As you know from 1 January 2021, there will be new requirements for placing medical devices on the Great Britain (GB) and Northern Ireland (NI) markets, regardless of whether you are using a CE mark or UKCA mark.
These requirements and timelines will differ slightly depending on where you are based and what you already have in place. To support you with this we have pulled together a simplified list to help you check if you have everything you need in place to register your products and have sufficient legal presence in all necessary parts of the UK to legally place your products on the whole of the UK market GB or NI.
To continue reading, please click on the following link;
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