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We focus on success through quality, because it is the essential basis for the trust placed in us by our customers.

Our quality principles and quality objectives are in line with our quality policy and thus ensure the best possible quality of our products and development services.

Our devices are developed and manufactured in accordance with the specifications of our established quality management system according to EN ISO 13485:2016, for which we have been certified since March 2019.

Our medical devices are developed and manufactured in full compliance with the essential requirements of the European Directive 93/42/EEC on medical devices and bear the CE mark.

Logo Med/Cert certified ISO 13485