Article L5462-6
For the criminal offences mentioned in this chapter, natural persons are also liable to the following additional penalties: 1° Display or dissemination of the decision handed down, under the condition…
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Showing 9991–10000 of 61025 articles for “Art. L 324-1 ss.”
For the criminal offences mentioned in this chapter, natural persons are also liable to the following additional penalties: 1° Display or dissemination of the decision handed down, under the condition…
I.-Placing on the market or putting into service on French territory a medical device or its accessories is punishable by five years' imprisonment and a fine of 375,000 euros: 1° Without the EU declar…
I.-Placing on the market or putting into service on French territory a device mentioned in Article 1 of Regulation (EU) 2017/746 is punishable by five years' imprisonment and a fine of €375,000: 1° Wi…
Legal entities declared criminally liable, under the conditions set out in article 121-2 of the French Criminal Code, for the offences set out in this chapter shall incur, in addition to the fine set…
For the criminal offences mentioned in this chapter, natural persons are also liable to the following additional penalties: 1° Display or dissemination of the decision handed down, under the condition…
Failure by the manufacturer, authorised representative or importer of devices referred to in Article 1 of Regulation (EU) 2017/745, whose registered office is located on French territory, to register…
Failure by the operator to subject a device mentioned in Article 1 of Regulation (EU) 2017/745 to maintenance obligations and quality controls pursuant to Article L. 5212-1 is punishable by two years'…
For a manufacturer, agent, distributor or importer of a device referred to in Article 1 of Regulation (EU) 2017/746 to carry out, cause to be carried out, disseminate or cause to be disseminated adver…
I.-If the manufacturer of a device referred to in Article 1 of Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 or, where applicable, its authorised representativ…
I.-If the manufacturer of a device referred to in Article 1 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 or, where applicable, its authorised representativ…
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