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Articles tagged with: UDI
UDI Labeling Requirement for Class I Devices
Class I devices without a UDI code on their label are no longer compliant with current regulations.
17/06/2025
Stefano Rusconi
Deadlines and exemptions
Manufacturers' duties
UDI
Affixing UDI on Medical Device Labels
Guidelines for UDI affixing process verification and validation obligations and our complete and compliant printing system.
06/12/2024
Dario Bortolotti
Software
Technical guide
UDI
UDI Registration Obligation for Healthcare Providers
The complete guide for healthcare providers and dentists for mandatory registration and storage of UDI codes from January 15, 2024.
15/01/2024
Matteo Valtorta
Manufacturers' duties
UDI
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
UDI Code Application Dates for Medical Devices
Regulation 2017/745 (MDR) defines the dates for compliance with the requirements for obtaining and applying the UDI code.
25/01/2022
Matteo Valtorta
Deadlines and exemptions
Legacy device
UDI
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
The Fabulous World of UDI
In an attempt to clarify, an overview of UDI requirements (UDI-DI, UDI-PI, and basic UDI) for medical devices.
12/03/2020
Matteo Valtorta
UDI
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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