bort medical Generation Mode D'emploi page 11

EN
the manufacturer and the Medicines & Healthcare products Regulatory
Agency (MHRA).
You can find our contact information in these instructions for use. You
can find the contact information for the national authority responsible for
your country under the following link: www.bort.com/md-eu-contact.
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: 10.2024
Medical device | Single patient – multiple use
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