20-006-024 20-006-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Nucleic Acid Test Cartridge LUMINEX CORPORATION
18 00840487101612 20-006-024 20-006-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Nucleic Acid Test Cartridge LUMINEX CORPORATION
19 00840487101612 20-006-024 20-006-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Nucleic Acid Test Cartridge LUMINEX CORPORATION
20 00840487101612 20-006-024 20-006-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Nucleic Acid Test Cartridge LUMINEX CORPORATION
21 00840487101612 20-006-024 20-006-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. Respiratory Pathogens Flex (RP Flex) Nucleic Acid Test Cartridge LUMINEX CORPORATION
22 00840487100486 I025C0197 I025C0197 The xTAG® Respiratory Viral Panel Fast (RVP FAST) is a qualitative nucleic acid The xTAG® Respiratory Viral Panel Fast (RVP FAST) is a qualitative nucleic acid multiplex test intended for the simultaneous detection and identification of multiple respiratory virus nucleic acids in nasopharyngeal swabs from individuals suspected ofrespiratory tract infections xTAG® RVP FAST (Respiratory Viral Panel Fast) LUMINEX MOLECULAR DIAGNOSTICS, INC
23 00840487100486 I025C0197 I025C0197 The xTAG® Respiratory Viral Panel Fast (RVP FAST) is a qualitative nucleic acid The xTAG® Respiratory Viral Panel Fast (RVP FAST) is a qualitative nucleic acid multiplex test intended for the simultaneous detection and identification of multiple respiratory virus nucleic acids in nasopharyngeal swabs from individuals suspected ofrespiratory tract infections xTAG® RVP FAST (Respiratory Viral Panel Fast) LUMINEX MOLECULAR DIAGNOSTICS, INC
24 00840487100486 I025C0197 I025C0197 The xTAG® Respiratory Viral Panel Fast (RVP FAST) is a qualitative nucleic acid The xTAG® Respiratory Viral Panel Fast (RVP FAST) is a qualitative nucleic acid multiplex test intended for the simultaneous detection and identification of multiple respiratory virus nucleic acids in nasopharyngeal swabs from individuals suspected ofrespiratory tract infections xTAG® RVP FAST (Respiratory Viral Panel Fast) LUMINEX MOLECULAR DIAGNOSTICS, INC
25 00840487100462 I019C0111 I019C0111 The xTAG® Respiratory Viral Panel (RVP) is a qualitative nucleic acid multiplex The xTAG® Respiratory Viral Panel (RVP) is a qualitative nucleic acid multiplex test intended for the simultaneous detection and identification of multiple respiratory virus nucleic acids in nasopharyngeal swabs from individuals suspected of respiratory tract infections. xTAG® RVP (Respiratory Viral Panel) LUMINEX MOLECULAR DIAGNOSTICS, INC
26 00840487100462 I019C0111 I019C0111 The xTAG® Respiratory Viral Panel (RVP) is a qualitative nucleic acid multiplex The xTAG® Respiratory Viral Panel (RVP) is a qualitative nucleic acid multiplex test intended for the simultaneous detection and identification of multiple respiratory virus nucleic acids in nasopharyngeal swabs from individuals suspected of respiratory tract infections. xTAG® RVP (Respiratory Viral Panel) LUMINEX MOLECULAR DIAGNOSTICS, INC
27 00840487100462 I019C0111 I019C0111 The xTAG® Respiratory Viral Panel (RVP) is a qualitative nucleic acid multiplex The xTAG® Respiratory Viral Panel (RVP) is a qualitative nucleic acid multiplex test intended for the simultaneous detection and identification of multiple respiratory virus nucleic acids in nasopharyngeal swabs from individuals suspected of respiratory tract infections. xTAG® RVP (Respiratory Viral Panel) LUMINEX MOLECULAR DIAGNOSTICS, INC
28 00840487100417 I051C0447 I051C0447 The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on the Luminex® MAGPIX® instrument for the simultaneous detection and identification of nucleic acids from multiple respiratory viruses and bacteria extracted from nasopharyngeal swabs collected from individuals with clinical signs and symptoms of a respiratory tract infection. NxTAG® Respiratory Pathogen Panel LUMINEX MOLECULAR DIAGNOSTICS, INC
29 00840487100417 I051C0447 I051C0447 The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on the Luminex® MAGPIX® instrument for the simultaneous detection and identification of nucleic acids from multiple respiratory viruses and bacteria extracted from nasopharyngeal swabs collected from individuals with clinical signs and symptoms of a respiratory tract infection. NxTAG® Respiratory Pathogen Panel LUMINEX MOLECULAR DIAGNOSTICS, INC
30 00840487100417 I051C0447 I051C0447 The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on the Luminex® MAGPIX® instrument for the simultaneous detection and identification of nucleic acids from multiple respiratory viruses and bacteria extracted from nasopharyngeal swabs collected from individuals with clinical signs and symptoms of a respiratory tract infection. NxTAG® Respiratory Pathogen Panel LUMINEX MOLECULAR DIAGNOSTICS, INC
31 00840487100417 I051C0447 I051C0447 The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on the Luminex® MAGPIX® instrument for the simultaneous detection and identification of nucleic acids from multiple respiratory viruses and bacteria extracted from nasopharyngeal swabs collected from individuals with clinical signs and symptoms of a respiratory tract infection. NxTAG® Respiratory Pathogen Panel LUMINEX MOLECULAR DIAGNOSTICS, INC
32 00840487100417 I051C0447 I051C0447 The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on the Luminex® MAGPIX® instrument for the simultaneous detection and identification of nucleic acids from multiple respiratory viruses and bacteria extracted from nasopharyngeal swabs collected from individuals with clinical signs and symptoms of a respiratory tract infection. NxTAG® Respiratory Pathogen Panel LUMINEX MOLECULAR DIAGNOSTICS, INC
33 00840487100417 I051C0447 I051C0447 The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on the Luminex® MAGPIX® instrument for the simultaneous detection and identification of nucleic acids from multiple respiratory viruses and bacteria extracted from nasopharyngeal swabs collected from individuals with clinical signs and symptoms of a respiratory tract infection. NxTAG® Respiratory Pathogen Panel LUMINEX MOLECULAR DIAGNOSTICS, INC
34 00840487100417 I051C0447 I051C0447 The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on The NxTAG® Respiratory Pathogen Panel is a qualitative test intended for use on the Luminex® MAGPIX® instrument for the simultaneous detection and identification of nucleic acids from multiple respiratory viruses and bacteria extracted from nasopharyngeal swabs collected from individuals with clinical signs and symptoms of a respiratory tract infection. NxTAG® Respiratory Pathogen Panel LUMINEX MOLECULAR DIAGNOSTICS, INC
35 00840487100158 50-10020 The ARIES® Flu A/B & RSV Assay is a polymerase chain reaction (PCR) based qualit The ARIES® Flu A/B & RSV Assay is a polymerase chain reaction (PCR) based qualitative in vitro diagnostic test for the direct detection and differentiation of influenza A virus, influenza B virus, and respiratory syncytial virus (RSV) nucleic acid in nasopharyngeal swabs (NPS) specimens from patients with signs and symptoms of respiratory tract infection in conjunction with clinical and laboratory findings. ARIES® Flu A/B & RSV Assay LUMINEX CORPORATION
36 00840487100158 50-10020 The ARIES® Flu A/B & RSV Assay is a polymerase chain reaction (PCR) based qualit The ARIES® Flu A/B & RSV Assay is a polymerase chain reaction (PCR) based qualitative in vitro diagnostic test for the direct detection and differentiation of influenza A virus, influenza B virus, and respiratory syncytial virus (RSV) nucleic acid in nasopharyngeal swabs (NPS) specimens from patients with signs and symptoms of respiratory tract infection in conjunction with clinical and laboratory findings. ARIES® Flu A/B & RSV Assay LUMINEX CORPORATION
37 00815381020161 RFIT-ASY-0130 RFIT-ASY-0130 IVD reagent kit containing 6 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
38 00815381020161 RFIT-ASY-0130 RFIT-ASY-0130 IVD reagent kit containing 6 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
39 00815381020161 RFIT-ASY-0130 RFIT-ASY-0130 IVD reagent kit containing 6 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
40 00815381020161 RFIT-ASY-0130 RFIT-ASY-0130 IVD reagent kit containing 6 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
41 00815381020161 RFIT-ASY-0130 RFIT-ASY-0130 IVD reagent kit containing 6 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
42 00815381020161 RFIT-ASY-0130 RFIT-ASY-0130 IVD reagent kit containing 6 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
43 00815381020161 RFIT-ASY-0130 RFIT-ASY-0130 IVD reagent kit containing 6 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
44 00815381020154 RFIT-ASY-0129 RFIT-ASY-0129 IVD reagent kit containing 30 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
45 00815381020154 RFIT-ASY-0129 RFIT-ASY-0129 IVD reagent kit containing 30 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
46 00815381020154 RFIT-ASY-0129 RFIT-ASY-0129 IVD reagent kit containing 30 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
47 00815381020154 RFIT-ASY-0129 RFIT-ASY-0129 IVD reagent kit containing 30 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
48 00815381020154 RFIT-ASY-0129 RFIT-ASY-0129 IVD reagent kit containing 30 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
49 00815381020154 RFIT-ASY-0129 RFIT-ASY-0129 IVD reagent kit containing 30 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC
50 00815381020154 RFIT-ASY-0129 RFIT-ASY-0129 IVD reagent kit containing 30 tests FilmArray® Respiratory Panel 2 (RP2) BIOFIRE DIAGNOSTICS, LLC