How The EU’s Device Nomenclature Operates: Free Of Charge And Accessible To All
Executive Summary
The EU’s device nomenclature is a vital key to operating the Eudamed database. A new EU document explains how it operates, who can use it and where to access the device naming scheme.
You may also be interested in...
Global Medtech Guidance Tracker: June 2021
Stay current on regulatory guidelines from around the world with Medtech Insight's Guidance Tracker. Forty-six documents have been posted on the tracker since its last update.
EU Regulatory Roundup, March 2024: Busy Agenda In Broad Range Of Key Areas
March was an important month for EU medtech regulation with an interesting spread of news relating to the Medical Device and IVD Regulations, the Batteries Regulation, the Artificial Intelligence Act and more.
EU’s Revised Phthalates Guideline Features New Annexes Focused On Alternatives
The effects of phthalates, plasticizers used in many medical devices, on the human endocrine system, have long been debated. But how safe are the alternatives? Updated guidelines give more insight.