Validated production for maximum precision and quality

... fast and variable, new developments, prototyping, small and large series

We have clean rooms with various processing stations at our disposal. All relevant work and test steps for products in medical engineering take place there. The clean-room workstations are subject to clean-room monitoring and bioburden determination and are regularly checked by an accredited microbiological institute.

All our products are subject to a quality management which is certified in compliance with EN ISO 9001:2008 und EN ISO 13485:2003 In addition to this, our fibre-optic medical devices and developments have their own CE number, CE 0535. The CE certification is reviewed each year by our notified body.

Our entire production steps are validated and verifiable. For our manufacturing processes we use only calibrated measuring and test equipment. This is subjected to a regular in-house calibration service which is checked by an external calibration institute.