Warning! Electric models have a
lifting mechanism that can lift the
user so high that it can pose a risk.
If the user cannot get out of the
device from its highest position,
then the seat height should never
be higher than the position at which
the patient’s feet touch the ground.
The only exception to this is cases
where the user can summon help via
a home-help alarm or telephone.
Warning! Only tested and approved
batteries and chargers from Mercado
Medic may be used with models
with electrical functions. If using
a different charger or different
batteries to those which are
provided alongside the device by
Mercado Medic AB, the CE marking
and Mercado Medic AB’s device
liability will cease to be valid for any
cases regarding the battery, charging
or other electronics of the device.
Warning! The device must not be
equipped with any accessories
or components other than those
approved by Mercado Medic.
To maintain the CE marking, no
individual modifications or changes
may be carried out without Mercado
Medic's approval. If unapproved
components are intended to be
used, see section 5.15. Individual
adaptation.
Warning! Do not plug any electrical
accessory, other than those
customised by Mercado Medic, into
the control system’s contacts. Non-
adapted components are at risk of
breaking and in turn injuring the
user. If unapproved components
are intended to be used, see section
5.15. Individual adaptation.
Warning! Installation, connection
or dismantling is not risk-free. If
components are handled incorrectly,
for example, crushing damage
may occur. This type of work may
therefore only be carried out
by a Mercado Medic authorised
technician.
Warning! All parts of the device must
be installed and fixed so that there is
no risk of small parts coming loose.
All cables must be secured with
cable ties to the device's structure to
minimise the risk of strangulation.
6.3. Expected service life
The expected service life of the device is ten
years when used in accordance with these
instructions for use. The expected service
life of the device is calculated from the date
of manufacture of the device. The date of
manufacture of the device can be found
on one of the silver labels on the device's
base and is in the format YYYY-MM (year
and month), see Figure 6.1. The label also
includes serial numbers and an identifier for
the device model (UDI-DI).
38
Instructions for use for medical work chairs in the REAL 9000 PLUS device range
Important safety information
21-08742-EN-01
2000m
150 kg
REAL 9000 PLUS
Basic UDI-DI: 732184D0019P
21-08974
-01
Tryffelslingan 14
SE - 181 57 Lidingö
www.mercado.se
Mercado
Medic AB
###### 001
90######AB
YYYY-MM
Identifi cation bar codes:
00123456700012345600123456701PV0000
Example label 123
Figure 6.1. Serial number, UDI-DI and date of manufacture on the
label.
Summary of Contents for REAL 9000 PLUS Series
Page 2: ...Space for device label with serial number...
Page 60: ......
