Other products from "CEPHEID"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 07332940003821 INFINITY 80-24 900-0496 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
2 07332940003937 GXIV-1-R 900-0510R OOI Real Time Nucleic Acid Amplification System 2 Certified Pre-Owned GeneXpert Dx System
3 07332940003838 INFINITY 80-16 900-0495 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
4 07332940003814 INFINITY 80-32 900-0497 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
5 07332940003975 INFINITY 80-72 900-0502 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
6 07332940003968 INFINITY 80-80 900-0503 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
7 07332940006860 INFINITY 48-48 900-0457 XPERT, GENEXPERT DX SYSTEM OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
8 07332940006853 INFINITY 48-40 900-0456 Additional catalog number: 900-0456R OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
9 07332940006846 INFINITY 48-32 900-0455 Additional catalog number: 900-0455R OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
10 07332940006839 INFINITY 48-24 900-0454 Additional catalog number: 900-0454R OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
11 07332940004002 INFINITY 80-48 900-0499 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
12 07332940004019 INFINITY 80-40 900-0498 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
13 07332940003999 INFINITY 80-56 900-0500 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
14 07332940003982 INFINITY 80-64 900-0501 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-80 System
15 07332940003449 GXIV-4 900-0065 XPERT, GENEXPERT DX SYSTEM OOI,NJR Real Time Nucleic Acid Amplification System,Nucleic Acid Amplification Assay Sys Real Time Nucleic Acid Amplification System,Nucleic Acid Amplification Assay System, Group B Streptococcus, Direct Specimen Test 1 GeneXpert Dx System
16 07332940002558 SWAB/A-50 SWAB/A-50 Xpert Vaginal/Endocervical Specimen Collection Kit; 50 pack LIO Device, Specimen Collection 1 Xpert Vaginal/Endocervical Specimen Collection Kit
17 07332940001032 GXCARBAR-10 GXCARBAR-10 Xpert Carba-R test; 10 test kit POC,PMY System, Nucleic Acid Amplification Test, Dna, Antimicrobial Resistance Marker, D System, Nucleic Acid Amplification Test, Dna, Antimicrobial Resistance Marker, Direct Specimen,System, Nucleic Acid Amplification Test, Dna, Carbapenem Non-Susceptible Gram Negative Organism, Colony 2 Xpert Carba-R
18 07332940007669 GXGBSLBXC GXGBSLBXC-120 GBS LB XC NJR Nucleic Acid Amplification Assay System, Group B Streptococcus, Direct Specimen Test 1 Xpert®
19 07332940007652 GXGBSLBXC GXGBSLBXC-10 GBS LB XC NJR Nucleic Acid Amplification Assay System, Group B Streptococcus, Direct Specimen Test 1 Xpert®
20 07332940008345 SWAB/G-50-US SWAB/G-50-US Swab Specimen Collection Kit PQA Vaginitis And Bacterial Vaginosis Nucleic Acid Detection System 2 Xpert®
21 07332940007072 XPRSMVP-10 XPRSMVP-10 Xpert Xpress MVP PQA Vaginitis And Bacterial Vaginosis Nucleic Acid Detection System 2 Xpert®
22 07332940007003 SWAB/G-50 SWAB/G-50 Xpert Swab Specimen Collection Kit; 50 pack QBD Microbial Nucleic Acid Storage And Stabilization Device 2 Xpert Swab Specimen Collection Kit
23 07332940006457 SWAB/F-100 SWAB/F-100 Nasal Sample Collect Kit for Viruses JSM Culture Media, Non-Propagating Transport 1 Xpert®
24 07332940002954 URINE/A-50 URINE/A-50 Xpert Urine Specimen Collection Kit; 50 pack LIO Device, Specimen Collection 1 Xpert Urine Specimen Collection Kit
25 07332940000936 GXHEMOSIL-10 GXHEMOSIL-10 Xpert HemosIL FII & FV kit; 10 test kit NPQ,NPR Test, Factor V Leiden Mutations, Genomic Dna Pcr,Test, Factor Ii G20210a Mutatio Test, Factor V Leiden Mutations, Genomic Dna Pcr,Test, Factor Ii G20210a Mutations, Genomic Dna Pcr 2 Xpert HemosIL FII & FV
26 07332940006044 XPRSFLU-10 XPRSFLU-10 Xpert Xpress Flu kit; 10 test kit OCC Respiratory Virus Panel Nucleic Acid Assay System 2 Xpert Xpress Flu
27 07332940001001 GXTV-10 GXTV-10 Xpert TV kit; 10 test kit OUY Trichomonas Vaginalis Nucleic Acid Amplification Test System 2 Xpert TV
28 07332940000974 GXNOV-10 GXNOV-10 Xpert Norovirus kit; 10 test kit PCH Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System 2 Xpert Norovirus
29 07332940000097 GXEV-100N-10 GXEV-100N-10 Xpert EV kit; 10 test kit OAI Assay, Enterovirus Nucleic Acid 2 Xpert EV
30 07332940005696 XPRSFLU/RSV-10 XPRSFLU/RSV-10 Xpert Xpress Flu/RSV kit; 10 test kit OCC Respiratory Virus Panel Nucleic Acid Assay System 2 Xpert Xpress Flu/RSV
31 07332940000783 GXFLU/RSV-10 GXFLU/RSV-10 Xpert FLU/RSV XC kit; 10 test kit OCC Respiratory Virus Panel Nucleic Acid Assay System 2 Xpert FLU/RSV XC
32 07332940004347 INFINITY48-24 900-0537 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-48s System
33 07332940004330 INFINITY 48-32 900-0538 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-48s System
34 07332940004323 INFINITY 48-40 900-0539 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-48s System
35 07332940004354 INFINITY48-16 900-0536 OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-48s System
36 07332940004316 INFINITY 48-48 900-0540 Additional catalog numbers: 900-0540L, 900-0540R OOI Real Time Nucleic Acid Amplification System 2 GeneXpert Infinity-48s System
37 07332940002565 SWAB/B-100 SWAB/B-100 Xpert Nasopharyngeal Sample Collection Kit; 100 pack JSM Culture Media, Non-Propagating Transport 1 Xpert Nasopharyngeal Sample Collection Kit
38 07332940002442 GXMRSA-120 GXMRSA-120 Xpert MRSA kit; 120 test kit NQX System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococc System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen 2 Xpert MRSA
39 07332940001728 GXMRSA-NXG-120 GXMRSA-NXG-120 Xpert MRSA NxG kit: 120 test kit NQX System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococc System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen 2 Xpert MRSA NxG
40 07332940001711 GXMRSA-NXG-10 GXMRSA-NXG-10 Xpert MRSA NxG kit; 10 test kit NQX System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococc System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen 2 Xpert MRSA NxG
41 07332940000196 GXMRSA-100N-10 GXMRSA-100N-10 Xpert MRSA kit; 10 test kit NQX System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococc System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen 2 Xpert MRSA
42 07332940000189 GXMRSA/SA-SSTI-10 GXMRSA/SA-SSTI-10 Xpert MRSA/SA SSTI kit; 10 test kit NQX System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococc System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen 2 Xpert MRSA/SA SSTI
43 07332940000141 GXMRSA/SA-BC-10 GXMRSA/SA-BC-10 Xpert MRSA/SA Blood Culture kit; 10 test kit NQX System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococc System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen 2 Xpert MRSA/SA Blood Culture
44 07332940000059 GXCDIFFICILE-120 GXCDIFFICILE-120 Xpert C. difficile test; 120 test kit LLH Reagents, Clostridium Difficile Toxin 1 Xpert C. difficile
45 07332940000035 GXCDIFFICILE-10 GXCDIFFICILE-10 Xpert C. difficile test; 10 test kit LLH Reagents, Clostridium Difficile Toxin 1 Xpert C. difficile
46 07332940006372 XPRSTREPA-10 XPRSTREPA-10 Xpert Xpress Strep A kit; 10 test kit PGX Groups A, C And G Beta-Hemolytic Streptococcus Nucleic Acid Amplification System 2 Xpert Xpress Strep A
47 07332940002503 XPRSTREPA-120 XPRSTREPA-120 Xpert Xpress Strep A kit; 120 test kit PGX Groups A, C And G Beta-Hemolytic Streptococcus Nucleic Acid Amplification System 2 Xpert Xpress Strep A
48 07332940000882 GXGBS-LB-10 GXGBS-LB-10 Xpert GBS LB kit; 10 test kit NJR Nucleic Acid Amplification Assay System, Group B Streptococcus, Direct Specimen Test 1 Xpert GBS LB
49 07332940000806 GXGBS-LB-120 GXGBS-LB-120 Xpert GBS LB kit; 120 test kit NJR Nucleic Acid Amplification Assay System, Group B Streptococcus, Direct Specimen Test 1 Xpert GBS LB
50 07332940007690 GX-IV R2 GX-IV R2 XPERT, GENEXPERT DX SYSTEM OOI,NJR Real Time Nucleic Acid Amplification System,Nucleic Acid Amplification Assay Sys Real Time Nucleic Acid Amplification System,Nucleic Acid Amplification Assay System, Group B Streptococcus, Direct Specimen Test 1 GeneXpert®
Other products with the same Product Codes "OOI, NJR"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00875197005950 08160104190 08160104190 cobas® Influenza A/B & RSV Nucleic acid test for use on the cobas® Liat® System ROCHE MOLECULAR SYSTEMS, INC.
2 00875197005783 07460082190 07460082190 cobas CTNG Positive Control Kit ROCHE MOLECULAR SYSTEMS, INC.
3 00875197005776 07460066190 07460066190 cobas CTNG Qualitative nucleic acid test for use on the cobas 6800/8800 Systems ROCHE MOLECULAR SYSTEMS, INC.
4 00875197005738 07958021190 07958021190 cobas PCR Media Dual Swab Sample Kit ROCHE MOLECULAR SYSTEMS, INC.
5 00875197005721 07958030190 07958030190 cobas&#x00AE PCR Media Uni Swab Sample Kit ROCHE MOLECULAR SYSTEMS, INC.
6 00875197005660 07402759190 07402759190 cobas Liat Cleaning Tool ROCHE MOLECULAR SYSTEMS, INC.
7 00875197005653 07402686190 07402686190 cobas® Influenza A/B &RSV Quality Control Kit for use on the cobas® Liat® System ROCHE MOLECULAR SYSTEMS, INC.
8 00875197005363 2.0 07102577190 cobas® 4800 CT/NG Test v2.0 ROCHE MOLECULAR SYSTEMS, INC.
9 00875197005356 2.0 07102569190 cobas® 4800 CT/NG Test v2.0 ROCHE MOLECULAR SYSTEMS, INC.
10 00875197004441 1.0 06768288190 cobas® MRSA/SA Controls and Cofactor Kit ROCHE MOLECULAR SYSTEMS, INC.
11 00875197004427 1.0 06768172190 cobas® MRSA/SA Test ROCHE MOLECULAR SYSTEMS, INC.
12 00875197004410 1.0 06768113190 cobas® MRSA/SA Test ROCHE MOLECULAR SYSTEMS, INC.
13 00875197003314 1.0 05235944190 cobas® 4800 CT/NG Test ROCHE MOLECULAR SYSTEMS, INC.
14 00875197003307 1.0 05235936190 cobas® 4800 CT/NG Test ROCHE MOLECULAR SYSTEMS, INC.
15 00875197003215 1.0 05235847190 cobas® 4800 System Control Diluent Kit ROCHE MOLECULAR SYSTEMS, INC.
16 00875197002997 1.0 05205743190 LightCycler® Advanced Lysis ROCHE MOLECULAR SYSTEMS, INC.
17 00875197002973 1.0 05205727190 LightCycler® MRSA Advanced Test ROCHE MOLECULAR SYSTEMS, INC.
18 00875197002911 1.0 05170516190 cobas® PCR Female Swab Sample Kit ROCHE MOLECULAR SYSTEMS, INC.
19 00875197002898 1.0 05170486190 cobas® PCR Urine Sample Kit ROCHE MOLECULAR SYSTEMS, INC.
20 00857573006409 10-0000-07R The Verigene® Processor SP is an instrument which integrates sample preparation, The Verigene® Processor SP is an instrument which integrates sample preparation, target amplification, and target hybridization within a single device as part of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications. (Refurbished) Verigene® Processor SP (Refurbished) NANOSPHERE, INC.
21 00857573006393 10-0000-02R The Verigene® Reader is the central control of the Verigene® System, a benchtop The Verigene® Reader is the central control of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications. (Refurbished) Verigene® Reader (Refurbished) NANOSPHERE, INC.
22 00857573006010 10-0000-07 The Verigene® Processor SP is an instrument which integrates sample preparation, The Verigene® Processor SP is an instrument which integrates sample preparation, target amplification, and target hybridization within a single device as part of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications. Verigene® Processor SP NANOSPHERE, INC.
23 00857573006003 10-0000-02 The Verigene® Reader is the central control of the Verigene® System, a benchtop The Verigene® Reader is the central control of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications. Verigene® Reader NANOSPHERE, INC.
24 00851458005099 NGDS-ASY-0006 NGDS-ASY-0006 FilmArray® NGDS Warrior Panel - IVD reagent Biothreat Detection Kit containing 30 tests. NGDS BIOFIRE DEFENSE, LLC
25 00851034007011 1 In-vitro multiplex assay used with the Biocode MDx 3000 for the detection of gas In-vitro multiplex assay used with the Biocode MDx 3000 for the detection of gastrointestinal pathogens. Gastrointestinal Pathogen Panel (GPP) Kit APPLIED BIOCODE, INC.
26 00851034007004 1 41-A0051 The BioCode MDx 3000 is an automated molecular diagnostic system for use with Ap The BioCode MDx 3000 is an automated molecular diagnostic system for use with Applied BioCode’s Barcoded Magnetic Beads (BMB) assays. BioCode MDx 3000 APPLIED BIOCODE, INC.
27 00840733102370 410500 410500 The revogene Carba assay performed on the revogene instrument is a qualitative i The revogene Carba assay performed on the revogene instrument is a qualitative in vitro diagnostic test designed for the detection and differentiation of the blaKPC, blaNDM, blaVIM, blaOXA-48-like and blaIMP gene sequences associated with carbapenem-non-susceptible pure colonies of Enterobacteriaceae, Acinetobacter baumannii, or Pseudomonas aeruginosa, when grown on blood agar or MacConkey agar. The revogene Carba C assay is intended as an aid for infection control in the detection of carbapenem-non-susceptible bacteria that colonize patients in healthcare settings. Revogene Carba C MERIDIAN BIOSCIENCE, INC.
28 00840733102363 410200 410200 The Revogene GBS LB assay performed on the Revogene Instrument is a qualitative The Revogene GBS LB assay performed on the Revogene Instrument is a qualitative in vitro diagnostic test designed to detect Group B Streptococcus (GBS) DNA from 18-24 hour LIM Broth enrichments of vaginal/rectal specimen swabs obtained from pregnant women. The Revogene GBS LB assay utilizes Automated sample processing and real-time polymerase chain reaction (PCR) to detect a cfb gene sequence specific to the Streptococcus agalactiae genome. The Revogene GBS LB assay is indicated for the identification of antepartum GBS colonization and does not provide susceptibility results. it is not intended to diagnose or monitor treatment of GBS infection. Culture isolates are needed for performing susceptibility testing as recommended for penicillin-allergic women. Revogene GBS LB MERIDIAN BIOSCIENCE, INC.
29 00840733102363 410200 410200 The Revogene GBS LB assay performed on the Revogene Instrument is a qualitative The Revogene GBS LB assay performed on the Revogene Instrument is a qualitative in vitro diagnostic test designed to detect Group B Streptococcus (GBS) DNA from 18-24 hour LIM Broth enrichments of vaginal/rectal specimen swabs obtained from pregnant women. The Revogene GBS LB assay utilizes Automated sample processing and real-time polymerase chain reaction (PCR) to detect a cfb gene sequence specific to the Streptococcus agalactiae genome. The Revogene GBS LB assay is indicated for the identification of antepartum GBS colonization and does not provide susceptibility results. it is not intended to diagnose or monitor treatment of GBS infection. Culture isolates are needed for performing susceptibility testing as recommended for penicillin-allergic women. Revogene GBS LB MERIDIAN BIOSCIENCE, INC.
30 00840733102332 610208 610208 The MOCK PIE is a re-usable PIE intended for use in conjunction with the Revogen The MOCK PIE is a re-usable PIE intended for use in conjunction with the Revogene instrument and the Revogene assays. The MOCK Pie simulates the presence of an assay PIE for thermal and rotational balance when the number of assay PIEs is lower than eight in a run. Revogene Mock Pie MERIDIAN BIOSCIENCE, INC.
31 00840733102325 410400 The revogene Strep A assay, performed on the revogene instrument, is an automate The revogene Strep A assay, performed on the revogene instrument, is an automated, qualitative in vitro diagnostic test that utilizes real-time polymerase chain reaction (PCR) for the direct detection of Streptococcus pyogenes (Group A B-hemolytic Streptococcus) nucleic acids from throat swab specimens. The revogene Strep A assay is intended for use as an aid in the diagnosis of the Group A Streptococcus infection.The revogene Strep A assay is intended for use in hospital, reference or state laboratory settings. Revogene Strep A MERIDIAN BIOSCIENCE, INC.
32 00840733102318 610210 610210 The system is a clinical multiplex instrument intended to measure and sort multi The system is a clinical multiplex instrument intended to measure and sort multiple signals generated my multiple probes, intercalating dyes, or other ligands in an assay from a clinical sample. Signals may be generated by fluorescence or other phenomena and may be measured using filters on a photodiode or other detector. It may integrate sample and/or reagent handling, amplification, dedicated instrument control, data acquisition software, raw data storage mechanisms and other essential hardware components along with the signal reader unit. The system is used with specific assays to comprise an assay test system. A real-time thermocycler is intended to identify and/or quantify the presence of specific sequences of double stranded DNA, amplified from a biological source and labeled with fluorescently labeled probes or through the use of intercalating dyes and detect using a high-power light-emitting diode (LED). Fluorescence emission is detected through the use of filters on a photodiode. The emission filters are optimized for use with specific fluorescent dyes. Revogene MERIDIAN BIOSCIENCE, INC.
33 00840733102264 480150 480150 The Alethia™ Group A Streptococcus (Group A Strep) assay, performed on the Aleth The Alethia™ Group A Streptococcus (Group A Strep) assay, performed on the Alethia™ Instrument, is a qualitative in vitro diagnostic test for the detection of Streptococcus pyogenes (Group A beta-hemolytic Streptococcus) in throat swab specimens. The Alethia™ Group A Strep assay utilizes loop-mediated isothermal DNA amplification (LAMP) technology to detect Streptococcus pyogenes by targeting a segment of the Streptococcus pyogenes genome. Results from the Alethia™ Group A Strep assay can be used as an aid in the diagnosis of Group A Streptococcal pharyngitis. The assay is not intended to monitor treatment for Group A Streptococcus infections. Alethia™ Group A Streptococcus MERIDIAN BIOSCIENCE, INC.
34 00840733102196 480350 480350 The Alethia Group B Streptococcus (GBS) assay, performed on the Alethia Incubato The Alethia Group B Streptococcus (GBS) assay, performed on the Alethia Incubator/Reader, is a qualitative in vitro diagnostic for the detection of Streptococcus agalactiae in enriched cultures obtained from vaginal/rectal swab specimens from antepartum women. Enriched cultures are obtained by 18-24 hour incubation of vaginal/rectal swab specimens in selective broth medium, either Lim Broth, TransVag Broth or Carrot Broth.The Alethia GBS assay utilizes loop-mediated isothermal DNA amplification (LAMP) technology to detect Streptococcus agalactiae by targeting a segment of the Streptococcus agalactiae genome. Results from the Alethia GBS assay can be used as an aid in establishing the GBS colonization status of antepartum women. This assay does not diagnose or monitor treatment for GBS infections.The Alethia GBS assay does not provide susceptibility results. Culture isolates are needed for performing susceptibility testing as recommended for penicillin-allergic women.Alethia Group B Streptococcus is intended for use in hospital, reference or state laboratory settings. The device is not intended for nonlaboratory point-of-care use. Alethia™ Group B Streptococcus MERIDIAN BIOSCIENCE, INC.
35 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.
36 00840733102127 479910 479910 The Alethia™ Group A Streptococcus (Group A Strep) External Control Kit contains The Alethia™ Group A Streptococcus (Group A Strep) External Control Kit contains Positive Reagent for use with the Alethia™ Group A Streptococcus DNA Amplification Assay. The External Positive Control Reagent is used in conjunction with the Alethia™ Sample Preparation Apparatus II/Negative Control III reagent provided with the Group A Strep Kit as part of routine Quality Control Testing. External controls are used as part of a routine quality control program. Alethia™ Group A Streptococcus External Control Kit MERIDIAN BIOSCIENCE, INC.
37 00840733102110 479900 479900 The Alethia GBS External Control Kit contains Positive and Negative Control Reag The Alethia GBS External Control Kit contains Positive and Negative Control Reagents for use with the Alethia Group B Streptococcus test kit. External controls are used as part of a routine quality control program. Alethia™ Group B Streptococcus External Control Kit MERIDIAN BIOSCIENCE, INC.
38 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.
39 00840733101663 610189 610189 Alethia™ is an automated isothermal amplification and detection system for use w Alethia™ is an automated isothermal amplification and detection system for use with Meridian Bioscience, Inc.’s Alethia Loop-Mediated Amplification assays. Alethia™ MERIDIAN BIOSCIENCE, INC.
40 00840733101342 280350 280350 The illumigene Group B Streptococcus (GBS) assay, performed on the illumipro-10, The illumigene Group B Streptococcus (GBS) assay, performed on the illumipro-10, is a qualitative in vitro diagnostic for the detection of Streptococcus agalactiae in enriched cultures obtained from vaginal/rectal swab specimens from antepartum women. Enriched cultures are obtained by 18-24 hour incubation of vaginal/rectal swab specimens in selective broth medium, either Lim Broth, TransVag Broth or Carrot Broth.The illumigene GBS assay utilizes loop-mediated isothermal DNA amplification (LAMP) technology to detect Streptococcus agalactiae by targeting a segment of the Streptococcus agalactiae genome. Results from the illumigene GBS assay can be used as an aid in establishing the GBS colonization status of antepartum women. This assay does not diagnose or monitor treatment for GBS infections. illumigene Group B Streptococcus MERIDIAN BIOSCIENCE, INC.
41 00840733101335 280150 280150 The illumigene Group A Streptococcus (Group A Strep) assay, performed on the ill The illumigene Group A Streptococcus (Group A Strep) assay, performed on the illumipro-10, is a qualitative in vitro diagnostic test for the detection of Streptococcus pyogenes (Group A beta-hemolytic Streptococcus) in throat swab specimens.The illumigene Group A Strep assay utilizes loop-mediated isothermal DNA amplification (LAMP) technology to detect Streptococcus pyogenes by targeting a segment of the Streptococcus pyogenes genome. Results from the illumigene Group A Strep assay can be used as an aid in the diagnosis of Group A Streptococcal pharyngitis. The assay is not intended to monitor treatment for Group A Streptococcus infections. illumigene Group A Streptococcus MERIDIAN BIOSCIENCE, INC.
42 00840733101328 279910 279910 The illumigene Group A Streptococcus (Group A Strep) External Control Kit contai The illumigene Group A Streptococcus (Group A Strep) External Control Kit contains Positive Reagent for use with the illumigene Group A Streptococcus DNA Amplification Assay. The External Positive Control Reagent is used in conjunction with the illumigene Sample Preparation Apparatus II/Negative Control III reagent provided with the Group A Strep Kit as part of routine Quality Control Testing. External controls are used as part of a routine quality control program. illumigene Group A Streptococcus External Control Kit MERIDIAN BIOSCIENCE, INC.
43 00840733101311 279900 279900 The illumigene GBS External Control Kit contains Positive and Negative Control R The illumigene GBS External Control Kit contains Positive and Negative Control Reagents for use with the illumigene Group B Streptococcus test kit. External controls are used as part of a routine quality control program. illumigene Group B Streptococcus External Control Kit MERIDIAN BIOSCIENCE, INC.
44 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.
45 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.
46 00840733101243 610172 610172 The illumipro-10 is an automated isothermal amplification and detection system f The illumipro-10 is an automated isothermal amplification and detection system for use with Meridian Bioscience, Inc. illumigene Loop-Mediated Amplification products. illumipro-10 MERIDIAN BIOSCIENCE, INC.
47 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.
48 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.
49 00840487101537 ARIES M12V1 The ARIES® System is a clinical multiplex test system that automates and integra The ARIES® System is a clinical multiplex test system that automates and integrates extraction of nucleic acid from a clinical sample, performs real -time PCR, and measuring and sorting multiple signals generated in an in vitro diagnostic assay. ARIES® System LUMINEX CORPORATION
50 00840487101490 10-0000-07R 10-0000-07R The Verigene® Processor SP is an instrument which integrates sample preparation, The Verigene® Processor SP is an instrument which integrates sample preparation, target amplification, and target hybridization within a single device as part of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications. (Refurbished) Verigene® Processor SP (Refurbished) LUMINEX CORPORATION