Certificates

Certification according to Directive 93/42/EC is an indispensible prerequisite for the CE marking of our medical device products classified Is, Im and IIa.

Our management system ensures that our medical device products meet the quality levels required by our customers, as well as the product safety standards required by law.

The success of this commitment to quality and safety of our products is evidenced by neutral, independent certifications and audits conducted in regular intervals.