Whitening Lase II - DMC Equipamentos
Contents
1. Ono ST ST Whitening Lase ttre retracts 055 ST J g 8 E User Manual Whitening Lase Il is device manufactured with the highest technology and all the devices are tested individually The device has the registration at the National He n the European market xillofacial area The surgeon must be qualified to the application of the equip related techniques The inadequate usage may cause irreversible damages alth Surveillance Agency Ag ncia Nacional de Vigilancia Sanitaria assuring this way the fulfillment of the national regulations This device also fulfills the require ments established by the European Community being able to be commercialized Whitening Lase Il was developed to be used by professionals of the oral and ma ment s The manufacturer recommends all manual reading before using the product DEVICE FUNCTIONS The Whitening Lase II device presents the following functions Emits red 660 nm and infrared 808 nm laser light with maximum power of 100mW for laser therapy Emits infrar2. 18 WHITENING LASE II User Manual Avoid device falling Keep the device a safe place avoiding hits and vibrations PROBLEMS AND POSSIBLE SOLUTIONS Error code Type of error Possible solutions Check for obstruction the microfan pon Locked Microfan Restart the device Contact the Manufacturer Clear air exits of the device Check the dental white High internal ning handpiece microfan functioning and of the com Error02 temperature erro mand box Contact the Manufacturer Error03 Current in the emitter error current above the specified Error04 Current in the emitter drivers error Error05 Current in the emitter error current below the specified Restart the device Error06 or Contact the Manufacturer reading of the emitters Error in the reading of the temperature sensors 08 emory reading failure Error09 emory writing failure Check if the A C Cable well connected Check with the A C cable disconnected from the power ER A The device do not turn of supply if the fuse is burnt according to the item FUSE VERIFICATION AND CHANGE PROCEDURE Check if the plug is working correctly DISCARDING After the product and its accessories life has expired it can cause environmental harm or can be used incorrectly In order to minimize these risks the client must discar
3. to be used in the procedure Use the navigation keys 2 5 and confirm with the 55 With the keys or will be possible to increase or decrease the power from 30 mW to 100mW in steps of 10 mW By using the key lt confirm the option chosen Having the power defined the next screen will be the choice between CONTINUOUS or PULSED emission The navigation between the options must be performed by the keys or 2 and the confirmation by the key Pulse Adjustment After choosing the pulsed mode in the previous item it will be allowed to adjust the number of pulses per second to be used With the keys r it is possible to vary between 10 pps and 100 pps pulses per second To confirm you must press the key Dosage Adjustment Then adjusting the dosage will be allowed and it may vary from 10 J cm minimum dosage to 1000 maximum dosage The adjustment must be performed by the keys and the confirmation key is Application In order to activate the laser you just need to press the button of the laser therapy handpiece Opting for the Assisted Mode With the keys r it will be possible to navigate between the preset therapies As you have chosen the therapy press the key Gs to confirm Later the display will show the minimum and the maximum dosage for the therapy Inside this range the professional may vary the value of the dosage by using the keys or 5 confirming wit
4. RF communication transmitters and the Whitening Lase II as recommen ded below according to the maximum output power of the communication devices Portable and mobile RF communication devices should not be used nearby any part of the Whitening Lase Il including cables with separation shorter than the recom mended calculates from the equation applicable to the ransmitter frequency Separation distance recommended D 10 10m D 10 10m 80 MHz up to 800 MHz D 20 20 Conducted RF 3 Vrms 800 MHz up to 2 5 GHz IEC 61000 4 6 150 kHz up to 80 MHz 3V Where P is the maximum output nominal power of the ransmitter in watts W according to the manufacturer of the transmitter and D Is the recommended separation distance in meters m Radiated RF 3 3 Vim IEC 61000 4 3 80 MHz up to 2 5 GHz t is recommended that the intensity of the field establi shed by the RF transmitter as determined by an elec romagnetic inspection at the local is smaller than the accordance level in each frequency range nterference may happen around the device marked with he following symbol Nominal maximum power of Separation distance according to the transmitter frequency m the transmitter W 150 kHz to 80 MHz 80 800MHz 800 MHz to 2 5 GHz 0 01 0 12 0 12 0 23 0 1 0 37 0 37 0 74 1 1 2 1 2 2 3 10 3 7 3 7 7 4 100 12 12 23 For transmitters with
5. for a mode where a series of exposures is available with certain duration and a certain v 4 Do not overturn frequency counting that the activation button is pressed Alternate Current Serial Number MO C Maximum Pilling 24 25 26 WHITENING LASE II User Manual WARRANTY A The devices manufactured and or commercialized by DMC have a 24 twenty four months war ranty from the date of the purchase against any manufacturing defect B The warranty covers only manufacturing defects or of material used in the manufacturing of the products The warranty DO NOT covers shipping expenses C The warranty is automatically cancelled in case of any electrical or physical abuse happen if the parts were altered or if applications different from those the device is developed for happened D In case of repaired devices out of the warranty period it will only be extended to the replaced parts E The causes of the defects more common come from physical shock applied to the device in these cases the warranty is cancelled F The DMC does not take any responsibility for personal or material damages from the misusage of the devices they manufacture and or commercialize it is the user s responsibility to provide safety procedures in order to avoid such problems G The DMC responsibility concerning to the use of the device and its consequences limits to the replacement of the amount
6. of the device The device will only be under the manufacturer warranty regulations if The assembling extensions adjusts modification or repair operations were performed by people authorized by them the electrical installation of the environment in focus is in accordance with the appropriate requirement device is used according to the instructions MDI Europa GMBH ALLL LOLOL T COCOTTE EC REP impigre sma n 30855 Langenhagen ALITTLE be ALITTI TN ALITTLE ON Ono TOLTOTTE TT TTL LITT Sto Carlos SP Zip Code 13562 030 CNPJ 02 827 605 0001 86 B B a B a Laser appliance for odontologic o o B A a m A a Phone 16 2107 2323 Fax 16 2107 2320 21 131 Rev 11 Review Date 05 02 2015
7. screen Restart time restarts the time of the previous application screen and Main Menu return to the Adjust Menu Operation Screen The choice of the option must be performed by the buttons or and the confirmation by the 55 If the user wants to interrupt the laser emission and LEDs at any moment of the application only press the button in the handpiece The device has a display with user friendly menu Warning messages be shown at it As the infrared laser emitter is not visible the device has a target light beam Attention Control usage or adjusts or execution of other procedures not specified here may result in harmful radiation FINALIZATION PROCEDURE In order to turn off the device the user must use the On Off switch located at the back panel SUPPLY ISOLATION In case of emergency or for maintenance purposes the supply plug A C Cable must be disconnected from the electrical power supply by removing it from the plug FUSE VERIFICATION AND CHANGE PROCEDURE Disconnect the A C cable from the electrical power supply and from the device By using a screwdriver undock both edges of the fuse holder lid see picture beside until it is possible to remove it with the hands Remove each one of the fuses and check if they are burnt observe if the fuse is dark of with the thread broken if necessary replace the fuse using a spare fuse provided or another from the same v
8. 1 IEC 60601 1 2 IEC 60601 1 4 and IEC 60685 1 Software version 8 10 WHITENING LASE II User Manual SAFETY IMPORTANT CAUTION If any component present damage it must be used Considering that the product is used by a qualified surgeon specific additional training is not necessary for the operation of the equipment apart from the reading and understanding of the instructions manual The use of part accessory or material not specified it is the user s entire responsibility The laser light is harmful to the eyes so the goggles must be used in order to protect them for everybody in the place where the session is happening The DMC provides three goggles along with the Whitening Lase II Only the goggles provided by the DMC may be used along with the device The model of the before mentioned goggle can be seen below Goggles Green lenses Never look directly to the laser light and more importantly do not direct the light to anybody unless he she is under treatment Reflexive surfaces may reflect the laser beam the eyes direction Never radiate tumor processes directly the laser can stimulate them Never radiate the infectious processes directly the laser can stimulate them Never radiate an undiagnosed injury not make extra oral applications in patients that take photosensitizing drugs any high intensity light can interact with the drug
9. alue and features see the item SPECIFICATIONS e Push the fuse holder with the hands until it locks PREVENTIVE MAINTENANCE The device must be calibrated at least every two years by the manufacturer If this maintenance is not performed the manufacturer does not take any responsibility for its safety gt the assistance services such as changes repairs calibration etc can only be performed by the manufacturer The circuit schemas components lists descriptions instructions for calibration and measurement are not available for people who are not qualified by the manufacturer If the maintenance or any other kind of assistance service if performed by unauthorized personnel the manufacturer do not take any responsibility for the safety of the device functioning n order to assure the safe usage of the product the user must inspect the integrity of the A C cable console and the handpieces in a daily basis that is check if this parts are not broken torn dirty etc Never open the command box At any problem contact the technical assistance of the DMC Equipment STORAGE AND TRANSPORTATION Store the device away from dust solar direct exposure near chemical products and cleaning agents device must be stored transported and used in the following environmental conditions e Temperature from 10 C 40 C Humidity from 30 to 75 e Atmospheric Pressure 700hPa to 1060hPa
10. an output nominal maximum power not listed above the separation distance recommended in meters can be determined by the equation applicable for the transmitter frequency Note 1 In 80 MHz up to 800 MHz the separation distance is applied for the highest frequency range Note 2 These guidelines cannot be applied in all situations The electromagnetic propagations are affected by the structure absorption and reflection objects and people NOTE 1 In 80 MHz 800 MHz applies to the higher frequency range NOTE 2 These guidelines cannot be applied in all the situations The electromagnetic propagation is affected by the structure absorption and reflection objects and people intensities of the field established by the fixed transmitters such as radio stations base telephone cell Phone wireless and mobile terrestrial radios amateur radio radio transmission AM and FM and TV transmitters do cannot be accurately foreseen theoretically In order to evaluate the electromagnetic environment due to the fixed RF transmitters it is recommended an electromagnetic inspection at the local If the measurement of the field intensity at the local in which Whitening Lase II is used exceeds the accordance level used above the Whitening Lase II should be observed to check if the operation is normal If an abnormal development if observed additional procedures may be necessary such as a reorienting or rearranging of the Whiteni
11. and provide spots at the radiation place Do not radiate the beam over the belly of women under three months of pregnancy The usage of flammable or oxidizable anesthetic gases such as the nitrous oxide 0 oxygen must be avoided Some materials for example cotton when saturated with oxygen may inflame by the high temperatures produced The adhesive solvents and flammable solutions used for cleaning and disinfection must evaporate before the device is used Only trained people can operate the device The inadequate usage can cause irreversible damages Only the components mentioned this manual used together with the device In case of ceasing the emission of the laser quickly the red button STOP front panel must be used It is not allowed the usage of the device by unauthorized and not qualified people aiming at avoiding the incorrect or inappropriate usage When not used Whitening Lase II must be turned off because when restarting it the access will only be permitted with the provided password The res ponsible professional must store this password in a way that not qualified and unauthorized people do not have access to it The device must not be used with wires and accessories that not provided by DMC because it can result in increase of the emissions or decrease of the immunity of the Device The Device must not be used too close of pilled over other devi
12. be assembled in the potential equalizer according to the picture beside HE LASER WARNINGS Side Panel Warnings The label below indicates the laser radiation exposure 10 9 to 60825 1 2007 10 Front panel warnings The label below illustrates the laser radiation warning a re LASER THERAPY HANDPIECE Lasers Activation Spacer Button This handpiece has two lasers one red and one infrared and must always used when the laser therapy applications are performed When this one is not being used it is important to keep it in its holder in order to not damage the optic fiber tip Spacer The spacer must be in contact with the target tissue in the moment of the application according to what can be seen below Target Tissue Laser Therapy Pen 11 WHITENING LASE II User Manual The spacer must be disinfected before using with alcohol 70 However after use it must be disposed In order to acquire extra spacers contact DMC Equipment DENTAL WHITENING HANDPIECE Handpiece LEDs and lasers Activation Button Handpiece fan This handpiece has three infrared lasers and six blue LEDs and it must be used in the dental white ning When it is not being used it is important to keep it in its holder in order to not get damaged How to apply the handpiece can be seen below PATIENT OPERATOR POSITION The equipment sha
13. ces If it is necessary we recommend that the Device is observed in order to check the Normal operation in the setup in which it is going to be used It does not exist an age limit concerning to the usage of the laser therapy handpiece However for the dental whitening the patient must be at least 18 years old In case of laser therapy the laser be applied under any tissue conditions However for dental whitening the patient must Be with a healthy gum with no inflammation and with no tartar Treat the teeth sensibility if have Check if he she has caries or permeation in the restorations The device is not designated to be used in an environment of oxygen In order to avoid the risk of electrical shock this device must be connected to only one power supply with grounding for protection The user must not connect the Cable A C plug in places that are difficult to access because it can make the device disconnection difficult None modification in this device is allowed The user must not connect the Cable A C plug in places that are difficult to access because it can make the device disconnection difficult WHITENING LASE II User Manual The manufacturer does not take any responsibility if the user uses a fuse and an A C cable different from the ones specified in this manual The user must be exposed to the noise the device does during the maximum period of 8 ho
14. d by a uninterruptable power lt 5 Ut supply or a battery gt 95 of voltage drops in Ut per 5 seconds Magnetic field in the su Magnetic fields in the supply frequency pply frequenc must be in specific levels of a typical pla i Am According ce in a hospital 17 typical IEC 61000 4 8 commerce NO E Ut is the supply voltage c a before the application of the trial level Table 2 Accordance Information to the electromagnet ic immunity requirements based on the table 202 60601 1 2 2007 21 22 WHITENING LASE II User Manual Guidelines and manufacturer statement Electromagnetic Immunity Device that is not from LIFE SUPPORT IEC 60601 1 2 2007 subcl 6 8 The Whitening Lase II is designated for the usage in electromagnetic environment specified below The client or user of the Whitening Lase II must assure that he she is using it in such environment Distance and minimum separation recommended between the RF portable and mobile communication devices and the Whitening Lase II Level of the Level of IEC 60601 accordance Electromagnetic Environment Guideline The Whitening Lase II is designated for using at the electromagnetic environment in which radiated RF disturbances are controlled The client or user of Whitening Lase II may help to prevent the electromagnetic interference keeping the mini mum distance between the portable or mobile
15. d the device according to what the local legislation determines BIOCOMPATIBILITY The part applied that touches the patient is in accordance with the requirements of the ISO 10993 1 LASER SUPPLY SYSTEM The laser therapy handpiece is composed by two diode lasers The light is conduced to the edge of the handpiece by optical fiber not replaceable The optical power emitted is controlled through electrical current that passes by the diodes The dental whitening handpiece is composed by three infrared diode lasers and six blue LEDs For the lasers the light is conduced to the edge of the handpiece by optical fiber not replaceable The blue light is transmitted directly through the LEDs The optical power emitted is controlled through the electrical current that passes through the diodes and through the LEDs Dental Whitening Optical Handpiece Fiber Dental Whitening Handpiece Optical Fiber Diode Laser gt Laser Output Current Current Monitor Monitor 1 8 1 Control Laser Output Diode Laser LEDs Output LEDs Signal Conditioner 4 Signal Conditioner Control Power Supply CALCULATION OF BEAM DIVERGENCE Standard IEC 60825 1 2007 The beam divergence is 0 45 rad 0 03 rad 19 20 WHITENING LASE II User Manual ELECTROMAGNETIC SAFETY STANDARD OF THE DEVICE Below the
16. ed laser light with power of 100mW and blue light for dental whitening DEVICE FUNCTIONING 4H Ho Ho w 5 gt he device has two handpieces one for laser therapy and another for dental whitening he laser therapy handpiece has a red laser and an infrared laser The red light red laser interacts nti inflammatory and healing properties th the soft tissues and the invisible light infrared laser with hard tissues These have analgesic he whitening handpiece has infrared lasers and blue LEDs The infrared lasers are used in the dental hitening in order to diminish the sensibility after the whitening and in order to activate the white ng gel by heating The blue LEDs have the function of activating the whitening gel thorough the eraction of the light dye NDICATIONS The equipment use indications be found below and in the equipment s assisted mode For any di fferent use the manufacturer must be prior contacted LASER THERAPY Soft Tissue Recovery Ulcer and Traumatic Ulcer Oral Manifestation of Systemic Diseases Lichen Planus Cheilitis Angular Gingivitis Postoperative ATM Dysfunction Bone Tissue Recovery Orthodontia Implantodonty Periodontitis WHITENING LASE II User Manual Extraction Traumatic Injury Biostimulation of bones Dental Tissue Recovery Dentine Hypersensibility Nerve Recovery Neuralgias Paresthesias Paralysis Pain Syndrome Other App
17. h the Application In order to activate the laser you just need to press the button of the laser therapy handpiece DENTAL WHITENING In this mode it is possible to select the application time which may vary from 30 seconds to 3 minu tes In order to change the values the keys or 5 must be used If the button is pressed in the dental whitening working screen will be available for the user the following options Go back to the previous work screen Enable or disable the laser in the dental whitening function Restart the application time Quit the dental whitening mode back to the main menu Application In order to activate the dental whitening handpiece just press its button WHITENING LASE II User Manual Operation Screen Dental Whitening Mode Enabled Disabled Laser a Dental Whitening Ea Dental Whitening screen Laser Enabled Selected laser Red Laser 660 nm 100 0 30 Selected power Applied energy counter Operation mode of the laser continuous or pulsed Laser on indicator Selected application time Laser therapy screen Important observations During the product usage the device will illustrate the time in a regressive way on the display If the user wants to go back to the main menu being on operation screen he she must press the button At this moment the following messages will be available Back returns to the previous
18. lications Alveolitis Edema Xerostomia Pericoronitis Anesthesia Geographic Tongue Simple Herpes Zoster Herpes Post endodontic DENTAL WHITENING PDT PHOTODYNAMIC THERAPY SPECIFICATIONS Infrared Laser Characteristics Wavelength 808 nm 10 Emitter useful power 100 mW 20 Pulse Duration Pulsed Mode 05 ms 50 ms Red Laser Target Laser Characteristics Wavelength 660 nm 10 Emitter useful power 0 5 mW 2 5 mW Red Laser Characteristics Wavelength 660 10 Emitter useful power 100 mW 20 Pulse Duration Pulsed Mode 05 ms 50 ms Blue Led Characteristics Wavelength 450 10 Emitter useful power 400 mW 20 The specified parameters not subject to m General Characteristics odifications due to time penetration Characteristics Specifications Voltage 90 240 V Power Input 50 VA Operation Mode Continuous Frequency Power 50 60 Hz Level of protection to the water and solid objects 220 Operation Mode of the lasers Continuous and pulsed operation Applied Part Laser therapy handpiece Nominal Current 2 Fuse l Voltage 250 V Breaking Capacity 35 A or L Size 17 cm depth x 13 cm width x 15 cm height Weight 1 28 Kg Fiber Diameter 600 u m Type of Current Alternating Current Manufactured and tested according to IEC 60601
19. ll be used in dental clinics It should be placed on a worktop and connected to a power supply network The hand pieces shall be positioned according to items Dental Whitening Handpiece and Lasertherapy Handpiece You can find images of the positions for the patient and the operator of the Whitening Lase II equipment below Dental Whitening Function Lasertherapy function Distance from the device for the operator patient Distance from the device for the operator patient 2cm from the target tissue DISINFECTION Command box device must be disconnected from the power supply before cleaning in order to avoid the user exposition to electrical shock command box must not be washed it will imply in warranty loss cleaning consists of using a soft cloth moistened with alcohol 70 Do not allow liquids to drain into the command box because it will damage it The device be cleaned disinfected multiple times with no damage Other items All the other Items used with the device must be cleaned with alcohol 70 INSTALL Connect the A C cable in the back part of the device Then insert the A C cable in the power supply The potential equalizer must be connected to the potential equalization bus of the power supply WHITENING LASE II User Manual BEFORE USAGE INSPECTION Check if all the items mentioned in the INSTALL are connected HOW TO USE A
20. ng Lase II Over the frequency range of 150 kHz up to 80 the field intensity should be lower than 3 V m Table 3 Accordance information to the electromagnetic immunity requirements for devices which aims at LIFE SUPPORT based on the Table 204 60601 1 2 2007 Table 4 separation distance between the device and the RF emission sources recommendations based on the Table 206 60601 1 2 2007 23 WHITENING LASE II User Manual SYMBOLS USED Laser Radiation Turn off the laser because of an emergency Terminal of power equalization ska 22 Temperature limits 10 C Applied part type B Humidity Limitation 30 Check the user s manual gt a Authorized Representative in the European Community Cauti aution 5 Fragile handle with care Protected against solid strange objects of 12 5 mm of diameter and not protected against water drain On with voltage Indicates the position for transport Off without Voltage ZN Keep away from sunlight Date of Manufacture Cnr Manufacturer Protect from heat and radioactive sources oO Continuous operation The laser device is selected for a mode where 44 the exposure is limited by the chosen dosage counting that Keep dry the activation button is pressed Repetitive Exposure The laser device is selected
21. re are tables that represent the adjustment to the regulation of electromagnetic immunity and emission Guidelines and Manufacturer Statement Electromagnetic Emission For all the Device and System IEC 60601 1 2 2007 subcl 6 8 3 201 a 3 Guidelines and Manufacturer Statement Electromagnetic Immunity For All Whitening Lase II 60601 1 2 2007 subcl 6 8 3 201 6 The Whitening Lase Il is designated for the usage in electrom The client or user of the Whitening Lase II must assure that h agnetic environment specified below e she is using it in such environment The Whitening Lase II is designated for the usage in electromagnetic environment specified below The client or user of the Whitening Lase must assure that he she is using it in such environment Level of the ABNT NBR Level of Accor Electromagnetic environment ABNT NBR CISPR 11 Harmonic Emissions 61000 3 2 Not applicable tha Emissions due to voltage loating scintillation EC 61000 3 3 Not applicable me Whi places that are not designated to domestic use or Immunity Trial Accordance Electromagnetic Environment Guideline Whitening Lase uses RF energy only for its internal RF Emissions Group 1 functions Thus its RF emissions are very low which is ABNT NBR IEC CISPR 11 According not likely that cause any interference in the electronic devices nearby RF Emissions Class A
22. s you activate the on off switch located in the back panel screens will be presented with some information like Device s name version serial number usage time and language selection option In order to select the language press and then or to alternate between the options available use the key to confirm The usage of the equipment is restrict to the user through a password By using the keys or insert the password provided in the warranty agreement to allow the device to complete its initiali zation Use the key to validate the choice of each number of the password got to the next digit and conclude after the insertion of the forth digit After the password confirmation the device accesses the Main Menu with the options Setup Menu and Operation Screen SETUP MENU In this screen it is possible to select the laser therapy and dental whitening modes In the laser the rapy it contains the options of the normal assisted and PDT mode In order to navigate between the options the keys or must be used and the key to confirm LASER THERAPY PDT In this therapy the device is set to act with the red laser in the power of 100 mW during1 minute and 30 seconds Application In order to activate the laser you just need to press the button of the laser therapy handpiece Normal Mode In this item it is possible to select the wave length of the red laser 660 nm or infrared 808 nm
23. tening handpiece handpiece Dental whitening handpiece output Laser therapy handpiece output WHITENING LASE II User Manual Key Increase the values and navigate through the available options Key CE Decrease the values and navigate through the options available Key Confirm select parameters and functions Key 29 Responsible for the immediate interruption of the laser when necessary BACK PANEL PARAMETERS 1 Microfan Air exit place must not be obstructed 1 2 Cable A C connector Place where cable A C O must be connected 3 Fuseholder Place where the device fuses are inserted 4 On Off Switch Turns on and off the command box 2 34 5 Potential equalizer This connector establishes an equipotential connection It is recommended that the grounding connection is done by qualified personnel 5 Equalizer Function potential equalizer function is to equalize the power between the different me tallic parts that can be touched simultaneously or reduce the power difference that may occur during the operation between the electromedical equipment housing and the conductive parts of other objects Kind of connector and cable Use the cable with the connector related to the code POAG K4FS KBT6DIN 100 Manufacturer Multi Contact How to Connect The connector before mentioned must
24. tening Lase is convenient for using all the are not directly connected to a public power su pply of low voltage that powers buildings used for domestic matter Table 1 Accordance information to the electromagn in the table 201 60601 1 2 2007 etic emission requirements based Immunity mial 60601 trial dance Guideline Floors must be made of wood concrete or Electrostatics discharge 6 kV per contact According ceramic If the floors are covered with syn ESD IEC 61000 4 2 8 kV through the air hetic material the relative humidity must be at least 30 Fast electric transitory 2 kV in the power lines Quality of the energy must be the one pulse train Burst IEC 1 kV in the input output According rom a hospital environment or typical 610004 4 lines commerce ote IEC 61000 4 5 1 kV line s to line commerce lt 5 U gt 95 of voltage drop in Ut per 0 5 cycles Quality of the energy must be the one Voltage drops short in 40 Ut from a hospital environment or typical 60 of voltage drops in Ut commerce If the user of the Whitening terruptjons Lase II demands continuous operation variations in the input per gt According aE sige supply line 70 Ut during energy interruption It is re 30 Of voltage drops in Ut commended that the Whitening Lase 11 IEC 61000 4 11 i per 25 cycles is supplie
25. urs day The air inputs and outputs must not be obstructed Do not apply any protective film in the handpieces SECUTIRY ITEMS OF THE DEVICE The device has some security items which include Sound signal emission while the laser is active Red emergency button front panel designated to interrupt immediately the laser output Security password which will allow the use of the device only by the responsible person e Indication in the display that the laser on by the symbol Target Beam Whitening Lase Il uses a target beam of low intensity This visible laser is designated to indicate the application point COMPONENTS LIST Whitening Lase 11 is constituted by the following parts PARTS AIC Cable Spacer Command Box 02 Fuses ACCESSORIES lt Electronic Media 03 Protection goggles Transportation Briefcase USER WARRANTY MANUAL AGREEMENT User Manua Warranty Agreement If the acquisition of any accessory is necessary it must be bought at DMC Equipment through the following codes AIC Cable 010130037 Goggles 050020001 Spacer 110030078 All the accessories and parts described above for exclusive use in the Whitening Lase II device FRONT PANEL PARAMETERS _ Location of laser openings Laser therapy Dental whi
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