Changing The Air Filter; Technical Specifications; Symbols That May Appear On The Product; General Warnings And Cautions Warnings - Resmed S8 Autoset Gebruikershandleiding
Cpap, apap, bilevel
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Weekly:
1.
Remove the air tubing and wash it in warm water and mild
detergent. Rinse thoroughly, hang and allow to dry.
2.
Before next use, reassemble the mask and headgear.
3.
Reconnect the air tubing.
Monthly:
1.
Clean the exterior of the fl ow generator with a damp cloth.
2.
Check the air fi lter for holes and blockage by dirt. Replace it
every six months, or more often in a dusty environment.
For information on cleaning your mask or humidifi er, refer to the
manual supplied with your mask or humidifi er.
WARNING
Beware of electric shock. Do not immerse the fl ow generator
or power cord in water. Always unplug the fl ow generator
before cleaning and make sure it is dry before reconnecting.
CAUTION
•
Do not hang the air tubing in direct sunlight as it may
harden over time and eventually crack.
•
Do not use bleach, chlorine, alcohol, or aromatic-based
solutions, moisturising or antibacterial soaps or scented
oils to clean the air tubing or the fl ow generator. These
solutions may cause hardening and reduce the life of the
product.
Changing the Air Filter
1.
Disconnect the power cord and air tubing.
2.
Remove the air fi lter from the air inlet at the back of the fl ow
generator.
3.
Put the new air fi lter into the air inlet with the blue side facing
out from the fl ow generator.
CAUTION
Do not wash the air fi lter.
Technical Specifi cations
Operating pressure range
Power supply
Operating temperature
Operating humidity
Storage and Transport
Temperature
Storage and Transport
Humidity
Atmospheric pressure
range
Additional Information
Additional technical specifi cations and information can be found
in the device-specifi c user guide on www.resmed.com on the
Products page under Service & Support.
Electromagnetic Compatibility
Product complies with all applicable electromagnetic compatibility
requirements (EMC) according to IEC60601-1-2, for residential,
commercial and light industry environments. The electromagnetic
compatibility tables for these ResMed devices can be found
on www.resmed.com on the Products page under Service &
Support. Click on the PDF fi le for your device.
Aircraft Use
Please consult ResMed and the medical services department of
your carrier if you intend to use your fl ow generator on an aircraft.
4 to 20 cm H
O (CPAP/APAP)
2
2 to 25 cm H
O (Bilevel)
2
Input range 100–240V, 50/60Hz
S8: 2.5A < 140VA (110W) (maximum
power consumption).
VPAP: 40VA (typical power
consumption), < 100VA (maximum
power consumption).
+5°C to +35°C
10–95% non-condensing
-20°C to +60°C
10–95% non-condensing
1,060 hPa (sea level) to 680 hPa
(2,591 m)
The manufacturer reserves the right to change these
specifi cations without notice.
Symbols that may Appear on the Product
Attention, consult accompanying documents
Type CF equipment
Class II equipment
Drip proof
IPX1
Name and address of manufacturer
Dangerous voltage
Environmental Information This device should be disposed
of separately, not as unsorted municipal waste. To dispose of your
device, you should use appropriate collection, reuse and recycling
systems available in your region. The use of these collection,
reuse and recycling systems is designed to reduce pressure
on natural resources and prevent hazardous substances from
damaging the environment. If you need information on these
disposal systems, please contact your local waste administration.
The crossed-bin symbol invites you to use these disposal
systems. If you require information on collection and disposal of
your ResMed device please contact your ResMed offi ce, local
distributor or go to www.resmed.com/environment.
General Warnings and Cautions
Warnings
•
Read the entire guide before using the fl ow generator.
•
The fl ow generator is NOT a life support ventilator and may
stop operating with power failure or in the unlikely event of
certain fault conditions.
•
Advice contained in this guide should not supersede
instructions given by the prescribing physician.
•
A patient should not connect a device to the data
communication port unless instructed to do so by their health
care provider or physician. Only ResMed products are designed
to be connected to the data communication port. Connecting
other devices could result in injury, or damage to the fl ow
generator. (Data communication ports are not available on all
devices.)
•
The fl ow generator should be used with masks (and
connectors)* recommended by ResMed, or by a physician
or respiratory therapist. A mask should not be used unless
the fl ow generator is turned on and operating properly. The
vent hole or holes associated with the mask should never be
blocked.
Explanation: The fl ow generator is intended to be used with
special masks (or connectors) which have vent holes to allow
continuous fl ow of air out of the mask. When the device is
turned on and functioning properly, new air from the device
fl ushes the exhaled air out through the mask vent holes.
However, when the device is not operating, insuffi cient fresh
air will be provided through the mask, and the exhaled air
may be rebreathed. Rebreathing of exhaled air for longer
than several minutes can, in some circumstances, lead to
suffocation. This applies to most models of positive airway
pressure devices.
* Ports may be incorporated into the mask or in connectors that are near
the mask.
•
In the event of power failure or machine malfunction, remove
the mask.
•
In certain fault conditions, pressures up to 30 cm H
APAP) or 40 cm H
O (Bilevel) are possible.
2
•
If oxygen is used with this device, the oxygen fl ow must be
turned off when the device is not operating. If oxygen has been
left on, turn off the device, then wait 30 minutes before turning
on the device again.
Explanation: When the fl ow generator is not in operation and
the oxygen fl ow is left on, oxygen delivered into the air delivery
3
O (CPAP/
2
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