Lipogel Medical Device for Atopic Skin

Since 2024, our lipogel medical device for atopic skin has been MDD certified The MDR (Medical Device Regulation), in force since May 2017 and fully applicable from May 2021, governs medical devices in Europe. Thanks to the extension of deadlines, devices compliant with the MDD Directive may continue to be marketed until December 31, 2027…

MDD Certification: Proctological Medical Devices

Topical gel and anal solution for the treatment of anorectal disorders The MDR (Medical Device Regulation), in force since May 2017 and fully applicable from May 2021, governs medical devices in Europe. Thanks to deadline extensions, devices compliant with the MDD Directive can continue to be marketed until December 31, 2027, for Class III and…

GFI Extends MDD Certificate for GERD Devices

Extension of MDD Certificate for Our Medical Devices for the Treatment of Gastroesophageal Reflux Disease (GERD) Based on Alginates The MDR regulation, effective from May 2017 and applicable from May 2021, governs medical devices in Europe. Deadline extensions allow the marketing of devices compliant with the Medical Devices Directive (MDD) until December 31, 2027, for…

GFI Extends MDR Compliance for Legacy Devices until 2028

MDR Transition Period Extension: FarmaImpresa Ensures Compliance for its Legacy Devices until 2028 The MDR (Medical Device Regulation), which came into force in May 2017 and has been applicable since May 2021, aims to create a robust and transparent regulatory framework for medical devices in Europe, ensuring safety and promoting innovation. However, because of concerns…