HiFlo User Manual - Clements Medical Equipment
Contents
1. 6 Description Me P 8 Installation and Operation 9 DDBEGS oicvivivUVUVUVUVUEVVIVIARIURUNUEUEUEMEMEEVEVEVEVE MAMMA 13 MatintenaBee 6 iiiiiMAM 15 Troubleshooting ccc eee ee cee eee tense ents 17 Diagnostic Setup cece cee eeeee tence eens 19 Disassembly and Repair 21 Warraney uu uiii bp dd dd dads 26 Contents 3 CLEMENTS Identification SUC 84112 HiFlo High Vacuum High Flow Suction Pump Intended Use To provide a continuous vacuum source within the stated operating vacuum range for the aspiration of fluids and particulate matter in medical procedures carried out by clinically trained and authorized personnel Uninterrupted Availability This equipment is mains powered If patient care requires the uninterrupted availability of a source of vacuum the clinical facility must make provision for either a backup power supply or standby suction units which are battery or manually powered Classifications GMDNS Code 36777 GMDNS Term Suction unit electric powered GMDNS Synonym Aspirator Device Class Class lla Electric Shock Class Equipment Protection Additional Electric Shock Protection Defibrillation proof Type BF Applied Part Sterilisation Not supplied in sterile state Anaesthetic Rating NOT Category AP NOT Category APG Operation Mode2. Continuous operation Classifications CLEMENTS Specifications HiFlo SUC 84112 Power Rating 220 240 V 5060Hz 380W Vacuum Range 0 to 93 kPa 0 to 697 mm Hg Max Flow Rate 55 litre min free air Motor Thermally protected PSC motor Pump Oil Less twin piston Ambient Continuous operation in ambient temperatures of 5 Requirement C to 35 C Filters Inlet disposable bacteria filter Exhaust clean bleached cotton wool 5g Internal disposable hydrophobic filter Collection Jar 2 x 2 litre autoclavable shatter resistant poly carbonate jars with non static polypropylene bungs and overflow shut off valves Regulator Needle Valve Gauge Bourdon tube type Dual Scale mm Hg kPa Accuracy 3 FSD Gauge Range 0 to 760 mm Hg graduated at 20 mm Hg 0 to 100 kPa graduated at 5 kPa Unit Width 406mm Depth 305mm Height 800mm Dimensions Weight 16 5kg Standard 25 C Sea Level 100kPa Conditions Environment Indoor Specifications CLEMENTS Transportation and Storage Environmental conditions for transportation and storage are shown in the following table In addition for vehicular transportation the unit should be packed in its original packaging and kept upright Parameter Minimum Maximum Temperature 10 C 40 C Humidity 60 RH 95 RH Barometric Pressure 700 mBar 1060 mBar Warning Symbols Legend The warning symbols marked on the e
3. Jar SUC 81099 1 litre or SUC 80312 2 litre Tubing SUC 80297 8x13mm Connect pump as shown in diagram Set vacuum control knob to maximum and switch on pump Occlude jar inlet and con firm that pump achieves the same maximum vacuum as in the previous vacuum check setup Any difference indicates leaks in jar or connections 2 Unoccluded flow check Jar SUC 81099 1 litre or SUC 80312 2 litre Vacuum Tubing SUC 80297 8x13mm Gauge Calibrated Collection Flowmeter Jar Connect pump as shown in diagram Set vacuum control knob to maximum and switch on pump Connect jar inlet to calibrated flow meter and note flow reading If flow is significantly below specification check internal tubing and pump itself or internal shutoff valve if fitted 20 Diagnostic Setup CLEMENTS Disassembly and Repair Dismantling The Pump The steps for dismantling the Pump are as follows 1 Disconnect the unit from the mains power supply 2 Remove Collection Jars and Suction Tubing 3 Remove the 4 screws from the base plate tabs at the rear of the unit and push the housing forward off the base plate 4 Remove the four cylinder head screws from each head Remove the cylinder heads 5 Check O ring pistons and replace if worn cracked or perished 6 Clean the inside of the cylinder head Check flapper valves and replace if worn cracked or perished 7 Reassemble pump Periodic Safety Check The following
4. Australia all other warranties expressed or implied and whether arising by virtue of statute or otherwise including any warranties implied by the Vienna Convention are hereby excluded BMDi TUTA Healthcare obligations under this warranty are limited to the repair or replacement of the product within the terms of this warranty and the total liability of BMDi TUTA Healthcare for loss or damage of every kind whether arising pursuant to the terms of the sale of the product or otherwise in connection with the product is limited to the amount paid by the purchaser to BMDi TUTA Healthcare for the product Apart from any liability imposed by Part VA of the Trade Practices Act BMDi TUTA Healthcare accepts no other liability for any loss or damage occasioned including consequential loss or damages in any way as a result of the use of the product The warranty does not extend to cover damage to the following parts as they are inherently prone to wear motor brushes This warranty does not extend to cover corrosion due to any cause nor to any damage to painted or anodised surfaces BMDi TUTA Healthcare will give the purchaser the benefit of any manufacturer s warranty in respect of any components in the product which were not manufactured by BMDi TUTA Healthcare if such a manufacturer s warranty is available Warranty 27
5. In termittently Thermal Overload Is Cutting In and Out Disconnect Mains Power And Wait For Unit To Cool Down Replacing the Hydrophobic Shut Off Valve Filter Transparent Filter Housing Filter Media To Patient To ensure there is no entry of fluid into the pump the Hydrophobic Shut Off Valve Filter MUST be fitted as shown above 18 Troubleshooting CLEMENTS Setup for Diagnostic and Performance Testing Note that the following arrangements are not used for actual suctioning applications They are specified to remove unnecessary variations when diagnosing faults and asa standard setup for performance measurement Vacuum Check Max 1 Unoccluded zero check 9 Vacuum Gauge Disconnect all items from inlet and with pump switched off confirm that gauge reads zero A non zero reading indicates a faulty gauge Set vacuum control knob to maximum switch on pump and confirm that gauge reads zero A non zero reading indicates obstruction in internal tubing or connections 2 Occluded vacuum check Vacuum Gauge Switch on pump and occlude inlet Note maximum vacuum reading 3 Occluded gauge check Vacuum Calibrated Gauge Vacuum Gauge Connect a calibrated vacuum gauge directly to inlet and repeat maximum vacuum reading Confirm that pump gauge reads within the specified tolerance Diagnostic Setup 19 CLEMENTS Flow Check 1 Occluded leak check
6. MHz to 800MHz IEC 61000 4 3 80MHz to d 7 E VP 800 MHz to 2 5GHz 2 5 GHz where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and dis the recommended separation distance in metre m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol Kw A Immunity Guidance Table 204 25 CLEMENTS Warranty BMDi TUTA Healthcare Pty Limited BMDi TUTA Healthcare warrants that this product is free from defects in workmanship and materials for a period of 12 months 3 months for batteries from the date of shipment by BMDi TUTA Healthcare or its authorised agent to the purchaser Subject to the conditions of this warranty if the product fails to operate for any reason within the warranty period and the product is returned to the place of purchase at the purchaser s expense BMDi TUTA Healthcare will repair or replace the product free of charge If a valid warranty claim is made within 30 days from the date of shipment then BMDi TUTA Healthcare will also reimburse the purchaser for reasonable freight costs in returning the product to the place of purchase Conditions of Warranty 1 The product must be returned to the place of purchase with proof of purchase 2 This warran
7. Regulator by turning the knob to obtain the required vacuum level as indicated on the Vacuum Gauge Check that there is no loss of vacuum in the Suction Tubing and fittings Connect the catheter to the patient Check the Collection Jars to ensure that suction is being applied correctly Please Note 12 Although the Collection Jars are fitted with Overflow Cut Off Valves the fluid levels should be monitored to prevent spill over into the pump unit The Hydrophobic Filter fitted to the inlet of the pump acts as a single use shut off valve to protect the pump It must be replaced if fluid has spilled over into the pump unit Always start the pump with Suction Tubing unoccluded Always clear any blockages before re starting the pump The pump motor is protected by a thermal overload mechanism that will stop the pump if the temperature exceeds a pre set level The mechanism will then automatically restart the Pump after the motor has cooled to the appropriate temperature Installation and Operation CLEMENTS If the motor thermal overload trips switch the power off at the mains switch This will prevent unexpected re starting of the pump when the thermal overload automatically resets upon cooling e If it is suspected that fluid may have entered the pump either by an external spill or by a jar overflow the unit must be taken out of service until the fault has been fixed and its continued electrical safety has been
8. SUC 89107 Kit for Pump Vacuum Controller Needle Valve Type SUC 89240 069 14 Regulator Knob Replacement Kit for Suction Pumps Regulator Knob Screw Spares CLEMENTS Maintenance IMPORTANT There are no user serviceable components inside Maintenance must be carried out by qualified personnel only To keep your Clements HiFlo High Suction Pump in good condition the following maintenance is recommended After Each Operation e Blue Bacterial Filter The blue bacterial filter is an important device to help protect the pump from moisture and bacteria taken from patient airways Clements recommend that the filter be changed every month or when the unit is used on infectious patients or when damp or discoloured Housing Wipe clean with a damp soapy cloth Do not immerse or allow liquid to enter the housing e Suction Tubing Suction Tubing should be sterilised with sterilants determined by local protocols and compatible with PVC tubing Suction Tubing may be autoclaved to a maximum of 121 C for 20 minutes At higher temperatures the Suction Tubing will discolour and lose shape e Collection Jars Place jars upright or up side down in autoclave not on their sides Autoclave to a maximum of 136 C for 10 minutes Do not use phenolic solutions as disinfecting agents in polycarbonate jars e Bung Disconnect float cage and float from Bung Place all items upright or up side down in autoclave not on
9. according to the WEEE directive 16 Maintenance Troubleshooting Fault Check CLEMENTS Rectify No Suction But Motor is Working Tubing Blocked Clear or Replace Overflow Cut Off Valve Closed Clear Replace or Empty Jar Hydrophobic Shut Off Valve Filter Blocked Replace Hy drophobic Shut Off Valve Filter Inlet Blocked Clear Vacuum Gauge De fective Replace Vacuum Gauge Regulator Blocked Clear or Replace Bung Not Sealing Adjust or Fit New Seal Regulator at Zero Adjust Setting No Suction Motor Not Working Mains Fuse Blown Replace Faulty Mains Power Lead Replace Power Not Turned On Turn On Unit Fuses Blown Replace Thermal Overload Acti vated Wait For Unit To Cool Down No Suction But Humming Can Be Heard From Motor Blockage In Pump Dismantle And Clean Pump Motor Windings Troubleshooting Replace Motor 17 CLEMENTS Fault Check Rectify Not Enough Suction Regulator Setting Too Low Adjust To Correct Set ting Leaks In Tubing or Fittings Tighten Connections Blockage In Tubing or Fittings Clear or Replace Hydrophobic ShutOff Valve Filter Blocked Replace Hy drophobic Shut Off Valve Filter Excessive Noise Coming From Pump Pump Worn Replace Pump Pump Incorrectly As sembled Assemble Correctly Pump Runs
10. confirmed The service department must also be notified of any potential biohazard Spares MUL 94003 702 Fuse T5 0 Amp 250V MUL 94004 000 Mains Power Switch Green Rocker SUC 80297 001 Kit Yellow Suction Tubing 20 Metre roll SUC 80301 2 litre Collection Jar for Suction Pumps SUC 80404 001 Single Use Plastic Handpiece pack of 10 SUC 84100 162 Blue Bacteria Filter Set of 12 SUC 84200 033 Bung Assembly with Overflow Cut Off Valve for 2 litre Collection Jar SUC 91005 415 User Manual for the HiFlo High Suction Pump Spares 13 CLEMENTS Spares SUC 37043 Cotton Wool for Suction Pumps Exhaust Filter Pack of 10 5 grams each SUC 80330 High Vacuum Gauge 0 100kPa SUC 84100 049 Exhaust Filter Assembly for Suction Pumps SUC 84100121 Resilient Motor Mount Pack of 4 SUC 84100 400 Hydrophobic Shut Off Valve Filter SUC 84100 505 Footswitch Kit for Suction Pumps with Switch Pneumatic Actuator SUC 84109 002 Motor and Pump for Hi Vac Hi Flo SUC 84200 501 Seal for Collection Jar Bung Set of 2 SUC 84200 502 Suction Inlet Nipple for 2 litre Jar Bung Set of 4 SUC 84200 503 Kit Grey Bung Float Chamber Set of 2 SUC 84200 518 Washer for Overflow Valve Pack of 4 SUC 84200 519 Blue Male Nipple for Bacteria Filter Pack of 10 SUC 84200 520 Blue Female Nipple for Bacteria Filter Pack of 10
11. safety checks should be performed at least every 24 months by a qualified person who has adequate training knowledge and practical experience to perform these tests Inspect the equipment and accessories for mechanical and functional damage Inspect the safety relevant labels for legibility Inspect the fuse to verify compliance with rated current and breaking characteristics Verify that the device functions properly as described in the instructions for use Test the protection earth resistance according IEC 60601 1 Limit 0 2 ohm Test the earth leakage current according IEC 60601 1 Limit NC 500 uA SFC 1000u4A The leakage current should never exceed the limit The data should be recorded in an equipment log If the device is not functioning properly or fails any of the above tests the device has to be repaired Disassembly and Repair 21 CLEMENTS Fuse Replacement The Pump is fitted with two cartridge fuses located in fuse holders that are accessible from outside the unit To replace the fuses use the following procedure 1 Disconnect the unit from the mains power supply 2 Locate the two fuse holders which are mounted on the rear side of the unit at the lower right hand side Lift off the fuse holder cover 4 Remove the old fuses and inspect them If they are blown replace them with new fuses Replace the fuse holder cover 6 Connect the unit to the mains power supply switch the power
12. CLEMENTS HiFlo High Vacuum High Flow Suction Pump SUC 84112 Q O N z ie qe u 0 SE Le NY ie E Ew px E 0 gt fe E Q User Manual Manual No SUC 91005 415 Issue 23 CLEMENTS Safety Thank you for purchasing this Clements HiFlo High Suction Pump For your safety it is imperative that this unit only be operated by authorised personnel in accordance with the instructions as described in this manual Operated in this way the HiFlo High Suction Pump will provide the standard of service specified Due to continual improvements in product design the HiFlo High Suction Pump may vary in detail from the descriptions in this manual In the event of further questions please contact your local distributor or BMDi TUTA Healthcare direct User Manual HiFlo High Suction Pump Manual Number SUC 91005 415 Issue 23 Copyright 2009 BMDi TUTA Healthcare Pty Ltd The information in this manual was originated by and is the exclusive property of BMDi TUTA Healthcare Pty Ltd It is furnished for customer information only and is not an authorisation or licence to make this product or to furnish this information to others BMDi TUTA Healthcare Pty Ltd taal Unit 4B 128 130 Francs Street Lidcombe NSW 2141 Australia Phone 61 2 9466 5300 Website www medaust com CLEMENTS Contents Classifications oo 3 ARR ARA EAR RA AT AR ARA 4 plz rP eclaloo MWM 5 Transportation and Storage
13. ce of all functions of the HiVac suction pump are considered essential performance for the purpose of electromagnetic immunity Table 201 Guidance and manufacturer s declaration electromagnetic emissions all equipment and systems Guidance and manufacturer s declaration electromagnetic emissions The HiVac suction pump is intended for use in the electromagnetic environment specified below The customer or user of the HiVac suction pump should assure that it is used in such an environment Emissions Test Compliance Electromagnetic environment guidance Harmonic Emissions Class A The HiVac suction pump is suitable for use in IEC 61000 3 2 all establishments including domestic establishments and those directly connected to the public low voltage power supply network Voltage fluctuations Complies that supplies buildings used for domestic flicker emissions purposes IEC 61000 3 3 RF emissions Complies The HiVac suction pump is not suitable for CSIPR 14 1 interconnection with other equipment Emissions Guidance Table 201 23 CLEMENTS Table 202 Guidance and manufacturer s declaration electromagnetic immunity for all equipment and systems Guidance and manufacturer s declaration electromagnetic immunity The HiVac suction pump is intended for use in the electromagnetic environment specified below The customer or user of the HiVac suction pump should assure that
14. ement Connect This Tube To The Patient Both Jars In Use Overflow Cut Off Valve in this Jar Only To connect the Collection Jars in a double jar arrangement use the following procedure and refer to the block diagram below 1 Place two clean jars in the holders ensuring that only one jar Jar 1 is fitted with an Overflow Cut Off Valve 2 Connect the SUCTION outlet with the Overflow Cut Off Valve of Jar 1 to the Bacteria Filter inlet on the main unit 3 Connect the PATIENT inlet of Jar 1 to the SUCTION outlet of the jar without an Overflow Cut Off Valve Jar 2 4 Connect the PATIENT inlet of Jar 2 to the Suction Tube leading to the patient Hydrophobic Shut Off Valve Blue Bacteria Filter Internal Filter External To Patient Overflow Cut Off Valve NO Overflow Cut Off Valve 5T Pump Jar 1 Jar 2 Installation and Operation 11 CLEMENTS Operation To operate the Pump follow the steps listed below 1 Place the pump on a level surface with a 15cm clearance from walls or other objects Install the Collection Jars and Suction Tubing in either the single jar or double jar arrangement as described in the Connecting The Collection Jars section on page 8 Connect the unit to the mains power supply and switch the power on at the mains supply outlet Press the Power Switch down into the ON position and the Motor will run Occlude the Suction Tubing and adjust the
15. it is used in such an environment Immunity Test IEC 61000 test level Compliance level not tested Electromagnetic environment guidance Electrostatic discharge ESD IEC 61000 3 4 Electrical fast transient burst IEC 61000 4 4 6 kV contact 8 kV air 6 kV contact 8 kV air 2 kV for power supply lines 1 kV for input output lines 2 kV for power supply lines 1 kV for input output lines Floors should be wood concrete or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 30 Mains power quality should be that of a typical commercial or hospital environment Surge IEC 61000 4 5 1 kV line s to line s 2 kV line s to earth 1 kV line s to line s 2 kV line s to earth Mains power quality should be that of a typical commercial or hospital environment Voltage dips short interruptions and voltage variations on power supply input lines IEC 61000 4 11 lt 5 Ur gt 95 dip in Ur for 0 5 cycle 40 Ur 60 dip in Ur for 5 cycles 70 Ur 30 dip in Ur for 25 cycles 5 96 Ur gt 95 dip in Ur for 5 sec 5 Ur gt 95 dip in Ur for 0 5 cycle 40 Ur 6096 dip in Ur for 5 cycles 70 Ur 30 dip in Ur for 25 cycles 5 Ur gt 95 dip in Ur for 5 sec Mains power quality should be that of a typical commercial or hospital environment The unit shut off during
16. on and ensure that the unit is operating correctly Electrical Wiring Diagram IEC INLET MAIN SWITCH LIGHT BLUE GREEN YELLOW 2 X 75 0 FUSES GREEN YELLOW PSC MOTOR 22 Disassembly and Repair CLEMENTS EMC Information Tables per EN60601 1 2 2001 09 Section 6 In accordance with EN 60601 1 2 2001 Medical electrical equipment Part 1 2 General requirements for safety Collateral standard Electromagnetic compatibility Requirements and tests 1 Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in the Accompanying Documents the following tables 2 Portable and Mobile RF Communications Equipment can affect Medical Electrical Equipment 3 The equipment or system should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary the equipment or system should be observed to verify normal operation in the configuration in which it is used The following tables provide information regarding the EMC characteristics of this Medical Electrical Equipment The compliance levels of immunity referred to in tables 202 and 204 have not been arrived at by testing but by declaration on the basis that the HiVac suction pump contains no electronic components and is inherently immune to the specified levels of electromagnetic disturbance The performan
17. quipment and their meanings are shown as follows N Attention consult accompanying documents e T F Defibrillation Proof Type BF applied part Dispose of product according to requirements of WEEE directive mm Transportation and Storage CLEMENTS Electromagnetic Interference This equipment generates uses and can radiate radio frequency energy and if not installed and used in accordance with the instructions may cause harmful interference to radio communications However there is no guarantee that interference will not occur in a particular installation If this equipment does cause harmful interference to radio or television reception which can be determined by turning the equipment off and on the user is encouraged to try to correct the interference by one or more of the following measures e Reorient or relocate the receiving antenna Increase the separation between the equipment and the receiver e Connect the equipment into an outlet on a circuit different from that to which the receiver is connected e Consult the dealer or an experienced radio TV technician for his or her help Changes or modifications to the equipment not expressly approved by Clements could void the user s authority to operate the equipment Electromagnetic Interference CLEMENTS Description The Clements HiFlo High Suction Pump is a mobile enclosed suction pump designed for high suction and high flow The main feat
18. ted with two Collection Jars it can either be connected in a single jar arrangement or a double jar arrangement With the single jar arrangement only one jar is in use at a time with the second jar on standby As one jar is filled it is disconnected so that it can be emptied and the other jar is connected The double jar arrangement allows both jars to be in use at the same time thus providing longer periods between changeover Installation and Operation 9 CLEMENTS Single Jar Arrangement Connect This Jar Tube To The Outlet Patient Jar Inlet Overflow Cut Spore Off Valves In Patient Both Jars Tube This Jar This Jar In Use On Standby To connect the Collection Jars in a single jar arrangement use the following procedure and refer to the block diagram below 1 Place two clean jars in the holders ensuring that both jars are fitted with an Overflow Cut Off Valve 2 Connect the SUCTION outlet of the jar to be used first to the Bacteria Filter inlet on the main unit 3 Connect the PATIENT inlet of the jar to be used first to the Suction Tube leading to the patient 4 When the first jar is full disconnect it and use steps 2 and 3 to connect the second jar Hydrophobic To Shut Off Valve Blue Bacteria Patient Filter Internal Filter External Overflow Cut Off Valves in BOTH Jars Suction s Jar in Jar on Use Standby 10 Installation and Operation CLEMENTS Double Jar Arrang
19. the gt 95 dip for 5 sec disturbance If the user of the HiVac suction pump requires continued operation during power mains interruptions it is recommended that the HiVac suction pump be powered from an uninterruptible power supply or battery Power frequency 50 60Hz magnetic field IEC 61000 4 8 3 A m 3 A m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment 24 Immunity Guidance Table 202 CLEMENTS Table 204 Guidance and manufacturer s declaration electromagnetic immunity for equipment and systems that are NOT life supporting Guidance and manufacturer s declaration electromagnetic immunity The HiVac suction pump is intended for use in the electromagnetic environment specified below The customer or user of the HiVac suction pump should assure that it is used in such an environment Immunity Test IEC 61000 Compliance Electromagnetic environment test level level guidance not tested Portable and mobile communications equipment should be used no closer to any part of the HiVac suction pump including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance Conducted RF 3 Vrms 3 Vrms d 8 5 V4 NP IEC 61000 4 6 150 kHz to 80 MHz Radiated RF 3 V m 3 V m d 3 5 E VP 80
20. their sides Autoclave all items to a maximum of 136 C for 10 minutes Note Do not use abrasive cleaning agents as this may damage plastic surfaces and reduce the expected performance of an item Maintenance 15 CLEMENTS After Every 100 Hours or 2 Months of Operation e Replace the Exhaust Filter 1 Remove the Exhaust Filter from the rear of the unit 2 Unscrew the caps and replace the cotton wool The filter takes 5 gram of bleached and teased out cotton wool Check all Suction Tubing and replace if it is perished soft or discoloured Also check the tubing nipples e Check the seal rings on the Bungs and replace them if they are hard cracked or perished Check the fit of the Bung in the Collection Jar Check the Overflow Cut Off Valve seals and replace them if they are perished or damaged IMPORTANT The preceding maintenance should also be carried out immediately after use with infectious patients Disposal and Recycling Waste Materials The contents of the collection jars suction tubing bacteria fil ter internal hydrophobic shut off filter or the cotton wool in the exhaust filter may contain biohazard wastes Handle using safe handling procedures which may include the use of rubber gloves and eye protection and dispose of according to local pro tocols for biohazard materials Recycling At the end of their service life the pump and accessories should be dismantled if necessary and disposed of
21. ty is only available to the original purchaser of the product 3 The product must not have had its serial number removed defaced or changed its casing opened its power supply altered or have been tampered with in any other way 4 This warranty does not cover inadequate or incorrect site preparation improper installation connection to the wrong voltage failure of the product due to misuse the use or operation of the product outside of the physical electrical or environmental specifications of the product use in a manner or environment in which the product is not designed to be used improper adjustment calibration or operation by the purchaser the use of accessories including consumables hardware or software which were not manufactured or approved in writing by BMDi TUTA Healthcare 26 Warranty 10 11 12 13 CLEMENTS any modifications of the product which were not authorised in writing by BMDi TUTA Healthcare any contamination or leakages caused or induced by the purchaser and inadequate or improper maintenance of the product This warranty does not cover normal wear and tear BMDi TUTA Healthcare will not be responsible for damage or loss caused during shipping In Australia apart from any warranties implied by the Trade Practices Act 1974 all other warranties expressed or implied and whether arising by virtue of statute or otherwise are hereby excluded Outside
22. ure of this unit is the low maintenance piston motor and pump assembly which can generate suction strengths from 0 to 675 mm Hg 90 kPa with flow rates up to 55 litres of Free Air Per Minute FAPM depending on the model and power supply The unit is mounted on large rubber wheels which make it easy to move to any part of a hospital The unit also has a storage compartment at the rear to house additional tubing handpieces and other items needed when using the pump Main Components of Unit Power Switch Exhaust Filter Vacuum Gauge Handle Regulator Control Knob Tube Storage Hooks Inlet Connection Storage Compartment a AIIN Pump Internal Description CLEMENTS Installation and Operation Installation The Clements HiFlo High Suction Pump is supplied with e 2x 2 litre Collection Jar with Bung Assembly e 1x 2 4 metre length of Suction Tubing e 1x0 4 metre length of Suction Tubing Important Remove strapping from motor before starting Ensure power is disconnected before opening unit WARNING This unit can generate high vacuums It must not be used for applications which require low vacuum Always check patient requirements before applying the Clements HiFlo High Suction Pump For applications which require low vacuum please contact your distributor for information about the Clements Low Suction range of products Connecting The Collection Jars Because the unit is fit
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