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Showing 9811–9820 of 61869 articles for “Art. R. 512-39-1 et s.”
…nded for human consumption, no more than one month's treatment may be given in medicated feed. The veterinarian prescribing a medicated feed must ensure that the medicated feed prescribed and the feed…
…and reporting obligations laid down in this section apply without prejudice to those laid down for veterinary medicinal products authorised by the European Medicines Agency in Regulation (EC) No 726/2…
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…
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…
…ule which applies shall be the most stringent and the device shall be classified in the highest class.
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…
…ed the application. The Regional Prefect may suspend approval for a period not exceeding three months.
…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 proced…
…ournal officiel de la République française, are presumed to comply with the essential health and safety requirements set out in section 5 of this chapter. The standards mentioned in the first paragrap…
The presentation at scientific or technical meetings, exhibitions and demonstrations of in vitro diagnostic medical devices which do not comply with the provisions of this Title is authorised provided…
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