Hello all,
The following text appears in Directive 2007/47/EC preamble (emphasis not in the source):
Yet an official European Commission Consumer Affairs webpage (http://ec.europa.eu/consumers/sectors/medical-devices/market-surveillance-vigilance/eudamed/) states (emphasis in source):
Can someone kindly shed some light on this, and maybe some prospects for the future?

Ronen.
The following text appears in Directive 2007/47/EC preamble (emphasis not in the source):
(16) In support of transparency in Community legislation, certain information related to medical devices and
their conformity with Directive 93/42/EEC, in particular information on registration, on vigilance reports and
on certificates, should be available to any interested party and the general public.
their conformity with Directive 93/42/EEC, in particular information on registration, on vigilance reports and
on certificates, should be available to any interested party and the general public.
Who can access Eudamed?
Eudamed is a secure web-based portal acting as a central repository for information exchange between national competent authorities and the Commission and is not publicly accessible. Eudamed use is obligatory since May 2011.
Eudamed is a secure web-based portal acting as a central repository for information exchange between national competent authorities and the Commission and is not publicly accessible. Eudamed use is obligatory since May 2011.

Ronen.