Article R5221-18
…provisions of articles R. 5211-25 to R. 5211-29 are applicable to in vitro diagnostic medical devices.
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Showing 6051–6060 of 55286 articles for “Art. s. 389 et 389-1”
…provisions of articles R. 5211-25 to R. 5211-29 are applicable to in vitro diagnostic medical devices.
…edical device;e) An express invitation to read carefully the instructions given in the package leaflet accompanying the medical device or on the labelling supplied to the end user;f) Depending on the…
…R. 5211-1 to R. 5211-3. It is carried out on medical devices after they have been placed on the market.
…It is carried out on all in vitro diagnostic medical devices after they have been placed on the market, as well as on the in vitro diagnostic medical devices mentioned in article L. 5221-5.
…dical device; e) an express invitation to read carefully the instructions given in the package leaflet accompanying the in vitro diagnostic medical device or on the labelling supplied to the end user;…
…this local correspondent to the director general of the Agence nationale de sécurité du médicament et des produits de santé ; 2° For a healthcare professional who is aware of an incident or risk of i…
…article L. 5232-3 may only be supplied by service providers and equipment distributors who have competent staff according to the type of equipment or service concerned. Competent personnel include : a…
Designation as an inspector of the Agence nationale de sécurité du médicament et des produits de santé, as provided for in Article L. 5313-1, is the subject of a decision by the Director General.The l…
…ame of this correspondent to the Director General of the Agence nationale de sécurité du médicament et des produits de santé ; 2° For a healthcare professional who is aware of a failure or alteration…
…t's family or social environment insofar as it affects the way in which the patient is treated; 4° Methods and dates of admission and discharge; 5° The medical units which treated the patient; 6° The…
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