NeuMoDx - HPV Test Strip
For high volume screening applications, the HPV Risk/ QIAscreen assay is also available on a fully automated system as the NeuMoDx HPV Test Strip. The automated workflow on the NeuMoDx™ 96 and 288 Molecular Systems include DNA extraction, PCR amplification, fluorescent detection and result calculation. The analytical and clinical validations are performed according to the International “Meijer” HPV DNA Test Guidelines.
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Key Features
Key features of the NeuMoDx HPV DNA Test Strip on the NeuMoDx Molecular Systems.
- High throughput
- Ultra-fast results
- Easy to use. always ready
- IVD & LOT' in parallel
- True Random Access
- Cost efficiency
Assay and Instrument characteristics
- Walk away principle, once samples are loaded and the assay is started, there is no manual intervention, results are generated fully automatic.
- Automatic liquid handling of multiple specimen types, reagents, and buffers
- Assay runs with dried reagents in microfluid cartridge, which can be stored at room temperature – allowing one month on deck reagent storage
- Possibility to run different PCR assays simultaneously, there is independent nucleic acid extraction and PCR modules across all available locations of the instrument
- No batching required – continuous random access: flexibility to add additional samples at any time for any assay
- Time to first result: 60 minutes
- Test volume: 18 tests per hour, max 144 tests per 8 hour for the 96 system and 36 tests per hour and max 288 per 8 hours for the 288 system
- Identification of all consumables and specimen tubes by barcode reader, ensuring complete traceability
- Inventory management to automatically remove empty consumables and replace with new, when applicable
- Integration with LIS and automated test order verification by NeuMoDx Software
- Multi-language support for English, French, Italian, German, and Spanish
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