Real Time Nucleic Acid Amplification System
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Real Time Nucleic Acid Amplification System
APPLIED BIOCODE, INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
1 | 0 | - | ||
41-A0051 | 0 | - |
BIOFIRE DEFENSE, LLC | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
NGDS-ASY-0006 | 0 | - |
BIOFIRE DIAGNOSTICS, LLC | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
RFIT-ASY-0120 | 0 | - | ||
RFIT-ASY-0126 | 0 | - | ||
RFIT-ASY-0127 | 0 | - | ||
RFIT-ASY-0136 | 0 | - | ||
RFIT-ASY-0137 | 0 | - |
LUMINEX CORPORATION | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
10-0000-02 | 0 | - | ||
10-0000-02R | 0 | - | ||
10-0000-07 | 0 | - | ||
10-0000-07R | 0 | - | ||
50-10026 | 0 | - | ||
50-10041 | 0 | - | ||
ARIES M12V1 | 0 | - | ||
ARIES M6V1 | 0 | - | ||
CN-SW47 | 0 | - |
Luminex Molecular Diagnostics, Inc | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
I051C0447 | 0 | - |
Meridian Bioscience Canada Inc | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
410400 | 0 | - | ||
410500 | 0 | - |
MERIDIAN BIOSCIENCE, INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
279890 | 0 | - | ||
279910 | 0 | - | ||
279940 | 0 | - | ||
280150 | 0 | - | ||
280250 | 0 | - | ||
280550 | 0 | - | ||
410200 | 0 | - | ||
410400 | 0 | - | ||
410500 | 0 | - | ||
479890 | 0 | - | ||
479910 | 0 | - | ||
480150 | 0 | - | ||
480250 | 0 | - | ||
610172 | 0 | - | ||
610189 | 0 | - | ||
610208 | 0 | - | ||
610210 | 0 | - |
NANOSPHERE, INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
10-0000-02 | 0 | - | ||
10-0000-02R | 0 | - | ||
10-0000-07 | 0 | - | ||
10-0000-07R | 0 | - |
Roche Molecular Systems, Inc. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
05170486190 | 0 | - | ||
05170516190 | 0 | - | ||
05205727190 | 0 | - | ||
05205743190 | 0 | - | ||
05235847190 | 0 | - | ||
05235936190 | 0 | - | ||
05235944190 | 0 | - | ||
06768113190 | 0 | - | ||
06768172190 | 0 | - |
321 Results
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Name
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Description
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Verigene® Processor SP (Refurbished)
NANOSPHERE, INC.
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)
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Verigene® Reader (Refurbished)
NANOSPHERE, INC.
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)
0
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Verigene® Processor SP
NANOSPHERE, INC.
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.
0
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Verigene® Reader
NANOSPHERE, INC.
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.
0
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NGDS
BIOFIRE DEFENSE, LLC
FilmArray® NGDS Warrior Panel - IVD reagent Biothreat Detection Kit containing 30 tests.
0
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Gastrointestinal Pathogen Panel (GPP) Kit
APPLIED BIOCODE, INC.
In-vitro multiplex assay used with the Biocode MDx 3000 for the detection of gastrointestinal pathogens.
0
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BioCode MDx 3000
APPLIED BIOCODE, INC.
The BioCode MDx 3000 is an automated molecular diagnostic system for use with Applied BioCode’s Barcoded Magnetic Beads (BMB) assays.
0
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Revogene Carba C
MERIDIAN BIOSCIENCE, INC.
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.
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Revogene GBS LB
MERIDIAN BIOSCIENCE, INC.
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.
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Revogene Mock Pie
MERIDIAN BIOSCIENCE, INC.
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.
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Revogene Strep A
MERIDIAN BIOSCIENCE, INC.
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.
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Revogene
MERIDIAN BIOSCIENCE, INC.
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.
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Alethia™ Group A Streptococcus
MERIDIAN BIOSCIENCE, INC.
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.
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Alethia™ Mycoplasma Direct
MERIDIAN BIOSCIENCE, INC.
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.
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Alethia™ Group A Streptococcus External Control Kit
MERIDIAN BIOSCIENCE, INC.
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.
0
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Alethia™ Mycoplasma Direct External Control Kit
MERIDIAN BIOSCIENCE, INC.
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.
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Alethia™
MERIDIAN BIOSCIENCE, INC.
Alethia™ is an automated isothermal amplification and detection system for use with Meridian Bioscience, Inc.’s Alethia Loop-Mediated Amplification assays.
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illumigene Group A Streptococcus
MERIDIAN BIOSCIENCE, INC.
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.
0
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illumigene Group A Streptococcus External Control Kit
MERIDIAN BIOSCIENCE, INC.
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.
0
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illumigene Mycoplasma Direct External Control Kit
MERIDIAN BIOSCIENCE, INC.
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.
0
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illumigene Mycoplasma Direct
MERIDIAN BIOSCIENCE, INC.
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.
0
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illumipro-10
MERIDIAN BIOSCIENCE, INC.
The illumipro-10 is an automated isothermal amplification and detection system for use with Meridian Bioscience, Inc. illumigene Loop-Mediated Amplification products.
0
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illumigene Mycoplasma
MERIDIAN BIOSCIENCE, INC.
"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.
0
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illumigene Mycoplasma External Control Kit
MERIDIAN BIOSCIENCE, INC.
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.
0
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ARIES® System
LUMINEX CORPORATION
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.
0
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Verigene® Processor SP (Refurbished)
LUMINEX CORPORATION
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)
0
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Verigene® Processor SP
LUMINEX CORPORATION
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.
0
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Verigene® Reader (Refurbished)
LUMINEX CORPORATION
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)
0
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ARIES® Group A Strep Assay
LUMINEX CORPORATION
The ARIES® Group A Strep Assay is a real-time polymerase chain reaction (PCR) based qualitative in vitro diagnostic test for the direct detection of Streptococcus pyogenes (Group A ß-hemolytic Streptococcus) in throat swab specimens from patients with signs and symptoms of pharyngitis.
0
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SYNCT™ Software
LUMINEX CORPORATION
The SYNCT Software is a desktop application that can be utilized by an end-user on a standalone computer, providing users the ability to operate general functions such as Order Management, with or without a Laboratory Information System (LIS), viewing test results, reviewing and preparing test reports, performing software administrative functions, and providing security control for permitted functions.
0
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NxTAG® Respiratory Pathogen Panel
Luminex Molecular Diagnostics, Inc
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.
0
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Verigene® Reader
LUMINEX CORPORATION
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.
0
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ARIES® M1 System
LUMINEX CORPORATION
The ARIES® M1 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.
0
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ARIES® Extraction Kit
LUMINEX CORPORATION
The ARIES® Extraction Kit is intended to extract nucleic acid from human biological specimens and universal transport media (UTM).
0
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FilmArray® Respiratory Panel 2 plus (RP2plus)
BIOFIRE DIAGNOSTICS, LLC
IVD reagent kit containing 6 tests
0
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FilmArray® Respiratory Panel 2 plus (RP2plus)
BIOFIRE DIAGNOSTICS, LLC
IVD reagent kit containing 30 tests
0
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FilmArray® Respiratory Panel (RP) EZ
BIOFIRE DIAGNOSTICS, LLC
IVD reagent kit containing 30 tests.
0
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Revogene® Strep A
Meridian Bioscience Canada Inc
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 obtained from patients with signs and symptoms of pharyngitis. The Revogene Strep A assay is intended for use as an aid in the diagnosis of Group A Streptococcus infection.
0
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Revogene® Carba C
Meridian Bioscience Canada Inc
The Revogene® Carba C 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 test utilizes automated real-time Polymerase Chain Reaction (PCR).The Revogene Carba C assay should be used in conjunction with other laboratory tests including phenotypic antimicrobial susceptibility testing. A negative Revogene Carba C assay result does not preclude the presence of other resistance mechanisms.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. The identification of a blaIMP, blaNDM or blaVIM metallo-B-lactamase gene (i.e., the genes that encode the IMP, NDM and VIM metallo-B-lactamases, respectively) may be used as an aid to clinicians in determining appropriate therapeutic strategies for patients with known or suspected carbapenem non-susceptible infections.