Article R4311-89
In addition to its Chairman, the Disciplinary Chamber of First Instance shall comprise :1° Where the total number of nurses on the most recently published roll is less than or equal to 10,000, six ful…
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Showing 7051–7060 of 38200 articles for “Art. R. 210-6”
In addition to its Chairman, the Disciplinary Chamber of First Instance shall comprise :1° Where the total number of nurses on the most recently published roll is less than or equal to 10,000, six ful…
…stance is announced by the National Council under the same conditions as those laid down in article R. 4311-58.Candidates shall make their candidacy known under the conditions laid down in Chapter V o…
Any person who sterilizes with a view to placing on the market CE-marked medical devices designed by their manufacturer to be sterilized before use or systems or kits referred to in Section 10 of this…
…evices with an approved type described in an EC type-examination certificate referred to in Article R. 5211-41 or with the technical documentation referred to in Article R. 5211-39 under the condition…
…nce, for class II a medical devices or class I medical devices, the provisions laid down in Article R. 5211-49 apply subject to the following modifications: 1° For class II a medical devices, the auth…
…check the manufacturing processes. The decision of the approved body is notified to the manufacturer. It contains the conclusions of the inspection and a reasoned assessment. The manufacturer ensures…
…evices with an approved type described in an EC type-examination certificate referred to in Article R. 5211-41 or with the technical documentation referred to in Article R. 5211-39 under the condition…
As part of the procedure applicable to custom-made medical devices, the manufacturer must draw up documentation including the name and address of the manufacturer, the place or places of manufacture,…
For Class IIa medical devices or Class I medical devices, the provisions of Article R. 5211-46 apply subject to the following modifications: 1° For class II a medical devices, the authorised body veri…
…check the manufacturing processes. The decision of the approved body is notified to the manufacturer. It contains the conclusions of the inspection and a reasoned assessment. In addition, for a class…
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