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Commission Decision (EU) 2018/1617 of 25 October 2018 concerning a measure adopted by France pursuant to Council Directive 93/42/EEC with regard to the Terrafor and Defiligne medical devices (notified under document C(2018) 6943) (Text with EEA relevance.)
Commission Decision (EU) 2018/1617 of 25 October 2018 concerning a measure adopted by France pursuant to Council Directive 93/42/EEC with regard to the Terrafor and Defiligne medical devices (notified under document C(2018) 6943) (Text with EEA relevance.)
Publication metadata
- Published:
- Corporate author(s): Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs (European Commission) , European Commission
- Subject: France , gastrointestinal disease , health risk , lead , market approval , marketing standard , medical device , product safety , withdrawal from the market
- IMMC : C(2018)6943/992985
- CELEX : 32018D1617
- OJ : JOL_2018_270_R_0003
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