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,for, Item ID-
- #1271003
- Providers like you icon 12
- Sekisui Diagnostics #MTRX-RDR-GEN2
Respiratory Test Reader Metrix®
READER, METRIX GEN 2 D/S
Features
- The Metrix® Gen 2 Reader is a compact device that can fit in the palm on your hands
- It is a reusable reader designed for use with the Metrix® COVID-19 Test and the Metrix® COVID-19 & Flu Test
- The Metrix Reader is a compact reusable electronic device that utilizes nucleic acid amplification technology, similar to PCR
- More …
Product Details Email
Product Specifications
| McKesson # | 1271003 |
|---|---|
| Manufacturer # | MTRX-RDR-GEN2 |
| Brand | Metrix® |
| Manufacturer | Sekisui Diagnostics |
| Country of Origin | Unknown |
| Analyzer Type | Handheld |
| Application | Respiratory Test Reader |
| Buy American Act (BAA) Compliant | No |
| Contents 1 | (1) Metrix Gen 2 Reader (Reusable), Power Adapter, USB-C Power Cord, Quick Start Guide |
| For Use With | For Metrix COVID-19 / Flu Test |
| Power Source | Battery Pack, USB-C |
| Purchase Program Type | Standard Purchase Agreement |
| Readout Type | LED Display |
| Sample Type | Nasal Swab Sample |
| Test Name | COVID-19 / Flu A / Flu B |
| Time to Results | 20 Minute Results |
| Trade Agreement Act (TAA) Compliant | No |
| UNSPSC Code | 42271505 |
| User Interface | LED Display |
Features
- The Metrix® Gen 2 Reader is a compact device that can fit in the palm on your hands
- It is a reusable reader designed for use with the Metrix® COVID-19 Test and the Metrix® COVID-19 & Flu Test
- The Metrix Reader is a compact reusable electronic device that utilizes nucleic acid amplification technology, similar to PCR
- It is intended to analyze specific FDA-authorized Metrix Tests and provide the results of those tests
- The Metrix® Reader box includes a reusable reader, power adapter, USB-C power cord, and Quick Start Guide
- This product has been authorized only for the detection and differentiation of nucleic acid from SARS-CoV-2, influenza A, and influenza B, not for any other viruses or pathogens
- For use with specific Metrix tests under EUA, sold separately
- The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. §360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner
- Minimal Hands-On Time – Can be performed in a CLIA-waived setting in a few simple steps
- Convenient – No maintenance or calibration, ready for tesing any time
More Information
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