Ask us anything - GS1 standards for Unique Device Identification (UDI)

UDI (Unique Device Identification) regulations for medical devices are a global requirement. Each regulation has barcode requirements and they often reference jargon and acronyms that it is important to understand in order to implement correctly. 

In this webinar we will start with a glossary and a short introduction to the concept of UDI, before opening up for your questions. Whilst we are not regulatory experts, we can guide you through the regulations using over a decade of experience speaking with medical device manufacturers and the MHRA. 

This session focuses on UDI – if you’re looking for guidance on allocating your numbers and understanding which numbers your trading partners require, please join our Ask us anything: product identification webinar. if you’re looking for guidance and best practice on creating barcodes, please join our Ask us anything: barcodes webinar.

Please note: This webinar is for GS1 UK members only. If you are not already a GS1 UK member, unfortunately you will not be able to join the webinar.