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First demonstration of the new Systec HX-150 autoclave

Innovations in the field of autoclaves at the Systec and Evidencia booth.

First presentation of the 2nd generation of the Systec H-Series.

Together with Evidencia GmbH, Systec presented autoclaves & validation processes at MEDICA 2019. Systec H-Series autoclaves new generation

From 18th to 21st November, emerging companies havel presented their technologies and processes at Medica 2019. Of course, Systec, the world’s leading manufacturer of laboratory autoclaves, and its partner company Evidencia GmbH   have been part of the action. While Evidencia introduced innovative concepts for qualifying and validating equipment and sterilization processes, there was particularly eager anticipationat Systec of the launch of their first product from the redesigned Systec H-Series: the new and improved Systec HX-150 autoclave.

More efficient work with the new generation of autoclaves

The Systec HX-150 autoclave is the world’s first device from the new, improved Systec H-Series – a new generation of autoclaves in a new design, with a completely overhauled interior, and a touchscreen control that has been newly developed from scratch. This combination guarantees more precise work, easier to maintain equipment, shorter and more efficient process times.

In addition, the new autoclaves come with an Ethernet port as standard and optional Wi-Fi hardware to optimise updating processes, remote maintenance, and remote control of the devices via a computer network. An integrated USB port allows the automated export of documentation data in CSV or PDF format. The volume of the extended internal memory also allows storage of up to 10 years of documentation data. This eliminates the need for separate programs for documentation and archiving that are the otherwise necessary. This integrated documentation function is also interesting from a regulatory point of view, because the new generation of the Systec H- Series thereby automatically fulfils an essential point of the FDA guideline CFR 21 Part 11. Additional features of the series also serve in this regard to satisfy regulatory requirements from the pharmaceutical industry, such as automatically distributed, tamper-proof signatures for the PDF and CSV files that are generated, and the tracking of all actions, adjustments, and alerts using AuditTrail.

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