by Eleni Stavridou | Jun 2, 2022 | Allgemein
Latest world news on coming UDI regulatory submissions – from GUDID to Egypt About the recorded online session Latest world news on coming UDI regulatory submissions – from GUDID to Egypt In this Online Session we will give a short panorama of what needs...
by Eleni Stavridou | Apr 21, 2022 | Allgemein
Simple and quick GUDID registration for class I devices About the recorded online session Simple and quick GUDID registration for class I devices Meet the 24th September 2022 GUDID deadline for class I products with atrify – simple and quick UDI registration in the...
by Eleni Stavridou | Nov 11, 2021 | Allgemein
How to connect GS1 members to UDI databases — EUDAMED About the recorded online session How to connect GS1 members to UDI databases — EUDAMED The EU Commission database EUDAMED is now live with 2 more modules!In this online session atrify wants to focus on the...
by Eleni Stavridou | Okt 29, 2021 | Allgemein
UDI Registration in EUDAMED — Why and How to use It now (EN) About the recorded online session UDI Registration in EUDAMED — Why and How to use It now The European Database on Medical Devices (EUDAMED) Device Registration and UDI Database module is available for use...
by Eleni Stavridou | Mrz 12, 2021 | Allgemein
Evolving UDI Product Data Requirements (EN) About the recorded Online Session The International Medical Device Regulators Forum (IMDRF) set out basic UDI requirements in their guidance document Unique Device Identification (UDI) of Medical Devices. As regulators,...
