At Manningham Medical Centre, you can find all the data about Danish Medical Devices Certification. 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.


Medical devices - Danish Medicines Agency

    https://laegemiddelstyrelsen.dk/en/devices
    Updated 01 November 2022. Medical devices are products which are used to diagnose, prevent, relieve or treat a disease, disability, injury, etc. There are more than 500,000 different types of medical devices available, covering anything from wheelchairs and glasses to pacemakers, mobile phone apps and state-of-the-art surgical equipment.

Registration and marketing - Danish Medicines Agency

    https://laegemiddelstyrelsen.dk/en/devices/registration-and-marketing/
    The device must be classified pursuant to the applicable rules and which are specified in Annex VIII of EU regulation 2017/745 on medical devices or Annex VIII of …

Certification of Medical Devices - Compliance, Testing, Approval

    https://presafe.dk/
    Presafe Denmark A/S offers global market access with certification services according to the European medical device directive, ISO13485 standard, IVD directive, the Canadian …

MDR: How are medical devices regulated in Denmark?

    https://mdlaw.eu/mdr/mdr-how-are-medical-devices-regulated-in-denmark/
    The Danish Authority must be notified of any changes to the information previously notified. All the notifications are kept in an electronic register. Clinical Trials. …

Global Testing & Certification of Medical Devices & EX …

    https://presafe.dk/about-presafe-denmark
    Presafe Denmark A/S (formerly DGM Denmark A/S) provides global market access certifying the safety and quality of products and systems according to international safety …

Denmark Medical Device Registration - DHMA Approval

    https://arazygroup.com/medical-device-registration-denmark/
    REGULATORY AUTHORITY: Devices are regulated by the EU list of Competent Authorities.In Denmark, devices are regulated by the Danish Health and …

Registration of healthcare professionals - Danish Patient …

    https://en.stps.dk/en/health-professionals-and-authorities/registration-of-healthcare-professionals/
    All information of importance to the assessment of your application for authorisation will be processed electronically by the Danish Patient Safety Authority, and if required by …

Overview of Medical Device Regulations …

    https://www.regdesk.co/overview-of-medical-device-regulations-in-denmark/
    The Danish Medicines Agency charges two annual fees and one registration fee. The registration fee is equal to either 1,159 DKK ($176 USD) for manufacturers or 1,147 DKK ($175 USD) for …

About Medicoindustrien | Medicoindustrien

    https://medicoindustrien.dk/content/about-medicoindustrien
    Medicoindustrien is the industry association for companies in Denmark which develop, manufacture, sell or otherwise take an interest in medical devices. Medicoindustrien's …

EUROPA - European Commission - Growth - Regulatory …

    https://ec.europa.eu/growth/tools-databases/nando/index.cfm?fuseaction=notifiedbody.notifiedbody&refe_cd=EPOS%5F43865&version_no=2
    DS Certificering A/S - Danish Medical Devices Certification Kollegievej, 6 DK-2920 Charlottenlund Country : Denmark Phone : +45/72.24.59.00 Fax : +45/72.24.59.03 Email …



Need more information about Danish Medical Devices Certification?

At Manningham Medical Centre, we collected data on more than just Danish Medical Devices Certification. There is a lot of other useful information. Visit the related pages or our most popular pages. Also check out our Doctors page.