USER MANUAL FOR SUCTION UNIT MOD.VACUTRON AS
Contents
1. _ Variabilita del AN comando manuale di regolazione vuoto A N Attenzione consultare la documentazione annessa P se 7X Corrente alternata D Terra di protezione R Classe I Tipo B Accensione messa in tensione O Spegnimento messa fuori tensione MN VACUTRON EN Mar 2010 2 22. 5 A Functioning continuous Noise lower than 50 dB Max vacuum 160 mmHg 5 which corresponds to 217 cmH O Vacuum regulation rotative compensation switch and vacuum regulator for checking in cmHg and cmH 0 Flow rate 8 l min Protection against the liquid penetration normal Cooling system normal Dimensions length x depth x height cm 32x32x30 Weight kg 8 Standard jar VMLT 1 capacity 900 ml or VMLT 2 capacity 1800 ml Tubing patient n 1 mt1 3 7x12 in silicone filter and connections for the jars n 1 cm 30 6x11 in silicone Mains cable section 3x0 75 mm length mt2 Environmental conditions For usage For transport and storage Temperature C 10 35 Temperature C 40 70 Humidity 30 75 Humidity 10 95 Pressure hPa 700 1060 Pressure hPa 500 1060 SWITCHES AND CONTROL DEVICES General main switch Vacuum regulator Vacuum regulator for checking Functioning selection only mod VACUTRON AS 130 Rotative switches for the regulation of the active and passive functioning times only mod VACUTRON AS 130 F B eit mm TOOVERFILL JAR TO UNIT ia A ALL APPARECCHIO AL TROPPOPIENO BOTT ALL APPARECCHIO AL PAZENTE ALLAPPARECCHO SE ALPAZENTE I Souk 1 sg U 2 8 U
3. USER MANUAL FOR SUCTION UNIT MOD VACUTRON AS 120 AS 130 0051 ed March 2010 This suction unit is manufactured by ALSA Apparecchi Medicali Castel Maggiore Bologna Italy which is responsible for its functioning reliability and safety but only if the installation the additions the calibrations and the changes are performed by authorized people and if the usage takes place in an environment which complies with the IEC CEI regulations and in accordance with the instructions for use On request the company will distribute the electrical drawings and all information required In accordance with the European regulation for the medical devices CE 93 42 and the procedures of the quality system for the after sale check of production the users have to communicate to the company all the problems even the smallest ones related to this unit in order to allow the technicians to intervene as soon as possible INSTRUCTIONS FOR USE AND REGULATIONS According to the International Directives EN 10079 1 this is a portable suction unit with a low vacuum level and a low flow rate it is suitable only for drainage in the hospitals and at home Emergency In order to stop suddenly the suctioning operation disconnect the tubing unit jar PRELIMINARY RULES see the drawings in the second page a Check the mains power it must correspond to the technical data on the rear of the unit b Place the jar on the unit and verify that the cap is well f
4. itted by pressure and that the overflow device moves without impedances Provide for the connection unit jar by using the appropriate tubing OPERATION RULES use the unit in vertical position and make sure that the ventilation areas are not obstructed nor at a distance of less than 20 cm from the other objects 1 Switch the unit on with the general mains switch 2 Ad just the vacuum at the desired level as indicated into the section Suction Regulation Suction regulation into the mod VACUTRON AS 120 continuous suctioning The regulation of the suctioning can be operated through the activation of the pedal switch rotative and multi turns max in clockwise it automatically compensates the vacuum just in case of variations of the power supply placed on the top of the device it is equipped with control vacuum regulator at double range 250 cmHg and 3 5 m H 0 Before using the unit it is possible to select the max vacuum which cannot be exceeded by activating the device with the suction tube completely closed and by operating on the regulator in order to select the level that has been chosen Suction regulation into the mod VACUTRON AS 130 continuous suctioning The regulation of the suctioning is the same as per the previous model AS 120 but it must be considered that this unit can work both in continuous and intermittent modes Thus before regulating the suctioning you should select with the time key on
5. izable solutions like Cydex The unit must be cleaned with a solution based on neutral soap by paying attention that the liquid does not go inside then the unit must be dried with a cloth When the unit is not used for a certain period of time it must be kept in a dried place without dust and at a medium temperature not too high nor too low as for the functioning No liquid substance must be spilt on it It is advisable to check the unit regularly every year at least with authorized personnel It is better to call directly the manufacturer s technicians MN VACUTRON EN Mar 2010 1 2 The transfer transport of the unit must be operated by keeping it in vertical position Check of the overflow device Verify that the floating bar moves without any obstacle and that the internal gasket is in well conditions to do so you should unscrew the ring nut which carries the bar It is advisable to replace this basket every 500 hours of functioning Do not intervene personally on the suctioning group use the technical qualified service DISPOSAL All the materials the consumables included must be eliminated according to the different National Laws TECNICAL DATA Directives CEI EN 60601 1 and CEI EN 10079 1 Classification CEI EN 10079 1 portable suction unit for medical usage with a low vacuum and a low flow rate Class I type B Power supply absorption and fuses 230 V 50 Hz 90 mA T0
6. ter must be connected as indicated into the drawings point F by following the instructions printed on the filter itself it has an obligatory connection side The whole group coupling tubing is made of silicone sterilizable rubber and so it can be connected or disconnected by a simple pressure and with extreme facility During the cleaning it must not be wet and above all if it is the case the interior membrane must be dried because otherwise the aspiration capacity is completely blocked In optimal conditions by suctioning with the regulator selected at the max level of vacuum on the vacuum device it is possible to put a vacuum of 10 15 cmHg which increases when the filter tends to become obstructed at the same time the aspiration force decreases The filter replacement must be operated after 30 treatments the number can be higher or lower as it depends on the aspirated substances anyway it cannot be more than 50 times RAPID CHECK OF THE TUIBING JARS ETC In order to check the status of the tubing the connections etc every time you use the unit it is advisable to switch it on by reaching the max level of vacuum to verify that all parts are well connected and not damaged or obstructed CLEANING STERILIZATION MAINTENANCE AND TRANSPORT The jar with the cap both of them are unbreakable all the tubing with the connections as well as the cannulae are sterilizable in autoclave for 20 min at 121 C or with cold steril
7. the front panel the continuous functioning CONT or the intermittent functioning INT With the rotative switches it is possible to select also the length of the active and passive functioning times Both of them can be regulated separately from 30 to 180 sec Overflow device All jars are equipped with an overflow device which avoids the possible aspiration of the liquid into the pump by interrupting the functioning itself the aspiration stops when the vacuum into the jar is finished It is really important that the device is in very good conditions and well clean and efficacious Emptying of the jars In order to empty a full jar you should take it by keeping it in vertical position do not take it through the cap Then a Start the emptying procedure through the hole for the connection tubing patient b Take the cap away for the final stage of the emptying procedure only when the jar is quite completely empty ANTIBACTERIAL FILTER WITH SUPPLEMENTARY OVERFLOW DEVICE The antibacterial filter in a unique block can be autoclavable code GP F or R F as spare part that is sterilizable 30 50 times in autoclave with a cycle of 121 20min or disposable code GP FM or R FM as spare part Both the sterilizable and the disposable filters have an efficiency level of 99 97 for all particles 20 3 micron These filters can block the liquids that s the reason why they are considered as a second overflow device The fil
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