We are your specialist for customised user interfaces in the OR. With our high level of expertise and decades of experience, we can meet the specific demands of medical disciplines while supporting you in gaining international approvals for your medical device.
In order to enable our customers to concentrate on their own core competence – the development and production of high-quality medical equipment – we offer comprehensive support and advice surrounding documentation, certification and validation in accordance with all the relevant medical standards.
As an optional extra, we provide MDR-2017/745-compatible documentation which can then be easily integrated in the overall documentation of the medical system. Within the framework of the "FDA Establishment Registration" (21 CFR 807), we are registered with the FDA as a "Contract Manufacturer", giving our customers proof that their user interfaces were produced by an FDA-registered specialist.