Download our white paper on nanomaterials today!
The new EU Medical Devices Regulation (MDR) and IVD Regulation (IVDR) do include specific classification rules for devices that consist of or incorporate nanomaterials. For medical device manufacturers, it is important that they can identify the use of nanomaterials in their devices to ensure that they meet the requirements of these new regulations.
At SAXOCON we have the expertise and tools for identifying and characterising nanomaterials and providing you with the required documentation for your final finished device.
Fill out the form below to read about their consequences for regulations and your manufacturing process.