We are happy to inform you that the Notified Body BSI UK certified the first device – classified as a IIa device – under Rule 20 of the new regulatory framework of the MDR – EU 2017/745. More information can be found on the BSI News section.
In view of Brexit, we look forward to more certifications from Notified bodies based in the EU 27. We will keep you informed in our MDlaw News section.
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