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Regulatory information regarding medical devices

Medical devices - Register. Clinical investigation. Classification. Placing on the market. Free sales certificate. Notified body. Administrative and advisory responsibilities related to legislation for medical devices.

Registration for medical devices	https://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/registration-for-medical-devices	Registration for medical devices	Registration for Norwegian manufacturers and Norwegian authorised representatives of medical devices (not distributors).	1580
Clinical investigation of medical devices	https://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/clinical-investigation-of-medical-devices	Clinical investigation of medical devices	Regulatory guidance on clinical investigations of medical devices.	1581
Classification of medical devices	https://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/classification-of-medical-devices	Classification of medical devices	Risk classification of a medical device is deciding what type of conformity assessment procedure should be used before the device is placed on the marked.	1582
Placing on the market of medical devices	https://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/placing-on-the-market-of-medical-devices	Placing on the market of medical devices	Procedure and responsibility related to CE marking and placing on the market of medical devices.	1583
Free Sales Certificate (English)	https://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/free-sales-certificate-english	Free Sales Certificate (English)	Free Sales Certificate to Norwegian manufacturers of medical devices.	1584
Notified Body	https://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/notified-body	Notified Body	Notified body has the task to conduct conformity assessments, i.e. to assess whether a medical device complies with the regulatory requirements.	1585

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