UDI
EUDAMED Requirements of Legacy Device Registration in UDI…
MDR 2017/745 and IVDR 2017/746 EU laws establish an EU identification system for medical devices based on a Unique D…
EUDAMED Vigilance Requirements and Steps
One of the modules of EUDAMED is Vigilance and Market Surveillance. EUDAMED will become mandatory for device Actors,…
Singapore UDI Phase – 1 Implementation
The Health Sciences Authority of Singapore will implement the UDI system, a global system for tracking and identifyi…
China UDI Requirements
Unique device identifier refers to a series of codes constituted of numbers, letters and/or symbols and established …
UDI & EUDAMED Explained under EU MDR
What is UDI?
Unique Device Identification (UDI) intended to assign a unique identifier to medical devices within …
Get the latest updates from DDi
Explore Topics
Most Used Tags
The First Step
Let's talk about how DDi can help you