EU MDR Annex XVI Introduces New Burdens for Products Without an Intended Medical Purpose

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EU MDR Annex XVI Introduces New Burdens for Products Without an Intended Medical Purpose     Adopted in 2017, the EU Medical Device Regulation (MDR) brought a host of changes. In its Annex XVI, for example, the regulation expands its scope to take in new product groups referred to as “products without an intended medical purpose”—in …

EU MDR Annex XVI Introduces New Burdens for Products Without an Intended Medical Purpose Read More »