No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 30014613339144 | Coronavirus | M124 | SARS-CoV-2 Direct Assay | QJR | Reagents, 2019-novel coronavirus nucleic acid | Lyra | |
2 | 30014613339090 | Coronavirus | M120 | Lyra SARS-CoV-2 Assay | QJR | Reagents, 2019-novel coronavirus nucleic acid | Lyra | |
3 | 30014613338727 | 01-124210 | 01-124210 | L-DFA RSV/MPV Antigen Control Slides | LJG | QUALITY CONTROL SLIDES | 1 | D3 Fastpoint |
4 | 30014613338710 | 01-124110 | 01-124110 | L-DFA Influenza A/Influenza B Antigen Control Slides | LJG | QUALITY CONTROL SLIDES | 1 | D3 Fastpoint |
5 | 30014613336440 | M311 | M311 | Solana GBS Assay | NJR | Nucleic acid amplification assay system, group b streptococcus, direct specimen test | 1 | Solana |
6 | 30014613337003 | M123 | M123 | Solana RSV+hMPV Control Set | OHQ | Multi-analyte controls unassayed | 1 | Solana |
7 | 30014613336990 | M122 | M122 | Solana Flu A+B Control Set | OHQ | Multi-analyte controls unassayed | 1 | Solana |
8 | 30014613336983 | M118 | M118 | Solana HSV 1+2/ VZV Control set | OHQ | Multi-analyte controls unassayed | 1 | Solana |
9 | 30014613336167 | M308 | M308 | Solana Bordetella Complete | OZZ | Bordetella pertussis dna assay system | 2 | Solana |
10 | 30014613336150 | M307 | M307 | Solana C. difficile Assay | OZN | C. Difficile Toxin Gene Amplification Assay | 2 | Solana |
11 | 30014613336143 | M306 | M306 | Solana RSV/hMPB Assay | OCC | Respiratory virus panel nucleic acid assay system | 2 | Solana |
12 | 30014613336136 | M305 | M305 | Solana Strep A/C & G Assay | PGX | Groups A, C and G beta-hemolytic streptococcus nucleic acid amplification system | 2 | Solana |
13 | 30014613336105 | M302 | M302 | Solana HSV 1+2/ VZV Assay | PGI | Herpes virus (VZV, HSV1, HSV2), DNA Detection Assay for cutaneous and mucocutane Herpes virus (VZV, HSV1, HSV2), DNA Detection Assay for cutaneous and mucocutaneous lesion samples | 2 | Solana |
14 | 30014613330929 | 01-215010 | 01-215010 | D3 Duet DFA RSV Screening Reagent | LKT | RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA | 1 | D3 Duet |
15 | 30014613330912 | 01-215002 | 01-215002 | D3 Duet DFA RSV Screening Reagent 2ML | LKT | RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA | 1 | D3 Duet |
16 | 30014613330905 | 01-210000 | 01-210000 | D3 Duet DFA RSV/Respiratory Virus Screening Kit | LKT | RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA | 1 | D3 Duet |
17 | 30014613330899 | 01-205010 | 01-205010 | D3 Duet DFA Influenza A Screening reagent | LKT | RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA | 1 | D3 Duet |
18 | 30014613330882 | 01-200000 | 01-200000 | D3 Duet DFA Influenza A/Respiratory Virus Screening kit | GNW | ANTISERA, CF, INFLUENZA VIRUS A, B, C | 1 | D3 Duet |
19 | 30014613330875 | 01-123504 | 01-123504 | L-DFA Parainfluenza Virus/Adenovirus Reagent | GNY,OMG,GQS,LKT,GNS | ANTISERA, FLUORESCENT, ADENOVIRUS 1-33,Antisera, fluorescent, human metapneumovi ANTISERA, FLUORESCENT, ADENOVIRUS 1-33,Antisera, fluorescent, human metapneumovirus,ANTIGENS, CF (INCLUDING CF CONTROL), PARAINFLUENZA VIRUS 1-4,RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,ANTISERA, HAI, INFLUENZA VIRUS A, B, C | 1 | D3 Fastpoint |
20 | 30014613330868 | 01-123304 | 01-123304 | L-DFA RSV/MPV Reagent | LKT,OMG,GQS,GNS,GNY | RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,Antisera, fluorescent, human RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,Antisera, fluorescent, human metapneumovirus,ANTIGENS, CF (INCLUDING CF CONTROL), PARAINFLUENZA VIRUS 1-4,ANTISERA, HAI, INFLUENZA VIRUS A, B, C,ANTISERA, FLUORESCENT, ADENOVIRUS 1-33 | 1 | D3 Fastpoint |
21 | 30014613330851 | 01-123104 | 01-123104 | L-DFA Influenza A/Influenza B Reagent | LKT,GNY,GQS,GNS,OMG | RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,ANTISERA, FLUORESCENT, ADENO RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,ANTISERA, FLUORESCENT, ADENOVIRUS 1-33,ANTIGENS, CF (INCLUDING CF CONTROL), PARAINFLUENZA VIRUS 1-4,ANTISERA, HAI, INFLUENZA VIRUS A, B, C,Antisera, fluorescent, human metapneumovirus | 1 | D3 Fastpoint |
22 | 30014613330844 | 01-122006 | 01-122006 | Re-Suspension Buffer | LKT,GNY,OMG,GNS,GQS | RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,ANTISERA, FLUORESCENT, ADENO RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,ANTISERA, FLUORESCENT, ADENOVIRUS 1-33,Antisera, fluorescent, human metapneumovirus,ANTISERA, HAI, INFLUENZA VIRUS A, B, C,ANTIGENS, CF (INCLUDING CF CONTROL), PARAINFLUENZA VIRUS 1-4 | 1 | D3 Fastpoint |
23 | 30014613330837 | 01-120002.B2 | 01-120002.B2 | FASTPOINT RSV/MPV KIT BX 2 | LKT,OMG | RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,Antisera, fluorescent, human RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,Antisera, fluorescent, human metapneumovirus | 1 | D3 Fastpoint |
24 | 30014613330820 | 01-120002.B1 | 01-120002.B1 | FASTPOINT RSV/MPV KIT BX 1 | LKT,OMG | RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,Antisera, fluorescent, human RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,Antisera, fluorescent, human metapneumovirus | 1 | D3 Fastpoint |
25 | 30014613330813 | RSV/MPV ID Kit | 01-120002 | D3 FASTPOINT RSV/MPV KIT | OMG,LKT | Antisera, fluorescent, human metapneumovirus,RESPIRATORY SYNCYTIAL VIRUS, ANTIGE Antisera, fluorescent, human metapneumovirus,RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA | 1 | D3 Fastpoint |
26 | 30014613330806 | 01-120001.B2 | 01-120001.B2 | FASTPOINT FLUA/B KIT BX 2 | GNW | ANTISERA, CF, INFLUENZA VIRUS A, B, C | 1 | D3 Fastpoint |
27 | 30014613330790 | 01-120001.B1 | 01-120001.B1 | FASTPOINT FLUA/B KIT BX 1 | GNW | ANTISERA, CF, INFLUENZA VIRUS A, B, C | 1 | D3 Fastpoint |
28 | 30014613330783 | 01-120001 | 01-120001 | FASTPOINT FLUA/B KIT | GNW | ANTISERA, CF, INFLUENZA VIRUS A, B, C | 1 | D3 Fastpoint |
29 | 30014613330776 | 01-120000.B2 | 01-120000.B2 | D3 FASTPOINT LDFA VIR IDKIT BX | LKT,GNS,GNY,GQS,OMG | RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,ANTISERA, HAI, INFLUENZA VIR RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,ANTISERA, HAI, INFLUENZA VIRUS A, B, C,ANTISERA, FLUORESCENT, ADENOVIRUS 1-33,ANTIGENS, CF (INCLUDING CF CONTROL), PARAINFLUENZA VIRUS 1-4,Antisera, fluorescent, human metapneumovirus | 1 | D3 Fastpoint |
30 | 30014613330769 | 01-120000.B1 | 01-120000.B1 | D3 FASTPOINT LDFA VIR IDKIT BX | GQS,OMG,GNS,LKT,GNY | ANTIGENS, CF (INCLUDING CF CONTROL), PARAINFLUENZA VIRUS 1-4,Antisera, fluoresce ANTIGENS, CF (INCLUDING CF CONTROL), PARAINFLUENZA VIRUS 1-4,Antisera, fluorescent, human metapneumovirus,ANTISERA, HAI, INFLUENZA VIRUS A, B, C,RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,ANTISERA, FLUORESCENT, ADENOVIRUS 1-33 | 1 | D3 Fastpoint |
31 | 30014613330752 | Respiratory Virus ID Kit | 01-120000 | D3 FASTPOINT RESP VIRUS ID KIT | GQS,OMG,GNS,LKT,GNY | ANTIGENS, CF (INCLUDING CF CONTROL), PARAINFLUENZA VIRUS 1-4,Antisera, fluoresce ANTIGENS, CF (INCLUDING CF CONTROL), PARAINFLUENZA VIRUS 1-4,Antisera, fluorescent, human metapneumovirus,ANTISERA, HAI, INFLUENZA VIRUS A, B, C,RESPIRATORY SYNCYTIAL VIRUS, ANTIGEN, ANTIBODY, IFA,ANTISERA, FLUORESCENT, ADENOVIRUS 1-33 | 1 | D3 Fastpoint |
32 | 30014613311218 | M121 | M121 | QMol HSV 1+2/VZV Control Set | OHQ | Multi-analyte controls unassayed | 1 | Quidel Molecular |
33 | 30014613311195 | M119 | M119 | QMol Trichomonas Control Set | JJX | Single (specified) analyte controls (assayed and unassayed) | 1 | Quidel Molecular |
34 | 30014613311171 | M117 | M117 | QMol Bordetella Control Set | JJX | Single (specified) analyte controls (assayed and unassayed) | 1 | Quidel Molecular |
35 | 30014613311164 | M116 | M116 | QMol GBS Control Set | JJX | Single (specified) analyte controls (assayed and unassayed) | 1 | Quidel Molecular |
36 | 30014613311157 | M115 | M115 | QMol Parainflu Control Set | OHQ,JJX | Multi-analyte controls unassayed,Single (specified) analyte controls (assayed an Multi-analyte controls unassayed,Single (specified) analyte controls (assayed and unassayed) | 1 | Quidel Molecular |
37 | 30014613311102 | M110 | M110 | QMol Adeno Control Set | JJX | Single (specified) analyte controls (assayed and unassayed) | 1 | Quidel Molecular |
38 | 30014613311096 | M109 | M109 | QMol HSV 1+2 Control Set | OHQ | Multi-analyte controls unassayed | 1 | Quidel Molecular |
39 | 30014613311089 | M108 | M108 | QMol CDIFF Control Set | JJX | Single (specified) analyte controls (assayed and unassayed) | 1 | Quidel Molecular |
40 | 30014613311072 | M107 | M107 | QMol RSV+HMPV Control Set | OHQ | Multi-analyte controls unassayed | 1 | Quidel Molecular |
41 | 30014613311065 | M106 | M106 | QMol FLUA+B Control Set | OHQ | Multi-analyte controls unassayed | 1 | Quidel Molecular |
42 | 30014613311034 | M103 | M103 | Lyra RSV+HMPV Assay | OEM,OCC | Human metapneumovirus (hmpv) rna assay system,Respiratory virus panel nucleic ac Human metapneumovirus (hmpv) rna assay system,Respiratory virus panel nucleic acid assay system | 2 | Lyra |
43 | 30014613311003 | M100 | M100 | Lyra FLU A+B Assay | OOI,OZE,OCC | real time Nucleic acid amplification system,Influenza A and influenza B multiple real time Nucleic acid amplification system,Influenza A and influenza B multiplex nucleic acid assay,Respiratory virus panel nucleic acid assay system | 2 | Lyra |
44 | 30014613338703 | 01-00020 | 01-00020 | CMV Antigen Control Slides | LJG | QUALITY CONTROL SLIDES | 1 | D3 |
45 | 30014613338697 | 01-00010 | 01-00010 | Chlamydia Antigen Control Slides | LJG | QUALITY CONTROL SLIDES | 1 | D3 |
46 | 30014613338680 | 01-00070.v2 | 01-00070.v2 | hMPV Antigen Control Slides | LJG | QUALITY CONTROL SLIDES | 1 | D3 |
47 | 30014613338673 | 01-00060 | 01-00060 | VZV Antigen Control Slides | LJG | QUALITY CONTROL SLIDES | 1 | D3 |
48 | 30014613338666 | 01-00100 | 01-00100 | HSV-1/HSV-2 Antigen Control Slides | LJG | QUALITY CONTROL SLIDES | 1 | D3 |
49 | 30014613338659 | 01-002007b | 01-002007b | Mounting Fluid (pH 8.0-8.4) | LEB | MOUNTING MEDIA | 1 | D3 |
50 | 30014613338642 | 01-014010 | 01-014010 | Respiratory Virus Antigen Control Slides (8 well slide, 7 viruses, 1 negative well) | LJG | QUALITY CONTROL SLIDES | 1 | D3 |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 03573026403997 | 69-010B-US | ADENOVIRUS R-gene® KIT US is a RT-PCR test is to aid in the diagnosis of respira ADENOVIRUS R-gene® KIT US is a RT-PCR test is to aid in the diagnosis of respiratory Adenovirus infection in humans in conjunction with other clinical and laboratory findings. | ARGENE® ADENOVIRUS R-gene KIT US | BIOMERIEUX SA | |
2 | 00875197005950 | 08160104190 | 08160104190 | cobas® Influenza A/B & RSV Nucleic acid test for use on the cobas® Liat® System | ROCHE MOLECULAR SYSTEMS, INC. | |
3 | 00875197005653 | 07402686190 | 07402686190 | cobas® Influenza A/B &RSV Quality Control Kit for use on the cobas® Liat® System | ROCHE MOLECULAR SYSTEMS, INC. | |
4 | 00875197005639 | 07402660190 | 07402660190 | cobas® Influenza A/B Quality Control Kit for use on the cobas® Liat® System | ROCHE MOLECULAR SYSTEMS, INC. | |
5 | 00875197005608 | 07341890190 | 07341890190 | cobas® Influenza A/B Nucleic acid test for use on the cobas® Liat® System | ROCHE MOLECULAR SYSTEMS, INC. | |
6 | 00857573006324 | 20-011-024 | The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a mult 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 | NANOSPHERE, INC. | |
7 | 00857573006294 | 20-011-020 | The Verigene® Respiratory Virus Plus Nucleic Acid Test (RV+) on the Verigene® The Verigene® Respiratory Virus Plus Nucleic Acid Test (RV+) on the Verigene® System is a qualitative nucleic acid multiplex test intended to simultaneously detect and identify multiple respiratory virus nucleic acids in nasopharyngeal (NP) swab specimens from individuals with signs and symptoms of respiratory tract infection. | Respiratory Virus Plus (RV+) Amplification Tray | NANOSPHERE, INC. | |
8 | 00857573006263 | 20-009-024 | The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a mult 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 | NANOSPHERE, INC. | |
9 | 00857573006232 | 20-009-020 | The Verigene® Respiratory Virus Plus Nucleic Acid Test (RV+) on the Verigene The Verigene® Respiratory Virus Plus Nucleic Acid Test (RV+) on the Verigene® System is a qualitative nucleic acid multiplex test intended to simultaneously detect and identify multiple respiratory virus nucleic acids in nasopharyngeal (NP) swab specimens from individuals with signs and symptoms of respiratory tract infection. | Respiratory Virus Plus (RV+) Extraction Tray | NANOSPHERE, INC. | |
10 | 00857573006164 | 20-006-024 | The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a mult 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 | NANOSPHERE, INC. | |
11 | 00857573006133 | 20-006-020 | The Verigene® Respiratory Virus Plus Nucleic Acid Test (RV+) on the Verigene The Verigene® Respiratory Virus Plus Nucleic Acid Test (RV+) on the Verigene® System is a qualitative nucleic acid multiplex test intended to simultaneously detect and identify multiple respiratory virus nucleic acids in nasopharyngeal (NP) swab specimens from individuals with signs and symptoms of respiratory tract infection. | Respiratory Virus Plus (RV+) Nucleic Acid Test Cartridge | NANOSPHERE, INC. | |
12 | 00857167005030 | ePlex Respiratory Panel (RP) | EA001012 | ePlex Respiratory Panel Kit, 12 test, IVD | ePlex System | GENMARK DIAGNOSTICS, INC. |
13 | 00857167005023 | ePlex Respiratory Panel (RP) | KT022006 | ePlex Sample Delivery Device RP Panel | ePlex System | GENMARK DIAGNOSTICS, INC. |
14 | 00857167005016 | ePlex Respiratory Panel (RP) | KT022287 | Respiratory Panel Cartridge | ePlex System | GENMARK DIAGNOSTICS, INC. |
15 | 00851458005112 | 1.5 | FLM1-ASY-0121 | NGDS FilmArray Instrument | FILMARRAY | BIOFIRE DEFENSE, LLC |
16 | 00851458005068 | JRPD-ASY-0137 | JRPD-ASY-0137 | JBAIDS IVD Influenza A & B Detection Kit | JBAIDS | BIOFIRE DEFENSE, LLC |
17 | 00851034007073 | 01 | 63-R0001 | In-vitro multiplex assay used with the Biocode MDx 3000 for the detection of res In-vitro multiplex assay used with the Biocode MDx 3000 for the detection of respiratory pathogens. | BioCode Respiratory Pathogen Panel | APPLIED BIOCODE, INC. |
18 | 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 |
19 | 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 |
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 | 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 |
22 | 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 |
23 | 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 |
24 | 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 | |
25 | 00815381020161 | RFIT-ASY-0130 | RFIT-ASY-0130 | IVD reagent kit containing 6 tests | FilmArray® Respiratory Panel 2 (RP2) | BIOFIRE DIAGNOSTICS, LLC |
26 | 00815381020154 | RFIT-ASY-0129 | RFIT-ASY-0129 | IVD reagent kit containing 30 tests | FilmArray® Respiratory Panel 2 (RP2) | BIOFIRE DIAGNOSTICS, LLC |
27 | 00815381020147 | RFIT-ASY-0120 | RFIT-ASY-0120 | IVD reagent kit containing 30 tests. | FilmArray® Respiratory Panel (RP) EZ | BIOFIRE DIAGNOSTICS, LLC |
28 | 00815381020079 | RFIT-ASY-0125 | RFIT-ASY-0125 | IVD reagent kit containing 6 tests. | FilmArray® Respiratory Panel (RP) | BIOFIRE DIAGNOSTICS, LLC |
29 | 00815381020062 | RFIT-ASY-0124 | RFIT-ASY-0124 | IVD reagent kit containing 30 tests. | FilmArray® Respiratory Panel (RP) | BIOFIRE DIAGNOSTICS, LLC |
30 | B540FAB1100CWC0 | FAB1100CW-C | FAB1100CW-1 | The Accula™ Flu A / B Control Kit is intended for in vitro diagnostic use in qua The Accula™ Flu A / B Control Kit is intended for in vitro diagnostic use in qualitycontrol testing with the Accula™ Flu A / B Test. | Accula Flu A / B Control Kit | MESA BIOTECH, INC. |
31 | B540FAB1100CW0 | FAB1100CW | FAB1100CW | The Accula™ Flu A / B Test performed on the Accula Dock is a molecular in vitro The Accula™ Flu A / B Test performed on the Accula Dock is a molecular in vitro diagnostic test utilizing polymerasechain reaction (PCR) and lateral flow technology for the qualitative, visual detection and differentiation of influenza A andinfluenza B viral RNA. The Accula Flu A / B Test uses a nasal swab specimen collected from patients with signs andsymptoms of respiratory infection. Accula Flu A / B assay is intended as an aid in the diagnosis of influenza infectionsin conjunction with clinical and epidemiological risk factors. The assay is not intended to detect the presence of influenzaC virus. | Accula Flu A / B Test | MESA BIOTECH, INC. |
32 | B540D20010 | D2001 | D2001 | The Programming Cassette is an accessory to the Accula Dock and facilitates repr The Programming Cassette is an accessory to the Accula Dock and facilitates reprogramming of the Dock’s embedded firmware. When firmware updates are needed, the firmware will be stored onto Programming Cassettes and sent to end users, who will load the Programming Cassette into their Dock and re-program its firmware | Accula Programming Cassette | MESA BIOTECH, INC. |
33 | B540D20000 | D2000 | D2000 | The Accula Dock is an electronic module which executes in vitro diagnostic tests The Accula Dock is an electronic module which executes in vitro diagnostic tests on compatible Test Cassettes. It consists of anelectro-mechanical interface to a single Test Cassette. The Dock contains all electrical systems, controls and logic necessary toorchestrate in-vitro diagnostic tests within the inserted Test Cassette. | Accula Dock | MESA BIOTECH, INC. |
34 | B54010400 | 1040 | 1040 | The Silaris™ RSV Test performed on the Silaris™ Dock is a molecular in vitro dia The Silaris™ RSV Test performed on the Silaris™ Dock is a molecular in vitro diagnostic test utilizing polymerase chainreaction (PCR) and lateral flow technologies for the qualitative, visual detection of respiratory syncytial virus (RSV) viral RNA.The Silaris RSV Test uses a nasal swab specimen collected from patients with signs and symptoms of respiratory infection.The Silaris RSV Test is intended as an aid in the diagnosis of RSV infection in children and adults in conjunction with clinicaland epidemiological risk factors. | Silaris RSV Supplemental Pack | MESA BIOTECH, INC. |
35 | B54010350 | 1035 | 1035 | The Silaris™ Influenza A&B Test performed on the Silaris Dock is a molecular in The Silaris™ Influenza A&B Test performed on the Silaris Dock is a molecular in vitro diagnostic test utilizing polymerasechain reaction (PCR) and lateral flow technology for the qualitative, visual detection and differentiation of influenza A andinfluenza B viral RNA. The Silaris Influenza A&B Test uses a nasal swab specimen collected from patients with signs andsymptoms of respiratory infection. Silaris Influenza A&B assay is intended as an aid in the diagnosis of influenza infectionsin conjunction with clinical and epidemiological risk factors. The assay is not intended to detect the presence of influenzaC virus. | Sialris Influenza A&B Supplemental Pack | MESA BIOTECH, INC. |
36 | B54010290 | 1029 | 1029 | The Silaris RSV Control Kit is intended for in vitro diagnostic use in quality c The Silaris RSV Control Kit is intended for in vitro diagnostic use in quality control testing with the Silaris RSV Test | Silaris RSV Control Kit | MESA BIOTECH, INC. |
37 | B54010280 | 1028 | 1028 | The Silaris Starter Pack contains two (2) Silaris Influenza A&B kits and one (1) The Silaris Starter Pack contains two (2) Silaris Influenza A&B kits and one (1) Silaris Dock for the purposes of starting up a clinical location. | SilarisTM Influenza A&B Starter Pack | MESA BIOTECH, INC. |
38 | B54010270 | 1027 | 1027 | The Silaris™ Influenza A&B Test performed on the Silaris Dock is a molecular in The Silaris™ Influenza A&B Test performed on the Silaris Dock is a molecular in vitro diagnostic test utilizing polymerasechain reaction (PCR) and lateral flow technology for the qualitative, visual detection and differentiation of influenza A andinfluenza B viral RNA. The Silaris Influenza A&B Test uses a nasal swab specimen collected from patients with signs andsymptoms of respiratory infection. Silaris Influenza A&B assay is intended as an aid in the diagnosis of influenza infectionsin conjunction with clinical and epidemiological risk factors. The assay is not intended to detect the presence of influenzaC virus. | Silaris Influenza A&B Test | MESA BIOTECH, INC. |
39 | B54010240 | 1024 | 1024 | The Silaris™ Influenza A&B Control Kit is intended for in vitro diagnostic use i The Silaris™ Influenza A&B Control Kit is intended for in vitro diagnostic use in qualitycontrol testing with the Silaris™ Influenza A&B Test. | Silaris Influenza A&B Control Kit | MESA BIOTECH, INC. |
40 | 30014613336143 | M306 | M306 | Solana RSV/hMPB Assay | Solana | DIAGNOSTIC HYBRIDS, INC. |
41 | 30014613336068 | M300 | M300 | Solana Infulenza A+B Assay | Solana | DIAGNOSTIC HYBRIDS, INC. |
42 | 30014613311133 | Adenovirus Assay | M113 | Lyra Adenovirus Assay | Lyra | QUIDEL CORPORATION |
43 | 30014613311034 | M103 | M103 | Lyra RSV+HMPV Assay | Lyra | DIAGNOSTIC HYBRIDS, INC. |
44 | 30014613311003 | M100 | M100 | Lyra FLU A+B Assay | Lyra | DIAGNOSTIC HYBRIDS, INC. |
45 | 20816101025552 | MOL2660 | Simplexa™ Flu A/B & RSV Positive Control Pack | DIASORIN MOLECULAR LLC | ||
46 | 20816101025545 | MOL2650 | Simplexa™ Flu A/B & RSV Direct | DIASORIN MOLECULAR LLC | ||
47 | 20816101025538 | MOL2600 | Simplexa™ Flu A/B & RSV | DIASORIN MOLECULAR LLC | ||
48 | 15420045509320 | AMR CTRLS, PANTHER FUSION, IVD | PRD-04338 | PANTHER FUSION | HOLOGIC, INC. | |
49 | 15420045509313 | FLU A B RSV CTRLS, PANTHER FUSION, IVD | PRD-04336 | PANTHER FUSION | HOLOGIC, INC. | |
50 | 15420045509290 | AMR KIT, PANTHER FUSION, 96T, IVD | PRD-04330 | PANTHER FUSION | HOLOGIC, INC. |