Registration for medical deviceshttps://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/registration-for-medical-devicesRegistration for medical devicesRegistration for Norwegian manufacturers and Norwegian authorised representatives of medical devices (not distributors). 1580
Clinical investigation of medical deviceshttps://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/clinical-investigation-of-medical-devicesClinical investigation of medical devicesRegulatory guidance on clinical investigations of medical devices. 1581
Classification of medical deviceshttps://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/classification-of-medical-devicesClassification of medical devicesRisk 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 deviceshttps://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/placing-on-the-market-of-medical-devicesPlacing on the market of medical devicesProcedure 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-englishFree Sales Certificate (English)Free Sales Certificate to Norwegian manufacturers of medical devices. 1584
Notified Bodyhttps://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/notified-bodyNotified BodyNotified 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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