bort medical X-Walker Achillo Manual De Instrucciones página 11

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 responsible national body in 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: 01.2023
Medical device | Single patient – multiple use
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