Medical Devices: Delegated acts on well-established technologies published
Delegated acts establishing criteria and procedures for well-established technologies under the MDR have been published.
EC Medical Devices · EU-wideDelegated acts establishing criteria and procedures for well-established technologies under the MDR have been published.
EC Medical Devices · EU-wideEuropean Commission updates the manual on borderline and classification decisions for medical devices and in-vitro diagnostics.
EC Medical Devices · EU-wideFAQ clarifying how MDR, IVDR and the AI Act interact in the regulation of AI-enabled medical devices and diagnostics.
EC Medical Devices · EU-wideCommission Delegated Regulation (EU) 2025/788 amends Delegated Regulation (EU) 2023/2197 regarding the application date.
EC Medical Devices · EU-wideRevised guidance on implementing the Master UDI-DI solution for contact lenses under MDR requirements.
EC Medical Devices · EU-wideEuropean Commission releases version 3.5 of a monitoring dashboard tracking medical device availability and notified body data across the EU market.
EC Medical Devices · EU-wideMDCG position paper on implementation timelines for Master UDI-DI requirements for optical devices.
EC Medical Devices · EU-wideMedical devices and In Vitro Diagnostic medical devices (IVDs) have a fundamental role in saving lives by providing innovative healthcare solutions for the diagnosis, prevention, monitoring, prediction, prognosis, tre...
EC Medical Devices · EU-wide