Product Comparison


  Cepheid GXIV-4-CLIA

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Abbott Rapid Dx North America LLC IDNOWINTRORAP Binx Health 3.001.001
McKesson # 1153473 1137479 1137476 941195 1184010
Description Molecular Analyzer GeneXpert® Xpress CLIA Waived Molecular Analyzer QIAstat-Dx CLIA Non-Waived Molecular Analyzer QIAstat-Dx CLIA Non-Waived Molecular Analyzer Alere™ i CLIA Waived Molecular Analyzer Binx io® CLIA Waived Sample Dependent
Manufacturer # GXIV-4-CLIA90028149002813IDNOWINTRORAP3.001.001
Brand GeneXpert® XpressQIAstat-DxQIAstat-DxAlere™ ibinx io®
Manufacturer CepheidQiagen LLCQiagen LLCAbbott Rapid Dx North America LLCBinx Health
Invoice DIAGNOSTIC SYSTEM, GENEXPERT XPRESS IV 4MODULE CONFIGURATIONANALYZER, DIAG ANALYTICAL MODULE QIASTAT DXANALYZER, DIAG OPERATIONAL MODULE QIASTAT DXID NOW INTRO KIT, INSTR/SCANNER/PRINTER/CABLE/ LAB PLACEMENTANALYZER, MOLECULAR DIAGNOSTICBINX IO D/S
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Comparison

CLIA Classification CLIA Waived for Female Vaginal Swabs / Male Urine
CLIA Classified CLIA WaivedCLIA Non-WaivedCLIA Non-WaivedCLIA WaivedCLIA Waived Sample Dependent
Contents 1 GeneXpert Instrument, Ext. CD-ROM DrivePower Supply Adapter, Barcode Scanner, Alere Universal Printer, Alere™ i USB Drive, Instrument User Manual, and Intrument Quick Start Guide
Country of Origin UnknownUnknownUnknownUnited StatesGermany
Dimensions 11-1/2 X 16 X 18 Inch153 X 307 X 428 mm234 X 326 X 517 mm8.15 X 5.71 X 7.64 Inch
For Use With For Single-Use Disposable CartridgeFor QIAstat-DX AnalyzerFor QIAstat-DX Analyzer
Power Source 100 V, 50/60 Hz90 to 264 VAC, 50/60 Hz90 to 264 VAC, 50/60 Hz12V Power Supply
Purchase Program Type Standard Purchase AgreementStandard Purchase AgreementStandard Purchase AgreementPlacement Promotion BundleStandard Purchase Agreement
Readout Type Color Touch DisplayDigital Readout, Printout
Sample Capacity Single Sample Capacity
Sample Type Vaginal Swab / First Catch Urine Sample
Test Name Extensive PCR Test MenuInfectious DiseasesChlamydia Trachomatis / Neisseria Gonorrhoeae (CT / NG)
Time to Results 20 to 30 Minutes15 Minute Results30 Minute Time to Results
UNSPSC Code 4111584341115843411158434111580741115843
User Interface Touchscreen Tablet, Barcode ScannerTouchScreen
Weight 41 lbs.16 kg5 kg3.0 kg
Analyzer Type BenchtopBenchtopBenchtopBenchtopBenchtop
Application Molecular AnalyzerMolecular AnalyzerMolecular AnalyzerMolecular AnalyzerMolecular Analyzer
Features and Benefits
  • The GeneXpert Dx System automates and integrates sample preparation, nucleic acid amplification, and detection of the target sequence in simple or complex samples using real-time Polymerase Chain Reaction (PCR)
  • 4-module configuration
  • Front-line Access and Control
  • Reduced footprint - built in barcode scanner and touchscreen tablet
  • Built-in redundancy - each module operates as its own independent analyzer
  • Run up to 4 tests at one time
  • No specialized training or daily maintenance required
  • Operator and QC lockout available
  • Remote IT troubleshooting
  • Simplified remote printing
  • Single-use, self-contained cartridge reduces waste and risk of contamination
  • The system is suited for in vitro diagnostic and research based applications that require hands-off processing of patient samples (specimens) and provides both summarized and detailed test results data in tabular and graphic formats
  • The GeneXpert system can only be used with the GeneXpert cartridge
  • Module contains the hardware and software for sample testing and analysis
  • Module enables interaction with the QIAstat-Dx Analyzer
  • Alere™ i is a rapid, instrument-based, isothermal system for the qualitative detection of infectious diseases
  • Our unique Alere™ i isothermal nucleic acid amplification technology provides molecular results in just minutes, allowing you to make effective clinical decisions sooner
  • The Alere™ i Instrument is factory calibrated and does not require any further calibration and verification
  • Includes Power Supply Adapter, Barcode Scanner, Alere Universal Printer, Alere™ i USB Drive, Instrument User Manual, and Intrument Quick Start Guide
  • Binx io is the first ever, FDA-cleared, molecular point-of-care platform that enables clinicians to test and treat women and men for the most common STIs, chlamydia and gonorrhea, in a single office visit
  • Binx io is a small, desktop instrument that processes a single-use, assay-specific cartridge with no sample preparation necessary
  • The binx io has been cleared by the FDA for use in point-of-care and clinical laboratory settings for the rapid and accurate detection of chlamydia and gonorrhea in vaginal swab and first catch urine samples collected by either a clinician or patient
  • 3.30.21 CLIA waived for binx health io Instrument (use with female vaginal swabs and male urine) for both Chlamydia and Neisseria gonorrhoeae