Service features

Eudamed registration and UDI

We manage the registration of manufacturers, importers, distributors and medical devices on to the Eudamed database. We also secure and support the use of the UDI code (UDI-DI, UDI-PI and basic UDI).

Context and introduction

The 2017/745 medical device regulation (MDR) requires the registration of businesses (manufacturers, importers and distributors) on the Eudamed database.
In addition, each product must be identified by a UDI code registered on the database prior to commercial release, with the guarantee that information will be updated over time.

01

Securing UDI

We secure the UDI code (UDI-DI, UDI-PI and basic UDI) by dealing with the awarding bodies authorised by the European Union and, once secured, we support clients in managing and using codes on labels and packaging.

02

Eudamed database

We manage registration and updating information on the Eudamed database for businesses (manufacturers, distributors, and importers) and medical devices. In addition, we deal with the publication of all information required for monitoring and oversight purposes.

03

Summary of safety

We manage publication in the Eudamed database of the summary of safety and clinical performance of implantable and class III medical devices.

Contact us

Requirement analysis.

Use the details in the contact section to get in touch so that we can give you more information, organise an initial meeting, create a bespoke service, or put together a dedicated quote.