Sideinnhold
The Norwegian Register for Medical Devices
Log into the Register for Medical devices
Norwegian manufacturers and authorised representatives are obliged to register their Medical device in the Norwegian Register for Medical Devices.
Registration should be performed at the start time of the placing on the marked of the medical device. A declaration of conformity should therefore be issued before registration takes place.
Manufacturers and authorised representatives localised in other Member States cannot register in the Norwegian Register for Medical Devices. Distributors and importers are not obligated to register.
How to register
To register in the Norwegian Register for Medical Devices for the first time, the manufacturer or authorised representative must fill out a form. The contact person will then receive username and password by e-mail. The form is only available in Norwegian. If you are unable to use the form, please contact NoMA at MSOD@legemiddelverket.no.
If you are already registered, please log in with your username and password.
EUDAMED
EUDAMED is scheduled to be fully functional in Q1 2024. Registration will be mandatory two years after the database is fully functional. The Norwegian Medicines Agency encourages Norwegian manufacturers, authorised representatives, importers and notified bodies to register before mandatory registration enters into force. Voluntary registration in EUDAMED does not replace the obligation to register in the national register.
