bort medical 215 870 Mode D'emploi page 14

EN
Duty of notification
If a serious worsening of the state of health occurs when using the medical device, you
are obliged to notify the specialist dealer or us as 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 appointed authority 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: 10.2021
Medical device | Single patient – multiple use
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