Essential checklist for all businesses that sell medical devices within the European Union to pass customs with no delays, decrease liability, increase safety and be able to sell your medical device within the EU.
You want to import, trade and/or sell your medical device on the European market? Do you want to make sure that your instructions for use, packaging, technical file, product marking & labelling and declaration of conformity comply with the requirements of the European Union to avoid problems at customs or to decrease liability? We have developed this checklist to make it happen.
With the checklist you can verify if your instructions for use, packaging, technical file, product marking & labelling and declaration of conformity complies with:
For questions, please contact us at info@instrktiv.com.
All our checklist have a 14-day, no-reason-required guarantee. So if you are not satisfied for any reason, just let us know and we’ll refund your money. As we believe that our product really helps you to create better instructions, we don’t think it’ll come to that. But as soon as you have any doubts whether our product is the right fit for you, just put your mind at ease. We will help you to get the results you want, or we will give you your money back!
