Directive 98/79/EC Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices
Publication Year
1998
Document Status
Withdrawn
Abstract
Ensures the safety, CE marking, and free market access of in vitro diagnostic medical devices.
Document History
Source: Office for Official Publications of the European Communities. Only European Community's legislation printed in the Official Journal of the European Communities is deemed to be authentic. Consolidated version dated 11-01-2012. Repealed by Regulation (EU) 2017/746.
Publisher Information
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