Regulation (EU) 2017/746/EU Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU
Publication Year
2017
Document Status
Current
Abstract
Specifies the safety, performance, and 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 10-01-2025. Repealing Directive 98/79/EC and Commission Decision 2010/227/EU.
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