Comparison |
CLIA Classification |
| | | | CLIA Waived for Female Vaginal Swabs / Male Urine |
CLIA Classified |
CLIA Waived | CLIA Non-Waived | CLIA Non-Waived | CLIA Waived | CLIA Waived Sample Dependent |
Contents 1 |
GeneXpert Instrument, Ext. CD-ROM Drive | | | Power Supply Adapter, Barcode Scanner, Alere Universal Printer, Alere™ i USB Drive, Instrument User Manual, and Intrument Quick Start Guide | |
Country of Origin |
Unknown | Unknown | Unknown | United States | Germany |
Dimensions |
11-1/2 X 16 X 18 Inch | 153 X 307 X 428 mm | 234 X 326 X 517 mm | 8.15 X 5.71 X 7.64 Inch | |
For Use With |
For Single-Use Disposable Cartridge | For QIAstat-DX Analyzer | For QIAstat-DX Analyzer | | |
Power Source |
100 V, 50/60 Hz | 90 to 264 VAC, 50/60 Hz | 90 to 264 VAC, 50/60 Hz | 12V Power Supply | |
Purchase Program Type |
Standard Purchase Agreement | Standard Purchase Agreement | Standard Purchase Agreement | Placement Promotion Bundle | Standard Purchase Agreement |
Readout Type |
Color Touch Display | | | Digital Readout, Printout | |
Sample Capacity |
| | | Single Sample Capacity | |
Sample Type |
| | | | Vaginal Swab / First Catch Urine Sample |
Test Name |
Extensive PCR Test Menu | | | Infectious Diseases | Chlamydia Trachomatis / Neisseria Gonorrhoeae (CT / NG) |
Time to Results |
20 to 30 Minutes | | | 15 Minute Results | 30 Minute Time to Results |
UNSPSC Code |
41115843 | 41115843 | 41115843 | 41115807 | 41115843 |
User Interface |
Touchscreen Tablet, Barcode Scanner | | | TouchScreen | |
Weight |
41 lbs. | 16 kg | 5 kg | 3.0 kg | |
Analyzer Type |
Benchtop | Benchtop | Benchtop | Benchtop | Benchtop |
Application |
Molecular Analyzer | Molecular Analyzer | Molecular Analyzer | Molecular Analyzer | Molecular 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
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- Module contains the hardware and software for sample testing and analysis
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- Module enables interaction with the QIAstat-Dx Analyzer
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- 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
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- 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
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