At Manningham Medical Centre, you can find all the data about Dutch Competent Authority Medical Devices. We have collected data about general practitioners, medical and surgical specialists, dental, pharmacy and more. Please see the links below for the information you need.


Registration of a medical device or IVD | Medical …

    https://english.igj.nl/medical-technology/market-authorisation/registration-and-deregistration
    Manufacturers may place a medical device or in vitro diagnostic device (IVD) in Europe only if it complies with the statutory requirements. The Health and Youth Care Inspectorate (IGJ) is responsible for monitoring, and supervising compliance alongside oversight counterparts from the other European Member Stat… See more

Rules for manufacturing and using medical devices

    https://business.gov.nl/regulation/medical-devices/
    The Dutch National Implants Registry (in Dutch) registers the implants that patients in the Netherlands have received, such as artificial hip joints, artificial cardiac pacemakers or …

Medical devices: MDR and IVDR in the Netherlands

    https://business.gov.nl/sector-specific/care-and-animal-care/medicines-and-medical-technologies/medical-devices-mdr-and-ivdr/
    Medical devices includes many products and services: from bandages to medical apps to pregnancy tests. The new European regulations may have serious implications for …

List of Competent Authorities for Medical Devices - AKRN

    https://akrnconsulting.com/list-member-states-competent-authorities-for-medical-devices/
    The competent authority belongs to the government of the Member State of the European Union (EU) and their responsibility is to transposes the requirements of …

National competent authorities (human) | European …

    https://www.ema.europa.eu/en/partners-networks/eu-partners/eu-member-states/national-competent-authorities-human
    List of national competent authorities in the EEA. Information on coronavirus …

Notifications | Medical devices and in vitro diagnostic

    https://english.farmatec.nl/medical-devices/notifications
    There are three types of notifications: notifications of 'new' medical devices and in vitro diagnostic medical devices (IVDs) which are being marketed for the first time in …

CAMD - Competent Authorities for Medical Devices : CAMD

    https://www.camd-europe.eu/
    The European Competent Authorities for Medical Devices (CAMD) met for its 51st meeting in Prague on the 20th – 21st October 2022 under the Czech Presidency of the Council of …

Competent authority: CCMO or Ministry of Health, …

    https://english.ccmo.nl/investigators/research-with-a-medicinal-product-extra-review-competent-authority/competent-authority-ccmo-or-ministry-of-health-welfare-and-sport
    the competent authority (CCMO or Ministry of Health, Welfare and Sport). The CCMO acts as competent authority for research with a medicinal product that is reviewed by an …

Home | Health and Youth Care …

    https://english.igj.nl/
    In the Netherlands, some pharmacies provide prescription medicines to people who live in other EU member states. Those pharmacies typically use mail-order services to deliver the prescribed …

Medical Device Registration and Approval in Netherlands

    https://arazygroup.com/medical-device-registration-netherlands/
    REGULATORY AUTHORITY: Devices are regulated by the EU list of Competent Authorities. In the Netherlands, devices are regulated by the Ministry of Health, Welfare …



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