Most of Neskrid's products are medical devices and are therefore certified in accordance with Regulation EU/2017/745 on Medical Devices (MDR). To comply with this, Neskrid has fully set up NOCS on the basis of this standard. Amongst other things, all required data and declarations are retained for 10 years in our own database. In addition, each product has its own unique code. To ensure full compliance, Neskrid is also registered with EUDAMED (European Databank on Medical Devices) and holds its own SRN registration number.