| 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 | Will be updated according to MDR - please see norwegian version | 1581 | |
| Classification of medical devices | https://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/classification-of-medical-devices | Classification of medical devices | Will be updated according to MDR - please see norwegian version | 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 | |
| Exemption from the conformity assessment procedure | https://legemiddelverket.no/english/medical-devices/regulatory-information-regarding-medical-devices/exemption-from-the-conformity-assessment-procedure | Exemption from the conformity assessment procedure | | 2476 | Information regarding exemption from the conformity assessment procedure |
| 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 | |
