The reprocessing of single-use devices referred to in Article 17 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017, their placing on the market and their use are prohibited.
Home | French Legislation Articles | French Public Health Code | Legislative part | Part five: Health products | Book II: Medical devices, in vitro diagnostic medical devices and other products and articles regulated in the interests of public health | Title I: Medical devices | Chapter I: Legal status of medical devices. | Article L5211-3-2 of the French Public Health Code
The reprocessing of single-use devices referred to in Article 17 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017, their placing on the market and their use are prohibited.
Le retraitement de dispositifs à usage unique mentionné à l’article 17 du règlement (UE) 2017/745 du Parlement européen et du Conseil du 5 avril 2017, leur mise sur le marché et leur utilisation sont interdits.
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is a Registered Trademark of
PETROFF LAW FIRM (SELARL LEGASTRAT)
182, rue de Rivoli
75001, Paris France
RCS Paris n°814433470
Paris Bar Registration n° (Toque) C2396
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is a Registered Trademark of
PETROFF LAW FIRM (SELARL LEGASTRAT)
182, rue de Rivoli
75001, Paris France
RCS Paris n°814433470
Paris Bar Registration n° (Toque) C2396
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