Eu Medical Device Directive 2007 47 Ec

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EUR-Lex - 32007L0047 - EN - EUR-Lex - Europa

https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX%3A32007L0047

DIRECTIVE 2007/47/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL. of 5 September 2007. amending Council Directive 90/385/EEC on the approximation of the …

Medical Device Directive (MDD), Directive 2007/47/EC - Lexparency

https://lexparency.org/eu/32007L0047/

Directive 2007/47/EC of the European Parliament and of the Council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member …

Directive 2007/47/EC of the European Parliament and of …

https://www.legislation.gov.uk/eudr/2007/47/contents

Directive 2007/47/EC of the European Parliament and of the Council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member …

Medical Devices Directive - Wikipedia

https://en.wikipedia.org/wiki/Medical_Devices_Directive

B COUNCIL DIRECTIVE 93/42/EEC of 14 June …

https://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=CONSLEG:1993L0042:20071011:en:PDF

M5 Directive 2007/47/EC of the European Parliament and of the Council of 5 September 2007 L 247 21 21.9.2007 1993L0042 — EN — 11.10.2007 — 005.001 — 1 B …

21.9.2007 EN Official Journal of the European Union …

https://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2007:247:0021:0055:en:PDF

Directive 2001/83/EC (10). (6) It is necessary to clarify that software in its own right, when specifically intended by the manufacturer to be used for one or more of the …

IMPLEMENTATION OF DIRECTIVE 2007/47/EC …

https://ec.europa.eu/docsroom/documents/10264/attachments/1/translations/en/renditions/pdf

Commission's services shall guide a uniform practice throughout the EU. Since Directive 2007/47/EC is addressed to the Member States, preliminary transposition into national ...

GUIDELINES ON MEDICAL DEVICES - European …

https://ec.europa.eu/docsroom/documents/10336/attachments/1/translations/en/renditions/pdf

Directive 90/385/EEC , as amended by Directive 2007/47/EC Directive 93/42/EEC , as amended by Directive 2007/47/EC Interpretative Documents MEDDEV 2.7.1 Rev. 3; …

MEDICAL DEVICES Guidance document …

https://ec.europa.eu/docsroom/documents/10337/attachments/1/translations/en/renditions/native

The present MEDDEV is part of a set of guidelines relating to questions of application of EU Directives on medical devices. They are not legally binding. ... Directive 2007/47/EC: 2: …

EUR-Lex - 31993L0042 - EN - EUR-Lex - Europa

https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:31993L0042

1. In the case of devices falling within Class III, other than devices which are custom-made or intended for clinical investigations, the manufacturer shall, in order to affix the CE …

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