EHRET HOT-AIR Sterilizers are developed to fulfil the high demands on hot-air sterilization and depyrogenation especially for pharmaceutical production as well as for hospital and pharmacy purposes. With this, various solutions for dry heat sterilization methods under GMP conditions are at customers hands.

Hot-Air Sterilizers differ generally from Drying Ovens in view of control technique. Basis and leading idea of construction and design are the regulations for the pharmaceutical production (GMP, PIC/s, ISO 14644, etc.).

The fabrication of Hot-Air Sterilizers is carried out entirely in the EHRET factory in accordance to ISO-certified work flow and basing on corresponding SOPs fpr design, production, qualification and documentation.

EHRET Hot-Air Sterilizers class 100 and 10.000 are manufactured in accordance to the FDA and GMP standards and the relevant standards in effect.

The stated cleanroom class conditions are granted during the complete sterilisation cycle at a temperature range from 5°C above ambient temperature up to 200°C with all units, optionally up to 280°C.