Regulation (EU) 2017/745: what changes for medical device traceability?

Loss of traceability of DMs poses a serious health risk to patients and users. The new European Parliament Regulation provided a common strategy, based on internationally recognized principles, through the establishment of a unique device identification system (UDI system). Read the full article…

Date: 06.2020   Source: iss.it

103 thoughts on “Regulation (EU) 2017/745: what changes for medical device traceability?”

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