The Veriti™ Dx Thermal Cycler is the First Applied Biosystems® Endpoint Thermal Cycler for In Vitro Diagnostic Use* The Veriti™ Dx Thermal Cycler is classified as a US FDA Class I Medical Device. It conforms to IVDD (98⁄79⁄EC) requirements and is CE IVD–labeled in Europe. The instrument is manufactured to ISO 13485 and GMP requirements. |
Innovative 96-Well VeriFlex™ Block TechnologyVeriFlex™ Blocks on the Veriti™ Dx Thermal Cycler provide a better-than-gradient approach to PCR optimization. With six independent Peltier blocks, you can precisely set and control the temperature in each block, giving you maximal versatility, flexibility, and confidence in your diagnostic development.
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Control at Your Fingertips
The powerful yet simple-to-operate user interface on the Veriti™ Dx system is driven by the 6.5-inch VGA touch screen. The easy viewing and large navigation buttons put programming of the Veriti™ Dx Thermal Cycler at your fingertips. A convenient USB port is also built into all Veriti™ Dx systems to simplify data transfer and software updates.
Brochures, User Guide, & Other Documents
Service & Support
Life Technologies provides award-winning service options for Applied Biosystems® thermal cyclers. The Veriti™ Dx system includes installation and Installation Qualification/Operational Qualification (IQ/OQ) by our factory-trained field service engineers. This helps ensure that your Veriti™ Dx instrument meets our stringent performance specifications and gives you the reliable results you expect.
Service Plans
- Rapid Exchange minimizes interruptions from unplanned instrument downtime
- Global Repair Center provides a cost-efficient way to maximize uptime and achieve superior performance
Support
Innovative 96-Well VeriFlex™ Block TechnologyVeriFlex™ Blocks on the Veriti™ Dx Thermal Cycler provide a better-than-gradient approach to PCR optimization. With six independent Peltier blocks, you can precisely set and control the temperature in each block, giving you maximal versatility, flexibility, and confidence in your diagnostic development.
|
Control at Your Fingertips
The powerful yet simple-to-operate user interface on the Veriti™ Dx system is driven by the 6.5-inch VGA touch screen. The easy viewing and large navigation buttons put programming of the Veriti™ Dx Thermal Cycler at your fingertips. A convenient USB port is also built into all Veriti™ Dx systems to simplify data transfer and software updates.
Brochures, User Guide, & Other Documents
Service & Support
Life Technologies provides award-winning service options for Applied Biosystems® thermal cyclers. The Veriti™ Dx system includes installation and Installation Qualification/Operational Qualification (IQ/OQ) by our factory-trained field service engineers. This helps ensure that your Veriti™ Dx instrument meets our stringent performance specifications and gives you the reliable results you expect.
Service Plans
- Rapid Exchange minimizes interruptions from unplanned instrument downtime
- Global Repair Center provides a cost-efficient way to maximize uptime and achieve superior performance
Support
The Veriti™ Dx Thermal Cycler is Available in Three Formats:
| Veriti™ Dx 96-Well Fast Thermal Cycler | Veriti™ Dx 96-Well Thermal Cycler | Veriti™ Dx 384-Well Thermal Cycler | |
|---|---|---|---|
| Block Format | 0.1 mL Alloy | 0.2 mL Alloy | 0.02 mL Aluminum |
| Features | Fast 0.1 mL format and sample block; enabled to run Fast chemistry | Standard 0.2 mL format and sample block provide enhanced performance and durability | High-throughput, single-block system optimized for low-volume |
| Max Block Ramp Rate | 5.00 ºC/Sec | 3.9 ºC/Sec | 3.7º C/Sec |
| Max Sample Ramp Rate | 4.25 ºC/Sec | 3.35 ºC/Sec | 3.1º C/Sec |
| Enabled to run FAST Chemistry | Yes | Yes | No |
| PCR Volume Range | 10-30 µL | 10-80 µL | 5-20 μL |
| VeriFlex™ Blocks | 25 °C (5 °C Zone-to-Zone) | 25 °C (5 °C Zone-to-Zone) | N/A |
*The Veriti™ Dx Thermal Cycler is available for in vitro diagnostic use in the United States of America and Europe and other selected countries only. The customer is responsible for any validation of assays, reagents, and consumables, and compliance with any regulatory requirements that pertain to their procedures and instrument use.
