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.
Available in three formats to suit your thermal cycling needs: standard 96-well, Fast 96-well, and standard 384-well. All three systems feature an exceptionally easy-to-operate color touch screen to simplify instrument setup and use.
The Veriti™ Dx instrument is only available for sale in the US, Europe, and other selected countries.
*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.
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