-
,for, Item ID-
- #1184027
- Providers like you icon 28
- Binx Health #2.555.009
Molecular Analyzer Binx io® CLIA Waived
STARTER PACK, DEMO BINX IO IN STRUMENT D/S
Features
- binxo io® Instrument Demo Starter Pack
- Starter Kit: binx io Instrument (3.001.001), CT / NG Test Cartridges (1.002.110), io Male Urine Speciment Kit (5.002.001), io Vaginal Swab Specimen Collection Kit (5.012.001)
- First ever FDA 510(k), CLIA-Waived CT/NG molecular test for males and females, enabling same-visit diagnosis and treatment
- More …
Product Details Email
Product Specifications
| McKesson # | 1184027 |
|---|---|
| Manufacturer # | 2.555.009 |
| Brand | binx io® |
| Manufacturer | Binx Health |
| Country of Origin | United Kingdom |
| Analyzer Type | Benchtop |
| Application | Molecular Analyzer |
| Buy American Act (BAA) Compliant | No |
| CLIA Classification | CLIA Waived |
| CLIA Classified | CLIA Waived |
| Contents 1 | binx io Instrument, binx io CT / NG Assay Cartridges, Vaginal Swab Specimen Collection Kit, Male Urine Specimen Collection Kit |
| Dimensions | 275 X 277 X 384 mm |
| Is_ECAT | Y |
| Is_GSA | N |
| Is_VA | N |
| Number of Tests | 10 Tests |
| Power Source | 100 to 240VAC, 50/60Hz |
| Purchase Program Type | Standard Purchase Agreement |
| Sample Type | Vaginal Swab / First Catch Urine Sample |
| Test Name | Chlamydia Trachomatis / Neisseria Gonorrhoeae (CT / NG) |
| Time to Results | 30 Minute Time to Results |
| Trade Agreement Act (TAA) Compliant | Yes |
| UNSPSC Code | 41115822 |
| User Interface | Touchscreen Display |
| Weight | 10.2 kg |
Features
- binxo io® Instrument Demo Starter Pack
- Starter Kit: binx io Instrument (3.001.001), CT / NG Test Cartridges (1.002.110), io Male Urine Speciment Kit (5.002.001), io Vaginal Swab Specimen Collection Kit (5.012.001)
- First ever FDA 510(k), CLIA-Waived CT/NG molecular test for males and females, enabling same-visit diagnosis and treatment
- 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
- The binx health io CT/NG Assay is intended for use with female vaginal swab specimens, collected either by a clinician or self-collected by a patient in a clinical setting, or male urine specimens, as an aid in the diagnosis of symptomatic or asymptomatic Chlamydia trachomatis and/or Neisseria gonorrhoeae infection
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