Rossmax V3 Bedienungsanleitung

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Model: V3

Suction Unit

www.rossmax.com

Rossmax Swiss GmbH,

Widnauerstrasse 1, CH-9435 Heerbrugg, Switzerland

IN3V30000000000XX

Warranty Card

This instrument is covered by a 2 year guarantee from the purchase date. The guarantee

is valid only on presentation of the guarantee card completed by the dealer confirming

purchase date or the receipt. Suction unit accessories are not included. Opening

or altering the instrument invalidates the guarantee. The guarantee does not cover

damage, accidents or noncompliance with the instruction manual. Please contact your

local seller/dealer or www.rossmax.com.

Customer Name: ____________________________________________________

Address: ___________________________________________________________

Telephone: _________________________________________________________

E-mail address: ______________________________________________________

Product Information

Date of purchase: ___________________________________________________

Store where purchased:

____________________________________________________________________

Float (12a) PP O O X

Connecting tubing

(Ø1/4”, 180 cm) (16) PVC O X X

Connecting tubing

(Ø8 mm, 14 cm) (14) Silicone O O X

O: Applicable, X: Not applicable

Note:

1. The collection canister and tubing after disinfecting should be dated and stored

in clean and dry areas to avoid recontamination.

2. Do not use any cleaners or disinfectants that contain ammonia, benzene and/or

acetone to clean the unit.

3. Dispose of the solution following the instructions provided by the disinfectant

manufacturer.

4. Dispose of the suction catheter in accordance with the local laws and regulations.

Collection canister – 1400 ML

Filter

Silicone and PVC tubing

Maintenance

Rules for returning and repairing

Microbial contamination

Accessories (optional)

Technical Specications

Troubleshooting

Electromagnetic Compatibility Information

Symbols

The collection canister consists of an overow valve, a bottle in PC (polycarbonate)

material and must be replaced if there are visible signs of the damage.

Note:

1. Keep the device vertical to allow the overow valve to function correctly.

2. Do not overturn the collection canister during use, in order to prevent the

intervention of the overow valve; should this occur, switch the aspirator o

and detach the tubing connected to the antibacterial lter.

3. To accelerate aspiration and simplify cleaning, it is recommended to put water

in the collection canister before using.

4. Suction at the patient is automatically obstructed when the liquid level reaches

the overow valve located on the underside of the canister lid.

5. Contents of the container should be emptied when automatic overow valve is

activated. Further suctioning could cause damage to the vacuum pump.

The antibacterial lter supplied with Rossmax aspirators must be strictly replaced

for each new patient, or if overow occurs or the lter is saturated. Should

the aspirator be used on the same patient, the lter for single-patient use is

recommended to be replaced after every application. It should also be replaced if

the unit is used with a patient whose risk of contamination is unknown. The lter

cannot be sanitized, disinfected, or sterilized.

Note:

1. Do not use the aspirator without the antibacterial lter, the unit could be

damaged. From a bacteriological point of view, it becomes dangerous for the

patient.

2. Do not substitute any other material for this antibacterial lter. Substitution may

lead to contamination or poor performance; use only Rossmax lters.

The tubing is recommended to be single use, but the number of cycles of

disinfection and/or cleaning is strictly linked to the employment of the said tubing.

Therefore, after each cleaning cycle, it is up to the nal user to verify whether the

tubing is suitable for reuse. The component must be replaced if there are visible

signs of the decay of the tubing.

The suction equipment does not need maintenance or lubrication. It is, however

to inspect the unit and accessories before each use.

DANGER:

Electric shock hazard. Do not attempt to open or remove cabinet, there are no

user-serviceable internal components. If service is required, return the device to

your local distributor or authorized Rossmax service center. Opening or tampering

with the unit will void warranty.

Rossmax requires the following procedures to be carried out to protect

the instrument and the safety of all who come in contact with it.

Before returning an instrument for repair, the external surfaces and all accessories

MUST be carefully disinfected with a cloth soaked in methylated spirits or

hypochlorite-based solution. The instrument and accessories should then

be placed in a bag with a note outlining the disinfection undertaken. Failure

to follow this procedure will result in the instrument being returned to the

purchaser unrepaired. Instruments returned for repair MUST be accompanied

by a description of the problem. Rossmax will not be responsible for damage

caused through improper use. To avoid such damage, please read the instruction

carefully. Rossmax will not be responsible for damage of accessories. Accessories

will be replaced at the customer’s expense

In the presence of pathologies with the risk of infection and microbial contamination,

we recommend personal use of the accessories, collection canister, connecting

tubing and antibacterial lter and all accessories should be thoroughly cleaned

and disinfected after each use.

Note: Use only with original Rossmax accessories.

Name Model No.

Connecting PVC tubing (Ø1/4”-length

180cm) SU_AC_001_00

Collection canister (1400ml) SU_AC_003_00

Antibacterial lter kit (Antibacterial lter +

2 Silicone tubing Ø8mm-length 14cm) SU_AC_004_00

Antibacterial lter SU_AC_005_00

Connecting Silicone tubing

(Ø8mm-length 14cm) SU_AC_006_00

AC/DC switching Adaptor (12V/2A)

(EU plug) SU_AD_001_00

(MODEL No.: UES24 LCP-120200SPA)

AC/DC switching Adaptor (12V/2A)

(US plug) SU_AD_002_00

(MODEL No.: UES24 LCP-120200SPA)

AC/DC switching Adaptor (12V/2A)

(UK plug) SU_AD_003_00

(MODEL No.: UES24 LCP-120200SPA)

Suction class: High Vacuum / Low Flow

Adaptor: Input: 100-240V, 50/60Hz; Output: DC 12V 2.0A

Max. vacuum @ pump inlet: -73 kPa/ -550 mmHg (mmHg for reference only)

Max air ow @ pump inlet: 16L/min

Power Consumption: ≤ 24W

Collection canister: 1,400 ml

Weight: Approx. 1.92 (kgs)

Machine dimension (with-

out collection canister): 363 (W) × 175 (D) × 254.5 (H) mm (Incl. rubber pad)

Operating conditions: Temperature: min: 10°C; max. 40°C;

Relative humidity: ≤90% non-condensing

Atmospheric pressure: Min. 700 hPa; max. 1060 hPa

Storage and transportation

conditions:

Temperature min: -20°C; max. 60°C;

Relative humidity: ≤90% non-condensing

Atmospheric pressure: Min. 700 hPa; max. 1060 hPa

IP Classication: IP21: Protection against harmful ingress of water

and particulate matter

If, after checking the described conditions below the device is still not working

properly, we recommend that you consult your local distributor or authorized

Rossmax service center.

Problem Possible cause Solution

The device does not

work

The AC adaptor has not

been correctly inserted

into the socket of the

device or the power

socket

Correctly insert the AC

adaptor into the sockets

Power switch has not

been activated.

Check if the power switch

is turned to the “I” (ON)

position

Lack of suction

The collection canister

lid has not been correctly

positioned on the canister

Correctly position the

collection canister lid

Leaks or cracks in canister

assembly Replace the canister

Filter blocked Replace the filter

Blocked float Incrustation on the float

Remove the canister

lid and overflow valve

and extract the float.

Continue by carrying out

the cleaning procedures

as described in the

paragraph “Sanitization,

Disinfection operations”

Vacuum power poor

and/or non-existent

Vacuum flow adjustment

knob/ vacuum regulator

completely open

Fully close the adjustment

knob and check the

vacuum power

Filter blocked Replace the filter

Connecting tubing to

the device or collection

canister is clogged, bent,

disconnected or broken;

or suction catheter is

twisted or blocked

Check the condition

of the tubing, replace

it if blocked or broken

and correctly connect it

as per the Assembling

Procedures of this manual

Canister lid overflow valve

closed or blocked

Unblock the overflow

valve, keep the device

upright

Dirty, blocked or

damaged pump

Take the device to

your local distributor

or authorized Rossmax

service center

Class II device

Type BF applied part

Attention: check the instructions before using this device

+More vacuum

SN Device serial number

Risk: Electrocution.

Consequence: Death.

Do not use the device while taking a bath or a shower

ΙSwitch on

ΟSwitch o

Direct current

1639 CE Marking medical ref. Dir 93/42/EEC amended by 2007/47/EC

Date of manufacture

Manufacturer

Attention: Consult accompanying documents

WARNING: The symbol on this product means that it’s an electronic

product and following the European directive 2012/19/EU the elec-

tronic products have to be disposed on your local recycling centre for

safe treatment.

OBM_IB_SU-V3_

EN_SW_ver2138

1. This device needs to be installed and put into service in accordance with the information provided

in the user manual.

2. WARNING: Portable RF communications equipment (including peripherals such as antenna cables

and external antennas) should be used no closer than 30 cm (12 inches) to any part of the V3,

including cables specied by the manufacturer. Otherwise, degradation of the performance of this

device could result.

If higher IMMUNITY TEST LEVELS than those specied in Table 9 are used, the minimum separation

distance may be lowered. Lower minimum separation distances shall be calculated using the

equation specied in 8.10.

Manufacturer’s declaration-electromagnetic immunity

The V3 is intended for use in the electromagnetic environment specied below. The customer or

the user of the V3 should assure that is used in such and environment.

Immunity test IEC 60601 test level Compliance level Electromagnetic environment-guidance

Conducted RF

IEC 61000-4-6

3 Vrms:

0,15 MHz – 80 MHz

6 Vrms: in ISM and

amateur radio

bands between

0,15 MHz and 80

MHz

80 % AM at 1 kHz

3 Vrms:

0,15 MHz – 80

MHz

6 Vrms: in ISM and

amateur radio

bands between

0,15 MHz and 80

MHz

80 % AM at 1 kHz

Portable and mobile RF communications

equipment should be used no closer to any

part of the V3 including cables, than the

recommended separation distance calcu-

lated from the equation applicable to the

frequency of the transmitter.

Recommended separation distance:

d = 1,2 √P, d = 1,2 √P 80MHz to 800 MHz, d

= 2,3 √P 800MHz to 2,7 GHz

Where P is the maximum output power rat-

ing of the transmitter in watts (W) accord-

ing to the transmitter manufacturer and d

is the recommended separation distance in

metres (m).

Interference may occur in the vicinity of

equipment marked with the following sym-

bol:

Radiated RF

IEC 61000-4-3

10 V/m

80 MHz – 2,7 GHz

80 % AM at 1 kHz

10 V/m

80 MHz – 2,7 GHz

80 % AM at 1 kHz

NOTE1: At 80 MHz and 800 MHz, the higher frequency range applies.

NOTE2: These guidelines may not apply in all situations. Electromagnetic propagation is aected by

absorption and reection from structures, objects and people.

More information on EMC compliance of the device can be obtained from Rossmax website: www.

rossmax.com.

Introduction

Intended Use

Preliminary Remarks

Warnings and Safety Instructions

DANGER, WARNING, CAUTION, NOTE/ATTENTION STATEMENT

Instructions for Use

Cleaning, Sanitization, Disinfection operations

We thank you for purchasing our Aspirator V3 which is adaptable to your needs. It is

very important that the health care worker and/or the patient read and understand

the information for use and maintenance.

Suction unit (Aspirator) V3 can be used to remove unwanted uids or infectious

materials from the airway or respiratory support system in health care structures like

hospitals and home care. The device generates suction (aspiration) which allows

uids to be extracted through connecting PVC tubing connected to a collection

canister which retains the uids until they can be properly disposed of. Use of

the device must be prescribed by a doctor. Carefully follow the recommended

operations and procedures outlined in this instruction guide to ensure proper

functioning and maximize the life of the device.

This Suction unit (Aspirator) complies with the European regulations and bears

the CE mark “CE 1639”. The quality of the device has been veried and conforms

to the provisions of the EC council directive 93/42/EEC amended by 2007/47/EC

(Medical Device Directive), Annex I essential requirements and applied harmonized

standards.

EN ISO 10079-1: 2015 Medical suction equipment - Part 1: Electrically powered

suction equipment.

Suction unit (Aspirator) V3 is EMC-tested in conformity with the requirements of IEC

60601-1-2 and can be used in the vicinity of other EMC-tested devices that fulll

the requirements as outlined in the IEC 60601-1-2 standard. Untested HF sources,

radio networks or the like can impair the function of the device and should not

be operated in combination with the Aspirator V3. The suction equipment is not

suitable for use in an MRI environment. Please read and observe these warning

and safety instructions before operation. These instructions for use must be kept

with the device for later reference. Please note that these instructions for use are

a general guide for the use of the product. Medical matters must be addressed by

a physician. Rossmax considers himself only responsible for the eect on BASIC

SAFETY, reliability and performance of the Aspirator V3 if it is used in accordance

with the instructions for use.

Important Safeguards

This is a medical device and must be used by qualied users. It must be

operated as indicated in this user instruction manual.

Read All Instructions Before Using This Device.

Save These Instructions.

The manufacturer makes every eort to ensure that every product is of the highest

quality and safety; however, as for any electrical appliances, basic safety regulations

must always be observed in order to avoid harming persons and things.

DANGER: Urgent safety information for hazards that will cause serious injury or

death.

WARNING: Important safety information for hazards that draws attention to a

potential danger.

CAUTION: Indicates correct operating or maintenance procedures to prevent

damage to the product or other property.

Note/Attention: Indicates information to which users should pay special

attention.

DANGER:

1. The device is intended exclusively for the collection of NON-ammable or NON-

corrosive uid materials in medical applications only. This unit should not be used

in the presence of a ammable anaesthetic mixture with air, or with oxygen or

nitrous oxide.

2. Do not use outdoors or operate where aerosol (spray) products are being used or

where oxygen is being administered in a closed environment such as an oxygen

reservoir.

3. Do not handle the AC/DC switching adaptor plug with wet hands or use

the unit when taking a bath or shower. Never submerge the device in any liquids.

4. Do not use the unit if the plug or AC adaptor are worn or wet and remove or touch

the immersed device. If by chance it falls into water, do not attempt to remove

the device from the water while the plug is still connected; disconnect the mains

switch, pull the plug out of the socket. Bring the device to your local distributor

or authorized Rossmax service center immediately. Do not attempt to make the

device work before it has been thoroughly checked by qualied personnel and/

or authorized Rossmax service center.

5. Do not place or store the device where it can fall or be pulled into a tub or sink.

Warning:

1. The medical device must NOT be used in the operating theater, for

drainage or thoracic drainage and nasogastric suction.

2. Never operate this product if a) it has a damaged cord or plug, b) it is not working

properly, c) it has been dropped or damaged, d) it has been dropped into water.

The device must be checked before each use in order to detect malfunctions

and / or damage caused by transport and / or storage and do not connect to

power if damage is apparent. Before each use, the accessories must be carefully

inspected to ensure the absence of dust, incrustation, clots or liquid substances

both inside the connecting tubing and the collection canister. Furthermore, they

must be cleaned following the instructions rigorously as stated in the “cleaning,

sanitization, disinfection “. We recommend personal use of the accessories, the

collection canister, the connecting tubing and antibacterial lter to prevent risk of

contagious infection.

1. Assembling procedures

1-1. Connect one end of connecting silicone tubing (Ø8mm,14cm), with the

antibacterial lter marked “IN” side, to the VACUUM inlet of the collection

canister marked in yellow

1-2. Connect the other end, with the antibacterial lter marked “OUT” side, to the

“AIR INLET” connector of the suction unit marked in yellow.

1-3. Connect the connecting PVC tubing (Ø1/4”,180 cm) to the “PATIENT” inlet of

the collection canister.

1-4. Connect the AC adaptor with the AC adaptor jack on the right side of the

unit.

Note:

1. Use only the authorized Rossmax AC adaptor with this aspirator.

2. Ensure that the FLUID SIDE or IN marker on the lter is on the side facing

the collection canister and t into the “VACUUM” inlet. A wrong connection

may cause immediate destruction in case of contact with sucked liquids.

2. Setup Before Use

2-1. Before each use, inspect the unit and accessories. If damaged, expired and/

or deteriorated, replace it at once.

2-2. Place the unit on a at, horizontal surface.

2-3. Plug the AC adaptor into the socket.

2-4. Place the switch to the “I” (ON) position.

2-5. Collapse the tubing with the antibacterial lter and check the vacuum

gauge to test that the unit makes vacuum without any leakage and this

level varies when the vacuum regulator is acted on.

2-6. Obstruct the connecting tubing and adjust the level of vacuum prescribed

by the doctor in the vacuum gauge turning the vacuum ow adjustment

knob/ vacuum regulator.

Note: The vacuum regulator can be used to set the level of vacuum required

(mmHg/kPa). Turn the regulator clockwise, in the “+” direction, to obtain

a higher vacuum; or anticlockwise for a lower vacuum; these values can

be read on the vacuum gauge.

Important: The vacuum values on the control decal are purely for

guidance; always refer to the reading shown on the vacuum

gauge.

Note: Gauge is for reference only. If the unit sustains a severe drop, accuracy of

the gauge must be checked.

2-7. Place the switch to the “O” (OFF) position.

Note:

1. The device is intended to be used on a at, horizontal surface in order for

the overow valve to function correctly and prevent liquids from entering

the suction pump. The device must be kept away from walls to allow for

adequate engine cooling.

2. In case unit is dropped, always transport unit with vacuum regulator rotated

fully clockwise.

3. Starting the Suction

3-1. Connect the suction catheter to the connecting PVC tubing (Ø1/4”, 180 cm)

Note: suction catheter and manual regulator are not supplied by

Rossmax.

Before using the device, the manufacturer advises you to clean and/or disinfect the

accessories. Switch o the device before any cleaning procedures and unplug the

AC adaptor from the socket.

Cleaning of the device

Use only a damp cloth with antibacterial soap (non-abrasive and with dissolvents of

any sort) to clean the external surfaces of the main unit.

Caution:

• Particular care should be taken to ensure that the internal parts of the device do

not get in touch with liquids.

• Do not submerge in water as this will result in damage to the vacuum pump.

• Do not use any cleaners or disinfectants that contain ammonia, benzene and/or

acetone to clean the unit.

Collection canister and connecting tubing

• Detach the suction catheter (18), the manual regulator (17) and the connecting

PVC tubing (16) from the collection canister.

• Disconnect the silicone tubing (14) from both the canister and the unit.

• Remove the canister from its holder. keep it upright, and empty it (in the WC at

home, in the biological waste container in the hospital) and clean it after each use.

Disassemble it as below:

1. Open the collection canister

2. Remove the overow valve(12) from the canister lid (11)

3. Remove the rubber valve and oat (12a) from the overow valve (12)

Sanitization, Disinfection operations

Warning:

• To prevent possible risk of infection from contaminated cleaning/disinfection

solutions, always prepare fresh solution for each cleaning cycle and discard solution

after each use.

• Contaminated devices must be thoroughly cleaned prior to disinfection.

• Personal protective equipment must be worn when handling contaminated

equipment, particularly tubing, lter and collection canister (protective clothing,

disposable latex gloves, mask, eye protection)

• If any liquid accidentally enters in the main unit or in the pump, the unit may be

damaged. For this reason, we recommend not to use the aspirator. The failure

should invalidate the guarantee under the manufacturer’s responsibility.

• In the event that contaminated uids have moved past the internal unit, remove

the tubing and the lter, clean the casing, and decontaminate the collection

canister. Return the device to your local distributor or authorized Rossmax service

center following “Rules for returning and repairing” paragraph.

1. Sanitization

Before and after each use, sanitize the collection canister and the connecting

tubing.

Rinse each part (7,11,12,12a,14,16) with clean, hot running water (<50°C) with

gentle dishwashing liquid (non-abrasive).

After cleaning, leave the parts to dry in an open, clean environment.

2. Disinfection

The accessories which can be disinfected are (7,11,12,12a,14).

You can choose one of the methods described below.

Method A: wash with a commercial disinfectant that must be an electrolytic

chloroxidizer (active principle: sodium hypochlorite) specic and

follow the instructions and dilution rates supplied by the disinfectant

manufacturer carefully.

Method B: boil each of the parts in water for 15~20 minutes, it is preferable to use

de-mineralized or distilled water to prevent calcium deposits.

It is eective on the parts that undergo this treatment only if the parts to be

treated have previously been sanitized. After cleaning, leave the parts to dry in an

open, clean environment.

Parts Material Sanitization Disinfection

Steam

Sterilization

(Gravity

autoclave)

Collection Canister

(7)

(Polycarbonate) O O X

Canister Lid (11) PP O O X

Overflow valve (12) PP O O X

Rubber valve (12a) Silicone O O X

Immediately Return the product to your local distributor or authorized Rossmax

service center for examination and repair.

3. For use only by medically trained persons who have been adequately trained in

suction procedures and in the use of aspirators.

4. Incorrect use can cause pain and injury to the patient.

5. Do not start the machine if you suspect the presence of explosive or inammable

liquids or gases, water inside the machine or environmental conditions that are

not within the specied limits.

6. Do not perform any maintenance operations while the device is being used on a

patient.

7. Replacement device must always be available if a breakdown of the device for

patients can lead to a critical situation (e.g. patients with acute dyspnoea or severe

catarrhal congestion),

8. The patient should be monitored regularly according to the physicians instructions

and facility guidelines. Objective indications or signs of a possible infection or

complication must be met immediately (e.g. fever, pain, redness, increased warmth,

swelling or purulent discharge). Non-observance can lead to considerable danger

for the patient. Monitoring the Aspirator V3 for operating status is a must.

9. Consult the indications for use and consider risk factors and contraindications

before using the Aspirator V3. Failure to read and follow all instructions in this

manual prior to use may result in serious or fatal injury of the patient.

10. In the presence of children and non self-sucient individuals, the device must be

used under the close supervision of an adult who has been adequately trained in

suction procedures and in the use of aspirators.

11. Some parts of the device are small enough to be swallowed by children; keep the

device out of the reach of children.

12. Do not use the provided tubing and AC adaptor for any other purpose than

those specied, as they can cause risk of strangulation. Be particularly attentive

with children and individuals with disabilities because they are often unable to

correctly assess risk.

13. Repairs must be done only by your local distributor or authorized Rossmax

service center. Unauthorized repairs void the warranty and may be hazardous for

the user.

Attention: Do not modify this device without authorization from Rossmax.

14. The lter used by the same patient is recommended to be replaced after every

application.

Attention: The antibacterial lter must be replaced for each new patient.

15. The suction catheter and the manual regulator are sterile, disposable products for

single use and must be replaced after every application.

Check the expiry date on the original packaging of the suction catheter and check

the integrity of the sterile packaging. If expired and/or deteriorated, replace it at

once.

Attention: The suction catheter and manual regulator are not supplied

by Rossmax.

Rossmax declines any responsibility for harm to the patient correlated to

the deterioration of the aforementioned sterile packaging due to THIRD

PARTY handling during the original packaging of the entire device

16. Do not use sterile accessories when the sterile packaging is damaged.

17. Do not connect this device to a passive drainage tube.

18. Do not operate the device on an obstructed, unstable surface to avoid incidents,

which may cause it to accidentally fall and lead to a malfunction and/or breakage.

Should there be signs of damage to the plastic parts, which may expose inner

parts of the device, do not connect the plug to the electrical socket. Do not

attempt to make the device work before it has been thoroughly checked by

qualied personnel and/or authorized Rossmax service center

19. Never obstruct the air inlet positioned on the device.

20. Use of the device in ambient conditions other than those specied in the manual

may seriously impair its safety and technical characteristics.

21. Before cleaning the device, pull the plug out of the xed mains socket.

22. The connecting tubing supplied with the canister must never come into direct

contact with the suction area.

23. Never use while drowsy or asleep.

24. Always unplug the product immediately after use.

25. Use the device only in dust-free conditions, otherwise treatment could be

compromised.

Caution:

1. Use only for the purpose intended. Don’t use for anything other than the

use dened by the manufacturer. The manufacturer will not be responsible for

damage due to improper use or connection to an electrical system not complying

with current regulations.

2. Do not tip the canister over while the device is working as the liquid may be

aspirated into the device causing pump damage. Should this occur, immediately

switch o the suction machine, then empty and clean the canister. Immediately

bring the device to your local distributor or authorized Rossmax service center.

3. Ensure that the connecting tubing and the canister lid have been carefully sealed

in order to avoid leakage of suction.

4. When the overow valve intervenes, suction is halted. Switch o the device, empty

the canister and carry out the cleaning procedures.

5. In the event of aspiration without the canister and/or antibacterial lter, or if it is

suspected that substances have entered the aspiration circuit, contact your local

distributor or authorized Rossmax service center at once.

6. Portable and mobile RF communications equipment can aect medical devices.

7. The AC adaptor provided has been specically designed for use with Rossmax

series aspirators. Never use the AC adaptor with other devices or for uses other

than that specied in this manual and never use Rossmax series aspirators with

other AC adaptor.

8. Before connecting the device always check that the electric data indicated on the

data label and the type of plug used.

9. The device casing is not waterproof. Do not wash the device under running water

or by immersion and keep it safe from being sprayed by water or other liquid.

10. Keep the AC/DC switching adaptor away from animals (for example, rodents)

which could damage the insulation.

11. Keep the device and AC/DC switching adaptor away from sources of heat, direct

sunlight or extreme hot locations.

12. When the liquid level reaches 50% of the total volume of the collection canister,

it is recommended to empty or change it before the overow valve acts, in this

way the risk of the entrance of humidity in the antibacterial lter is minimized.

3-2. Switch on the unit (ON/OFF switch)

3-3. Place your nger on the manual regulator to activate the suction, begin

suction on the patient using the suction catheter. The unit is ready to put

the suction catheter to the patient.

3-4. After application, switch o the device and remove the AC adaptor from

the mains socket. Perform the cleaning operations as described in the

“cleaning, sanitization, disinfection “paragraph.

Note: A 30-minute interval is recommended after each use. Do not operate the

device continuously for more than 30 minutes for a single use without

turning it o and following with a cooling period for at least 30 minutes

Produktspezifikationen

Marke:	Rossmax
Kategorie:	Nicht kategorisiert
Modell:	V3

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