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Showing 7041–7050 of 38229 articles for “Art. R 134-6”
The manufacture, possession and use of batches of Category A, B or C radioactive sources, high activity sealed sources as defined inAnnex 13-7, the management of radioactive waste as defined in Articl…
I.-For the nuclear activities referred to in Article L. 1333-10, the person responsible for the nuclear activity and, where applicable, the head of the establishment when a different person is involve…
I.-The following nuclear activities are subject to the declaration, registration or authorisation system mentioned in Article L. 1333-8, subject to the provisions of Article L. 1333-9: 1° For radioact…
I.-Subject to the provisions of Article R. 1333-107, the following are exempt from the authorisation, registration or declaration provided for in Article L. 1333-8: 1° The possession, manufacture, use…
I.-The results of the initial inspections provided for in Articles R. 4451-40 and R. 4451-44 are recorded in the safety register or registers referred to in Article L. 4711-5. II -The results of the o…
The employer shall make the results of the checks provided for in this section available to the health professionals referred to in the first paragraph of Article L. 4624-1 and to the Social and Econo…
A joint order of the ministers responsible for labour and agriculture shall specify: 1° The work equipment or categories of work equipment and the type of sealed radioactive sources for which the empl…
For medical devices other than those subject to clinical investigations, the certification procedures mentioned in Article R. 5211-14 are as follows: 1° The EC declaration of conformity ; 2° The EC de…
For medical devices to be subject to clinical investigations, the manufacturer must comply with the provisions of Title II of Book I of Part I of this Code.
For the purposes of placing a custom-made medical device on the market, the manufacturer shall follow the procedure defined in Article R. 5211-51. The Director General of the Agence nationale de sécur…
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