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Technical Specifications - Gemino 30 Gebruikershandleiding

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  • DUTCH, pagina 43
MB4100 Gemino 30
Hygiene measures when being
re-used:
Prior to the walker/rollator being re-used, it
must be carefully prepared. All surfaces which
come into contact with the user must be
treated with a disinfection spray.
To do this, you must use a disinfectant as
authorised/recommended in your country, for
rapid alcohol-based disinfection for medical
products and medical devices, which must be
disinfected quickly.
Please be aware of the manufacturer's
instructions for the disinfectant you are using.
In general, a complete disinfection cannot
be guaranteed on seams. We therefore
recommend that you dispose of seat and back
slings to avoid micro-bacterial contamination
with active agents according to your local
infection protection law.
Regular inspection
• Check that the brakes function correctly.
Adjust if necessary.
• Check that the wheels are in good condition
and that they have not been damaged.
• Ensure that the rollator is clean and that all
moving parts function correctly.
• Check and if necessary adjust all screwed
connections.
Repairs
Apart from small repairs to paintwork, the
replacement of wheels and the adjustment
of the brakes, all repairs must be undertaken
by qualified personnel at the supplier in your
municipality or at the technical aids centre.
For information about repairs and servicing,
contact the technical aids centre in your
county.
Storage
Store the rollator in a standing position.
The rollator can be kept outdoors.
Transport
Fold the rollator before transport. It should be
lifted and carried using the lifting handles.
Never lift the rollator by the brake cables or
the seat strap.

Technical specifications

Materials used
The rollator and most of the parts are
manufactured using a special aluminium alloy.
Areas of application
The rollator is intended for both indoor and
outdoor use on a flat and firm surface.
It has been developed for individuals with
reduced muscle strength, reduced movement,
reduced mobility and reduced stability.
The expected lifetime is 10 years.
Waste handling
Waste relating to packaging, parts of the
rollator or the rollator itself can be treated as
general waste. The main component of the
rollator is aluminium, which can be melted
down for reuse. The plastic and cardboard
used in the packaging can be recycled.
CE labelling
As the manufacturer, SUNRISE
MEDICAL, declares that this product
conforms to the Medical Device
Regulation (2017/745).
UKCA Labelling
As the manufacturer, SUNRISE
MEDICAL, declares that this product
conforms to the UK Medical Devices
Regulation 2002 No. 618.
Notice to the user and/or patient: Any serious
incident that has occurred in relation to the
device should be reported to the manufacturer
and the competent authority of the Member
State in which the user and/or patient is
established.
B4Me special adaptations
Sunrise Medical strongly recommends that
in order to ensure that your B4Me product
operates, and performs as intended by
the manufacturer; all the user information
supplied with your B4Me product is read and
understood, before the product is first used.
Sunrise Medical also recommends that
the user information is not discarded after
reading it, but it is kept safely stored for future
reference.
Medical Device Combinations
It may be possible to combine this Medical
device with one or more other Medical Device
or other product. Information on which
combinations are possible can be found at
www.Sunrisemedical.co.uk. All combinations
listed have been validated to meet the General
Safety and Performance Requirements, Annex
I Nr. 14.1 of the Medical Device Regulation
2017/745.
Guidance on the combination, such as
mounting, can be found at
www.SunriseMedical.co.uk.
English
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