3a health care Aspeed professional User manual

ISTRUZIONI D’USO

INSTRUCTION MANUAL

MANUEL D’INSTRUCTIONS

MONTAGE-UND GEBRAUCHSANWEISUNG

MANUAL DE INSTRUCCIONES

ASPEED

PROFESSIONAL

-0,5

-0,2

-0,3

-0,4

-0,1

1. Aspiratore

2. Cavo alimentazione

3. Interruttore I/O

4. Presa entrata-aria INLET

5. Maniglia di trasporto

6. Regolatore di vuoto

7. Vuotometro

8. Vaso da 1.000 ml

9. Dispositivo di protezione

10.Tappo per vaso

11.Filtro antibatterico

12.Tubo in silicone 50 cm

1. Aspirator

2. Netzkabel

3. I/O Schalter

4. Anschluss INLET

5. Tragegriff

6. Vakuumregler

7. Vakuummessgerät

8. Gefäß 1.000 ml

9. Schutzvorrichtung

10.Gefäßdeckel

11.Bakterienﬁlter

12.Silikonschlauch 50 cm

1. Aspirator

2. Power cord

3. ON/OFF Switch

4. Air inlet connector INLET

5. Trasportation handle

6. Vacuum regulator

7. Vacuum gauge

8. 1.000 ml Vessel

9. Protection device

10.Vessel plug

11.Antibacterial ﬁlter

12.50 cm silicon tube

1. Aspirador

2. Cable eléctrico

3. Botón ON/OFF

4. Toma entrada-aire INLET

5. Manija de transporte

6. Regulador de vacío

7. Vacuómetro

8. Vaso de 1.000 ml

9. Aparato de protección

10.Tapón para el vaso

11.Filtro antibacteriano

12.Tubo de silicona 50 cm

1. Aspirateur

2. Câble d’alimentation

3. Bouton Marche/Arrêt

4. Prise entree air INLET

5. Poignée de transport

6. Régulateur de vide

7. Vacuomètre

8. Vase de 1.000 ml

9. Dispositif de protection

10.Bouchon pour vase

11.Filtre antibactérien

12.Tube en silicone 50 cm

Fig - Abb. 1

364 7

1. Vaso di raccolta serigrafato 1.000 ml in policarbonato steri-

lizzabile

2. Tappo in polipropilene sterilizzabile

3. Guida galleggiante in polipropilene sterilizzabile

4. Corpo galleggiante in polipropilene sterilizzabile

5. Valvola in gomma sterilizzabile

6. Filtro antibatterico Monouso

7. Tubo in silicone sterilizzabile Ø 6x12 mm - Lunghezza 50 cm

8. Tubo in silicone sterilizzabile lungo Ø 6x12 mm - Lunghezza

130 cm

9. Sacca monouso

10.Cannula sterile monouso

11.Regolatore manuale sterile monouso

1. 1.000 ml collection vessel with serigraph,

made of sterilisable polycarbonate

2. Sterilisable polypropylene top

3. Sterilisable polypropylene ﬂoat guide

4. Sterilisable polypropylene ﬂoat body

5. Sterilisable rubber valve

6. Antibacterial ﬁlter

7. Sterilisable silicon tube Ø 6x12 mm - length 50 cm

8. Sterilisable silicon tube Ø 6x12 mm - length 130 cm

9. Disposable bag

10.Disposable sterile cannula

11.Disposable sterile manual regulator

1. Pot de collecte sérigraphié 1.000 ml en polycarbonate stérili-

sable

2. Bouchon en polypropylène stérilisable

3. Guide ﬂottant en polypropylène stérilisable

4. Corps ﬂottant en polypropylène stérilisable

5. Valve en caoutchouc stérilisable

6. Filtre antibactérien

7. Tuyau en silicone stérilisable Ø 6x12 mm 50 cm

8. Tuyau en silicone stérilisable Ø 6x12 mm 130 cm

9. Sac uniservice

10.Canule stérile uniservice

11.Régulateur manuel stérile uniservice

1. 1.000 ml Sekretgefäß, mit Siebdruck, aus sterilisierbarem

Polykarbonat

2. Sterilisierbarer Propylenstopfen

3. Schwimmführung aus sterilisierbarem Polypropylen

4. Schwimmkörper aus sterilisierbarem Polypropylen

5. Sterilisierbares Gummiventil

6. Antibakterieller Filter

7. Sterilisierbarer Silikonschlauch, Ø 6x12 mm - 50 cm

8. Sterilisierbarer Silikonschlauch, Ø 6x12 mm - 130 cm

9. Steriles Einwegbeutel

10.Steriles Einwegkatheter

11.Steriler Einweghandregler

1. Frasco de recogida gradado mediane serigraﬁa 1.000 ml de

policarbonato esterilizable

2. Tapón de polipropileno esterilizable

3. Guía del ﬂotador de polipropileno esterilizable

4. Cuerpo del ﬂotador de polipropileno esterilizable

5. Válvula de goma esterilizable

6. Filtro antibacteriano

7. Tubo de silicona esterilizable de Ø 6x12 mm de diámetro -

50 cm

8. Tubo de silicona esterilizable de Ø 6x12 mm de diámetro -

130 cm

9. Bolsa desechable

10.Cánula estéril desechable

11.Regulador manual estéril desechable

Fig - Abb. 2a

Fig - Abb. 2b

ASPEED PROFESSIONAL aspirator is a professional unit for outpatient use for secretion aspiration. It is equipped with Vacuum regulator

6, vacuum gauge 7, 1.000 ml vessels. with protection device, for the liquid intake on the suction pump, that interrupts the suction ﬂow. It is

lubrication-free, handy, easy to use, reliable, sturdy and quiet. The ASPEED PROFESSIONAL aspirator is supplied with the following ac-

cessories: 1.000 ml vessel with protection device, power supply cable, connection tube in sterilisable silicon Ø 6x12 short, connection tube in

sterilisable silicon Ø 6x12 long, sterile and single use cannula, sterile and single use manual regulator, single use bag, single use

antibacterial ﬁlter. N.B.: Only use genuine accessories supplied by 3A Health Care; the accessories supplied with the device

by the manufacturer have been tested and proven compliant with the latest current safety standards. WARNING! Correct

operation of the device is not guaranteed in the event of use of accessories other than those supplied.

INTENDED USE

Mains-operated medical /surgical aspirator intended for outpatient use.

Medical purposes: This product is intended for use for the aspiration of body ﬂuids.

Intended users of the product:

• Legally certiﬁed medical personnel (doctors, nurses and therapists).

• Users must also be able to understand the operation of the medical device, and the contents of the instruction manual, in general terms.

Intended patients for the product: People who need to remove body ﬂuids (saliva, blood, etc.).

Environment: This product is intended for outpatient use.

Expected duration: Duration may vary based on the operating environment. The lifetime of the device is 5 years and that of the collection

vessel and the silicone tubes 1 year or 30 sterilisation cycles. The cannula, manual ﬂow regulator, antibacterial ﬁlter and bag are disposable

devices and must therefore be replaced after each application. Frequent use of the product may shorten the duration.

Precautions for use: The warnings and cautions described in the instruction manual must be observed.

IMPORTANT WARNINGS

This is a medical device and it must be used only upon medical prescription. It must be used as described in this instruc-

tion manual. The user must read and understand in full the information regarding the use and maintenance of the unit. For

any question, do not hesitate to contact your preferred retailer.

MICROBIAL CONTAMINATION: due to pathologies with risk of microbial infection and contamination a personal use of the

accessories is recommended (ask your physician).

The manufacturer does anything possible to provide a product equipped with the highest quality and safety features, although, being it an

electric device, some fundamental safety directions must be observed:

• Kids and non self-sufﬁcient people must always use the device under strict supervision of a competent adult in his full-capacity and who has

read and understood this manual. Ensure that children do not use the device unsupervised some parts are small enough to be swallowed.

• The device must always be used by speciﬁcally trained staff who have read this manual.

• This device must only be used for its intended purpose: aspirator for outpatient and domestic use; any other use is considered improper

and dangerous and the manufacturer cannot be held responsible for any consequence of misuse.

• Never use adapters for voltages different from the voltage indicated on the data label on the bottom of the device.

• Keep the cable away from hot surfaces.

• This device is not suitable for use in presence of anaesthetic blend inﬂammable with air, oxygen, or nitrous oxide.

Never handle the power supply cable plug with wet hands, and never use the device in the bath or in the shower.

• Never leave the device near water, never immerse it in any liquid, never wet it, if it gets wet immediately unplug it from the power supply socket

before touching it. Do not use the device if the plug or the power supply cable are worn or wet (immediately send it to your preferred retailer).

• The device is not watertight.

• Always unplug the power supply cable immediately after use.

• Maintenance and/or repair must be carried out only by authorised personnel. Non-authorised repairs void the warranty.

• Ensure that the connections and vessel closing are performed carefully to prevent suction losses.

• Do not turn over the vessel while it is connected to the device in function, since the liquid would come into contact with the hydro phobic

antibacterial ﬁlter, immediately blocking suction; in case this happens, empty the vessel and replace the antibacterial ﬁlter.

• In the event of aspiration without the container and/or antibacterial ﬁlter, or if it is suspected that solid and liquid substances have entered

the aspiration circuit, it is necessary to send the device to the customer care service.

• In view of their length, the power cord and connection hose could constitute a strangulation hazard.

• The appliance is equipped with two safety fuses, easy to inspect in the event of a fault. They are located in the back of the appliance in the

panel socket. Before performing this operation remove the power supply plug.

• The pipe and the manual control of the ﬂow are sterile and single-use products: they must be replaced after each application. Check the

expiration date on the original packaging of the pipe and the suction ﬂow manual control and verify the integrity of the sterile packaging.

• The antibacterial ﬁlter is a single-use device and it must be replaced after each application.

• Before each use always perform the cleaning and disinfecting operations as mentioned in the paragraph “CLEANING AND DISINFEC-

TING OPERATIONS” of this instructions manual.

INSTRUCTION FOR USE

Before each use, verify that all the accessories are perfectly clean in accordance with the instructions of the section “CLEANING AND DISIN-

FECTING OPERATIONS”.

1. Connect the device as shown in ﬁgure 1 (page 2).

2. With the vacuum regulator 6you can set the depression value (bar). Rotate the knob towards «+» to increase the vacuum and rotate it

towards «-» to decrease it, the values can be read on the vacuum gauge 7.

3. Turn the device on by putting the switch on the «I» position (ON) 3.

4. After the application turn off the device and unplug the cable form the power supply socket and carry out the cleaning and disinfecting

operations as described in the “CLEANING AND DISINFECTING OPERATIONS” paragraph.

5. Secretion collection vessel - 1.000ml.

The 1.000 ml collection bottle 8supplied with the aspirator can be used in two ways: as a collection vessel which can be sterilised as shown

in ﬁgure 2a or as a collection vessel with disposable bag as illustrated in ﬁgure 2b.

5.1 Sterilisable secretion collection vessel (ﬁgure 2a).

The antibacterial ﬁlter 6must be inserted directly in the vessel’s lid 2. Never use the aspirator without the antibacterial ﬁlter,

since it is very dangerous for the patient. The collection vessel 1is supplied with overﬂow valve, lid and vessel in a see through

material (polycarbonate).

The antibacterial ﬁlter must be placed directly in the lid, only on the hole called VACUUM/VUOTO. The antibacterial ﬁlter protects the suc-

tion circuit from possible contaminants sucked during use. All the components of the vessel can be conventionally sterilised in autoclave

at a maximum temperature of 121° C, or by boiling them for 10 minutes. We recommend to replace the whole vessel every 30 sterilisation

cycles.

Do not turn over the vessel during use to prevent the backﬂow valve from being activated; if this happens turn off the aspirator and remove

the tube connected to the antibacterial ﬁlter. Never use the aspirator without the secretion collection vessel and/or without the antibacterial

ﬁlter.

5.1.1 Connection: connect one end of the short sterilisable silicon tube 7to the rubber holder of the antibacterial ﬁlter 6and put the latter

in the “VACUUM/VUOTO” input of the blue lid 2, connect the other end to the “INLET” input of the aspirator.

Connect one end of the sterilisable silicon tube 8to the “PATIENT/PAZIENTE” input of the blue lid; connect the sterile single-use manual

regulator 11 to the other end and connect the single-use sterile cannula 10 to the regulator.

5.2 Secretion collection vessel with single use bag (ﬁgure 2b).

The aspirator can be used with the 1.000 cc re-usable transparent secretion collection vessel 1and with the single use bag 9supplied. In

this case the antibacterial ﬁlter is integrated in the single-use bag, therefore the antibacterial ﬁlter 6and the blue lid with the valve 2should

not be used. The ﬁlter embedded in the bag, also prevents the reﬂux of the liquids sucked towards the aspirator when it is full, or when it is

inadvertently turned over.

In this case to restore the device to normal operation, the single use bag shall be replaced. For the cleaning and disin-

fecting operations of the tubes 7-8and vessel 1, sterilise the single parts in autoclave at a maximum temperature of 121° C, or by boiling

them for 10 minutes.

The bag is single use and it MUST be replaced after each use. The bag must be completely inserted in the vessel in order to

prevent any vacuum losses.

N.B.: maximum disposable bag usage vacuum: –0.75 bar (75 kPa).

5.2.1. Connection: connect one end of the short sterilisable silicon tube 7to the yellow rubber holder (VACUUM) of the bag 9and the

other end to the “INLET” input of the aspirator.

Connect one end of the long sterilisable silicon tube 8to the red rubber holder (PATIENT) of the bag 9and connect the sterile single-use

manual regulator 11 and the single-use sterile cannula 10 to the other end.

N.B.: only use the single use bags supplied by 3A - Code 3A1687.

CLEANING AND DISINFECTION OPERATIONS

N.B.: If using chemical disinfectants, follow the manufacturer’s instructions exactly.

• The cannula and the suction ﬂow manual control are sterile, single use products and must be replaced after every application.

• The antibacterial single use ﬁlter must be replaced after every application.

• Never leave the appliance in water or submerged; clean the external casing of the appliance using only a damp cloth with detergent (non

abrasive).

Single pump version

Low ﬂow, high vacuum device

Fuse

Protection against electric shock

T1, 6A - 250V

Class I

Supply voltage 230V ~ 50Hz 150VA

Adjustable vacuum level 0 ÷ -0,85 bar (85 kPa)

Air ﬂow approx. 15 l/min.

Dimensions 330 x 185 x 210(H) mm

Weight 3,5 kg approx.

Noise level approx. 53 dBA

Operation cycle Continuous use

Class of risk according to the 93/42/EEC directive

Operating Temperature/Humidity

Storage and Transport Temperature/Humidity

Operating-storage air pressure

IIa

+10° C to +40° C/10% to 95% RH

–25° C to +70° C / 10% to 95% RH

min. 690 hPa - max 1060 hPa

Double pump version

High ﬂow, high vacuum device

230V ~ 50/60Hz 100VA

approx. 22 l/min.

4,2 kg approx.

approx. 63 dBA

PERIODICAL CHECK FOR THE SAFETY OF THE DEVICE

ASPEED PROFESSIONAL does not need maintenance and/or lubrication, although it is required to perform some simple checks before each use:

• Check the integrity of the shell and the power supply cable.

• Using a ﬁnger, close the suction connector and verify that the vacuum level reaches 0.80 ÷ 0.85 bar approx.

• Verify that there is no disturbing noise that may be the symptom of a malfunction.

• Check that the cage is correctly positioned inside its housing. It must be aligned with the suction hole of the lid, so the valve of the ﬂoat can

obstruct it when the sucked liquid is too much against the maximum quantity that can be assimilated by the vessel (ﬁgure 2a).

• Check that the ﬂoat is mounted in the right position and that it is free to slide inside the cage (dirt and deposits can obstruct its movement).

PROBLEMS, CAUSES AND SOLUTIONS

PROBLEMS POSSIBLE CAUSES SOLUTIONS

Excessive noise Damaged pump or obstructions in the internal

suction duct Send to the customer care service

The unit turns on but it does not suck

- Damaged pump

- Vacuum regulator fully open. Connection

tubes disconnected and/or badly connected,

broken connection tubes. Container not in a

vertical position, full, or defective overﬂow

valve. Possible blockage of the hydraulic cir-

cuit inside the unit.

- Send to the customer care service.

- Check the position of the vacuum regula-

tor. Check the connections and the integri-

ty of the tubes. Position the container in a

vertical position, check the overﬂow valve

(blocked) and/or replace the silicon tubes.

The vacuum value cannot be adjusted

Damage to the internal hydraulic circuit or

obstruction of the connection tubes to the

aspiration unit

Send to the customer care service

The protection fuse is activated any time

the device is turned on Pump damaged or in short circuit Send to the customer care service

The vacuum gauge does not work Liquid penetrating the pneumatic circuit. Send to the customer care service

Note: if you experience faults or malfunctioning problems different to those listed above, always and exclusively contact authorised

assistance centres.

TECHNICAL SPECIFICATIONS

Piston electric-compressor, with thermal protection.

Electromagnetic Compatibility

Compliance levels according to EN 60601-1-2:2015 standard

- ESD immunity: 15 kV air, 8 kV contact (EN 61000-4-2)

- Burst immunity: 2 kV/100 kHz (EN 61000-4-4)

- Surge immunity (EN 61000-4-5): 1 kV common mode /2 kV differential mode

- Magnetic field (EN 61000-4-8): 30 A/m

- Immunity to rf currents in the 150 kHz-80 MHz range (EN 61000-4-6) 3 V modulation 80% 1 kHz

- RF emissions, CISPR 11: Class B

- Harmonics emissions, EN 61000-3-2: Class A

Rf field immunity (EN 61000-4-3):

Field (V/m) Frequency Modulation

3 80MHz 2700MHz 1kHz AM 80%

27 380MHz 390MHz 18Hz PM 50%

28 430MHz 470MHz 18Hz PM 50%

9 704MHz 787MHz 217Hz PM 50%

28 800MHz 960MHz 18Hz PM 50%

28 1700MHz 1990MHz 217Hz PM 50%

28 2400MHz 2570MHz 217Hz PM 50%

9 5100MHz 5800MHz 217Hz PM 50%

For transmitters with rated maximum output power not listed above, the recommended separation distance d in metres (m) may be determined using the equation

adopted for the transmitter frequency, where P is the maximum rated output power of the transmitter in Watts (W) stated by the transmitter manufacturer.

Notes:

(1) At 80 MHz and 800 MHz the highest frequency range applies.

(2) These guidelines might not apply in all situations.

Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

0,01 0,12 0,12 0,23

0,1 0,38 0,38 0,73

1 1,2 1,2 2,3

10 3,8 3,8 7,3

100 12 12 23

Rated maximum

output power

of transmitter

(W) from 150 kHz to 80 MHz

d = 1,2 √P from 80 MHz to 800 MHz

d = 1,2 √P from 800 MHz to 2,5 GHz

d = 2,3 √P

Separation distance (m) in relation to transmitter frequency

Warnings:

Although compliant with the EN 60601-1-2 standard, the ASPEED PROFESSIONAL medical device may interfere with other devices

in the vicinity. The device must not be used in proximity to or stacked on top of other equipment. Install the device well away from

other equipment that emits high frequencies (short waves, microwaves, electric scalpels, cell phones).

The device is intended for use in an electromagnetic environment in which radiated RF disturbances are under control. The customer

or user can help prevent electromagnetic interference by maintaining a minimum distances between mobile and portable RF communication

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

communication equipment.

SYMBOLS

Type B device

Ground protection

Safety fuse

Switch “OFF”

Switch “ON”

Alternating current

Do not use the unit when taking a bath or a shower

It is compulsory to carefully read the instructions before using this device

Keep dry

Single use

Sterilisation by ethyl oxid

3A HEALTH CARE S.r.l.

Via Marziale Cerutti, 90F/G

25017 Lonato del Garda (BS) - ITALY

DISPOSAL PROCEDURE (Dir. 2012/19/Ue-WEEE) The symbol on the bottom of the device indicates the separated collection

of electric and electronic equipment. At the end of life of the device, do not dispose it as mixed solid municipal waste, but dispose it

referring to a speciﬁc collection centre located in your area or returning it to the distributor, when buying a new device of the same type

to be used with the same functions. This procedure of separated collection of electric and electronic devices is carried out forecasting

a European environmental policy aiming at safeguarding, protecting and improving environment quality, as well as avoiding potential

effects on human health due to the presence of hazardous substances in such equipment or to an improper use of the same or of parts

of the same. Caution! The wrong disposal of electric and electronic equipment may involve sanctions.

Conforms to Directive 93/42/EEC for medical devices

Electromagnetic Compatibility

Compliance levels according to EN 60601-1-2:2015 standard

- ESD immunity: 15 kV air, 8 kV contact (EN 61000-4-2)

- Burst immunity: 2 kV/100 kHz (EN 61000-4-4)

- Surge immunity (EN 61000-4-5): 1 kV common mode /2 kV differential mode

- Magnetic field (EN 61000-4-8): 30 A/m

- Immunity to rf currents in the 150 kHz-80 MHz range (EN 61000-4-6) 3 V modulation 80% 1 kHz

- RF emissions, CISPR 11: Class B

- Harmonics emissions, EN 61000-3-2: Class A

Rf field immunity (EN 61000-4-3):

Field (V/m) Frequency Modulation

3 80MHz 2700MHz 1kHz AM 80%

27 380MHz 390MHz 18Hz PM 50%

28 430MHz 470MHz 18Hz PM 50%

9 704MHz 787MHz 217Hz PM 50%

28 800MHz 960MHz 18Hz PM 50%

28 1700MHz 1990MHz 217Hz PM 50%

28 2400MHz 2570MHz 217Hz PM 50%

9 5100MHz 5800MHz 217Hz PM 50%

For transmitters with rated maximum output power not listed above, the recommended separation distance d in metres (m) may be determined using the equation

adopted for the transmitter frequency, where P is the maximum rated output power of the transmitter in Watts (W) stated by the transmitter manufacturer.

Notes:

(1) At 80 MHz and 800 MHz the highest frequency range applies.

(2) These guidelines might not apply in all situations.

Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

0,01 0,12 0,12 0,23

0,1 0,38 0,38 0,73

1 1,2 1,2 2,3

10 3,8 3,8 7,3

100 12 12 23

Rated maximum

output power

of transmitter

(W) from 150 kHz to 80 MHz

d = 1,2 √P from 80 MHz to 800 MHz

d = 1,2 √P from 800 MHz to 2,5 GHz

d = 2,3 √P

Separation distance (m) in relation to transmitter frequency

Warnings:

Although compliant with the EN 60601-1-2 standard, the ASPEED PROFESSIONAL medical device may interfere with other devices

in the vicinity. The device must not be used in proximity to or stacked on top of other equipment. Install the device well away from

other equipment that emits high frequencies (short waves, microwaves, electric scalpels, cell phones).

The device is intended for use in an electromagnetic environment in which radiated RF disturbances are under control. The customer

or user can help prevent electromagnetic interference by maintaining a minimum distances between mobile and portable RF communication

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

communication equipment.

3A HEALTH CARE S.r.l.

Via Marziale Cerutti, 90F/G - 25017 Lonato del Garda (BS) - Italy

tel. +39 030 9133177 - fax +39 030 9919114

e-mail: [email protected] - www.3-a.it

3A3992 rev. 00 - 02/2018

PROCEDURA DI SMALTIMENTO (Dir.2012/19/Ue-RAEE) Il simbolo posto sul fondo dell’apparecchio indica la raccolta separata delle apparecchiature

elettriche ed elettroniche. Al termine della vita utile dell’apparecchio, non smaltirlo come rifiuto municipale solido misto ma smaltirlo presso un centro

di raccolta specifico situato nella vostra zona oppure riconsegnarlo al distributore all’atto dell’acquisto di un nuovo apparecchio dello stesso tipo ed

adibito alle stesse funzioni. Questa procedura di raccolta separata delle apparecchiature elettriche ed elettroniche viene effettuata in visione di una

politica ambientale comunitaria con obiettivi di salvaguadia, tutela e miglioramento della qualità dell’ambiente e per evitare effetti potenziali sulla salute

umana dovuti alla presenza di sostanze pericolose in queste apparecchiature o ad un uso improprio delle stesse o di parti di esse. Attenzione! Uno

smaltimento non corretto di apparecchiature elettriche ed elettroniche potrebbe comportare sanzioni.

ENTSORGUNGSVERFAHREN (RICHTLINIE 2012/19/Ue-Weee) Das Symbol auf dem Boden des Geräts gibt die getrennte Müllsammlung der elektrischen

und elektronischen Ausrüstungen an. Am Ende der Lebensdauer vom Gerät es nicht als gemischter fester Gemeindenabfall, sondern es bei einem

spezifischen Müllsammlungszentrum in Ihrem Gebiet entsorgen oder es dem Händler zurückgeben, wenn Sie ein neues Gerät desselben Typ mit

denselben Funktionen kaufen. Diese Prozedur getrennter Müllsammlung der elektrischen und elektronischen Ausrüstungen wird im Hinblick auf eine

zukünftige gemeinsame europäische Umweltschutzpolitik vorgenommen, welche darauf zielen wird, die Umwelt zu schützen und sichern, als auch die

Umweltqualität zu verbessern und potentielle Wirkungen auf die menschliche Gesundheit wegen der Anwesenheit von gefährlichen Stoffen in diesen

Vorrichtungen oder Missbrauch derselben oder von Teilen derselben zu vermeiden. Vorsicht! Die fehlerhafte Entsorgung von elektrischen und elektronischen

Vorrichtungen könnte Sanktionen mit sich bringen.

DISPOSAL PROCEDURE (Dir. 2012/19/Ue-WEEE) The symbol on the bottom of the device indicates the separated collection of electric and electronic

equipment. At the end of life of the device, do not dispose it as mixed solid municipal waste, but dispose it referring to a specific collection centre

located in your area or returning it to the distributor, when buying a new device of the same type to be used with the same functions. This procedure

of separated collection of electric and electronic devices is carried out forecasting a European environmental policy aiming at safeguarding, protecting

and improving environment quality, as well as avoiding potential effects on human health due to the presence of hazardous substances in such equipment

or to an improper use of the same or of parts of the same. Caution! The wrong disposal of electric and electronic equipment may involve sanctions.

PROCÉDURE D’ÉLIMINATION (Dir. 2012/19/Ue-WEEE) Le symbole placé sur le fond de l’appareil indique la récolte séparée des appareils électriques

et électroniques. A la fin de la vie utile de l’appareil, il ne faut pas l’éliminer comme déchet municipal solide mixte; il faut l’éliminer chez un centre de

récolte spécifique situé dans votre zone ou bien le rendre au distributeur au moment de l’achat d’un nouveau appareil du même type et prévu pour les

mêmes fonctions. Cette procédure de récolte séparée des appareils électriques et électroniques se réalise dans une vision d’une politique de sauvegarde,

protection et amélioration de la qualité de l’environnement et pour éviter des effets potentiels sur la santé humaine dus à la présence de substances

dangereuses dans ces appareils ou bien à un emploi non autorisé d’elles ou de leurs parties. Attention! Une élimination incorrecte des appareils

électriques pourrait impliquer des pénalités.

PROCEDIMIENTO DE ELIMINACIÓN (Dir.2012/19/Ue-RAEE) El símbolo colocado en el fondo del aparato indica la recogida separada de los equipos

eléctricos y electrónicos. Al término de la vida útil del aparato, no eliminar como residuo municipal sólido mixto sino eliminarlo en un centro de recogida

específico colocado en vuestra zona o entregarlo al distribuidor a la hora de comprar un nuevo aparato del mismo tipo y destinado a las mismas

funciones. Este procedimiento de recogida separada de los equipos eléctricos y electrónicos se realiza con el propósito de una política del medioambiente

comunitaria con objetivos de salvaguardia, defensa y mejoramiento de la calidad del medioambiente y para evitar efectos potenciales en la salud de

los seres humanos debido a la presencia de sustancias peligrosas dentro de estos equipos o a un uso inapropiado de los mismos o de algunas de

sus partes. Cuidado! Una eliminación no correcta de equipos eléctricos y electrónicos podría conllevar sanciones.