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Medical devices | European Medicines Agency

    https://www.ema.europa.eu/en/human-regulatory/overview/medical-devices
    The Medical Devices Regulation applies since 26 May 2021. Manufacturers must comply with the Regulation when placing new medical devices on the market. It repeals Directive 93/42/EEC on medical devices and the Directive 90/385/EEC on active …

Medical Device Regulation comes into application

    https://www.ema.europa.eu/en/news/medical-device-regulation-comes-application
    The Medical Device Regulation (MDR), which was adopted in April 2017, changes the European legal framework for medical devices and introduces new …

Directives - Public Health

    https://health.ec.europa.eu/medical-devices-sector/directives_en

    Medical Devices - Sector - Public Health

      https://health.ec.europa.eu/medical-devices-sector_en
      The following medical devices Directives were repealed and replaced by Regulation (EU) 2017/746 and Regulation (EU) 2017/745 respectively... New Regulations …

    New Regulations - Public Health

      https://health.ec.europa.eu/medical-devices-sector/new-regulations_en
      With effect from 26 May 2022, Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices replaces Directive …

    Medical devices - Internal Market, Industry, Entrepreneurship and …

      https://single-market-economy.ec.europa.eu/single-market/european-standards/harmonised-standards/medical-devices_en
      Guidelines related to medical devices regulations; European Commission contact point: Directorate-General for Health and Food Safety Medical devices Email Webpage on …

    Harmonised standards - Public Health

      https://health.ec.europa.eu/medical-devices-topics-interest/harmonised-standards_en
      For Regulation (EU) 2017/746 on in vitro diagnostic medical devices: Commission Implementing Decision (EU) 2022/729 of 11 May 2022 Commission …

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

      https://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=CONSLEG:1993L0042:20071011:en:PDF
      medical device as a general rule is governed by the present Directive and the placing on the market of the medicinal product is governed by Directive 65/65/EEC; …

    The European Union Medical Device Regulation – …

      https://eumdr.com/
      Publication of MDCG 2021-24 Guidance on classification of medical devices. The EUDAMED UDI/Devices and NBs & Certificates modules are now open for economic …

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

      https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:31993L0042
      Whereas this Directive covers the medical devices referred to in Council Directive 76/764/EEC of 27 July 1976 on the approximation of the laws of the Member States on …



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