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Services for Medical Device Registration in Greece - NEW!

Published 04 Nov 2011


In accordance with Greek transposition of MDD 93/42/EEC, as published in the Greek Government Gazette, number 2198, dated 2 October 2009; article 14, paragraph 1, all medical devices must be registered with the Greek Ministry of health (EOF) before being placed on the market in Greece.

Categories included in the requirement are:

• Class I, Is, Im
• Class IIa, IIb, III
• Custom Made Devices
• Kits

Registration Process

Please visit our Services for Device Registration in Greece page for additional information.

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