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Showing 6301–6310 of 66039 articles for “Art. R 581-52-1 to R 581-52-4”
Article R. 522-1 is applicable in the Wallis and Futuna Islands in the version resulting from Decree No. 2017-1313 of 31 August 2017.
The poison control centres referred to in article L. 6141-4 and the regional pharmacovigilance centres referred to in article R. 5121-167 shall transmit, without delay, to the Agence nationale de sécu…
I. - Subject to the adaptations provided for in II, Article R. 440-1 is applicable in the Wallis and Futuna Islands, in the version resulting from Decree no. 2014-498 of 16 May 2014.II. - For the appl…
I. - Subject to the adaptations provided for in II, Article R. 440-1 is applicable in New Caledonia in the version resulting from Decree no. 2014-498 of 16 May 2014.II. - For the application of I:1° A…
The CE mark is affixed under the responsibility of the manufacturer or his authorised representative. Its form and dimensions are laid down by order of the Minister for Health. The CE marking must be…
Any medical device placed on the market or put into service in France must bear the CE mark certifying that it meets the conditions set out in article R. 5211-17. However, CE marking is not required f…
The affixing of marks or inscriptions on a medical device, on its packaging or on the instructions for use which are likely to mislead as to the meaning or form of the CE marking is prohibited. Any ot…
The presentation, at scientific or technical meetings, exhibitions or demonstrations, of medical devices which do not comply with the provisions of this Title is authorised provided that a visible sig…
The CE marking may be affixed to a medical device only if it complies with the essential health and safety requirements referred to in Section 5 of this Chapter and has undergone the certification pro…
Medical devices which comply with the standards applicable to them, transposing the harmonised European standards, the references of which have been published in the Journal officiel de la République…
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