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Respiratory Test Kit ID NOW COVID-19 2.0 24 Tests CLIA Waived
- FDA-cleared ID NOW COVID-19 2.0 detects SARS-CoV-2 in 6–12 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
- Highly accurate, rapid molecular COVID-19 test
- 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
- Room temperature storage - run tests on demand, right out of the box
- For use with the ID NOW Instrument
- Materials required but not provided: ID NOW Instrument
Product Specs
| Item Number | 1232210 |
|---|---|
| Catalog Number | 192000 |
| UOM | KT |
| Level 1 Family Description | Lab-Waived Lab |
| Level 2 Category Description | Lab-Respiratory Testing |
| Level 3 Group Description | COVID Testing |
| Level 4 Sub-Category Description | COVID - Molecular |
| Application | Respiratory Test Kit |
| Brand | ID NOW |
| Buy American Act (BAA) Compliant | Yes |
| CLIA Classification | CLIA Waived |
| CLIA Classified | CLIA Waived |
| Contents 1 | (24) Test Bases, Sample Receivers, Transfer Cartridges, Patient Swabs, Positive Control Swab, Negative Control Swab, Package Insert, Quick Reference Instructions |
| Country of Origin | United States |
| For Use With | For ID NOW Instrument |
| Is_ECAT | N |
| Is_GSA | Y |
| Is_VA | N |
| Manufacturer | Abbott Rapid Dx North America LLC |
| Manufacturer # | 192000 |
| McKesson # | 1213540 |
| Number of Tests | 24 Tests |
| Purchase Program Type | Standard Purchase |
| Reading Type | Machine Read |
| Sample Type | Nasal Swab / Nasopharyngeal Swab Sample |
| Specialty | Molecular |
| Technology | Molecular (NAAT) Isothermal Technology |
| 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) |
| Trade Agreement Act (TAA) Compliant | Yes |
| UNSPSC Code | 41116144 |
- FDA-cleared ID NOW COVID-19 2.0 detects SARS-CoV-2 in 6–12 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
- Highly accurate, rapid molecular COVID-19 test
- 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
- Room temperature storage - run tests on demand, right out of the box
- For use with the ID NOW Instrument
- Materials required but not provided: ID NOW Instrument
Product Specs
| Item Number | 1232210 |
|---|---|
| Catalog Number | 192000 |
| UOM | KT |
| Level 1 Family Description | Lab-Waived Lab |
| Level 2 Category Description | Lab-Respiratory Testing |
| Level 3 Group Description | COVID Testing |
| Level 4 Sub-Category Description | COVID - Molecular |
| Application | Respiratory Test Kit |
| Brand | ID NOW |
| Buy American Act (BAA) Compliant | Yes |
| CLIA Classification | CLIA Waived |
| CLIA Classified | CLIA Waived |
| Contents 1 | (24) Test Bases, Sample Receivers, Transfer Cartridges, Patient Swabs, Positive Control Swab, Negative Control Swab, Package Insert, Quick Reference Instructions |
| Country of Origin | United States |
| For Use With | For ID NOW Instrument |
| Is_ECAT | N |
| Is_GSA | Y |
| Is_VA | N |
| Manufacturer | Abbott Rapid Dx North America LLC |
| Manufacturer # | 192000 |
| McKesson # | 1213540 |
| Number of Tests | 24 Tests |
| Purchase Program Type | Standard Purchase |
| Reading Type | Machine Read |
| Sample Type | Nasal Swab / Nasopharyngeal Swab Sample |
| Specialty | Molecular |
| Technology | Molecular (NAAT) Isothermal Technology |
| 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) |
| Trade Agreement Act (TAA) Compliant | Yes |
| UNSPSC Code | 41116144 |
$1,606.62
Respiratory Test Kit ID NOW COVID-19 2.0 24 Tests CLIA Waived—
$1,606.62
Description
- FDA-cleared ID NOW COVID-19 2.0 detects SARS-CoV-2 in 6–12 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
- Highly accurate, rapid molecular COVID-19 test
- 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
- Room temperature storage - run tests on demand, right out of the box
- For use with the ID NOW Instrument
- Materials required but not provided: ID NOW Instrument
Product Specs
| Item Number | 1232210 |
|---|---|
| Catalog Number | 192000 |
| UOM | KT |
| Level 1 Family Description | Lab-Waived Lab |
| Level 2 Category Description | Lab-Respiratory Testing |
| Level 3 Group Description | COVID Testing |
| Level 4 Sub-Category Description | COVID - Molecular |
| Application | Respiratory Test Kit |
| Brand | ID NOW |
| Buy American Act (BAA) Compliant | Yes |
| CLIA Classification | CLIA Waived |
| CLIA Classified | CLIA Waived |
| Contents 1 | (24) Test Bases, Sample Receivers, Transfer Cartridges, Patient Swabs, Positive Control Swab, Negative Control Swab, Package Insert, Quick Reference Instructions |
| Country of Origin | United States |
| For Use With | For ID NOW Instrument |
| Is_ECAT | N |
| Is_GSA | Y |
| Is_VA | N |
| Manufacturer | Abbott Rapid Dx North America LLC |
| Manufacturer # | 192000 |
| McKesson # | 1213540 |
| Number of Tests | 24 Tests |
| Purchase Program Type | Standard Purchase |
| Reading Type | Machine Read |
| Sample Type | Nasal Swab / Nasopharyngeal Swab Sample |
| Specialty | Molecular |
| Technology | Molecular (NAAT) Isothermal Technology |
| 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) |
| Trade Agreement Act (TAA) Compliant | Yes |
| UNSPSC Code | 41116144 |
