Suction Unit CAMI Askir30 Proximity User Manual
Contents
1. SUCTION UNIT NEW ASKIR30 PROXIMITY USER MANUAL CE 0123 medical suction 1 www medicalsuction co uk NEW ASKIR 30 Proximity Surgical aspirator is a portable unit working with 230V 50 Hz network electricity designed for the aspiration of bodily fluids in adult and children It s particularly suitable for nasal oral or tracheal aspiration of mucus catarrh or blood after minor surgical procedures and can be used in post operative therapy at home or conveniently transported from one hospital ward to another Easily portable equipment designed for continuous use Made of highly heat resistant electrically insulated plastic material in conformity with the latest European safety standard the product is supplied with a complete polycarbonate autoclavable jar with overflow valve and it is equipped with aspiration regulator and vacuum indicator located on the front panel The device with PROXIMITY function allows the device to be turned on or off through the infra red proximity sensor that can detect a hand passed within approximately ten centimetres of it It allows the operator to use the device without touching it The PROXIMITY function can be disabled for regular on off switch via button GENERAL WARNING READ INSTRUCTION MANUAL CAREFULLY BEFORE USE THE DEVICE IS FOR USE BY QUALIFIED PERSONNEL SURGEON PROFESSIONAL NURSE ASSISTANT THE USE OF THE DEVICE AT HOME IS RESTRICTED TO AN ADULT IN FULL POSSES2. plug remove the plug from the mains socket correctly e Preserve and use the medical device in environments protected from atmospheric factors and at a distance from heat sources Don t use the device thoracic drainage e In general it is advisable to use single or multiple adapters and or extensions Should their use be necessary you must use ones that are in compliance with safety regulations however taking care not to exceed the maximum power supply tolerated which is indicated on adapters and extensions 4 For repairs exclusively contact technical service and request the use of original spare parts Failure to comply with the above can jeopardise the safety of the device 5 Use only for the purpose intended Don t use for anything other than the use defined 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 regulation 6 The medical device requires special precautions regarding electromagnetic compatibility and must be installed and used in accordance with the information provided with accompanying documents NEW ASKIR 30 PROXIMITY device must be installed and used away from mobile and portable RF communication devices mobile phones transceivers etc that may interference with the device 7 Instrument and accessory discharging must be done according to current regulations in the country of use 8 WARNING Do not change this eq
3. RF transmitters an electro magnetic study of the site should be considered If the field intensity measured in the place where the device will be used surpasses the above mentioned applicable level of conformity the normal functioning of the device should be monitored If abnormal performance arises additional measures such as changing the device s direction or positioning may be necessary b The field intensity on an interval frequency of 150 kHz to 80 MHz should be less than 3 V m Recommended separation distance between portable and mobile radio communication devices The NEW ASKIR 30 PROXIMITY surgical aspirator is intended to operate in an electro magnetic environment where RF irradiated interferences are under control The client or operator of the NEW ASKIR 30 PROXIMITY device can help preven electro magnetic interference by keeping a minimum distance between the portable and mobile RF communication devices transmitters and the NEW ASKIR 30 PROXIMITY device as recommended below in relation to the radio communication maximum output power Maximum nominal Separation distance from the frequency transmitter m output power of the Transmitter W as kHz to 80 M A MHz to 800 M pi MHz to 2 5 GHz 3 5 V1 P 12 E1 P 23 E1 P Zoa f o f o E o f a For transmitters with a maximum nominal output power not shown L the recommended es distance in metres m can be calculated using the equation applicable to the transmitter frequency w
4. SION OF MENTAL FACULTIES AND OR HOME CARERS THE INSTRUMENT MUST NOT DISASSEMBLED FOR TECHNICAL SERVICE ALWAYS CONTACT CA MI SRL IMPORTANT SAFETY RULES Check the condition of the unit before each use The surface of the unit should carefully inspected for visual damage Check the mains cable and do not connect to power if damage is apparent E gt E gt gt gt 2 Before connecting the appliance always check that the electric data indicated on the data label and the type of plug used correspond to those of the mains electricity to witch it s to be connected 3 Respect the safety regulations indicated for electrical appliances and particularly e Use original components and accessories provided by the manufacturer to guarantee the highest efficiency and safety of the device e The device can be used only with the bacteriological filter e Never immerse the appliance into water e Position instrument on stable and flat surfaces e Position the device in a way that the air inlets on the back aren t obstructed e Don t use in the presence of inflammable substances such as anaesthetic oxygen or nitrous oxide e Don t touch the device with wet hands and always prevent the appliance coming into contact with liquids e Keep off the reach of children or not capable people without supervision e Don t leave the appliance connected to the power supply socket when not in use e Don t pull the power supply cable to disconnect the
5. amaged The aspiration tubes can be sterilized on autoclave using a sterilization cycle at 121 C 1 bar relative pressure 15 min The conical connector can be sterilized on autoclave using a sterilization cycle at 121 C 1 bar relative pressure 15 min DO NOT WASH STERILIZE OR PUT IN AUTOCLAVE THE ANTIBACTERIAL FILTER 5 www medicalsuction co uk PERIODICAL MAINTENANCE CHECKS The NEW ASKIR 30 PROXIMITY suction equipment does not need maintenance or lubrication It is however necessary to inspect the unit before each use With regard to training given the information contained in the user manual and since it is easy to understand the said device it doesn t appear to be necessary Unpack the instrument and always check integrity of plastic parts and feeding cable they might have been damaged during previous use Connect the cable to electrical network and turn the switch on Close the aspirator outlet with your finger and with suction regulator at maximum check that the vacuum indicators reaches at least 80kPa 0 80 bar Rotate the knob from right to left The vacuum indicator should go down 40kPa 0 40 bar Check that no loud noises are present A protection fuses F 1 x 1 6A L 250V reachable from exterior and situated in the plug protects the instrument For fuses replacing always the type and the range Before changing the fuse disconnect the plug from the power supply socket doesnt work External power source failur
6. ated 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 CAMI will not be responsible for damage caused through improper use To avoid such damage please read the instruction carefully Where CAMI determines that an instrument is faulty a replacement will be provided only if a SALES RECEIPT and STAMPED GUARANTEE are provided CA MI will not be responsible for damage accessories These may be replaced at the customer s expense 6 www medicalsuction co uk INSTRUCTION FOR USE e The device must be checked before each use in order to detect malfunctions and or damage caused by transport and or storage e The working position must be such as to allow one to reach the control panel and to have a good view of the empty indicator the jar and the antibacterial filter e tis recomended not to keep the device in your hands and or to avoid prolonged contact with the body of apparatus WARNING For proper use place the aspirator on a flat stable surface in order to have the full volume of use of the jar and better efficiency of the overflow device e Place the unit on a flat horizontal surface e Connect one end of the short silicon tube with antibacterial filt
7. device More than 850 hours of operation or 3 years in accordance with the standard conditions of testing and operation Shelf life maximum 5 years from the date of manufacture CLEANING OF ACCESSORIES Before using the device the manufacturer advises you to clean and or sterilize the accessories Washing and or cleaning the autoclavable jar as to be carried out as follows e Wear protection gloves and apron glasses and face mask if necessary to avoid contact with contaminating substances Disconnect the tank from the device and remove the said container from the support of the device Separate all the parts of the cover overflow device washer Disconnect all tubes from the jar and the protection filter Wash each part of the container from secretions under cold running bater and then clean every single part in hot water temperature not exceeding 60 C e Once again carefully wash each single part using if necessary a non abrasive brush to remove any deposits Rinse with hot running water and dry all parts with a soft cloth non abrasive It is possible to wash with commercial disinfectants by carefully following the instructions and dilution values supplied by the manufacturer After cleaning leave the parts to dry in an open clean environment e Dispose of the aspiration catheter according to that provided by local laws and regulations The silicone aspiration tubes and the conical fitting may be carefully washed in hot water temperat
8. e Check the external power source Unscrew the cap and insert the seal properly in its seat o Vacuum regulator set to e Turn the vacuum regulator clockwise and check the minimum value of the vacuum on the gauge Protection filter blocked or Replace the filter damaged Replace or reconnect the tubes check the jar Connection tubes blocked connections kinked or disconnected Empty the jar or disconnect the tube from the jar Shut off valve blocked or and unblock the shut off valve The unit twill only damaged work in the upright position Pump motor damaged Refer to authorised service personnel 5 The float doesn t If the cap has been washed ensure that the float is not partially Fit the float into it s place close detached 6 The float doesn t The float its covered by dirty Unscrewed the cap leave the and put in on autoclave close material Foam inside the jar Fill the jar to 1 3 full of ordinary water Faults 1 2 3 4 5 None of the procedures have Contact CA MI customer service 6 7 achieved the desired results If the overfill security system it s activated don t proceede with the liquid aspiration If the overfill security system doesn t work there are two cases 1 case If the overfill security system doesn t work the aspiration will be stopped by the bacteriological filter who avoid the liquid penetration inside the device 2 case If both the security system doesn t work there is the possibility that liq
9. er to the suction connector on the lid of the jar e The other tube already connected to the filter has to be connected to the VACUUM jar outlet where has been fixed the red float security float When the 90 of the volume of the jar is reached there is the activation of the security float the float close the aspiration connector on the jar to avoid liquid penetration inside the device WARNING Ensure that the FLUID SIDE or IN marker on the filter is on the side facing the collection jar lid and fitted into the VACUUM A wrong connection causes immediate destruction in case of contact with sucked liquids Filter assembling FLOW DIRECTION IN Fluid Inside Suction Pump Inlet jar Air Tube Connect the long silicone tube to the PATIENT jar outlet Connect the other end of the long silicon tube to the probe plastic connector then connect the suction probe to it Connect the power cord to the device then connect the plug to the electrical mains supply Push switch on position I to start suction Unscrew the lid of the jar and fill the jar 1 3 full or ordinary water this assists the unit to reach peak vacuum performance and makes clean up easier then re screw the lid on the jar correctly e During operation the jar has to be in vertical position to avoid overflow valve to cut off aspiration Should this happen switch off the device and disconnect the tube from the jar cover from VACUUM outlet e Once finished
10. function switches the card off 20 minutes after the motor is switched off if it is not switched back on again 7 www medicalsuction co uk Antibacterial Filter VACUUM Port Autoclavable Silicone Tube PATIENT Conical Fittings Port Infra Red Proximity Sensor Proximity Button I Proximity enabled NEKiRIQ blue LED F F o e eum ON OFF _ sh hn ol egulator s Knob Switch 500 Vacuum Indicator kPa Bar i Collection Jar pem 4 in Autoclavable PC K The PROXIMITY function starts aspiration with a simple movement of the hand without touching the device in this case it prevents and avoids possible cross contamination between patients as they treated in turns The unwanted approach of the hand to the Proximity sensors causes the device to switch off To reactivate the N function place the hand close to the sensors NOTE It is up to the end user to activate or deactivate the Proximity sensor With the Function off the device is activated deactivated by pressing the ON OFF key LED Button Signals ON OFF Button Near the front panel ke Proximity Button Switch ON OFF Ke LED located above the Proximity ke gt NEVER USE THE DEVICE WITHOUT JAR AND OR PROTECTION FILTER gt MAKE SURE THAT CHILDREN AND OR MENTALLY ILL PEOPLE DO NOT USE THE DEVICE WITHOUT ADULT SURVEILLANCE 8 www medicalsuction co uk RISK OF ELECTROMAGNETIC INTERFERENCE AND POSSIBLE REMEDIES Thi
11. he device doesn t Mains power quality should be that of a typical S UT gt 95 dip UT for Mains power quality should be that of a typical 0 5 cycle commercial environment or hospital If the user of Loss of voltage brief 40 UT gt 60 dip UT for the voltage interruptions 5 cycle surgical aspirator NEW ASKIR 30 PROXIMITY and variations TO UT gt 30 dip UT for request EN 61000 4 1 1 25 cycle that the appliance operates continuously the use lt 5 UT gt 95 dip UT for ofa 5 sec continuity unit is recommended Magnetic field The device doesn t me ae ene aE held should be measured in the intended installation location to EN 61000 4 8 change its state n me assure that it s sufficiently low Nota UT is the value of the power supply voltage The device doesnt Mains power quality should be that of a typical change its state commercial environment or hospital 9 www medicalsuction co uk Guidance and manufacturer s declaration Immunity Emissions The surgical aspirator NEW ASKIR 30 PROXIMITY is intended for use in the electromagnetic environment specified below The customers or the user of the surgical aspirator NEW ASKIR 30 PROXIMITY should assure that it s used in suc environment Level indicated m the Compliance Immunity Test EN m 1 1 2 Electromagnetic environment guidance Conducted Immunity 3Vrms 150kHz to V1 3Vrms The portable and mobile RF communication EN 61000 4 6 80Mhz devices including cables
12. here P is the maximum nominal output power of the transmitter i n Watt W depending on the transmitter s manufacturer Note 1 At80 MHz and 800 MHz the interval with the highest frequency is applied Note 2 These guide lines may not be applicable in all situations The electro magnetic propagation is influenced by the absorption and by the reflection from buildings objects and people 10 www medicalsuction co uk
13. inal packaging of the suction catheter and check the integrity of the sterile packaging CAMI declines any liability for injury to the patient correlated to the deterioration of the above mentioned sterile packaging due to handling of the original packaging by third parties WARNING Suction tubes for insertion in the human body purchased separately from the machine should comply with ISO 10993 1 standards on material biocompatibility Aspiration jar The mechanical resistance of the component is guaranteed up to 30 cycles of cleaning and sterilization Beyond this limit the physical chemical characteristics of the plastic material may show signs of decay Therefore we recommend that you to change it Silicone tubes the number of cycles of sterilization and or cleaning is strictly linked to the employment of the said tube Therefore after each cleaning cycle it is up to the final user to verify whether the tube is suitable for reuse The component must be replaced if there are visible signs of decay of the material constituting the said component Conical fitting the number of cycles of sterilization and the number of cleaning cycles is strictly linked to the employment of the said component Therefore after each cleaning cycle it is up to the final user to verify whether the fitting is suitable for reuse The component must be replaced if there are visible signs of decay in the material constituting the said component Service life of the
14. must not be used closer fornonlife supporting to the NEW ASKIR30 PROXIMITY device than the devices separation distance calculated by the equation applicable to the transmitter frequency ae ati separation distance Radiated Immunity 3V m 80MHz to 2 5GHz E1 3V m d 8 5 V1 P EN 61000 4 3 fornonlife supporting 12 E1 P from 80 MHz to 800MHz devices 23 E1 P from 800 MHz to 2 5 GHz hee P is the maximum nominal output voltage of the transmitter in Watt W depending on the manufacturer of the transmitter and the recommended separation distance n metres m The intensity of the field from the fixed RF transmitters as determined by an electro magnetic study a of the site could be lower than the level of conformity of b each frequency interval It is possible to check for interference in proximity to devices identified by the following symbol Note 1 At80 MHz and 800 MHz the interval with the highest frequency is applied Note 2 These guide lines may not be applicable in all situations The electromagnetic propagation is influenced by the absorption and by reflection from buildings objects and people a The field intensity for fixed transmitters such as the base stations for radiotelephones mobile and cordless and terrestrial mobile radio amateur radio devices radio AM and FM transmitters and TV transmitters can not be theoretically and accurately foreseen To establish an electro magnetic environment generated by fixed
15. push switch on O position and unplug e Remove the accessories and clean e Atthe end of each use place the device in its box away from dust WARNING The power supply cable plug is the element of separation from the electrical mains system even if the units equipped with a special on off switch button the power supply plug must be kept accessible once the device is in use so as to allow a further method of disconnection from the mains supply system PROXIMITY OPERATION e Connect the power supply cable to the device and insert the plug into the mains outlet e The motor will start up by pressing the on off button and will continue running until the button is pressed again The green LED on the button comes on when the motor is running e Press the Proximity key with blue LED to enable the motor s on off function through an infra red proximity sensor that detects the operator s hand within a distance of approximately ten centimetres This allows the operator to use the device without touching it or focusing his her attention on pressing the button e The on off key remains active even when the proximity function is enabled and can be used as an alternative e Press the relative button again to disable the Proximity function The function remains in memory meaning that if it was enabled when the device was switched off when it is switched back on again it will still be enabled whereas if it was disabled it will remain so The
16. r of the surgical aspirator NEW ASKIR 30 PROXIMITY should assure that it s used in such an environment The surgical aspirator NEW ASKIR 30 PROXIMITY only used Irradiated Conducted emissions RF energy only for its internal functioning Therefore its RF CISPR11 emissions are very low and are not cause interference in proximity of any Electronic appliances Harmonic emissions EN 61000 3 2 Class A The surgical aspirator NEW ASKIR 30 PROXIMITY can be used in all environments including domestic and those connected Voltage fluctuations flicker emissions bonclics directly to the public mains distribution that supplies power to EN 61000 3 3 p environments used for domestic scopes Guidance and manufacturer s declaration Immunity Emissions The surgical aspirator NEW ASKIR 30 PROXIMITY is intended for use in the electromagnetic environment specified below The customers or the user of the surgical aspirator NEW ASKIR 30 PROXIMITY should assure that it s used in such an environment Immunity Test meh ea te Compliance Level Electromagnetic environment guidance Electrostatic discharge 6kV on contact The device doesn t ESD 8kV in air change its state EN 61000 4 2 Electrical fast transient Floors should be wood conceret or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 30 2kV power supply lines burst 1kV for input output EN 61000 4 4 lines Surge T
17. s section contains information regarding the conformity of the compliance with the EN 60601 1 2 Standard The NEW ASKIR 30 PROXIMITY surgical aspirator is an electro medical device that requires particular precautions regarding electro magnetic compatibility and which must be installed and commissioned according to the electro magnetic compatibility information supplied Portable and mobile radio communication devices mobile phones transceivers etc may interfere with the medical device and should not be used in close proximity with adjacent to or on top of the medical device If such use is necessary and unavoidable special precautions should be taken so that the electro medical device functions properly in its intended operating configuration for example constantly and visually checking for the absence of anomalies or malfunctions The use of accessories transducers and cables different to those specified with the exception of transducers and cables sold by the appliance and system manufacturer as spare parts can lead to an increase in emissions or in a decrease of the immunity of the device or system The following tables supply information regarding the EMC Electromagnetic Compatibility characteristics of electro medical device Guidance and manufacturer s declaration electromagnetic Emissions The surgical aspirator NEW ASKIR 30 PROXIMITY is intended for use in the electromagnetic environment specified below The customers or the use
18. servation temperature 40 70 C Alternate current Mains frequency ON OFF Batch production Serial number Model Ref number He tingid Degree of protection an electrical device provides in the case of accidental or intentional contact with the human body or with objects and protection in the case of contact with water PENETRATION OF SOLIDS PENETRATION OF LIQUIDS dimension greater than 12mm of drops of water ACCESSORIES SUPPLIED IP21 DESCRIPTION CODE COMPLETE ASPIRATION JAR 1000cc RE 210001 02 CONICAL FITTING RE 210410 TUBES SET 6mm x 10mm TRANSPARENT SILICON ASPIRATION PROBE CH 20 25723 ANTIBACTERIAL AND HYDROPHOBIC FILTER SP 0046 The filter is produced with PTFE hydrophobic material to prevent fluids entering the pneumatic circuit It should be changed immediately if it becomes wet or if there is any sign of contamination or discolouration It should also be changed if the unit is used with a patient whose risk of contamination is unknown Don t use the suction unit without the protection filter If the suction unit is used in an emergency or in a patient where the risk of contamination is not know the filter must be changed after each use A www medicalsuction co uk Suction catheter Single use device to be used on a single patient Do not wash or re sterilize after use Reuse may cause cross infections Don t use after lapse of the sell by date Check the expiry date on the orig
19. the sample 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 CLEANING DEVICE Use a soft dry cloth with not abrasive and not solvent detergents To clean the device external parts always use a cotton cloth dampened with detergent Don t use abrasive or solvent detergents PARTICULAR CARE SHOULD BE TAKEN TO ENSURE THAT THE INTERNAL PARTS OF THE EQUIPMENT DO NOT GET IN TOUCH WITH LIQUIDS NEVER CLEAN THE EQUIPMENT WITH WATER During all clearing operations use protection gloves and apron if need be also wear a face mask and glasses to avoid getting in contact with contaminating substances after each utilization cycle of the machine 3 www medicalsuction co uk SYMBOLS Class 2 isolation equipment CE marking in conformity with EC directive 93 42 CEE and subsequent changes General warnings and or specifications Consult the instruction manual Manufacturer CA MI Srl Via Ugo La Malfa n 31 43010 Pilastro PR Italy Type B equipment Fuse Keep in a cool dry place Con
20. uid comes inside the device in this case return the device to CAMI technical service CA MI Srl will provide upon request electric diagrams components list descriptions setting instructions and any other information that can help the technical assistance staff for product repair 4 The Vacuum power on the patient side is either very low or absent WARRANTY CONDITIONS RULES FOR RETURNING AND REPAIRING This product is guaranteed for a period of 24 months from the date of purchase The warranty includes the repair or replacement of defect spare parts free of charge if the defect has been clearly described by the customer and determined by technical service Inspections on the part of the seller performed at the request of the customer and intended to determined whether the device is fully functional are not covered by the free of charge warranty service This service will be charged to the customer depending on the effort required The consumables components are not subject to warranty Consumable components are silicon tubes filters seals conical adaptor and suction catheter Also excluded from warranty is all damage resulting from improper handling wilful damage or improper care of the device The warranty shall expire if repairs and servicing are not carried out by technical service Before returning an instrument for repair the external surfaces and all accessories MUST be carefully disinfected with a cloth soaked in methyl
21. uipment without the permission of the manufacturer CA MI Srl None of electric or mechanical parts have been designed to be repaired by customers or end users Don t open the device do not mishandle the electric mechanical parts Always contact technical assistance 9 Using the device in environmental conditions different than those indicated in this manual may harm seriously the safety and the technical characteristics of the same 10 Use in Home Care Keep all accessories of the device out of reach of children under 36 months of age since they contain small parts that may be swallowed 2 www medicalsuction co uk 11 Do not leave the device unattended in places accessible to children and or persons not in full possession of mental faculties as they may strangle themselves with the patient s tube and or the power cable 12 The medical device is in contact with the patient by means of a disposable probe supplied with the device furnished with the relative CE compliance certification according to the requirements of regulation ISO 10993 1 thus no allergic reactions and skin irritations may occur 13 The product and its parts are biocompatible in accordance with the requirements of regulation EN 60601 1 14 Operation of the device is very simple and therefore no further explanations are required other than those indicated in the following user manual The manufactured cannot be held liable for accidental or indirect damages should the de
22. ure must not exceed 60 C After cleaning leave the parts to dry in an open clean environment When cleaning is complete reassemble the container for liquid aspirations according to the following procedure e Place the overflow valve into its seat in the cover under VACUUM connector e insert floating valve keeping the o ring towards the opening of the cage e Place the o ring into its seat around the cover e After completing assembling operations always make sue that cover seals perfectly to avoid vacuum leakages or liquid exit After disposing of disposable parts and disassembling the jar wash in running cold water and rinse thouroughly Then soak in warm water temperature shall not exceed 60 C Wash thouroughly and if necessary use a non abrasive brush to remove incrustations Rinse in running warm water and dry all parts with a soft cloth non abrasive The jar and the cover can be autoclaved by placing the parts into the autoclave and running one sterilization stem cycle at 121 C 1 bar relative pressure 15 min making sure that the jar is positioned upside down Mechanical resistance of the jar is guaranteed up to 30 cycles of sterilization and cleaning at the indicated conditions EN ISO 10079 1 Beyond this limit the physical mechanical characteristics of the plastic may decrease and replacement of the part is therefore recommended After sterilization and cooling at environment temperature of the parts make sure that these are not d
23. vice be modified repaired without authorization or should any of its component be damaged due to accident or misuse Any minimal modification repair on the device voids the warranty and does not guarantee the compliance with the technical requirements provided by the MDD 93 42 EEC and subsequent changes and its normatives TECHNICAL CHARACTERISTICS NEW ASKIR 30 PROXIMITY Typology MDD 93 42 EEC Medical Device Class Il a Classification UNI EN ISO 10079 1 230 V 50 Hz 107 VA F 1 x 1 6A 250 V Maximum suction aspiration without 80kPa 0 80 bar ar Minimum suction aspiration without Less 40kPa 0 40 bar jar Maximum flow without jar 40 l min 3 6 Ko Dimension 350 x 210 x 180 mm Functioning to 35 C and 110 NON STOP OPERATED operating voltage Working condition Room temperature 5 35 C Room humidity percentage 30 75 RH Altitude 0 2000m s l m Conservation condition Room temperature 40 70 C Room humidity percentage 10 100 RH Atmospheric pressure 500 1060 hPa IMPORTANT INFORMATION FOR CORRECT DISPOSAL OF THE PRODUCT IN ACCORDANCE WITH EC DIRECTIVE 2012 19 UE WEEE The symbol on the device indicates the separated collection of electric and electronic equipment At the end of life of the device don t 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
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