Customised private label medical devices according to MDR
LIVONDO offers the manufacture of private label medical devices in accordance with EU Regulation 2017/745 (MDR). Consulting, development, production, documentation, shipping and exemption from liability can be realised with our 360° services – with appropriate labelling.
Our aim is to always offer you first-class advice for your private label products. We cover all the necessary services to fulfil your specific requirements. With our expertise, we guide you through the entire process and combine our know-how of the EU Medical Device Regulation 2017/745 (MDR) and the Cosmetics Regulation (CIR) with our in-depth market knowledge. Thanks to our extensive experience in product development, product management and marketing, we provide you with optimal support for all relevant issues.
At LIVONDO, comprehensive service is not an additional offer, but a matter of course.
We can realise your individual product ideas from a minimum order quantity of 10,000 units. Our certified recipes, diverse production options and generous capacities enable rapid realisation and maximum flexibility.
Livondo – your partner for consulting, development and production
