- Condition: Factory New
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Learn more:
- MFR: Abbott Rapid Dx North America LLC Ships from MFI Medical
- MPN: 192000
- Phone: (800) 727-7846
Frequently asked questions
Does this test provide rapid molecular results?
Yes, it utilizes isothermal technology to deliver results significantly faster than traditional PCR methods. You can expect positive results in as little as 6 minutes and negative results in just 12 minutes.
Is this kit easy to use for staff?
Absolutely. It is designed for simplicity in high-throughput environments and features: <ul><li>Video-guided on-screen operation</li><li>Elimination of manual pipetting</li><li>Minimal training requirements</li></ul>
Can I test for other respiratory illnesses simultaneously?
Yes, the system supports diagnostic stewardship. Clinicians have the flexibility to add on Influenza A & B testing using the same patient sample, which streamlines the diagnostic process and reduces patient discomfort.
Does the kit require specialized storage conditions?
No, the kit is designed for convenience and supports room temperature storage (between 2°C to 30°C), ensuring it is ready for on-demand use whenever clinical needs arise.
What sample types are compatible with this test?
The ID NOW COVID-19 2.0 test kit is compatible with two common sample collection methods: <ul><li>Nasal Swab</li><li>Nasopharyngeal Swab</li></ul>
Are all necessary components included in the box?
Yes, each kit contains 24 complete test sets. Included in your purchase are: <ul><li>24 Test Bases, Sample Receivers, and Transfer Cartridges</li><li>Patient Swabs</li><li>Positive and Negative Control Swabs</li><li>Package Insert and Quick Reference Instructions</li></ul>
Is this system classified as CLIA-waived?
Yes, this product is CLIA-waived, making it an excellent choice for point-of-care settings like urgent care centers and professional clinics that require regulatory compliance and ease of operation.
What hardware is required to run these tests?
To perform these tests, you must have the ID NOW Instrument. Please note that the instrument is sold separately from this test kit.
Is this a high-quality, reliable testing solution?
The ID NOW COVID-19 2.0 is an FDA-cleared molecular diagnostic test manufactured by Abbott. It is designed to provide high-confidence, professional-grade results to assist in timely clinical decision-making.
Are these tests manufactured in the United States?
Yes, these test kits are manufactured in the United States and meet strict compliance standards, including BAA and TAA compliance requirements.