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- Frank`s Hospital Workshop
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1. TO UNIT ALL APPARECCHIO TO PATIENT AL PAZIENTE AF TO UNIT B k 6x11 mm A TO OVERFILL J AR gt BE ALL APPARECCHIO AL TROPPOPIENO BOTTIGLIONE REAR PANEL PANNELLO TO UNIT ALL APPARECCHIO ON M a a F STOP PN fi Hi PAR ea E PEDAL VR ww A Variability of aN vacuum regulation hand control gt Pedal switch D Ground protection Switching on O Switching off F 6x11 mm TO OVERFILL JAR AL TROPPOPIENO BOTTIGLIONE AN Warning see instruction manual LJ R Class I Type B IF NA Alternating current MN V S AS 200 March 1998 pag 3 di pag 3
2. OVERFILL The bacteriological filter able to stop even liquids and usable as a second safety overfill device is a in line filter device reusable and sterilizable 30 times by autoclave at 121 C for 20 min with retantion rating of 99 97 of all particules 0 3 micron The filter must be connected according to detail F and indications on the filter it has a specific side to the vacuum all the group connections tubing is made of silicon rubber sterilizable and so it can be assembled and disassembled very easily by means of a simple pressure During the cleaning the filter can t be wet Anyway if the device works the internal media filter must be dry because otherwise stops completely the suction power When the filter is new working at the maximum vacuum with the patient tubing opened on the vacuum gauge you can see a vacuum of 10 15 cmHg which raises while the media filter is getting obstructed at the same time the suction power decreases The filter must be replaced after about 30 times they can be more or less according to the material aspirated but in any case don t exceed 50 times QUICK CHECKING OF TUBINGS BOTTLES GASKETS AND SO ON To check tubing bottles caps gaskets pump and so on not damaged or obstructed it is advisable each time you use the unit to switch it on reaching the maximum vacuum with patient tubing closed CLEANING STERILIZATION MAINTENANCE AND TRANSPORT Attention at the moment of sale the acce
3. VORTEX S AS 200 INSTRUCTION MANUAL Edition 1 March 1998 This unit is manufactured by ALSA APPARECCHI MEDICALI S R L CASTEL MAGGIORE BOLOGNA ITALY which guarantees its safety reliability and performances only if the installation recalibrations and repairs are performed by personnel authorized by ALSA and if the unit is used in compliance with given instructions in an area that meets all the applicable IEC requirements The Manufacturer will supply on demand the electric diagrams and any further information needed This manual must be kept with the unit Please read this entire manual carefully to become familiar with each of the controls and features before making any attempt to use the equipment clinically and ask for it again if it is missing If any questions arise regarding the information contained in this manual according to your specific needs please contact the Manufacturer directly or through the local distributor before using the unit VERY IMPORTANT In accordance with the requirements of the European directive for medical devices 93 42 CEE and with the procedures of Company Quality System for the after sale control of the production the users are pleased to inform the Manufacturer about every however small problem of this unit INDICATIONS AND GUIDELINES FOR POWER SETTINGS According to the international rules EN 10079 1 this equipment is a transportable suction unit with high vacuum low flow for hospital and domi
4. cile use It is indicated For out patients departments first aid departments or to the bed of patients not for drainage starting from setting of 300 mmHg For pharyngeal suction starting from setting of 300 mmHg For O R L suction starting from setting of 400 mmHg For neonatal mucous extraction starting from setting of 100 mmHg For every kind of need in gynaecological field starting from setting of 500 mmHg For endoscopic suction starting from setting of 400 mmHg For permanent tracheostomy suction starting from setting of 400 mmHg For extremely delicate suctions starting from setting of 150 mmHg For plastic surgery starting from setting of 300 mmHg In any case this suction unit must be used under direct control of personnel thoroughly trained in the techniques and problems of medical suction and it is advisable before using the equipment to check carefully its performance without trusting blindly to previous experience with other similar units VERY IMPORTANT 1 Use rigid suction tips tube curettes only when the field is under direct visual control otherwise use only soft catheter tubes 2 For suction on delicate tissues use only suction tips with finger vacuum regulation this system grants more safety intermittent suction and if necessary the immediate reduction of suction power 3 Emergency if necessary you can obtain quick stop of suction power by disconnecting the handle B of th
5. e tubing apparatus bottle CANNULAS OR SUCTION TIPS use always cannulas or suction tips according to ISO 10993 1 Rules PRELIMINARY INSTRUCTIONS please see details on last page a Check that power input corresponds to the technical data label on the back of the unit b Put the bottle bottles on the unit checking the cap should be well inserted and well pressed and the relative over fill device the floating must freely work c Connect the unit to the bottle by using the relative intermediate tubing for the model with 2 bottles please see design no 2 then connect the patient tubing d In order to use the pedal switch STOP PN an accessory on request you have to insert in the tubing the ring nut O and the gasket N during the shipping screwed in the plastic part M and so without activating the pedal you have to insert the tubing and the gasket in the plastic part M tightening the threaded ring nut INSTRUCTIONS FOR USE the unit must be used in vertical position without obstructing the air cooling areas not less of 20 cm from the walls 1 Switch on the unit by the main switch 1 2 Select with the switch ASPIRATION on the back of the apparatus the type of working position CONT working without pedal switch position INT working only activating the pedal switch 3 Set the vacuum power as indicated in the paragraph Suction setting SUCTION SETTING To set the desi
6. red suction power use the manual control 2 rotary multi turn maximum vacuum clockwise with the relative vacuum gauge 3 and according to the same way but with the patient tubing closed you can preset the maximum vacuum not to be exceeded before using the unit OVERFILL DEVICE the unit can be provided with a supplementary outside overfill device The bottle has a specific overfill device which prevents the aspiration of liquid into the pump without stopping the unit but interrupting the connection between bottle and vacuum pump MN V S AS 200 IN March 1998 pag 1 dipag 3 This overfill device must be in good condition well cleaned and efficient with floating freely working CHANGING OVER AND EMPTYING OF THE BOTTLES To change the aspiration from a bottle to another one when the apparatus is supplyed with 2 bottles see design no 2 in the last page you have to remove from the cap of the first bottle the blue part of the side A of the connection apparatus bottle and the connection of the tubing suction patient P inserting them in the relative points of the cap of the other bottle To empty the full bottle you have to take it up in a vertical position you have not to take it from the cap and then start emptying the liquid through the hole for the connection of patient tubing Take away the cap only at the end when the bottle is nearly empty BACTERIOLOGICAL FILTER WITH FUNCTION OF SUPPLEMENTARY
7. ssories even reusable suction accessories on request are not sterile Bottles with caps both unbreakable tubing with connectors gaskets suction accessories are sterilizable by autoclave at 121 C for 20 min or by means cold sterilizer solutions i e Cydex The bacteriological filter is sterilizable by autoclave at 121 C for 20 min but can t be wet when cleaning The overfill device can be sterilized by means cold sterilizer solutions i e Cydex obviously you have to remove it first The unit may be cleaned with mild soap solution but take great care that fluid does not enter the system Wipe dry When the unit is not used keep it in a dry dust free area at room temperature and take care not to spill any liquid onto the system It is advisable to submit the unit for a periodic annual inspection better to the manufacturer Move the equipment around the working area keeping it in vertical position Check overfill device Before using the equipment you have to verify the overfill device with the floating freely working and the inside gasket better if changed after a working period of 500 hours well cleaned and in good conditions to perform this control you can unscrew the ring nut floating holder Never operate on the pump please contact trained technical assistance DISPOSAL all the materials including consumer materials must be disposed off according to the different National Rules TECHNICAL FEATURES Unit mee
8. ts Safety Rules CEI EN 60601 1 and CEI EN 10079 1 Classification CEI EN 10079 1 mobile unit for medical suction high vacuum low flow Classification I type B Input voltage absorption fuses please see technical data label on the back of the unit Working mode temporary max 90 min 15 sec max vacuum 15 sec no vacuum Aspiration pump with thermal protection max vacuum 650 mmHg 5 about 0 86 bar 86 kPa Vacuum setting rotary regulator on front panel with vacuum gauge Pedal switch pneumatic water and explosion proof Working noise less than 60 dB Casing protection against liquids common not protected Cooling convention cooling with fan on vacuum pump Dimensions cm 32x32x30 Weight kg 8 Collection container bottle VMLT 2 capacity ml 1800 1 or 2 pcs Tubing silicon rubber made patient length m 2 7x12 mm intermediate cm 30 6x11 mm Power cord section 3x0 75 mm lenght 2 m MN V S AS 200 IN March 1998 pag 2 dipag 3 ATMOSPHERIC CONDITIONS of use Temperature C 10 35 Humidity 30 75 Pressure hPA 700 1060 of transport and storage Temperature C 40 70 Humidity 10 95 Pressure hPA 500 1060 CONTROLS 1 Main switch 2 Working selector 3 Vacuum control On the back socket with fuse holders socket for pedal switch and working selector
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