20-06583-UK
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3
IMPORTANT INFORMATION & CLASS
The REAL chair has replaceable components, accessories and functions with setting options for individual custo-
misation. The chair must only be used by the person for whom it was prescribed and for the purpose for which it is
intended. The chair is intended for indoor use and must not be exposed to water, other fluids or chemicals. Nor should
it be exposed to high temperatures, prolonged and intense sunlight or other forms of radiation. The chair must not be
equipped with any accessories or components other than those approved by Mercado Medic AB. To maintain the CE
marking, modifications or changes must not be carried out without Mercado Medic AB’s approval. Repairs and other
technical measures may only be carried out by personnel authorised by Mercado Medic AB. Read this manual carefully
before using the chair for the first time.
NOTE!
The electrical functions may be used for max. 10 % of the time (max. 6 mins/hour).
Exceeding this limit may result in damage to the chair.
EXPECTED SERVICE LIFE
The expected service life of the Product is ten years when used in accordance with the instructions in this manual.
The Product's date of manufacture can be found together with the serial number on one of the silver labels on the
Product's chassis, marked with Lev/Del and stated in the format YYWW (number of year and week).
As a user of the Product, you should contact your prescriber, technical aids centre or distributor if the Product
shows reduced or altered performance.
After the expected service life, it is important to make an overall assessment of the Product before continuing
to use it. After the expected service life, Mercado Medic AB cannot guarantee the suitability and safety of the
product, as Mercado Medic AB has no control over how the product has been used and wear and tear. The overall
assessment of the Product should be carried out by the healthcare organisation if the product is prescribed,
and, as a minimum, should take into account how the Product has been used, the condition of the Product and
its component parts, whether the Product has been reconditioned and been serviced, when this occurred, what
actions have been taken on these occasions and the reason for the actions.
In markets outside Sweden and Norway where a distributor has sold the Product directly to the user (where
applicable), and therefore there is no responsible prescriber, periodic maintenance must be carried out according
to instructions in the section Reconditioning and Service in addition to the overall assessment above.
After the expected service life, Mercado Medic AB cannot guarantee the provision of spare parts. CE marking is
not affected by expected service life.