bort medical AktiVen Serie Mode D'emploi page 14

EN
Disposal
Upon the termination of use, the product must be disposed of
in accordance with the corresponding local requirements.
Declaration of conformity
We confirm that this device conforms with the requirements of
REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT
AND OF THE COUNCIL. You can find the current declaration of
conformity under the following link:
www.bort.com/conformity
Status: 03.2024
Medical device | Single patient – multiple use
12