Comparison |
CLIA Classification |
| | | | CLIA Waived for Female Vaginal Swabs / Male Urine |
CLIA Classified |
CLIA Non-Waived | CLIA Non-Waived | CLIA Non-Waived | CLIA Waived | CLIA Waived Sample Dependent |
Contents 1 |
Single Module Instrument with Desktop, Reagent | | | 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 |
4 X 11.7 X 12 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 |
1.5 A at 100 V, 0.75 A at 200 V | 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 |
| | | Digital Readout, Printout | |
Sample Capacity |
| | | Single Sample Capacity | |
Sample Type |
Dye Sample | | | | Vaginal Swab / First Catch Urine Sample |
Test Name |
Extensive PCR Test Menu | | | Infectious Diseases | Chlamydia Trachomatis / Neisseria Gonorrhoeae (CT / NG) |
Time to Results |
| | | 15 Minute Results | 30 Minute Time to Results |
UNSPSC Code |
41115843 | 41115843 | 41115843 | 41115807 | 41115843 |
User Interface |
| | | TouchScreen | |
Weight |
| 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 |
- 1 Reaction site
- Fully integrated and automated single module on-demand molecular diagnostic system
- Single module instrument
- Heating ramp rates (max.): 10°C/sec from 50 to 95°C
- Cooling ramp rates (max.): 2.5°C/sec from 95 to 50°C
- Temperature duration accuracy: ± 1.0 sec From programmed time
- Temperature accuracy: ± 1.0°C from 60 to 95°C
- Melt curve programmable ramp rates: 0.01°C/seconds to 1.0°C/seconds
- The GeneXpert® system fully integrates and automates sample extraction, amplification and detection — all in one 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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