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Eudamed: a step towards a single market for medical devices in Europe

This article was originally published in SRA

Executive Summary

The fact that the use of Eudamed, the European databank for medical devices, is to become mandatory throughout the EU in May 2011, is good news for the industry. There are, however, certain problems associated with it and, in its present format it will do little to improve the current situation in which the many different national registration systems that exist are hindering the development of a genuine single market for medical devices.

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Eudamed: a step towards a single market for medical devices in Europe

The fact that the use of Eudamed, the European databank for medical devices, is to become mandatory throughout the EU in May 2011, is good news for the industry. There are, however, certain problems associated with it and, in its present format it will do little to improve the current situation in which the many different national registration systems that exist are hindering the development of a genuine single market for medical devices.

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