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EUR-Lex - 31993L0016 - EN - EUR-Lex - Europa
- https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX%3A31993L0016
- Council Directive 93/16/EEC of 5 April 1993 to facilitate the free movement of doctors and the mutual recognition of their diplomas, certificates and other evidence of formal …
EUR-Lex - l23021 - EN - EUR-Lex - Europa
- https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=LEGISSUM%3Al23021
- Council Directive 93/16/EEC of 5 April 1993 to facilitate the free movement of doctors and the mutual recognition of their diplomas, certificates and other evidence of …
ANNEX I Medical Device Directive - ESSENTIAL …
- https://lexparency.org/eu/31993L0042/ANX_I/
- If parts of a device (or a device itself) intended to administer and/or remove medicines, body liquids or other substances to or from the body, or devices intended for transport and …
MEDICAL DEVICES Guidance document …
- https://ec.europa.eu/docsroom/documents/10337/attachments/1/translations/en/renditions/native
- Conformity assessment is the method by which a manufacturer demonstrates that their devices comply with the requirements of Directive 93/42/EEC. The classification of the …
B COUNCIL DIRECTIVE 93/42/EEC of 14 June …
- https://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=CONSLEG:1993L0042:20071011:en:PDF
- COUNCIL DIRECTIVE 93/42/EEC of 14 June 1993 concerning medical devices THE COUNCIL OF THE EUROPEAN COMMUNITIES, Having regard to the …
Council Directive 93/42/EEC of 14 June 1993 concerning …
- https://eur-lex.europa.eu/legal-content/EN/LSU/?uri=CELEX%3A31993L0042
- In 2013, the Commission adopted an implementing act, Implementing Regulation (EU) No 920/2013 on designating and supervising notified bodies under …
ANNEX IX Medical Device Directive - CLASSIFICATION …
- https://lexparency.org/eu/31993L0042/ANX_IX/
- Rule 3. All non-invasive devices intended for modifying the biological or chemical composition of blood, other body liquids or other liquids intended for infusion into the body …
2019 - 2024 - europarl.europa.eu
- https://www.europarl.europa.eu/doceo/document/TA-9-2023-0052_EN.pdf
- continue to comply with Directive 90/385/EEC or Directive 93/42/EEC can lawfully be placed on the market or put into service. (3) Also due to the impact of the COVID-19 …
MEDICAL DEVICES : Guidance document
- https://ec.europa.eu/docsroom/documents/10288/attachments/1/translations/en/renditions/pdf
- The medical devices directives (MDD, AIMD, [draft IVD]) each require a statement given on the label and/or the information provided with the device on any time limitation on the …
Council Directive 93/42/EEC of 14 June 1993 concerning …
- https://www.legislation.gov.uk/eudr/1993/42/data.htm
- ‘ If the appliance is at the same time a medical device within the meaning of Directive 93/42/EEC and if it satisfies the essential requirements laid down therein for that device, …
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