MDR

Most Neskrid products are medical devices and certified under European Regulation EU/2017/745 for Medical Devices (MDR). To meet the relevant requirements, Neskrid has set up NOCS entirely on the basis of this standard. All required data and statements, for example, are kept for 10 years in our own database. Moreover, most products have their own unique code. To safeguard all processes, Neskrid is also registered with EUDAMED (European Databank on Medical Devices) and has its own SRN registration number.