To Whom it May Concern
NO-xx/xxxx
Date: xx.xx.xxxx

Certificate of Free Sale

The Norwegian Medical Products Agency as competent authority for medical devices hereby declares that the following manufacturer has its registered place of business in Norway:

Eventuell produksjonssted på vegne av norsk produsent

Adresse

Land	– stryk dette avsnittet hvis det ikke er aktuelt.

For	Produsent

SRN:

Adresse

Adresse

Norway

We have been notified that the following medical devices bear the CE-mark in accordance with Regulation (EU) 2017/745/Regulation (EU) 2017/746:

Product Name	Certificate number	Basic UDI-DI
Identisk med navn i Samsvarserklæring og Utstyrsregister	Dersom relevant

The precondition for medical devices to be CE-marked in accordance with Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices is to meet the essential requirements for safety. A CE-marked medical device may be marketed within the European Union/European Economic Area without any approval from the Norwegian Medical Products Agency, and may be exported without any restrictions.

This certificate is valid until xx. Month xxxx

Raymond Ludvigsen	Jørgen Bryn

Senior Adviser	Consultant