Article summary
The European Commission has published a Q&A on the European Medical Device Nomenclature (EMDN), which will be used by manufacturers to register medical devices in the EUDAMED database. The Q&A explains what the EMDN is, how it was created, the key principles behind it and how to access it. It also explains the structure of the EMDN, which includes clustering medical devices into three main levels, comprising categories, groups and types, as well as which of the levels users should assign their device to.
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