Tecan Freedom EVO-2 150 HID EVOlution Liquid Handler System with Software and Dongle

Insights by AMPTIUS | AMP Tech Instruments

Price and cost of ownership of Tecan Freedom EVO-2 150 HID EVOlution Liquid Handler System with Software and Dongle

Investing in the Tecan Freedom EVO-2 150 Liquid Handler provides laboratories with a highly flexible and automated solution for high-throughput workflows across genomics, proteomics, forensic HID applications, and clinical research. A new system is typically priced around $93,000, while a certified refurbished unit averages approximately $25,000, offering substantial cost savings without compromising performance. The Freedom EVO-2 150 features a configurable deck layout, precise liquid handling capabilities, and integration with advanced modules, allowing labs to scale and customize workflows efficiently. It includes essential control software and dongle for seamless operation and protocol compliance. Ongoing costs include consumables such as tips and tubing, routine maintenance of pipetting components, and periodic software updates, with service contracts recommended to maintain reliability. A refurbished system delivers a cost-effective pathway to automation, enabling laboratories to enhance productivity and throughput while staying within budget.

Tecan EVO-2 150 HID Liquid Handler: A Core Tool for Modern Laboratory Automation

The Tecan Freedom EVO-2 150 Liquid Handler is a versatile, automated platform designed to streamline complex liquid handling tasks across genomics, proteomics, forensics, clinical diagnostics, and pharmaceutical research. It supports workflows such as DNA extraction, PCR setup, ELISA preparation, and NGS library construction, all controlled through EVOware software for precise, customizable, and validated protocol execution. Commonly integrated with thermocyclers, microplate readers, and magnetic bead processors, it enhances end-to-end sample preparation efficiency. The system aligns with regulated workflows including forensic STR analysis under ISO 18385, qPCR-based testing guided by Centers for Disease Control and Prevention and World Health Organization, clinical standards such as Clinical Laboratory Improvement Amendments and College of American Pathologists, as well as AOAC, ISO, and FDA/EMA method validation frameworks, making it a reliable solution for high-throughput, compliance-driven laboratory environments.