Systec News and Events

First demonstration of the new Systec H series

Written by Systec | Mar 11, 2026 8:38:38 AM

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

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

Systec presented autoclaves & validation processes with Evidencia GmbH at MEDICA 2019.

From November 18 to 21, 2019, up-and-coming companies 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 were also there again. While Evidencia presented innovative concepts for the qualification and validation of devices and sterilization processes, Systec's presentation of the first product from the revised Systec H series was eagerly awaited this year: The new and improved Systec HX-150 autoclave.

More efficient work with the new generation of autoclaves

The Systec HX-150 is the world's first device from the new, improved Systec H-series - a new generation of autoclaves with a new design, a completely redesigned interior and a touchscreen control developed from scratch. This combination guarantees more precise work, more maintenance-friendly devices and shorter and more efficient process times.

In addition, the new autoclaves have an Ethernet connection as standard and optional WLAN hardware to optimize updating, 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 documentation data to be stored for up to 10 years. This eliminates the need for separate programs for documentation and archiving. This integrated documentation function is also interesting from a regulatory point of view, as the new generation of the Systec H series automatically fulfills an essential point of the FDA directive CFR 21 Part 11. In this context, other functions of the series serve to fulfill regulatory requirements from the pharmaceutical industry, such as automatically distributed, tamper-proof signatures of the generated PDF and CSV files as well as the tracking of all measures, adjustments and alarms using AuditTrail.