Apex Digital Domus Auto Manuale utente

AUTO

Instruction Manual

Model No.: 9P-077520 PLEASE READ ALL INSTRUCTIONS BEFORE USE.

User’s manual .................................................................P. 1

Manual de Instrucciones

...............................................

P. 18

Instruções de Utilização

................................................

P. 35

Instructions d'utilisation................................................P. 52

Gebrauchsanleitung

......................................................

P. 69

Nederlands

Gebruikershandleiding ..................................................P. 86

Italiano

Manuale di istruzioni ....................................................P.103

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IMPORTANT SAFEGUARDS

READ ALL INSTRUCTIONS BEFORE USE

DANGER - To reduce the risk of electrical shock:

1. Always unplug this product immediately after using.

2. Do not use while bathing.

3. Do not place or store product where it can fall or be pulled into a tub or sink.

4. Do not place in or drop into water or other liquids.

5. Do not reach for a product that has fallen into water. Unplug immediately.

NOTEs, CAUTIONs AND WARNINGs:

NOTE - Calls attention to useful information, tips, reminders.

CAUTION - Calls attention to correct operating or maintenance procedures in order to prevent

damage to or destruction of the equipment or other property.

WARNING - Calls attention to a potential danger that requires correct operating procedures or

practices in order to prevent personal injury.

WARNING - To reduce the risk of burns, electrical shock, fire, or injury:

1. This product should never be left unattended when plugged in.

2. Evaluate patients for entrapment risk according to protocol and monitor patients appropriately.

3. Close supervision is necessary when this product is used on or near children. Electrical burns or

choking accident may result from a child swallowing a small part detached from the device.

4. Use this product only for its intended use as described in this manual. Do not use other mattress not

recommended by the manufacturer.

5. Never operate this product if it has a damaged cord or plug, if it is not working properly, if it has been

dropped or damaged, or exposed to water. Return the product to a service center for examination

and repair.

6. Keep the cord away from heated surfaces.

7. Never block the air openings of this product. Never place the product on a soft surface, such as a

bed or couch, where the air openings may become blocked. Keep the air openings free of lint, hair,

and other similar particles.

8. Never drop or insert any object into any opening or hose on this product.

9. Do not modify this equipment without authorization of the manufacturer.

10. Mattress covers have passed skin sensitization and skin irritation test. However, If you suspect that

you may have had or are having an allergic reaction, please consult a physician immediately.

11. Do not leave long lengths of tubing around the top of your bed. It could lead to strangulation.

CAUTION –

1. If there is a possibility of electro-magnetic interference with mobile phones, please increase the

distance (3.3m) between devices or turn off the mobile phone.

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SYMBOL Definitions

Authorized representative in the European community.

Catalog, reorder or reference number

Manufacturer

Complies with standards protecting against electric shock for type BF equipment.

Attention, you should read the accompanying information carefully!

Attention – Observe proper Disposal of Electrical & Electronic Equipment (WEEE):

This product should be handed over to an appropriate collection point for the

recycling of electrical and electronic equipment. For more detailed information about

the recycling of this product, please contact your local city office, household waste

disposal service or the retail store where you purchased this product.

Consult operating instructions for use

Protected against solid foreign objects of 12,5 mm and greater; Protection against

vertically falling water drops

Class II

Temperature limitation/temperature range

Dry clean, Any Solvent Except Trichloroethylene

Do Not Iron

Tumble Dry, Normal, Low Heat

Do Not Tumble Dry

Do Not Bleach

Do Not Dry Clean

Machine wash, regular / normal, 95 degrees C (203 degrees F)

Machine wash, regular / normal, 60 degrees C (140 degrees F)

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1. INTRODUCTION

This manual should be used for initial set up of the system and for reference purposes.

1.1 General Information

This system is a high quality, affordable mattress system, suitable for the treatment and prevention of

pressure ulcers. This product has been tested and successfully approved for the following standards:

1.2 Intended Use

This product is intended:

 to help and reduce the incidence of pressure ulcers while optimizing patient comfort.

 for long term home care of patients suffering from pressure ulcers.

 for pain management as prescribed by a physician.

NOTE: This equipment is not suitable for use in the presence of flammable anesthetic

mixture with air or with pure oxygen or nitrous oxide.

EN 60601-1

EN 60601-1-2

EN 55011 Class B

IEC61000-3-2

IEC 61000-3-3

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2. PRODUCT DESCRIPTION

2.1 Pump and Mattress System

1. CPR

2. Pump unit

3. Mattress System

4. Quick Connector

2.2 Pump Unit

Front

1. Quick Connectors

2. Front Panel

Rear

1. Power Switch

2. Power Cord

3. Hanger

4. Air Filter

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2.3 Front panel

1. Pressure Adjust

The function can automatically adjust the mattress pressure based on the patient’s weight. To

remind user the process is on-going, the function LED lights will be periodically flashed from left to

right until the Ready LED turn on permanently (the process is completed). There are three

conditions will trigger this function to ensure the appropriate pressure setting for the patient.

A) Press the Auto-Adjust button for 2 seconds, system will automatically re-adjust the

pressure setting.

B) The system will automatically start Auto-Adjust immediately after the initial mattress

inflation is completed.

C) While the system detects a significant change in patient’s weight on the mattress (e.g.

patient Ingress) for a period of time, the system will automatically run the function again.

While the process is completed, system will return to previous setting automatically. To disable

this function, press Auto-Adjust button again.

NOTE: During the Auto-Adjust operation, it is normal that system will go through a

series of inflation and deflation.

2. TUNING

The Tuning function is to fine-tune the system auto-adjusted preset pressure. Three Tuning levels

are available. “0” is system auto-adjusted preset pressure. “+” is one level higher than preset

pressure, and “-” is one level lower than preset pressure.

NOTE: The Tuning function is only available in alternate and static mode.

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3

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3. THERAPY

The Therapy button allows you to choose one of the therapy modes. There are four selectable

therapy modes available. Continually press Therapy button to select a desired mode:

A. MaxFirm

The surface will go into Max firm automatically when the power switch is turned on. This

insures the pump is able to reach its maximum operating pressure. Once the max

pressure level is reached, the pump will automatically switch into alternating mode. User

can also use this function during patient transfers or nursing procedures for better support.

This mode will last for 20 minutes and then it will return to previous setting automatically.

To disable this function, press Maxfirm button again.

B. Alternate

The mattress will alternate every 10 minutes under this therapy mode.

C. Static

Non-alternating mode, all of the air cells is equally inflated.

D. Seat Inflate

The seat inflate features additional supports to the patient during upright position.

4. Alarm Mute

Press alarm mute button to temporary suspend the low-pressure alarm (LED light and buzzer).

Should the situation not resolved within 5 mins, the alarm shall resume to notify the patient.

A. PFA (Power Failure Alarm)

During power failure situation, the Power Failure LED light will lit on with buzzer.

By pressing the mute button to disable both buzzer and LED.

B. Low Pressure Indicator

When low pressure LED lights up, the pressure inside of air mattress is below normal.

Please refer to troubleshooting.

C. Tech. Support

This feature will light during mechanical failure situation. User can notify the technician

for repair.

Alternate

Static

Alternate+Seat Inflate

Static+Seat Inflate

MaxFirm

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5. Panel Lock

If the control panel remains untouched for 5 minutes, a green LED will light and the control panel

will lock all settings. This will prevent the settings from being accidently changed during normal

operation. To unlock, simply press the Panel lock button for three seconds.

3. INSTALLATION

Unpack the box and check the package contents for completeness.

Package Content List

 Mattress unit x 1 (may not be included if only pump unit is purchased)

 Pump Unit x 1

 User Manual x 1

Inspect equipment for damage which may have occurred during shipment. If there is damage, please

contact your dealer immediately.

3.1 Pump & Mattress Installation

1. Place the mattress or pad on top of the bed frame.

Please note for the foot end. If it is an overlay system

(mattress height less than 8”), please make sure there

is a foam or a current mattress underneath.

WARNING: The overlay mattress must be applied

on the underlying mattress.

2. Hang the pump onto bed rail (foot-end), and adjust

hangers to best upright position of the pump, or place

the pump on a flat surface.

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3. Connect air hose connectors from air mattress to the

pump unit. When a "click" sound is felt or heard, the

connection is completed and secured.

NOTE: Check and ensure the air hoses are not

kinked or tucked under mattress.

4. Plug the power cord into electrical outlet.

NOTE:

1. Make sure the pump unit is suitable for the local

power voltage. Do not position the equipment

so that it is difficult to operate the disconnecting

device

2. The plug is also used to disconnect the device.

CAUTION: The pump can only be applied to the

mattress recommended by the

manufacturer. Do not use it for any

other purpose. (Applied part: air

mattress)

5. Then turn the main power switch to ON position.

NOTE: You can unplug the unit to power-off the device.

CAUTION: The pump supplied with the mattress can only be used for mattresses

recommended by the manufacturer. Do not use it for any other purpose.

(applied part: air mattress)

NOTE: (For models WITHOUT the low-air-loss function) During power outages, you

can cover the Quick Connector with the transport cap to maintain air pressure

inside the air cells.

NOTE: After installation, make sure any excess cord or tubing is removed from

possible foot traffic to avoid accidental tripping. All EQUIPMENT should be

positioned to always allow unhindered patient access by physicians and

caregivers.

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4. OPERATIONS

NOTE: Always read the operating instructions before use.

4.1 General operation

1. Switch on the main power switch found on the

side of the pump.

2. Once the pump begins delivering air into the

mattress it will take approximately 30 minutes to

fully inflate the mattress.

3. Every time when mattress is first setup for use, It

will be forced to execute Maxfirm for the quickest

inflation. The low-pressure indicator (yellow LED)

will light up when the mattress is not fully inflated

at initial inflation. If the appropriate pressure is

reached, the low-pressure indicator (yellow LED)

will go off.

4. When the initial inflation (Maxfirm process) is

completed, the system will automatically enter

the Auto-Adjust process.

5. According to the weight and height of the patient,

the system will automatically adjust an

appropriate pressure setting to ensure the

patient’s comfort, and then enter to alternating

mode.

4.2 Emergency CPR Operations

CPR must be performed on a firm surface. Therefore, if an

emergency CPR situation occurs with the patient on the

mattress, the mattress must be quickly deflated. This is

done by quickly pulling on the CPR tag located at the head

of the mattress on the patient’s right-side. The quick

connector found from the pump unit can also be

disconnected to hasten deflation.

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4.3 Low Pressure Function

When an abnormal low pressure is occurred, the Low Pressure indicator (yellow LED) will light up.

Check that connections are correctly made and that they are correctly installed as per installation

instructions.

NOTE - If the pressure level is consistently low, check for any leakage (tubes or connecting

hoses). If necessary, replace any damaged tubes or hoses. Or contact local

qualified dealer for repair.

If the pump unit is equipped with alarm buzzer, the alarm will buzz and the Low Pressure indicator

light up when air pressure is below normal. To mute the alarm, simply press the button on the

panel. However, the low pressure indicator remains until the low-pressure fault condition is solved.

4.4 Static Mode

Press the button to suspend the alternating mode of mattress. By pressing this button again,

the mattress will be back to alternating therapy mode.

4.5 Alarm Mute

When low-pressure situation occurred, both the LED light and buzzer will sound off to warn the

patient. By pressing the button, it will temporary mute the buzzer so the care giver may check for

possible air leaks. Should the situation not resolved within 3 minutes; the alarm will resume to

beep.

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5. CLEANING

It is important to follow the cleaning procedures before first-time use with any patient; this is to avoid the

possibility of transmission of pathogens between patients and caregivers.

Wipe down the pump unit with a damp cloth pre-soaked with a mild detergent. Avoid contact with dust

and proximity to dusty areas. Make sure that any cleaning agents you use will not harm or corrode the

plastic casing on the pump unit.

CAUTION: Do not immerse or soak the pump unit in liquids.

Wipe-down the mattress unit with a damp cloth pre-soaked with warm water containing a mild detergent.

Avoid dust and proximity to dusty areas. The cover may also be cleaned using sodium hypochlorite

diluted in water. All components should be air dried thoroughly before use.

CAUTION: Do not use phenolic based products for cleaning.

CAUTION: Do no dry the mattress in direct sunlight.

The carrying bag (if available) should be turned inside-out and completely wiped-down using

disinfectant solutions. Allow it to air-dry thoroughly and then turn it back and wipe down the outside of

the bag with disinfectant solutions.

Cover Material: Nylon/PU

Cover Material: Silver+ Nylon/PU

Cover Material: Stretch

6. MATTRESS STORAGE

1. Lay the mattress on a flat surface, upside-down.

2. Roll-up the mattress starting from the head until you reach the foot of the mattress.

3. Use the straps at the end of the mattress and stretch them around the mattress to prevent it from

unraveling.

Note: Do not fold, crease or stack the mattresses.

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7. MAINTENANCE

7.1 General

1. Check the main power cord and plug for abrasions or excess wear.

2. Check the mattress cover for signs of wear or damage.

3. Disconnect the air tube from the mattress. Then check the airflow coming from the two air outlets

on the pump. They should be alternately delivering air when the pump is set at “alternate” mode.

4. Check the air hoses for kinks or breaks. For replacement, please contact your local distributor.

7.2 AIR FILTER REPLACEMENT

1. Open the air filter cap located at the back of pump.

2. The filter is reusable and can be washed gently with a mild

detergent and water. Dry the filter before use.

3. Check and replace air filter regularly if environment is dirty.

8. EXPECTED SERVICE LIFE:

The products are intended to offer safe and reliable operation when use or installed according to the

instructions provided by Apex Medical. Apex Medical recommends that the system be inspected and

serviced by authorized technicians if there are any signs of wear or concerns with device function and

indication on products. Otherwise, service and inspection of the devices generally should not be

required.

9. TROUBLE SHOOTING

Problem

Solution

Power is not ON

‧ Check if the plug is connected to mains.

Alarm is on

‧ Check if the power is suddenly shut down.

‧ Check if the CPR is sealed.

‧ Check if the connection between air tube connector to pump unit is

tightly secured.

‧ Check if all tubing connections along mattress are secured.

Patient is bottoming out

‧ Pressure setting might be inadequate for the patient, adjust comfort

range 1 to 2 levels higher and wait for a few minutes for best comfort.

Mattress form is loose

‧ Check if all the snap buttons or straps of mattress are all securely

fastened.

‧ Check if the mattress is fixed to the bed frame by straps.

No air produced from some

air outlets of the air tube

connector

‧ This is normal since there is alternating mode. Air outlets take turns

to produce air during their cycle time.

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10. TECHNICAL DESCRIPTION

SPECIFICATIONS:

Item

Specification

Power Supply (Note: See

rating label on the product)

AC 220-240V 50 Hz, 0.08A (for 230V system)

Fuse Rating

T1AL, 250V

Cycle time

Fixed

Dimension (L x W x H)

29 x 18.5 x 12.6 (cm) / 11.4" x 7.3" x 5.0"

Weight

2.3 Kg or 5.1 lb

Environment

Temperature

Operation:10° C to 40° C (50° F to 104° F)

Storage: -15° C to 50° C (5° F to 122° F)

Shipping: -15° C to 70° C (5° F to 158° F)

Humidity

Operation: 10% to 90% non-condensing

Storage: 10% to 90% non-condensing

Shipping:10 % to 90% non-condensing

Atmospheric

Pressure

Operation: 700 hPa to 1013.25 hPa

Storage: 50 – 106 kPa

Shipping: 50 – 106 kPa

Classification

Class II, Type BF, IP21

Applied Part: Air Mattress

Not suitable for use in the presence of a flammable

anesthetic mixture (No AP or APG protection)

Mattress

Specification

Model

5"+ 3” Replacement

8” Replacement

Dimension (L x W x H)

200 x 90 x 12.5 cm

/ 78.7" x 35.4" x 5"

200 x 90 x 20.3 cm

/ 78.7” x 35.4” x 8”

Weight

5.6 kg or 12.5 lb

6.9 kg 15.2 lb

Max. Support Weight

180 Kg

200 Kg

Pressure Range

6 comfort levels setting.

NOTE:

1. Consult the distributor or EU representative for further technical documents.

2. These specifications are also applicable for other regions operating with the same

power supply.

3. Mattress dimensions and weight is measured without foam;

4. The manufacturer reserves the right to modify the specifications without notice.

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APPENDIX A: EMC INFORMATION

Guidance and Manufacturer’s Declaration- Electromagnetic Emissions:

This device is intended for use in the electromagnetic environment specified below. The user of this

device should make sure it is used in such an environment.

Emissions Test

Compliance

Electromagnetic Environment-Guidance

RF emissions

CISPR 11

Group 1

The device uses RF energy only for its internal function.

Therefore, its RF emissions are very low and are not

likely to cause any interference in nearby electronic

equipment.

RF emissions

CISPR 11

Class B

The device is suitable for use in all establishments,

including domestic establishments and those directly

connected to the public low-voltage power supply

network.

Harmonic emissions

IEC61000-3-2

Class A

Voltage fluctuations /

Flicker emissions

IEC61000-3-3

Complies

Guidance and Manufacturer’s Declaration- Electromagnetic Immunity:

This device is intended for use in the electromagnetic environment specified below. The user of this

device should make sure it is used in such an environment.

Immunity Test

IEC60601 test

level

Compliance

Electromagnetic

Environment-Guidance

Electrostatic Discharge

(ESD) IEC61000-4-2

±6kV contact

±8kV air

±6kV contact

±8kV air

Floors should be wood,

concrete or ceramic tile. If

floors are covered with

synthetic material, the relative

humidity should be at least

30%.

Electrical fast transient/

burst

IEC61000-4-4

±2kV for power

supply line

±1kV for input/out

line

±2kV for power

supply line

±1kV for input/out

line

Mains power quality should be

that of a typical commercial or

hospital environment.

Surge

IEC61000-4-5

± 1 kV line(s) to

line(s)

± 2 kV line(s) to

earth

± 1 kV line(s) to

line(s)

Mains power quality should be

that of a typical commercial or

hospital environment.

Voltage dips, short

interruptions and voltage

variations on power supply

input lines

<5 % U

T

(>95 % dip

in U

T

)for 0,5 cycle

40 % U

T

(60 % dip

in U

T

)for 5 cycles

<5 % U

T

(>95 % dip

in U

T

) for 0,5 cycle

40 % U

T

(60 % dip

in U

T

) for 5 cycles

Mains power quality should be

that of a typical commercial or

hospital environment. If the

user of this device requires

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IEC61000-4-11

70 % U

T

(30 % dip

in U

T

)for 25 cycles

<5 % U

T

(>95 % dip

in U

T

)for 5 sec

70 % U

T

(30 % dip

in U

T

) for 25 cycles

<5 % U

T

(>95 % dip

in U

T

) for 5 sec

continued operation during

power mains interruptions, it is

recommended that the device

be powered from an

uninterruptible power supply or

a battery.

Power frequency

(50/60Hz) magnetic field

IEC61000-4-8

3 A/m

Power frequency magnetic

fields should be at levels

characteristic of a typical

location in a typical commercial

or hospital environment.

NOTE: U

T

is the a.c. mains voltage prior to the application of the test level

Guidance and Manufacturer’s Declaration - Electromagnetic Immunity:

This device is intended for use in the electromagnetic environment specified below. The user of this

device should make sure it is used in such an environment.

Immunity Test

IEC60601 test level

Compliance

Electromagnetic

Environment-Guidance

Conducted RF

IEC 61000-4-6

Radiated RF

IEC 61000-4-3

3Vrms150 kHz to 80

MHz outside ISM

bands

a

3 V/m 80 MHz to

2.5 GHz

3 Vrms

3 V/m

Portable and mobile RF

communications equipment should

be used no closer to any part of this

device, including cables, than there

commended separation distance

calculated from the equation

applicable to the frequency of the

transmitter.

Recommended separation distance

Pd 2.1

150kHz to 80MHz

Pd 2.1

150kHz to 80MHz

Pd 3.2

80 MHz to 2.5G MHz

Where P is the maximum output

power rating of the transmitter in

watts (W) according to the

transmitter manufacturer and d is

the recommended separation

distance in meters (m).

b

Field strengths from fixed RF

transmitters, as determined by an

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electromagnetic site survey

c

, should

be less than the compliance level in

each frequency range

d

.

Interference may occur in the vicinity

of equipment marked with the

following symbol:

NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.

NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by

absorption and reflection from structures, objects and people.

a/ The ISM (industrial, scientific and medical) bands between 150 kHz and 80 MHz are 6,765 MHz to

6,795 MHz; 13,553 MHz to 13,567 MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz.

b/ The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz and in the

frequency range 80 MHz to 2.5 GHz are intended to decrease the likelihood that mobile/portable

communications equipment could cause interference if it is inadvertently brought into patient areas.

For this reason, an additional factor of 10/3 is used in calculating the recommended separation

distance for transmitters in these frequency ranges.

c/ Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless)

telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast

cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to

fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field

strength in the location in which the device is used exceeds the applicable RF compliance level

above, the device should be observed to verify normal operation. If abnormal performance is

observed, additional measures may be necessary, such as reorienting or relocating the device.

d/ Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

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Recommended separation distances between portable and mobile RF communications

equipment and this device:

This device is intended for use in an electromagnetic environment in which radiated RF disturbances

are controlled. The customer or the user of this device can help prevent electromagnetic interference by

maintaining a minimum distance between portable and mobile RF communications equipment

(transmitters) and this device as recommended below, according to the maximum output power of the

communications equipment

Rated maximum

output power

of transmitter

W

Separation distance according to frequency of transmitter m

150 kHz to 80 MHz

Pd 2.1

80 MHz to 800 MHz

Pd 2.1

800 MHz to 2,5 GHz

Pd 3.2

0.01

0.12

0.23

0.1

0.38

0.73

1

1.2

2.3

10

3.8

7.3

100

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For transmitters rated at a maximum output power not listed above, the recommended separation

distance d in meters (m) can be estimated using the equation applicable to the frequency of the

transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to

the transmitter manufacturer.

Note 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by

absorption and reflection from structures, objects, and people.

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IMPORTANTES MEDIDAS DE SEGURIDAD

LEER TODAS LAS INSTRUCCIONES ANTES DEL USO

PELIGRO – Para reducir el riesgo de choque eléctrico:

1. Desenchufar siempre el producto inmediatamente después de utilizarlo.

2. No utilizarlo durante el baño.

3. No colocar o almacenar el producto donde pueda caer al suelo o dentro de un lavabo o

fregadero.

4. No meterlo en agua ni en otros líquidos.

5. No intentar coger un producto que haya caído al agua. Desenchufar inmediatamente.

SIGNIFICADO DE LAS LLAMADAS NOTA, PRECAUCIÓ N Y AVISO:

NOTA: Indica información a la que deberá prestar una atención especial.

PRECAUCIÓ N: Indica los procedimientos necesarios para un correcto funcionamiento y

mantenimiento con el fin de evitar daños o destrucción al equipo, sus componentes o

a otros bienes.

AVISO: Llama la atención de algún posible peligro que requiera un procedimiento de uso correcto con

el fin de evitar daños personales.

ADVERTENCIA – Para reducir el riesgo de quemaduras, choque eléctrico, incendios o lesiones:

1. No dejar desatendido nunca este aparato cuando esté enchufado.

2. Evaluar en los pacientes el riesgo de que queden atrapados de acuerdo con el protocolo y

hacerles un seguimiento adecuado.

3. Cuando se utilice el equipo en o cerca de niños o personas discapacitadas, mantenga un

estrecho control sobre el mismo. Se podrían producir quemaduras eléctricas o asfixia si un niño

se traga una pequeña pieza desprendida del aparato.

4. Utilícelo sólo para el uso indicado en este manual. No utilice otros colchones no recomendados

por el fabricante.

5. No haga funcionar el equipo si: Tiene un cable o enchufe estropeados, no funciona normalmente,

se ha caído o dañado o ha entrado en contacto con agua o líquidos. Devuelva el equipo al punto

de venta donde lo adquirió para su examen y reparación.

6. Mantenga el cable de red lejos de cualquier fuente de calor.

7. No bloquear nunca las entradas de aire de este producto. No colocar nunca el producto en

superficies mullidas, como camas o sillones ya que podrían bloquearlas igualmente. Mantener

las entradas de aire libres de hilos, pelos y otras partículas similares.

8. No introducir ni dejar entrar ningún objeto en las entradas o en el tubo de este producto.

9. No modificar este equipo sin la autorización del fabricante.

10. Las fundas del colchón han superado la prueba de irritación y sensibilización de la piel. Sin

embargo, si sospecha que puede haber tenido o estar teniendo una reacción alérgica, consulte

inmediatamente con un médico.

11. No dejar largos trozos de tubo en la parte superior de la cama. Podría provocar

estrangulamiento

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