MB4400 Gemino 30 Parkinson
Cleaning the brakes
Clean the brake blocks and brake springs
regularly.
Cleaning the basket
The basket can be removed and washed
separately. Machine wash 60°, hand wash 40°
or disinfection.
To disinfect; use approved chemical
disinfectant. Do not use heat disinfection.
Conditions that could damage the
rollator
The rollator should not be used at
temperatures below -35 °C or above 60
°C. No specific requirements are made in
connection with humidity or air pressure.
No further requirements are made regarding
storage conditions.
Screws and nuts
Screws and nuts can become loose over
time. Therefore, remember to check and if
necessary retighten all screws and nuts on a
regular basis. A thread-locking product, such
as Loctite Blue No. 243, may be used.
If self-locking nuts have been removed they
lose some of their locking ability and should
be replaced.
Hygiene measures when being
re-used:
Prior to the 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.
Changing batteries
Once a year the batteries need to be
replaced, depending on the usage of the
laser. First unplug the pushbutton and
laser from the electronics box. Unclick the
electronics box from the baseplate and
replace the 3 AA batteries with high quality
AA batteries. Reassemble the electronics
box back on the baseplate by clicking it
into position. Take care that the slots for the
pushbutton and laser plug face to the ground.
Plug the laser and pushbutton back in and
the rollator is ready for use again.
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.
English
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 laser light must be treated
as hazardous 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.
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