GS1 Norway recommends atrify's UDI Solution for EUDAMED registration

13 Jun 2022

Even if the mandatory registration of medical devices in EUDAMED still seems a long way off until 2023, many experts recommend already dealing with the complex requirements now and start testing and registering in time.

GS1 Norway officially recommends using the atrify UDI Solution since registration via the EUDAMED portal itself can often be difficult and complicated.

The atrify UDI Solution supports medical device manufacturers to register their products quickly, easily and compliantly in EUDAMED. No matter whether via M2M, the manual user interface or with the Excel Bulk Upload

Start with the UDI registration in Eudamed now and get free advice from our experts.

Read more about GS1 Norway's recommendation for an easy EUDAMED registration.

Click here for more information about registering your data in EUDAMED with atrify's UDI Solution.

Team atrify

Team atrify

Team atrify is all of us at atrify. We understand the problems manufacturers face in data management. Data optimization and internal system integration are our core competencies. We advise and implement the requirements for both commercial and regulatory use of the data in a system.

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