Portable Suction Unit CAMI Askir 36BR User Manual
Contents
1. SUCTION UNIT NEW ASKIR36 BR D Sarr USER MANUAL C 0123 medical suction 1 www medicalsuction co uk ASKIR 36BR is a surgical aspirator with the following electrical features 14V 4A with AC DC adapter mod UE60 140429SPA3 of FUHUA input 100 240V 50 60Hz 100VA or Internally powered equipment Pb Battery 12V 4A or with cigarette lighter adapter 12V 4A ASKIR 36BR is a desk type electric suction unit for the aspiration of body liquids oral nasal and tracheal aspiration in adults or children The appliance is designed for easy transport and almost continuous use The unit is operated by means of an electronic power management system also monitoring the internal battery operation and status Provided with acoustic alarm and LED system indicating low battery level and battery charge status The unit is equipped with suction regulator on the front panel and polycarbonate autoclavable jar complete with overflow valve Thanks to these characteristics and to its functions this device is particularly suitable for different applications utilization in hospital wards for tracheotomy for suction of body liquids and for minor surgery GENERAL WARNING j READ INSTRUCTION MANUAL CAREFULLY BEFORE USE ONLY HIGHLY QUALIFIED STAFF USE RESERVED A THE INSTRUMENT MUST NOT BE DISASSEMBLED FOR A TECHNICAL SERVICE ALWAYS CONTACT CA MI IMPORTANT SAFETY RULES Check the condition of the unit before each use The surface of the un2. 12 Operation of the device is very simple and therefore no further explanations are required other than those indicated in the following user manual 13 The lead battery integrated in the device is not to be considered as an ordinary domestic waste Such a component must disposed of in a specific collection centre in order to be recycled 2 www medicalsuction co uk 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 pe A The manufactured cannot be held liable for accidental or indirect damages should the device be modified repaired IMPORTANT INFORMATION FOR CORRECT DISPOSAL OF THE PRODUCT IN ACCORDANCE WITH EC DIRECTIVE 2002 96 EC In respect of art 13 Decreto Legislativo 25 Luglio 2005 n 151 Actuation of European directives 2002 95 EC 2002 96 EC and 2003 108 EC for reduction in use of dangerous substances in the electric and electronic device and for garbage disposal The symbol as over applied on the device or its packaging means that at the end of its useful life the product must not be disposed of with domestic waste At the end of device useful the user will must deliver it to the able collecting centres for electric and electronic garbage or give back to the retailer in the mome
3. Air Tube 7 www medicalsuction co uk 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 To avoid the risk of electric shock this equipment must only be connected to a supply mains with protective earth If the state of the protective conductor of the installation to which the medical device in question is connected appear to be dubious the use of equipment with a internal battery is recommended gt gt 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 Antibacterial Filter Autoclavable Silicone Tube Conical Fittings LED Indicator of Battery Status Vacuum Regulator Knob ON OFF Switch Vacuum Indicator kPa Bar Collection Jar A sy Autoclavable oy Operation using cigarette lighter DC 12V Connect the device s external plug 12V to the ligther plug with the cigarette lighter cable Check the battery power status of the vehicle before the cigarette lighter cable Press the switch to start suction Press the switch to the I position to turn it on WARNING Only use
4. Close the aspirator outlet with your finger and with suction regulator in maximum vacuum position check that the vacuum indicators reaches 80kPa 0 80 bar minimum internal battery Rotate the knob from right to left and check the aspiration regulating control The vacuum indicator should go down 25kPa 0 25 bar Verify that loud noises are not present these can indicate wrong functioning The device is protected by a safety fuse F 10A L 250V situated in the cigarette lighter cable When replacing always check the type and value as indicated Internally the device is protected see electrical specifications by two fuses T 15A L 125V that cannot be reached from the outside Therefore contact the manufacturer to request the assistance of an authorized and qualified technician when they need to be replaced If it s replaced make sure that its replacement is always the same type and value as indicated The device is made up of a lead battery which cannot be accessed by outside In order to replace it consult the technical staff authorised by the manufacturer Faulty Cass O o o sowon O O OOOO positioning the equipment power switch on 0 internal problem 3 No aspiration Jar Cap badly screwed down Unscrewed the cap then rescrew it correctly 4 No aspiration Lid seal not in its seat Unscrew the cap and insert the seal properly in its seat the float is not partially detached 8 No aspiration due to flow Filter blocked Replace filt
5. inner parts of the energised 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 qualified personnel and or the CA MI technical service department Don t use in the presence of inflammable substances such as anaesthetic oxygen or nitrous oxide Don t touch the device with wet hands and always prevent the appliance coming into contact with liquids Don t leave the appliance connected to the power supply socket when not in use Don t pull the power supply cable to disconnect the plug remove the plug from the mains socket correctly Store and use the device in places protected against the weather and far from any sources of heat After each use it is recommended to store the device in its own box away from dust and sunlight Don t use the device thoracic drainage In general it is inadvisable 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 the 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 wil
6. m output power of the Transmitter W 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz d 3 5 V VP d 12 E VP d 23 E P Sear o ooo 0 E EC 1 1 l 10 For transmitters with a maximum nominal output power not shown above the recommended separation distance in metres m can be calculated using the equation applicable to the transmitter frequency where P is the maximum nominal output power of the transmitter in Watt W depending on the transmitter s manufacturer Note 1 At 80 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 WARRANTY CONDITIONS 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
7. on contact The device doesn t Floors should be wood conceret or ceramic tile If floors are discharge ESD 8kV in air change its state covered with synthetic material the relative humidity should IEC EN 61000 4 2 be at least 30 Electrical fast 2kV power supply The device doesn t Mains power quality should be that of a typical commercial transient burst lines change its state environment or hospital EN 61000 4 4 1kV for input output lines Surge 1kV differential The device doesn t Mains power quality should be that of a typical commercial EN 61000 4 5 mode change its state environment or hospital Loss of voltage brief 5 UT gt 95 dip UT Mains power quality should be that of a typical commercial voltage interruptions for 0 5 cycle environment or hospital If the user of the surgical aspirator and variations 40 UT gt 60 dip ASKIR 36BR request that the appliance operates EN 61000 4 1 1 UT for 5 cycle continuously the use of a continuity unit is recommended 70 UT gt 30 dip UT for 25 cycle lt 5 UT gt 95 dip UT for 5 sec Magnetic field 3A m The device doesn t The power frequency magnetic field should be measured in EN 61000 4 8 change its state the intended installation location to assure that it s sufficiently low Nota UT is the value of the power supply voltage Guidance and manufacturer s declaration Immunity Emissions The surgical aspirator ASKIR 36BR is intended for use in the electr
8. wet or if there is any sign of contamination or discolouration If 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 Available under request with different versions with complete jar 2000cc 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 WARNING Suction tubes for insertion in the human body purchased separately from the machine should comply with ISO 10993 1 standards on material biocompatibility WARNING The medical device is provided without a specific suction probe If this device must be used with a specific suction probe the end user is responsible for making sure it complies with the EN 10079 1 regulation 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 u
9. ED will flash red turns off when the begin the battery recharge cycle immediately battery is flat operation LED signal comes on N NEVER USE THE DEVICE WITHOUT JAR AND OR PROTECTION FILTER RISK OF ELECTROMAGNETIC INTERFERENCE AND POSSIBLE REMEDIES This section contains information regarding the conformity of the compliance with the EN 60601 1 2 Standard The ASKIR 36BR 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 c
10. VACUUM HIGH FLOW Power Feeding 14V 4A with AC DC adapter mod UE60 140429SPA3 of FUHUA input 100 240V 50 60Hz 100VA or Internally powered equipment Pb Battery 12V 4A or with cigarette lighter adapter 12V 4A Current Consumption Maximum Suction Pressure without jar Minimum Suction Pressure without jar Maximum Suction Flow without jar Insulation Class when used with the AC DC adapter Class mod UE60 140429SPA3 Insulation Class when used with an Internal batte Internally Powered Equipment Insulation Class when used with a car cigarette lighter Class II cable Size Battery Holding Time Battery Time Charge Accuracy of Vacuum Indicator Working Condition Room temperature 5 35 C Room humidity percentage 10 93 RH Atmospheric pressure 800 1060 hPa Conservation condition and Transport Room temperature 25 70 C Room humidity percentage 0 93 RH Atmospheric pressure 500 1060 hPa 3 www medicalsuction co uk SYMBOLS Class II isolation equipment only when connected to a car cigarette lighter cable C 1 9 CE marking in conformity with EC directive 93 42 EEC and 0 3 subsequent changes Warning consult the instruction manual Consult the instruction manual Manufacturer CA MI S r l Via Ugo La Malfa nr 13 43010 Pilastro PR Italia Keep in a cool dry place Conservation temperature 40 70 C Applied Part type BF suction probe Battery DEHP Phthalates Suct
11. 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 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 10 www medicalsuction co uk Recommended separation distance between portable and mobile radio communication devices and the monitor The ASKIR 36BR surgical aspirator is intended to operate in an electro magnetic environment where RF irradiated interferences are under control The client or operator of the ASKIR 36BR device can help prevent electro magnetic interference by keeping a minimum distance between the portable and mobile RF communication devices transmitters and the ASKIR 36BR device as recommended below in relation to the radio communication maximum output power Maximum nominal Separation distance from the frequency transmitter
12. ace Connect the short silicon tube with antibacterial filter to the suction connector The other tube with one end connected to the antibacterial filter with the other end to jar s lid connector where has been fixed the red 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 the avoid liquid penetration inside the device Connect the long silicon tube to the other jar s lid connector Connect the other end of the long silicon tube to the probe plastic connector then connect the suction probe to it Connect the switching adapter to the device with the appropriate connector and insert the power cable plug to the power socket To start the treatment press the I switch to turn it on Set the desired vaccum value Bar kPa with the appropriate vacuum regulator Turning the handle clockwise increase the vacuum value these values can be read on the vacuum indicator instrument To suspend and or terminate the treatment press the switch againg and pull the plug out from the power socket Unscrew the jar s lid and fill the jar 1 3 full or ordinary water this for an easy cleaning operations and an rapid reaching of the functionally vacuum then rescrew the lid on the jar correctly To extract the accessories and start with cleaning Filter assembling Mod NEW ASKIR 36BR FLOW DIRECTION Ye IN Fluid Inside Suction pump Inlet Jar
13. er leakage of mucus 9 The Vacuum power on the Vacuum regulator set to minimum Turn the vacuum regulator clockwise and check the patient side is either very low Protection filter blocked or damaged value of the vacuum on the gauge or absent Connection tubes blocked kinked or Replace the filter disconnected Replace or reconnect the tubes check the jar Shut off valve blocked or damaged connections Pump motor damaged Empty the jar or disconnect the tube from the jar and unblock the shut off valve The unit twill only work in the upright position Contact the technical service 10 Noisy Technical internal problem Contact the technical service Faults 1 2 3 4 5 6 7 None of the remedies has achieved Contact the seller or CA MI After sales Assistance 8 9 10 the desired results 6 www medicalsuction co uk The device is made up of a lead battery which cannot be accessed by outside In order to replace it consult the technical staff authorised by the manufacturer USE ONLY THE RECOMMENDED BATTERIES FROM CA MI THE USE OF OTHER BATTERIES ARE NOT RECOMMENDED AND INVOLVING THE CANCELLATION OF WARRANTY In the event that the service personnel has to replace the internal battery pay special attention to the polarity of the same component The polarities are indicated directly on the battery 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 tw
14. haracteristics of the electro medical device Guidance and manufacturer s declaration electromagnetic Emissions The surgical aspirator ASKIR 36BR is intended for use in the electromagnetic environment specified below The customers or the user of the surgical aspirator ASKIR 36BR should assure that its used in such an environment Compliance Electromagnetic environment guidance Irradiated Conducted emissions Group 1 The surgical aspirator ASKIR 36BR only used RF energy only for its CISPR11 internal functioning Therefore its RF emissions are very low and are not cause interference in proximity of any Electronic appliances Irradiated Conducted emissions Class B CISPR11 The surgical aspirator ASKIR 36BR can be used in all environments including domestic and those connected directly to Harmonic emissions EN 61000 3 2 Class A the public mains distribution that supplies power to environments used for domestic scopes Voltage fluctuations flicker Complies emissions EN 61000 3 3 9 www medicalsuction co uk Guidance and manufacturer s declaration Immunity Emissions The surgical aspirator ASKIR 36BR is intended for use in the electromagnetic environment specified below The customers or the user of the surgical aspirator ASKIR 36BR should assure that it s used in such an environment Immunity Test Level indicated by Compliance Level Electromagnetic environment guidance the EN 60601 1 2 Electrostatic 6kV
15. ion catheter a a a a a i DEHP On Off O Batch Production Serial Number Model Ref Number Degree of protection an electrical device provides in the case of accidental or i ntentional contact with the human body or with objects ang protection in the case of contact with water 1st DIGIT 2nd DIGIT PENETRATION OF SOLIDS PENETRATION OF LIQUIDS Protected against solids having a Protected against the vertical dimension greater than 12mm 4 www medicalsuction co uk CLEANING OF THE 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 ACCESSORIES SUPPLIED DESCRIPTION COMPLETE ASPIRATION JAR 1000cc CONICAL FITTING TUBES SET 6 mm x 10 mm ASPIRATION PROBE CH20 ANTIBACTERIAL FILTER Antibacterial Filter The filter is produced with PTFE hydrophobic material to prevent fluids entering the pneumatic circuit It should be changed immediately if it becomes
16. it should carefully inspected for visual damage Check the mains cable and do not connect to power if damage is apparent 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 Use original components and accessories provided by the manufacturer to guarantee the highest efficiency and safety of the device The device can be used only with the bacteriological filter Never immerge the appliance into water Do not place or store the aspirator in places where it may fall or be pulled into the bathtub or washbasin In the event it is accidentally dropped do not attempt to remove the device from the water whilst the plug is still connected disconnect the mains switch remove the plug from the power supply and contact the CA MI technical service department Do not attempt to make the device work before it has been thoroughly checked by qualified personnel and or the CA MI technical service department Position the device on stable and flat surfaces in a way that the air inlets on the back aren t obstructed To avoid incidents do not place the aspirator on unstable surfaces 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
17. l 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 the accompanying documents the ASKIR 36BR device must be installed and used away from mobile and portable RF communication devices mobile phones transceivers etc that may interference with the said device 7 Instrument and accessory discharging must be done according to current regulations in the country of use 8 WARNING Do not change this equipment 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 The medical device is in contact with the patient by means of a disposable probe not supplied with the device Suction tubes for insertion in the human body purchased separately from the machine should comply with ISO 10993 1 standards on material biocompatibility 11 The product and its parts are biocompatible in accordance with the requirements of regulation EN 60601 1
18. n 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 upsidedown 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 damaged 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 N DO NOT WASH STERILIZE OR PUT IN AUTOCLAVE THE ANTIBACTERIAL FILTER MAINTENANCE The ASKIR 36BR suction equipment does not need maintenance or lubrication It is however 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 AC DC switching adapter feeding cable they might have been damaged during previous use Connect cable to electrical network and turn switch on
19. nt of equivalent new device purchasing one against one Disposing of the product separately prevents possible negative consequences for the environment and for health deriving from inadequate disposal It also allows the recovery of materials of witch its made up in order to obtain an important saving of energy and resources and to avoid negative effects to the ambient and health In case of abusive disposal of device by user will be applied administrative endorsements in compliance with current standard Pt DISPOSAL OF WASTE BATTERIES Directive 2006 66 EC This symbol on the battery or on the packaging indicates that the battery provided with this product shall not be treated as household waste By ensuring these batteries are disposed of correctly you will help prevent potentially negative consequences for the environment and human health which could otherwise be caused by inappropriate waste handling of the battery The recycling of the materials will help to conserve natural resources At the end of their life hand the batteries over to the applicable collection points for the recycling of waste batteries For more detailed information about recycling of this product or battery please contact your local Civic Office your household waste disposal service or the shop where you purchased the product TECHNICAL CHARACTERISTICS Model ASKIR 36BR Typology MDD 93 42 EEC Class Ila Medical device UNI EN ISO 10079 1 Classification HIGH
20. o 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 liquid comes inside the device in this case return the device to CA MI 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 CA MI TECHNICAL SERVICE CA MI DOES NOT GIVE GUARANTEE IF INSTRUMENT AFTER THE TECHNICAL BEFORE EVERY CHECKING OPERATION IN CASE OF ANOMALIES OR BAD FUNCTIONING PLEASE CONTACT SERVICE CHECKING APPEARS TO BE TAMPERED INSTRUCTIONS The device must be checked before each use in order to detect malfunctions and or damage caused by transport and or storage 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 It is recommended 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 Operation using with AC DC switching adapter Place the unit on a flat horizontal surf
21. omagnetic environment specified below The customers or the user of the surgical aspirator ASKIR 36BR should assure that it s used in such an environment Immunity Test Level indicated by Compliance Level Electromagnetic environment guidance the EN 60601 1 2 3Vrms 150kHz to 80Mhz for non V1 3 Vrms The portable and mobile RF communication devices lifesupporting including cables must not be used closer to the ASKIR devices 36BR device than the separation distance calculated by the Conducted Immunity EN 61000 4 6 equation applicable to the transmitter frequency 3V m 80MHz to E1 3V m Recommended separation distance Radiated Immunity 2 5GHz for non d 3 5 V1 P EN 61000 4 3 lifesupporting d 12 E1 P from 80 MHz to 800MHz devices d 23 E1 P from 800 MHz to 2 5 GHz Where 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 in metres m The intensity of the field from the fixed RF transmitters as determined by an electro magnetic study of the site could be lower than the level of conformity of each frequency interval b Note 1 At 80 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 reflection from buildings objects and people
22. ser 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 device More than 1000 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 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 water and then clean every single part in hot water temperature not exceeding 60 C Once again caref
23. 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 RULES FOR RETURNING AND REPAIRING UNDER NEW EUROPEAN RULES CA MI 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 CA MI will not be responsible for damage caused through improper use To avoid such damage please read the instruction carefully Where CA MI 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 11 www medicalsuction co uk
24. the originally supplied or recommended replacement cigarette liqther cables view the chapter Important Safety Rules WARNING Before using the device check the battery power status Before each use proceed with charging the battery To maintain the device in good conditions recharge the battery every 3 months when not in use Recharging operations to be able to charge the internal battery it is necessary to connect the universal switching adapter mod UE 60140429SPA3 of FUHUA to the electric network for approx 120 to 150 minutes with the main switch to position 0 The battery s autonomy when fully charged is approx 60 minutes with continued operations 8 www medicalsuction co uk TAB INDICATOR LIGHTS DURING OPERATIONS When an external power supply regardless of the state of the battery charger and when the device is working after having turned it on the LED stays in a FIXED GREEN position LED Signal Phase Problem Cause Solution Flashing Green Led Battery recharge running Steady Greed Led During recharge Recharging cycle Remove power supply complete Steady Red Led During battery Flat battery Start recharging cycle operation WARNING During this signal you will hear a long continuous beep duration of sound 0 8 sec sound frequency every 8 5 sec which notifies the user regarding the battery discharge Flashing Red Led Device automatically Battery completely flat When the device is restarted the L
25. ully 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 Dispose of the aspiration catheter according to that provided by local laws and regulations 5 www medicalsuction co uk The silicone aspiration tubes and the conical fitting may be carefully washed in hot water temperature 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 Place the overflow valve into its seat in the cover under VACUUM connector Insert floating valve keeping the o ring towards the opening of the cage Place the o ring into its seat around the cover 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 thoroughly soak in warm water temperature shall not exceed 60 C Wash thoroughly and if necessary use a non abrasive brush to remove incrustations Rinse in running warm water and dry all parts with a soft cloth no
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