For effective treatment, it is always necessary to identify the cause of the problem and choose the right product. The medical device may be a tool, apparatus, device, software, or other article intended by a manufacturer for use in humans for the purpose of diagnosing, preventing, monitoring, treating or alleviating the disease and other purposes.
A definition that specifies what is a medical device is part of the Medical Device Act No. 268/2014 Coll. Medical devices are subject to strict EU and national approval procedure. Other than approved EPs - which are CE marked - must not be shipped to the market.
Medical devices we market help to assist the patients in the field of urology, urology, uro-gynecology, gynecology and other areas.