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Services for Device Registration in LATVIA - NEW!

Published 17 Oct 2011

Background

Under the Latvian Regulation No. 581 adopted on 2 August 2005 by Cabinet of Ministers, three categories of medical devices require to be registered with the State Agency of Medicines of Latvia (ZVA) at the time of being put into service within Latvian territory. (Please see Article 1 General Provision, paragraph 20 of the Regulation No. 581)

Categories of medical devices concerned by this obligatory communication are:

1. Class IIb medical devices
2. Class III medical devices
3. Active implantable medical devices (AIMDD)

Registration Process

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

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