Get ready for class I registration
– Let us show you how!
This eBook covers the following topics:
- What is GUDID?
- EUDAMED and FDA’s GUDID: What’s the difference?
- Checklist: How and when do you need to get ready for GUDID
- GUDID is just the beginning: See what countries are on the horizon and how a Global data readiness strategy can ensure future success.
Start preparing for the registration of Class I devices in GUDID now and be compliant in time
After the GUDID (FDA) registration for medical devices of classes II and III having been mandatory for several years now, the deadline is now also getting closer for class I medical devices and unclassified medical devices. We will show you how to get ready in time.
Download free eBook now
Regardless of whether you are based in the US or selling to the US market: If you want to continue selling your class I medical devices in the US, you need to register your products in time. Our eBook shows you how to get ready.