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3 steps to Classifying Medical Devices in the EU

Posted on by Congenius

To classify a medical device in the EU, the intended use needs to be articulated, before defining and categorising the device according to MDR 2017/745.

Download our fact sheet below to learn more about the three important steps to take when looking to classify your medical device in the EU. And if you’re looking for information on classifying your medical device in the US, click here.

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