With the mediCAD® solution, mediCAD Hectec GmbH establishes an innovative milestone in the support of orthopedic surgery worldwide.
By automatically archiving of all necessary information and providing continuous traceability of findings (Kein Komma) of the surgical preparation and follow-up care, mediCAD® offers the ideal opportunity for optimally prepared, professionally executed and revision-proof documented surgery with corresponding recorded follow-up care. With mediCAD, you have the opportunity to plan your operations efficiently and precisely to achieve optimal results.
MDR certification is therefore a decisive success for us as a manufacturer. It demonstrates that we meet all medical device requirements and thus ensure the highest standards of quality and safety. Our goal is to always provide you with the best possible products and services to enable you and your patients to receive optimal and individualized treatment.
Our sales team is always available to provide you with further information on mediCAD and our MDR certification. Simply contact us at sales@medicad.eu.
We are proud to be one of the first medical device manufacturers to be able to meet the strict requirements of the new EU Medical Devices Regulation (MDR) and guarantee you the latest state of the art technology and compliance with all medical regulations and guidelines at all times.