Suppliers of medical devices

The Unique Device Identifier (UDI) is a medical device identification system used by various regulators worldwide.

Thanks to the UDI, medical devices are uniquely identified, which increases patient safety and efficiency. This allows better management of medical device recalls and will reduce medical errors.

Benefits for your company

worldwide
Recognised worldwide
processus
Efficient and effective processes
legal
Compliant with the legislation

What would you like to do?

identify-EN
share EN
UDI EN

Why use My Product Manager?

prise en charge

Centralised management

one to many

One-to-many

compliant

Full administrative support

Useful information

MDR

Unique Device Identifier (UDI)

What is an UDI? Which standards should be used? 

 

Stappenplan

Step-by-step plan

Follow our step-by-step plan to create a Unique Device Identifier (UDI-DI)

Step 1

Knowledge center

Documents, legal texts, articles, guides and organisations in the healthcare sector

trainings

Follow our training courses

GS1 offers useful training to help you

Which regulation do apply?

EU regulations Medical Devices Regulation (MDR) & in vitro diagnostics (IVDR)

UK regulations National Health Services (NHS)

US regulations Food and Drug Administration (FDA)

Other regulations

Contact the sector helpdesk

Need technical information?