That's alright, but please be aware that when you are talking to companies about these, they might not be aware as the MDR is a large document taking a lot of companies focus but this is a very small paragraph in it. Provide hem as much information about it and suggest that they talk to their regulatory team about it. As companies are so use to sending IFU's with all product taking it out for a large order will be unusual for them and would be a change in the processes that they are likely to have in place
