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Showing 10791–10800 of 39241 articles for “Art. al. 6”
Failure to comply with 1° of article L. 5231-2 to manufacture, sell, offer for sale, display or import tube feeding bottles is punishable by a fourth-class fine. Natural persons guilty of the offence…
The following is punishable by the fine laid down for fifth class offences: 1° For a health establishment, an inter-hospital syndicate, a health cooperation group or an association mentioned in articl…
The Agence nationale de sécurité du médicament et des produits de santé carries out an inspection of each blood establishment at least once every two years. The purpose of these inspections is to ensu…
As part of the EC type-examination procedure, the manufacturer must submit to an authorized body for examination a representative sample, known as the type, of the production envisaged in order that t…
The Director General of the Agence Nationale de Sécurité du Médicament et des Produits de Santé may require the communication of all information essential for checking the accuracy of the advertised c…
At the request of the Director General of the Agence nationale de sécurité du médicament et des produits de santé, the manufacturer or its authorised representative shall provide any information relat…
The certificate is issued by the person responsible for transferring the second-hand medical device to the transferee.
In application of Article L. 5212-1, the list of medical devices subject to compulsory maintenance, the list of medical devices subject to internal quality control and the list of medical devices subj…
In vitro diagnostic medical devices, other than in vitro diagnostic medical devices undergoing performance evaluation, are classified in two categories: 1° In vitro diagnostic medical devices whose re…
…and on ways of avoiding incorrect operation and eliminating the risks inherent in the installation; 6° To reduce to a minimum, if they are connected to or equipped with an energy source, the risks of…
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