Hello, I'm new to the forum and more familiar with registration of IVD's. My company wishes to register a class 1 medical device and in the guidance notes to the RG2 form there is not an applicable generic code number. However, searching the MHRA registration database I have found a suitable code assigned to a similar product from another manufacturer by MHRA. Can I use this code, or do I have to send details of my product for MHRA for them to then assign the code, as this code isn't listed in the guidance notes? Hope this makes sense!