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Showing 1391–1400 of 4074 articles for “Art. no 16-26395”
…products in a Member State of the European Community or a party to the Agreement on the European Economic Area. However, all or part of this experience may have been acquired either in one or more est…
…horised body to which the conformity certification procedures have been entrusted, in France or in another Member State of the European Union or party to the Agreement on the European Economic Area.
In order to comply with the requirements relating to design and manufacture, in vitro diagnostic medical devices are designed, manufactured and packaged in such a way as to meet the following objectiv…
…considered to be persons who are neither manufacturers or their agents or users of medical devices nor patients. In particular, distributors of medical devices fall into this category if they are awa…
…d results before release and during use, the making available, use and traceability of in vitro diagnostic medical devices and their sale. Similarly, it carries out any investigations or work necessar…
…irector General referred to in Article L. 5322-2 which are communicated to the Ministers for the Economy, Health and Social Security for information fifteen days before their notification is set by or…
The purpose of the vigilance exercised over the software mentioned in 18° of Article L. 5311-1 and the devices mentioned in 19° of the same article, used in medical biology laboratories, is to monitor…
…who, in the course of his duties within a health care establishment, observes one or more cases of nosocomial infections, informs, on the one hand, the practitioner responsible for the area of activi…
The agenda for meetings of the National Committee is set by the minister(s) responsible for social action, health and social security.
The interventions of the SMUR and those of the SMUR branches mentioned in article R. 6123-5 are triggered and coordinated by the SAMU. The mobile emergency and resuscitation structure team informs the…
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