TīmeklisThe European Database on Medical Devices ( EUDAMED) is the IT system developed by the European Commission as an integral part of MDR and IVDR implementation. It aims to enhance transparency about medical devices, including better access to information for the public and healthcare professionals, and enhancing coordination … Tīmeklis2024. gada 25. sept. · The European Commission's EUDAMED has various ways for you to add your Device data. This video explains the EUDAMED options and we make our expert recommenda...
MDCG 2024-5 - Public Health
TīmeklisThis site uses cookies to offer you a better browsing experience. Find out more on how we use cookies. TīmeklisRegistration of legacy devices in EUDAMED April 2024 This document has been endorsed by the Medical Device Coordination Group (MDCG) established by Article … umich research study
DocsRoom - European Commission
Tīmeklis2024. gada 21. apr. · EUDAMED Actor 注册模块将上线,如何申请和维护SRN. 2024年8月,MDCG发布了关于Actor registration模块与SRN的使用的立场文件MDCG 2024-15 [1] 文件透露MDCG已经于2024年3月12日同意将EUDAMED各个模块分开独立上线运行,其中的Actor registration模块将于2024年12月1日上线运行。. 届时 ... Tīmeklisbsi客户门户网站. 我们目前正在变更将文档上传至bsi客户门户网站的方式,bsi 客户可使用该门户网站来上传警戒报告和技术文档。 该门户网站将加入附加功能,以便制造商根据 eudamed 要求上传单个文件。 制造商可根据证书编号提交 ss(c)p 文件,同时指定 ss(c)p 文件涵盖的基本 udi-di。 TīmeklisThe Actor registration is the first of the six EUDAMED modules. The Commission is not in a position to require the use of the Actor registration module until EUDAMED is … umich residency application