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Showing 7231–7240 of 14914 articles for “Art. 6 mars 1996”
The registrars and the National Institute of Industrial Property are authorised to respond to any statistical requests.
Requests for information relating to the future status of files may be made by subscription. They entail the issue of an extract or a copy, either at regular intervals, the frequency of which may not…
I. - The articles R. 5211-13 to R. 5211-15, with the exception of its first paragraph, article R. 5211-18 and article R. 5211-18-1 are applicable in French Polynesia subject to the adaptations provide…
I.-The results of the initial inspections provided for in Articles R. 4451-40 and R. 4451-44 are recorded in the safety register or registers referred to in Article L. 4711-5. II -The results of the o…
…his section available to the health professionals referred to in the first paragraph of Article L. 4624-1 and to the Social and Economic Committee. It shall provide the Social and Economic Committee w…
…ody referred to in Article R. 4724-1 of the body referred to in Articles R. 4451-40 and R. 4451-44; 6° The organisational and resource requirements necessary for the independent and objective performa…
…e-examination ; 4° EC verification; 5° EC declaration of conformity, production quality assurance ; 6° EC declaration of conformity, product quality assurance ; 7° The declaration relating to custom-m…
For medical devices to be subject to clinical investigations, the manufacturer must comply with the provisions of Title II of Book I of Part I of this Code.
For the purposes of placing a custom-made medical device on the market, the manufacturer shall follow the procedure defined in Article R. 5211-51. The Director General of the Agence nationale de sécur…
In the case of active implantable medical devices or medical devices in Class III or Class II b, the manufacturer shall take all necessary measures to ensure that the manufacturing process guarantees…
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