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Articles tagged with: Eudamed
Obtaining and Implementing UDI: the Complete Guide
All the details regarding the UDI code for medical devices, issuing bodies, and methods of obtaining and applying.
28/03/2023
Dario Bortolotti
Eudamed
Technical guide
UDI
Medical Device Registration in Eudamed: the Guide
All the steps to independently register UDI codes of medical devices in Eudamed, the European database.
22/03/2023
Dario Bortolotti
Eudamed
Manufacturers' duties
Technical guide
Eudamed Actor Registration: the Complete Guide
All the steps to independently register an economic operator in Eudamed, the medical device database.
28/01/2023
Dario Bortolotti
Eudamed
Manufacturers' duties
Technical guide
Registering UDI Codes in Eudamed
The latest Eudamed update allows for the registration of medical device UDI codes. How to access the registration module.
15/10/2021
Matteo Valtorta
Eudamed
Legacy device
UDI
All about Eudamed, the European Database for Medical Devices
The unique, publicly accessible database providing an up-to-date picture of the lifecycle of medical devices in Europe.
25/05/2021
Matteo Valtorta
Deadlines and exemptions
Eudamed
The CND, when Italy is Top of the Class in Europe
The European Commission has decided to adopt the Italian National Classification of Devices as the official nomenclature in Eudamed.
22/04/2021
Matteo Valtorta
Eudamed
Ministry of Health
Eudamed: Mandatory Registration from December 2020
Manufacturers, authorized representatives, system and procedure pack producers, and importers must register in Eudamed's Actor registration module.
27/10/2020
Matteo Valtorta
Deadlines and exemptions
Eudamed
Manufacturers' duties
Eudamed: the Commission Publishes the Official Link
The official link to Eudamed, the medical device database, has been published on the European Commission's website.
03/10/2020
Matteo Valtorta
Eudamed
Servizi
European Medical Device Regulation Consulting
CE Marking for Medical Devices
ISO 13485 and MDSAP Quality System
Technical Documentation
UDI and Eudamed Registration
Training Courses
European Medical Device Regulation Consulting
CE Marking for Medical Devices
ISO 13485 and MDSAP Quality System
Technical Documentation
UDI and Eudamed Registration
Training Courses
Home
Company
Work Method
Blog
Contact
Home
Company
Work Method
Blog
Contact
English
Services
European Medical Device Regulation Consulting
CE Marking for Medical Devices
ISO 13485 and MDSAP Quality System
Technical Documentation
UDI and Eudamed Registration
Training Courses
European Medical Device Regulation Consulting
CE Marking for Medical Devices
ISO 13485 and MDSAP Quality System
Technical Documentation
UDI and Eudamed Registration
Training Courses
Home
Company
Work Method
Blog
Contact
Home
Company
Work Method
Blog
Contact
English
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