Suction Unit CAMI Askir20 User Manual
Contents
1. 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 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 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 functionality vacuum then rescrew the lid on the jar correctly 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 push switch on O position and unplug Remove the accessories and clean NEVER USE THE DEVICE WITHOUT JAR AND OR PROTECTION FILTER MAKE SURE THAT CHILDREN AND OR MENTALLY ILL PEOPLE DO NOT USE THE DEVICE WITHOUT ADULT SURVEILLANCE ALWAYS PLACE THE DEVICE IN POSITIONS FOR EASY DISCONNECTION RULES FOR RETURNING AND REPAIRING COMPLYING WITH THE NEW EUROPEAN RULES CA MI Srl INDICATES THE IMPORTANT POINTS TO PROTECT INSTRUMENT AND OPERATORS HYGIENE THESE RULES MUST2. SUCTION UNIT NEW ASKIR20 NEW ASKIR 1 USER MANUAL CE 0123 medical suction www medicalsuction co uk NEW ASKIR 20 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 GENERAL WARNINGS ZN READ INSTRUCTION MANUAL CAREFULLY BEFORE USE ZN ONLY HIGHLY QUALIFIED STAFF USE RESERVED N 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 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 th
3. 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 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 Assemble the jar as follows e 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 e After completing assembling operations always make sue that cover seals perfectly to avoid vacuum leackages or liquid exit The aspiration tubes can be sterilized on autoclave using a sterilization cycle at 120 C The conical connector can be sterilized on autoclave using a sterilization cycle at 121 C The device is ready for a new employment now ZN DO NOT WASH STERILIZE OR PUT IN AUTOCLAVE THE ANTIBACTERIAL FILTE
4. BE RESPECTED IN ORDER TO GUARANTEE HYGIENE AND SAFETY TO ALL THE PEOPLE OPERATING WITH THE INSTRUMENT TO OBTAIN QUALITY AND WELL BEING CA MI warrants its product for 24 months after purchasing date Every returned instrument will be hygienically checked before repairing If CA MI finds instrument not suitable for repairing due to clear signs of internal or external contamination the same will be returned to customer with specification of NOT REPAIRED INSTRUMENT accompanied by an explanation letter CA MI will decide if contamination is due to bad functioning or misuse If contamination is due to bad functioning CA MI will substitute the instrument only if a SALE RECEIPT and STAMPED GUARANTEE accompany the same CA MI is not responsable for contaminated accessories they will be substitute at customer s expenses For this reson it is COMPULSORY to carefully disinfect the external part of the instrument and accessories with a cloth soaked in methylated spirits or hypochlorite based solutions Put the instrument and accessories in a bag with indication of disinfecting We also request to specify the kind of fault in order to speed up repairing procedures To this end please read the instructions carefully in order www medicalsuction co uk to avoid damaging the equipment through improper use Always specify the fault encountered so that CA MI Srl can establish whether it falls into the category of the faults covered by the guarantee www medicalsucti
5. R ACCESSORIES SUPPLIES The filter is produced with PTFE hydrophobic material witch prevents fluids entering the pneumatic circuit When the filter is wet it s not possible to use the unit therefore the filter should be changed immediately In case of possible contamination or discolouration change the filter immediately Don t use the suction unit without the protection filter fitted 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 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 WARNING Suction tubes for insertion in the human body purchased separately from the machine should comply with ISO 10993 1 standards on material biocompatibility PERIODICAL MAINTENANCE CHECKS The NEW ASKIR 20 suction equipment does not need maintenance or lubrication It is necessary to check functioning and instrument before every use Unpack the instrument and always check integrity of plastic parts and feeding cable they might have been damaged during previous use Connect cable to electrical network and turn switch on Close the aspirator outlet with your finger and with suction regulator in maximum vacuum position check
6. al interruptions and variations 40 Ur for 05 cycle environment or hospital If the user of the surgical aspirator NEW IEC EN 61000 4 11 70 U7 for 25 cycle ASKIR 20 request that the appliance operates continuously the use lt 5 Ur for 5 sec of a continuity unit is recommended Magnetic field 3A m The power frequency magnetic field should be measured in the IEC EN 61000 4 8 intended installation location to assure that it s sufficiently low Conducted Immunity 3Vrms 150kHz to 80MHz IEC EN 61000 4 6 for appliances that aren t life supporting Irradiated Conducted 3V m 80MHz to 2 5 GHz IEC EN 61000 4 3 for appliances that aren t life equipment Nota Ur is the value of the power supply voltage CLEANING OF ACCESSORIES To clean the plastic housing of the device wear disposable latex gloves and clean with denaturated alcohol or hypoclorite solutions 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 jar from the device e Disconnect all tubes from the jar and the protection filter Empty and dispose of the content and of the suction catheter according to the laws in force in your country e Separate all parts of the cover overflow valve o ring After disposing of disposable parts and disassembling the jar wash in running cold water and rinse thouroughly Then
7. ar Fill the jar to 1 3 full of ordinary water Faults 1 2 3 4 5 6 7 None of the remedies has Contact the seller or CA MI After sales Assistance achieved the desired results Service 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 liquid comes inside the device in this case return the device to CA MI technical service BEFORE EVERY CHECKING OPERATION IN CASE OF ANOMALIES OR BAD ZN FUNCTIONING PLEASE CONTACT CA MI TECHNICAL SERVICE CA MI DOES NOT GIVE GUARANTEE IF INSTRUMENT AFTER THE TECHNICAL SERVICE CHECKING APPEARS TO BE TAMPERED www medicalsuction co uk INSTRUCTION FOR USE e Place the unit on a flat horizontal surface e Connect the end of the short silicon tube with antibacterial filter to the suction connector 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
8. e mains electricity to witch it s to be connected 3 Ifthe plug supplied with the appliance is incompatible with the mains electricity socket contact qualified staff for replacement of the plug with a suitable type The use of simple or multiple and or extension adapters is not generally recommended Whenever their use is indispensable use those in compliance with safety regulations however paying attention not to exceed the maximum power supply limits which are indicated on the adapters and extensions 4 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 immerge the appliance into water e Place 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 O 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 plug remove the plug from the mains socket correctly e Preserve and use the medical de
9. ironment guidance e Irradiated Conducted Group 1 The surgical aspirator NEW ASKIR 20 only used RF energy only for its internal emissions functioning Therefore its RF emissions are very low and are not cause CISPR11 interference in proximity of any Electronic appliances Irradiated Conducted emissions Class B The surgical aspirator NEW ASKIR 20 can be used in all environments including CISPR11 domestic and those connected directly to the public mains distribution that Harmonic emissions IEC EN Class A supplies power to environments used for domestic scopes 61000 3 2 Voltage fluctuations flicker Complies emissions IEC EN 61000 3 3 www medicalsuction co uk Guidance and manufacturer s declaration electromagnetic Immunity The surgical aspirator NEW ASKIR 20 is intended for use in the electromagnetic environment specified below The customer or the user of the surgical aspirator NEW ASKIR 20 should assure that it s used in such an environment Immunity Test Compliance Electromagnetic environment guidance Electrostatic discharge ESD 6kV on contact Floors should be wood concrete or ceramic tile If floors are IEC EN 61000 4 2 8kV in air covered with synthetic material the relative humidity should be at least 30 IEC EN 61000 4 4 environment or hospital IEC EN 61000 4 5 environment or hospital Loss of voltage brief voltage 5 Ur for 0 5 cycle Mains power quality should be that of a typical commerci
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11. that the vacuum indicators reaches 75kPa 0 75 bar minimum 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 A protection fuses F 1 x 1 6 A 250V reachable from exterior and situated in the plug protects the instrument For fuses replacing always the type and the range Type of fault work External power source failure Check the external power source Lid seal not in its seat Unscrew the cap and insert the seal properly in its seat 4 The Vacuum power on the e Vacuum regulator set to e Turn the vacuum regulator clockwise and check the value patient side is either very low minimum of the vacuum on the gauge or absent Protection filter blocked or Replace the filter damaged Replace or reconnect the tubes check the jar connections Connection tubes blocked Empty the jar or disconnect the tube from the jar and kinked or disconnected unblock the shut off valve The unit twill only work in the Shut off valve blocked or upright position damaged e Refer to authorised service personnel Pump motor damaged e 5 The float doesn t close If the cap has been washed Insert the float into it s place ensure that the float is not partially detached 6 The float doesn t close The float it s covered by dirty Unscrewed the cap leave the and put in on autoclave material Foam inside the j
12. vice in environments protected from atmospheric factors and at a distance from heat sources e Don t use the device thoracic drainage 5 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 6 This medical device must be destined exclusively for the use for witch it has been designed ad described in this manual Any different use must be considered incorrect and therefore dangerous the manufacturer will not be responsible for damage due to improper use or connection to an electrical system not complying with current regulations 7 Particular precautions must be made concerning electromagnetic compatibility The medical device must be installed and used according to information supplied with the accompanying documents 8 Instrument and accessories discharging must be done following current law regulations in every country of use 9 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 10 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 The manufactured cannot be held liable for accidental or indirect damages should the device be modified repaired without authori
13. zation or should any of its component be damaged due to accident or misuse AN 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 www medicalsuction co uk TECHNICAL CHARACTERISTICS Model fe NEWASKIR20 Typology MDD 93 42 EEC Maximum suction aspiration without jar 75kPa 0 75 bar Regolable from 75kPa 0 75 Bar to 10kPa 0 10 Bar Maximum flow without jar 16 l min Weight 2 5 Kg 350 x 210 x 180 mm voltage Room humidity percentage 30 75 RH Altitude 0 2000m s l m Room humidity percentage 10 100 RH Class 2 isolation equipment CE marking in conformity with EC directive 93 42 CEE and subsequent changes Manufacturer CA MI Srl Via Ugo La Malfa n 31 43010 Pilastro PR Italy Warning consult the instruction manual 4 ee E Hz To preserve in place coolness and dry land Conservation temperature 40 70 C ON OFF OZ 0 Please note tecnica specifications may vary upon the manufactures s discretion Guidance and manufacturer s declaration electromagnetic Emissions The surgical aspirator NEW ASKIR 20 is intended for use in the electromagnetic environment specified below The customer or the user of the surgical aspirator NEW ASKIR 20 should assure that its used in such an environment Complianc Electromagnetic env
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