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Showing 3871–3880 of 4146 articles for “Art. 1649 B”
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…
…nded use means the use for which a medical device is intended according to the information provided by the manufacturer in the labelling, the instruction leaflet or promotional material; 2° Placing on…
…part of the procedure for the EC declaration of conformity, product quality assurance, for class II b medical devices, the manufacturer must submit an application to the authorized body for assessment…
1. Notwithstanding the provisions of
For the application of the legislative provisions of Book I to the Wallis and Futuna Islands:1° In article L. 2112-4, the words: "of the Member States of the European Union" are replaced by the words:…
…r the application in the French Southern and Antarctic Territories of the legislative provisions of Book I:1° In article L. 2112-4, the words: "of the Member States of the European Union" are replaced…
From 2004, public establishments of inter-municipal cooperation with their own tax status receive a compensation grant equal to the amounts due in respect of 2003 pursuant to I of D of article 44 of t…
I.-The collège de résolution may suspend any obligation to pay or deliver financial instruments resulting from a contract to which a person referred to in I of Article L. 613-34 is bound if all of the…
I.- Are applicable in the Wallis and Futuna Islands, subject to the adaptation provisions provided for in II and III, the provisions of the articles mentioned in the left-hand column of the table belo…
…authorisation holder and any pharmaceutical company exploiting a medicinal product in France shall build up a safety stock intended for the national market referred to in article L. 5121-29, in accor…
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