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Abbott 2IDNOW15C Respiratory Test Kit, COVID-19 2.0 Molecular Diagnostic Rapid, 15 X 24 Tests, For ID Now Instrument US
Contents Include: (2) ID NOW Instruments (NAT024), (15) ID NOW COVID-19 2.0 Test Kits (192000)
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Item#: Abb-2IDNOW15C-EA
$18,859.31
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| Dealer # | 1249538 |
| Manufacturer # | 2IDNOW15C |
| Brand | ID NOW |
| Manufacturer | Abbott Rapid Dx North America LLC |
| Country of Origin | United States |
| Application | Respiratory Test Kit |
| CLIA Classification | CLIA Waived |
| CLIA Classified | CLIA Waived |
| Contents 1 | (2) ID NOW Instruments (NAT024), (15) ID NOW COVID-19 2.0 Test Kits (192000) |
| For Use With | For ID Now Instrument US |
| Number of Tests | 15 X 24 Tests |
| Product Dating | McKesson Acceptable Dating: we will ship >= 90 days |
| Purchase Program Type | Promotion |
| Reading Type | Machine Read |
| Sample Type | Nasal Swab / Nasopharyngeal Swab Sample |
| Specialty | Molecular |
| Technology | Isothermal Nucleic Acid Amplification Technology (NAAT) |
| Test Format | Cartridge Format |
| Test Kit Type | Rapid |
| Test Name | COVID-19 2.0 |
| Test Type | Molecular Diagnostic |
| Time to Results | 6 Minute Results (Positive), 12 Minute Results (Negative) |
| UNSPSC Code | 41116144 |
Features
- )ID NOW Promotion: (15) COVID-19 2.0 Kits (427000) + (2) each ID NOW instrument (NAT024)
- FDA-cleared ID NOW COVID-19 2.0 detects SARS-CoV-2 in 612 minutes with the option to add on the ID NOW Influenza A & B 2 test without collecting another sample
- Product ships with minimum 30 days dating
- Each COVID-19 2.0 Kit contains: (24) Test Bases, (24) Sample Receivers, (24) Transfer Cartridges, (24) Nasal Swabs, Positive and Negative Control Swabs, Product Insert and Quick Reference Instructions
- The ID NOW platform uses isothermal technology to provide molecular results faster than PCR for more timely and informed clincial decisions
- CLIA-waived; requires minimum training with easy on-screen video-guided operation and no manual pipetting required
- ID NOW Platform gives you the power to decide which tests to run based on patient presentation, circulating prevalence and seasonality of infectious diseases
- Easily add on Flu A & B testing based on clinical necessity, supporting diagnostic stewardship
- Diagnostic Stewardship: Right tests at the right time for optimal care and fewer unnecessary tests
- Unique ID NOW Instrument isothermal nucleic acid amplification technology provides molecular results in just minutes, allowing you to make effective clinical decisions sooner
- A key new feature of the ID NOW COVID-19 510(k) product and the supporting software update v7.1 provides customers with the flexibility to use a new sequential testing workflow; the sequential workflow will allow customers to have the option to add-on an ID NOW Influenza A & B 2 test after a COVID-19 result is received, using the same patient sample
- The new sequential testing workflow feature and the updated 510(k) labeling will apply to existing ID NOW COVID-19 2.0 EUA product after upgrading to software update v7.1; by performing this software update, it enables the sequential workflow for any ID NOW COVID-19 2.0 EUA product you may have in inventory
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