LM-ProPower UltraLED Manual
Contents
1. 1 kV differential mode mode IEC 61000 4 4 Mains power quality should be that of a typical commercial or hospital 32 IEC 61000 4 5 Voltage dips short interruptions and voltage varaiations on power supply input lines IEC 61000 4 11 Power frequency 50 60 Hz magnetic field IEC 61000 4 8 2 kV common mode 5 Yo U 595 dip in Ur for 0 5 cycle 40 Yo Ur 60 dip in Ur for 5 cycles 70 Yo U 30 Yo dip in Ur for 25 cycles 5 Yo Ur gt 95 dip in Ur for 5 sec 2 kV common mode lt 5 Yo Ur gt 95 dip in Ur for 0 5 cycle 40 Yo Ur 60 dip in Ur for 5 cycles 70 Yo U 30 dip in Ur for 25 cycles 5 Yo Ur gt 95 dip in Ur for 5 sec NOTE Uy is the a c mains voltage prior to application of the test level environment Mains power quality should be that of a typical commercial or hospital environment If the user of the LM ProPower requires continued operation during power mains interruption it is recommended that the LM ProPower be powered from an uninterruptible power supply or battery Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment Warranty and declaration Guidance and manufacturer s declaration electromagnetic immunity The LM ProPower is intended for use in the electromagnetic environment specified below The customer or the user of the LM ProPo2. Use the LM ProPower Fixer to check that the water hose inside the handpiece has not stuck in the autoclave Insert the Fixer carefully into the handpiece from the hose connector side To avoid the hose getting stuck the water adjustment on the handpiece should be set to fully open before sterilization in autoclave 7 Ifthe problem still remains contact your dealer for support and indicate Error Code E S04 F Tip does not fit smoothly onto the handpiece 1 Clean handpiece threads with compressed air and try with a new tip 2 Ifthe problem still remains the threads of the handpiece may be damaged and the handpiece needs to be replaced Contact your dealer and indicate Error Code E S06 G Difficulty to remove the ErgoGrip from the handpiece 1 Grab the ErgoGrip gently near the lens and at the same time twist and slide it off the handpiece 2 Ifthe problem still remains replace the ErgoGrip H Handpiece is overheated during use 1 Check that the fluid flow is sufficient at least 20 ml min 2 Ifthe problem still remains replace the handpiece and contact your dealer l Weak or no LED light 1 Check that lens in the ErgoGrip is clear and clean Clean or replace 1f necessary 2 If you have an additional handpiece try replacing the handpiece 3 Ifthe problem still remains contact your dealer for support and indicate Error Code E S03 2 LM cao Technical data 7 Technical data LM Instruments Oy Man
3. ted at both ends and 1s not damaged The blue light next to the ON key is Check that the scaler handpiece is properly flashing alternately with three other connected blue lights on the control panel Three yellow lights are flashing in The Working Mode has not been selected sequence Select the working mode by pressing one of the keys next to the yellow lights The light next to the C key 1s flas The cleaning function has been activated hing Wait until the cleaning process has finished and the light stops flashing C No tip vibration 1 Check that the tip is firmly tightened Preferably use a torque wrench and tighten clockwise until the torque wrench slides The torque wrench prevents the tip from being over tightened 2 Check that the green light below the keys on the control panel is lit If it is not lit please see Section A on page 25 3 Check that the device has been turned on by pressing the ON key and that the blue light next to the ON key 1s lit 4 Check that the Working Mode has been selected by pressing one of the Working Mode keys and that one of the yellow lights on the control panel is lit If you have an additional handpiece try replacing the handpiece If you have an additional foot control cable try replacing the foot control cable If you have an additional foot control try replacing the foot control go ID A If the problem still remains contact your dealer for support and indicate Error C
4. 13 2 4 Medicament bottle annen senen eeen eenen 14 2 5 Symbols on the equipment aaneen vennen eenn 15 3 Molo sn AA 16 3 1 General installation instructions nnee enn 16 3 2 Version for tap water 2 Q XQXX aa 16 3 3 General installation instructions continued 17 4 Operating instructions aaan an nnen eenn nenn menen 18 del OENE vennen EE 18 5 Cleaning and maintenance an nnnann nennen 22 5 1 General cleaning procedure aan vaan nennen 22 5 2 Recommended cleaning procedure 23 Dis MANI ENANC wamre nnn 24 6 Troubleshooting UltraLED 25 TeenniCal data aan NABANG 28 8 Warranty and Declaration of conformity 30 8 1 Warranty OS AGANG 30 8 2 Declaration of conformity ana en 31 Ba ENG IOUIO ANCO se anko ea en 32 LM rene LM cac Safety Safety Intended use This scaler is designed for dental purposes It 1s designed for removal of tartar or calculus on teeth and other dental work where the ultrasonic vibration is beneficial The unit should only be used by licensed dental proffesionals trained in the proper use of scaling devices Do not use it for applications where it is not intended If you are unsure about your application please contact your local dealer or place of purchase General requirements Service of the product is only to be performed by authorized service personnel The product must be connecte
5. 4 3 Check that the power cord is connected and the unit is in stand by mode the green indicator lamp 1s illuminated 4 1 General 1 Gently slide the ErgoGrip on to the scaler handpiece 2 Carefully place the tip in the torque wrench 3 Use the torque wrench and screw the tip clockwise on to the scaler handpiece Tighten until resistance and the torque wrench slides The torque wrench prevents the tip from being overtightened LM cao A WARNING Atip that is bent altered worn more than 2 mm will loose performance and must be exchanged Prolonged use may cause tip breakage and injury to the patient The operator should be aware of that ultrasonic in struments with small diame ters are subject to breakage at any time If not used cor rectly or with too much po wer or force the instrument WILL break Do not use nickel titanium files since they easily break at high frequenses LM scene Operating instructions 4 Turn on the UltraLED scaler by ON key on the keyboard The blue indicator lamp illuminates and the scaler is activated 5 The indicators next to the working modes are flashing to remind Caution that a working mode has to be selected If several blue indicators are Without cooling fluid the flashing instead check that the scaler hand piece is connected If the maximum operating time problem remains concern the trouble shooting section Check the re for the scaler handpiece is ded
6. a comfortable relaxed grip as well as an excellent feel LM ProPower is highly adaptable to any procedure or user approach It is not only an outstanding scaling and cleaning device but it also brings power and versatility to endodontics implantology restorative treatments minimally invasive treatments and apical surgery 9 D UltraLE _ pa 5 a NG LM Equipment description 1 AC power input 2 Fuse holder 3 Water hose coupling optional 4 Foot control connection 5 Type plate 2 2 Control panel 19 A c oo 1 1 Cleaning key 2 POWER ON key 3 POWER OFF key 13 e O 6 4 Working mode 1 key 0 to 40 power O 5 Working mode 2 key 0 to 70 power Ke W 066 6 Working mode 3 key 0 to 100 power 7 StandBy indicator 8 POWER ON indicator 9 Dry mode indicator Ultra LED 10 Irrigation mode indicator 11 Working mode 1 indicator 12 Working mode 2 indicator 13 Working mode 3 indicator 14 Cleaning mode indicator LM scene Equipment description 2 3 Foot control Connection for foot control cable OFF position ON position N Diagnostic function turn LED light ON or OFF by a single click on the pedal Irrigation position Zero power position Maximum power position CO N Oo ao Power regulation 13 Equipment description 2 4 Medicament bottle optional LM ProPower has a medica
7. aka eee 1 Verify that the water supply can be turned off 2 Verify that the water pressure conforms to the data in the Technical data 3 Verify that the water supply fulfills the medical demands of hygiene 4 Unscrew the nut from the nipple and thread it on the hose 5 Push the hose onto the coupling nipple 6 Tighten the nut firmly and insure that the hose is securely attached to the unit 7 Connect the other end of the hose to the water supply LM irene A WARNING The unit must be connec ted to an AC power outlet provided with a protective ground USA and Canada The power cord and plug must be classified as Hos pital Grade Installation 3 3 General installation instructions continued e Verify that the voltage rating on the rear side match the voltage of the AC power outlet e Verify that the AC power outlet is provided with a protective ground e Connect the power cord to the unit and the AC power outlet All indicator lamps will illuminate for a short period during a self check of the unit e The unit is standby when the green indicator lamp is illuminated 17 Operating instructions 4 Operating instructions Preparations bottle version 1 Fill the medicament bottle with water or medicament solution according to the Medicaments that can be used listed on page 29 2 Screw the bottle connector onto the bottle and push it onto the con nector See picture in section 2
8. lips cheeks and tongue out of the way of the tip and perform treatment according to How to use the scaler lon on nex Not section on next page At low power settings there will be no spray Increase the water flow if the handpiece feels too warm 19 Operating instructions How to use the UltraLED scaler The side of the tip end shall be applied to the tooth so that the movement of the tip is parallel to the surface of the tooth The first 2 mm of the tip are the most efficient Place the tip on the tooth surface before activating the foot control The power is regulated with the foot control from 0 to 100 within each working mode Normal scaling rarely requires more than 50 power level of each working mode However hard to remove calculus might require a higher power setting Ensure that contact between the tip and the tooth surface 1s maintained during scaling Keep moving the tip slowly back and forth and let the instrument do the work Use short and long strokes so that the whole surface of each tooth is scaled The tip 1s normally aimed towards the toothpocket To keep the tip working parallel to the surface of each tooth it is important to follow the anatomy of the tooth With the correct power setting appropriate pressure against the tooth approximately 20 grams but not exceeding 50 and the tip operating parallel to the surface treatment will be gentle quiet and efficient If during the treatmen
9. predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the LM ProPower is used exceeds the applicable RF compliance level above the LM ProPower should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the LM ProPower Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m 33 Warranty and declaration 34 The LM ProPower is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the equipment can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the LM ProPower as recommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter m Rated maximum output power of 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz transmitter d 1 2VP d 1 2VP d 2 3VP For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres m can be estimated using the equation applicable to the frequency of the transmitter where P is the maximum output power rat
10. the Authorized Dealer or customer or any other person for or on account of any injury loss or damage of any kind or nature sustained by or any damages assessed or asserted against or any other liability incurred by or imposed upon the handling use operation maintenance or repairs of Products by anyone other than the Manufacturer This exclusion of liability does not apply pursuant to the laws on product liability in case of personal injury and property damage to privately used objects resulting from the Products 30 LM scene A WARNING No modification of this equipment is allowed Warranty and declaration 6 2 Declaration of conformity The manufacturer hereby declares that the LM ProPower UltraLED unit Class I type B according to EN60601 1 equipped with original acces sories conforms to the essential requirements of the Medical Device Directive 93 42 EEC with reference to the following harmonized standards IEC 60601 1 Third edition 2005 EN 60601 1 2006 Classification Medical products Class Ia C os37 31 Warranty and declaration 8 3 EMC Guidance and manufacturer s declaration Guidance and manufacturer s declaration electromagnetic emissions The LM ProPower is intended for use in the electromagnetic environment specified below The customer or the user of the LM ProPower should assure that it is used in such an environment Emissiontest Compliance Electromagnetic environment guid
11. to correct or circumvent the errors or to repair or replacement of defective parts of Products by the Manufacturer EXW Manufacturer s factory providing that a written claim of the defect 1s sent to the Manufacturer within the warranty period and the original part is returned to Manufacturer s factory by the Authorized Dealer and Manufacturer s inspection establishes the existence of such a defect The customer must contact the Authorized Dealer from whom the products were purchased to request repair or replacement under this warranty and a written claim of the defects and send the original Product the Authorized Dealer This warranty is void if service or repair is performed by persons not authorized by the manufacturer Any Products not manufactured by the Manufacturer carries only such warranty if any as given by any manufacturer thereof This warranty is the Manufacturer s only warranty 1n respect of the Products and the Manufacturer disclaims all other warranties whether of merchantability fitness for particular purpose or otherwise guarantees and liabilities express or implied arising by law or otherwise In no event shall the Manufacturer be liable for any general consequential or incidental damages loss of use or loss of profits by reason of the manufacturer s negligence or otherwise in connection with the sale delivery installation repair or use of the Products The Manufacturer shall have no liability whatsoever to
12. LM LMProP gt UltraLED USER MANUAL LM rene This manual is valid for LM ProPower 100721741 LM ProPower 100731751 LM ProPower 10072174 lus LM ProPower 10073175 lus LM ProPower 100721741jp LM ProPower 100731751jp Important Read this manual carefully before using the product How to read this manual Each chapter starts with a section with general instructions which 1s followed by sections with additional information First read the general section and then proceed to the section that applies to your product If there are any questions regarding the contents of this manual please contact LM Instruments Oy Manufacturer Marketing and Sales LM Instruments Oy PL 88 Norrbyn rantatie 8 FI 21601 Parainen Finland Telephone 358 2 4546 400 Fax 358 2 4546 444 E mail info lm dental com Internet www lm dental com Copyright Copyright 2014 LM Instruments Oy All rights reserved The contents of this manual may be changed without notice No part of this manual may be reproduced in any form or by any means without permission in writing from LM Instruments Oy C 0537 LM scene Contents SO ee 5 Consignes de securite Canada 7 L ATID AGING ane kid eee AA 9 1 1 General content of delivery aaneen nnen 9 1 2 Content OF introkits a sista ak pite 10 2 Equipment description a 11 2 1 General description aa 11 2 2 Control panakaw AGE ooo ee ekate ei 12 2o FOOLGONMO iii boat w kan ti et iya a
13. ance The LM ProPower uses RF energy only for its internal function Group 1 Therefore it s RF emissions are very low and are not likely to cause any interference in nearby electronic equipment RF emissions CISPR 11 RF emissions CISPR 11 Class B The LM ProPower is suitable for use in all establishments including domestic establishments and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Harmonic emissions Nakanalicabia IEC 61000 3 2 PP Voltage fluctuations flicker emissions IEC 61000 3 3 Guidance and manufacturer s declaration electromagnetic immunity The LM ProPower is intended for use in the electromagnetic environment specified below Not applicable The customer or the user of the LM ProPower should assure that it is used in such an environment l IEC 60601 Electromagnetic environment Immunity test Compliance level i test level guidance Electrostatic 6 kV contact ica Floors should be wood concrete or discharge ESD 7 ceramic tile If floors are covered with synthetic material the relative humidity should be at least 30 8 kV air 8 kV air IEC 61000 4 2 Mains power quality should be that of a typical commercial or hospital environment Electrical fast transient burst 2 kV for power supply lines 2 kV for power supply lines 1 kV for input output 1 kV for input output lines lines Surge 1 kV differential
14. d to electricity and water supply meeting the requirements specified in the Technical data section page 28 The product needs special precautions regarding EMC Elektro Magnetic Compability and needs to be installed and put into service according to the EMC information provided on page 33 Portable and mobile RF Radio Frequency communications equip ment can affect the product Contraindications Do not use the scaler on patients with cardiac pacemakers The scaler may disturb the function of the pacemaker General precautions e The product is not suitable for use in the presence of flammable gases e Only use the product in combination with LM Instruments and Amdent scaler tips e If the handpiece tubing is damaged or worn out it must immedia tely be replaced to avoid exposing the user or the patient to elec tric hazard e Use the original packaging when returning equipment for service Warnings The product should not be used adjacent to or stacked with other equipment If adjacent or stacked use 1s necessary the product should be observ ed to verify normal operation in the configuration in which it will be used Safety Safety notices in this manual A Warning indicates a potentially dange rous situation Non observance may lead to NABANG death or injury A Caution indicates a potentially harmful situation Non observance may damage Santen the equipment Note indicates a situation where special notice should b
15. e observed Note LM feel the difference LM cac Consigne de securite Consigne de securite Canada Utilisation prevue Cet appareil a ultrasons est destin a des applications dentaires Il est con u pour liminer le tartre ou les calculs des dents et pour toute autre application dentaire ou les vibrations ultrasonores sont b n fiques Cet appareil doit tre exclusivement manipul par des professionnels dentaires dipl6m s ayant suivi une formation relative l utilisation correcte des dispositifs de d tartrage N employez pas cet appareil pour des applications pour lesquelles il n est pas con u Au cas ou vous ne seriez pas s r de son application veuillez contacter votre distributeur local ou le point de vente Conditions g n rales Le service du produit doit tre execut seulement par le personnel de service autoris avec les outils et le mat riel appropri s Le produit doit tre reli a l approvisionnement de l lectricit et l approvisionnement en eau r pondant aux exigences d finies dans la section Caract ristiques techniques la page 28 Le produit exige des pr cautions sp ciales concernant la CEM Compatibilit Electromagn tique et doit tre install et mis en service selon la page 33 L quipement de communication RF Radio Fr quence portable et mobile peut affecter le produit Contres indication N employez pas sur des patients avec les stimulateurs cardiaque
16. ibly the scaler handpiece and autoclave according to the clinic s routines End of the day e Run the automatic cleaning cycle with clean water See instructions on page 22 e Remove and wash medicament bottle and bottle cap at a maximum temperature of 65 C bottle version 23 LM Cleaning and maintenance Weekly bottle version e Run the automatic cleaning cycle with an anti microbial cleaning agent solution in the bottle See instructions on page 22 We recommend to use a separate bottle for the cleaning agent solution Concerning exposure times of cleaning agent follow instructions given by manufacturer e Before patient treatment to rinse the lines from cleaning agent solution put clean water in the bottle and run the automatic cleaning cycle until clean water comes out of the handpieces 5 3 Maintenance Power cord Inspect the power cord cables and the handpiece hose daily to insure that the equipment is in good condition without mechanical damage O rings bottle connector Lubricate the O rings regularly with a glycerine based water soluble lubricant Vaseline may also be used but it may shorten the durability time of the O rings Caution Tips A petroleum based lubricant When a tip is bent altered or worn more than 2 mm it will loose on the o rings may shorten performance and must be exchanged Check the tip length weekly their durability time by comparing the tip to a tip check card Excha
17. in line 2 The cleaning cycle starts and stops automatically after 80 seconds see picture Cleaning of the equipment components Wipe off with a soft cloth and use a surface disinfectant suitable for hard plastics Cover and control panel UltraLED lo a Wash at max 65 C Medicament bottle Cap for medicament bottle 22 LM cao Note Autoclaving the handpiece regularly may shorten the life time of the scaler hand piece IN Caution Before cleaning and steriliz ing the handpiece water control ring must be set to fully open dots in line see picture Note Always set the water flow to fully open before running the cleaning cycle dots in line see picture AN TAS Caution Do not sterilize any scaler accessories using dry heat or chemical autoclaves This may damage the material Cleaning and maintenance Autoclave in steam at 134 C max 135 C for at least 3 minutes Scaler tips Torque wrenches LM ErgoGrip Focus LED LM ProPower scaler handpiece 5 2 Recommended cleaning procedure Beginning of the day Run the automatic cleaning cycle with clean water See instructions on page 22 After each treatment e Run the automatic cleaning cycle with clean water See instructions on page 22 e Wipe off the cover control panel handpiece and the hose with a soft cloth Use a surface disinfectant suitable for hard plastics e Wash the ErgoGrip the tip and poss
18. ing of the transmitter in watts W according to the transmitter manufacturer NOTE 1 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people LM feel the difference 35 LMDental LM Instruments Oy PL 88 Norrbyn rantatie 8 FI 21601 Parainen Finland Tel 358 2 4546 400 Fax 358 2 4546 444 info lm dental com www lm dental com www lIm dental com Downloads 0314EN 9770035 G
19. ki Jethis ked het a tue allowed bra commended working mode that is marked on the tip an cooling down period of 8 choose the working mode by pressing the corresponding working minutes Operating without mode key on the keyboard cooling fluid for more than 2 minutes may cause over heating of the scaler hand piece After above cycle has been 6 A second press of the ON key activates the dry mode for scaling EPERE A IMOS Ine cae without water medicament handpiece has to cool down for at least 60 minutes 7 A third press of the ON key activates the irrigation mode The irrigation mode can also be activated in the scaling mode by pressing down the foot control in the leftmost position A 8 By pressing the ON key repeatedly it will toggle between normal scaling dry and irrigation mode WARNING e MY 2 Remember to choose the 9 Keep the handpiece over the cuspidor bowl and depress the foot right working mode if chang ing scaler tip during the control in the leftmost position and adjust the water flow with the treatment ring on the handpiece until the water 1s dripping from handpiece as in picture below Recommended flow 20 ml min New tips are not sterile upon delivery Sterilize before use according to the clinic s routines Keep the patient s lips cheeks and tongue out of the way of the activated tip since contact may cause burns because of friction heat 10 Keep the patient s
20. m chloride e Clorhexidine e Essential oils e Hydrogen peroxide 3 USP e Povidine iodine 10 solution e Saline solution e Sangurinara extract e Sodium hypochlorite 1 solution 29 LM sca Warranty and declaration 8 Warranty and Declaration of conformity 8 1 Warranty Terms The following warranty terms apply to the sale of LM Instrument Oy s products hereinafter Products to a purchasing company or individual by LM Instruments Oy hereinafter Manufacturer Manufacturer hereby warrants that the Products will be free from defects arising from faulty materi als or workmanship for a period of twenty four 24 months from the date of purchase by a customer from Manufacturer s authorized dealer hereinafter Authorized Dealer The warranty period is exceptionally three 3 months for products with a life inherently shorter than 24 months due to normal wear and tear for example tips of ultrasonic scalers tips of endodontic files This warranty shall not apply to Products or parts thereof which have been subject to abuse misuse negligence or accident or are not connected to proper power supply to which any modification alteration or attachment has been made without written consent of the Manufacturer or which are installed or operated violating instructions for installation use and maintenance which are normally consumed in operation The sole and exclusive remedy under this warranty shall be limited
21. ment dispenser system making the device independent of a fixed water supply connection The medicament bottle can be used for either medi cament solutions or ordinary clean water The unit contains an electrically driven air compressor When operating the unit the compressed air forces the fluid from the bottle through the hose and to the handpiece and the tip nozzle 1 Medicament bottle 2 Bottle connector 3 Depressurisation button The LM ProPower can be delivered either with the medicament dispenser system or with fixed water supply connection without the bottle and bottle connector 14 LM feel the difference LM rene 606660 FF Scaler Model LM ProPower 100731751 Type No 5609651 Senal Na XXXXX 3 L nat are uy PL a Va ti rzut e 33 FI2180 PAZAINEN CLASSIFIED TERTE b 9800163 A LG C os37 pi QO la Equipment description 2 5 Symbols on the equipment Working mode 1 0 to 40 power Working mode 2 0 to 70 power Working mode 3 0 to 100 power Irrigation mode Dry mode Automatic cleaning function Power ON Power OFF Example of type plate The type plate is placed on the back side of the scaler unit Medical electrical equipment classified by ETL with respect to electric shock fire mechanical and other specified hazards in accordance with the Safety Standards ANSI AAMI ES 60601 1 and CAN CSA C22 2 No 60601 1 08 Caution Consult accompanying documents C
22. nging fuses 1 Disconnect the power cord from the AC power outlet and the unit 2 Open the fuse holder on the rear side of the unit A WARNING Atip that is bent altered scratched or worn more than 2 mm will loose performan ce and must be exchan ged Prolonged use may cause tip breakage and inju ry to the patient The opera tor should be aware of that ultrasonic instruments with small diameters are subject to breakage at any time If not used correctly or with too much power or force the instrument WILL break 3 Inspect the fuses for damages Replace damaged fuses with new ones Verify the fuse specifications according to the Technical data section on page 28 4 Close the fuse holder 24 LM Eirene Troubleshooting 6 Troubleshooting UltraLED Type of problem Please see I Weak or no LED light Page 27 A Unit is not responding and no lights are lit on the control panel 1 Check that the power cord is connected properly and double check the voltage 120V 230V 2 Check the fuse and replace if necessary See Maintenance section of the user guide 3 Check that the wall outlet and the fuse panel of your clinic are OK 4 Ifthe problem still remains contact your dealer for support and indicate Error Code E X02 25 LM Eren Troubleshooting B Lights are flashing on the control panel Four blue lights on the control panel Check that the foot control cable 1s connec are flashing simultaneously
23. ode E S01 D Weak tip vibration 1 Check that the tip is firmly tightened Preferably use a torque wrench and tighten clockwise until the torque wrench slides The torque wrench prevents the tip from being over tightened 2 Check that the tip is not worn out Use a tip check card to evaluate wearing or try an unused tip Use original LM Instruments tips for reliable performance 3 Ifyou have an additional handpiece try replacing the handpiece 4 Ifthe problem still remains contact your dealer for support and indicate Error Code E S02 26 LM scene Troubleshooting E Insufficient or no water flow when foot switch is activated 1 Ifthe unit are equipped with a water bottle Check that the medicament water bottle is properly connected i e the cap is tightened and pushed in all the way onto the connector Check that the o rings on cap and connector are in good condition Replace o rings if worn O rings can be lubricated with a glycerine based lubricant or vaseline 2 Ifthe unit are connected with tap water Check that the tap water hose 1s properly connected to the back of the device and that the tap water system 1s OK tap valve is open and possible filter 1s OK 3 Check that dry mode is not activated 1 e that the blue light next to the crossed out water drop is not lit If it is lit press the ON key 4 Adjust the water control ring on the handpiece to fully open dots aligned Try with another tip nn
24. ompliance label indicating compliance with the Medical Device Directive 93 42 EEC 0537 is the ID number of the Notified Body VTT Withstands autoclave temperature 135 C 275 F Type B applied part according to the degree of protection against electrical shock Fuse Input Output Please do not throw the equipment into the domestic refuse Please use the re turn and collection systems available in your country for the disposal of this product The equipment can also be returned to the manufacturer for disposal 15 LM rene Installation 3 Installation 3 1 General installation instructions Checklist e Position the unit horizontally with the handpiece in the holder A and the hose hanging free Sauter e Position the unit where air is free to circulate on all sides and be i ie i Do not place the unit on or neath it Do not position the unit on a wall or next to a heat source ji next to a heat source Ex e Avoid placing the unit in the immediate vicinity of sources of cessive heat may damage electromagnetic radiation for example an electrosurgery equip HP Cae rence ment e Connect the foot control cable to the foot control and at the rear side of the unit _ a e Mount the scaler tubing in the groove underneath the unit as in picture A Caution Consult a qualified technici 3 2 Version for tap water optional an for connecting the scaler to the wat ly Connecting to the water supply MS
25. ry This chapter describes the components of the delivery and can be used as a check list when unpacking Con tact your place of purchase if anything is missing Fora description of the features of the equipment read the Equipment description sec tion on page 11 1 LM ProPower UltraLED unit Scaler handpiece connected to unit Scaler introkit see section 1 2 500 ml medicament bottle or water hose 6 mm 1 4 Foot control Foot control cable Power cord er a p o oe NO LM ProPower Fixer LMProPower UltraLED T ProPower Fixer Unpacking 1 2 Content of introkits Content of UltraLED Scaler introkit 3 x Scaler tips 3 x ErgoGrips 3 x Torque Wrenches 3 x Tip Check Cards LM feel the difference LM cac Equipment description 2 Equipment description 1 UltraLED Handpiece with an ErgoGrip and a tip mounted 2 Water flow control ring 3 Handpiece tubing 4 Control panel 5 Foot control 6 Medicament bottle 7 Depressurisation button 2 1 General description LM ProPower UltraLED is an effective piezoelectric scaler in a versatile and ergonomic appliance The device s LED lights advanced electronics quality and high durability LM DuraGradeMAX tips enhance the execution of procedures which require great precision Ergonomically designed ErgoGrip handpieces with soft silicone hand les give the user
26. s Le produit peut deranger la fonction du stimulateur Precautions generales e Le produit n est pas appropri pour Il usage en pr sence d un m lange anesth sique inflammable e Utilisez seulement le produit en combinaison avec des inserts de d tartreur de LM Instruments et Amdent e Si la tuyauterie de pi ce main est endommag e ou us e elle doit imm diatement tre substitu e pour viter d exposer Putilisateur ou le patient au risque lectrique Utilisez l original empaquetage en renvoyant le mat riel pour le service Avertissement Le produit ne doit pas tre utilis a proximit ou empil avec d autres quipements Si l usage adjacent ou empil est n cessaire le produit doit tre surveill pour une utilisation normale suivant la configuration dans laquelle il sera utilis Consigne de securite Notifications de surete en ce manuel A Warning indique une situation proba blement dangereuse La inobservance peut menerala mort ou des dommages WARNING Caution indique une situation probable ment nocive La inobservance peut endom mager le mat riel Caution Note d crit si on observe la notification sp ciale Note LM feel the difference LM cac Unpacking 1 Unpacking Carefully unpack your LM ProPower UltraLED unit and verify that all accessories and components are included according to the content lists below Note 1 1 General content of delive
27. t a squeaking sound is heard loud and dominat ing the pressure against the tooth might be too low or the tip not parallel to the surface of the tooth 20 LM feel the difference LM scene Operating instructions After treatment 1 Run the automatic cleaning function see instructions on page 22 Note 2 After the cleaning cycle is finished screw off the tip counter Always set the water flow to clockwise with the torque wrench fully open before running the cleaning cycle dots in line see picture 3 Squeeze the ErgoGrip gently at the top and at the same time slide it off the handpiece Do not squeeze too hard at the ErgoGrip as this can make the removal difficult AN Caution 4 Press the depressurization button bottle version Before cleaning and steriliz ing the handpiece water control ring must be set to fully open dots in line see picture 6 Clean and sterilize the equipment components according to the Cleaning and maintenance section on page 22 23 5 Pull the medicament bottle from the unit bottle version 21 LM cao Cleaning and maintenance 5 Cleaning and maintenance 5 1 General cleaning procedures Automatic cleaning function 1 Make sure the water control is fully open Place the scaler handpiece over the bowl and start the cleaning cycle by pressing the cleaning key C Note Always set the water flow to fully open before running the cleaning cycle dots
28. ufacturer PL 88 Norrbyn rantatie 8 FI 21601 Parainen FINLAND Model LM ProPower UltraLED l EN60601 1 Class 1 Type B n 93 42 EU Medical products class Ila LxWxH 270 x 140 x 165 mm without bottle Weight 2900 g 100 Vac 50 60 Hz Voltage 115 Vac 50 60 Hz 230 Vac 50 60 Hz T500 mAH 250 V 05x20 mm 100 Vac Primary fuse T400 mAH 250 V 05x20 mm 115 Vac T200 mAH 250 V 05x20 mm 230 Vac Power cord Separate with protective earth plug Power consumption Max 40 VA Scaler power consumption Max 24 VA Scaler power output Max 10 W 24 kHz 28 kHz automatic tuning Transport and storage 40 C to 70 C 40 F to 158 F Ambient temperature Operation 10 C to 40 C 50 F to 104 F Transport and storage 10 to 100 Relative humidity Operation 10 to 95 Water supply pressure 1 10 bar 0 1 1 0 MPa 14 5 145 PSI version conn to tap water Water consumption 10 50 ml min Bottle volume bottle version 500 ml Installation and service of the product is only to be performed by authorized service personnel by the manufacturer 28 LM scene A WARNING Immedately after using any kind of medicament in the medicament bottle run the automatic cleaning cycle with clean water in the med icament bottle for both the scaler and the polisher un til clean water comes out of the handpieces Technical data Medicaments that can be used e Clean water e Cetylpyridiniu
29. wer should assure that it is used in such an environment Immunity test IEC 60601 test level d ni Electromagnetic environment guidance Conducted RF IEC 61000 4 6 Radiated RF IEC 61000 4 3 3 Vrms 150 kHz to 80 MHz 3 V m 80 MHz to 2 5 GHz Portable and mobile RF communications equipment should be used no closer to any part of the LM ProPower including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance d 1 2VP d 1 2VP 80 MHz to 800 MHz d 23VP 800 MHz to 2 5 GHZ were P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and d is the recommended separation distance in metres m Field strengths from fixed RF transmitters as deter mined 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 NOTE 1 At 80 MHz and 800 MHz the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people Field strengths from fixed transmitters such as base stations fro radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast cannot be
Download Pdf Manuals
Related Search