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Showing 681–690 of 62812 articles for “Art. Futures margin and mark-to-market rules”
All in vitro diagnostic medical devices imported, placed on the market or put into service must bear the CE mark. However, CE marking is not required for devices undergoing a performance evaluation or…
…nder the responsibility of the manufacturer or his authorised representative, in a visible, legible and indelible manner on the in vitro diagnostic medical device where this is possible and appropriat…
…to the provisions of Article R. 5221-9, in vitro diagnostic medical devices which comply with the standards relating to them and transposing the harmonised European standards, the references of which…
The provisions of articles R. 5211-15, R. 5211-17, R. 5211-19 and R. 5211-20 are applicable to in vitro diagnostic medical devices.
…sions of this Title, decrees in the Council of State, issued after consultation with the employers' and employees' professional organisations concerned, shall determine : 1° The work equipment and mea…
Machinery and personal protective equipment subject to the relevant technical rules of Annexes I and II to this Title respectively, when designed and constructed in accordance with the standards liste…
In cases other than those mentioned in article R. 4311-12, a decree may make standards mandatory.
…utomatically preceded by an audible or visual warning signal. The exposed worker must have the time and the means to quickly remove himself from the risks generated by starting or possibly stopping th…
Work equipment is installed and equipped to prevent hazards from falling or flying objects such as machined parts, tooling, swarf and waste.
The protectors and protective devices provided for in articles R. 4324-1 and R. 4324-2 have the following characteristics: 1° They are of robust construction, adapted to the conditions of use; 2° They…
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