DKL CHAIRS D2-AVEO Operating Instructions Manual Download Page 1

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Operating Instructions

Manufacturer:
DKL CHAIRS GmbH
An der Ziegelei 3
D-37124 Rosdorf
+49 (0)551-50060
[email protected]
www.dkl.de

D2-AVEO

Form no.GEN-D2AVEO
Rev. 06 / 21.01.2022
Subject to change without
notice.

Summary of Contents for D2-AVEO

Page 1: ...perating Instructions Manufacturer DKL CHAIRS GmbH An der Ziegelei 3 D 37124 Rosdorf 49 0 551 50060 info dkl de www dkl de D2 AVEO Form no GEN D2AVEO Rev 06 21 01 2022 Subject to change without notice...

Page 2: ...cons Display 16 Icons Navigation Touch Display 17 Icons Setup 18 Moving the Treatment Chair 19 Putting the Treatment Unit into Operation 21 Creating a User 22 Managing Users 23 Main Menu Instruments 2...

Page 3: ...s on the unit Observe the operating instructions ON OFF Do not dispose of with household waste CE marking with iden ti cation number of the noti ed body Type B application part Manufacturing date Mode...

Page 4: ...uctor connection Protective earth Functional earth Symbols on the packaging Transport upright top Permissible temperature range Air humidity limitation Protect from moisture Do not stack Fragile N Con...

Page 5: ...ice complies with the provisions of Directive 93 42 EEC 0123 Responsibility of the manufacturer The manufacturer can only be held responsible for the impact on the safety reliability and performance o...

Page 6: ...uipment Do not use portable and mobile HF communication equipment such as mobile telephones during operation These can a ect medical electrical devices Risks due to electromagnetic elds The functional...

Page 7: ...ment unit before leaving the practice Hygiene and care before using the device Clean and disinfect the device immediately before or after each treatment Wear protective clothing The treatment unit is...

Page 8: ...hat are ISO 3964 DIN 13940 compatible and approved by the manufacturer For air powered instruments only use coupling systems according to ISO 9168 For air powered instruments only use coupling systems...

Page 9: ...nt unit are designed for intermittent operation in accordance with the dental treatment method Driving motors for patient chair and backrest duty cycle max 25 s ON 400 s OFF Permanently connected devi...

Page 10: ...water supply of the treatment unit install an angle valve with 2 outlets and 2 stop cocks The second outlet allows easy sampling of water for microbiological analysis Connection to the public drinkin...

Page 11: ...50 m Replace annually 210623 WBG Particle lter compressed air inlet 50 m Replace annually 210623 LBG Solid particle lter for the suction system Mesh size 1 mm In case of damage replace at least annua...

Page 12: ...12 Dimensions in Millimetres Treatment chair lowest position 370 mm highest position 880 mm...

Page 13: ...Treatment chair double jointed head rest 4 Treatment chair joystick 5 Foot controller doctor s device 6 Doctor s device 7 Assistant s device 8 Tray 9 Cuspidor 10 Operating lamp LED light 1 6 2 3 4 5...

Page 14: ...tor T Turbine connection M Micromotor S Syringe P Piezo Scaler Connecting the instrument hoses The instrument hoses can be connected or disconnected via a plug connection under the doctor s device Dep...

Page 15: ...Foot Controller The wireless S NW foot controller enables hands free operation of the instruments Only use high quality disposable AA Mignon LR6 1 5 V batteries You will nd further information on use...

Page 16: ...chair activate programme run Display lock Bell Cup ller Bowl rinser Touch Screen You can nd application lms at www youtube DKL Germany Playlist DKL CHAIRS L2 D2 SERIES DOCTOR S DEVICE WITH TOUCH SCRE...

Page 17: ...replace battery Foot controller wireless Information with selection option Error message further work is possible Error message no further work is possible Icons Navigation Touchscreen Add user Back...

Page 18: ...18 Icons Setup Touchscreen lock Manage users System Setup foot controller Setup touchscreen lock Sound ON Sound OFF except warning sounds Device information Language Setup service...

Page 19: ...amme position manually and then keep the respective programme key pressed for about 3 seconds until you hear a signal tone Now you have successfully saved your individual treatment position Saving pro...

Page 20: ...d rest Press the lever down to x the position of the double jointed head rest The release lever must always be pulled up completely to move the head rest When moving the back rest there is a risk of i...

Page 21: ...se The power switch connects the treatment unit with the power supply In the event of longer downtimes the treatment unit should be disconnected from the power supply The treatment unit contains a dev...

Page 22: ...er Activating a User The active user is displayed under My Favourites Con rm the user Six user pro les can be created Changing the User Activate My Favourites The active user is displayed under My Fav...

Page 23: ...vourites 6 Wireless foot controller VARIABLE or ON OFF 2 Documentation DOCU only with Implantmed 7 Display work mode 3 Setup 8 Display programme mode 4 Right left hand rotation 9 Speed rpm torque Ncm...

Page 24: ...ched o the coolant Adjusting the Coolant Spray on water Spray o Air only adjustment not possible with the piezo scaler Selection via push button 2 on the foot controller Changing the Coolant Settings...

Page 25: ...Activate the work display mode 7 on the touch screen Display speed intensity of the instrument while activated in bar structure Display speed intensity of the instrument while activated in Display of...

Page 26: ...the Roto Quick coupling and turbine see also operating instructions of W H Dentalwerk B rmoos GmbH Primea Advanced Air Setting the speed Activate the speed on the touchscreen 9 Decrease increase setti...

Page 27: ...e P1 Continue this process for the desired number of programmes P1 to P6 back Setting the transmission con guring the programme Transmission ratio Activate deactivate transmission Setting the speed Ac...

Page 28: ...Incorrectly selected speeds and torque values endanger the patient Treatment errors e g the breaking of a le can occur as a result of incorrect settings Observe the manufacturer s speci cations for th...

Page 29: ...ue this process for the desired number of programmes P1 to P6 back Setting the power Activate power on the touchscreen 9 Decrease increase Activate the start signal at the foot controller 1 Put the sc...

Page 30: ...the 2 seals on the inner body and the metal tube of the nozzle with Vaseline grease Cleaning the syringe Clean the sleeve and nozzle under running water or using alcohol based solutions Sterilisation...

Page 31: ...maximum hygiene To blow water into the operating eld just press the left button on the handpiece symbol water To insu ate air into the operating eld just press the right button on the handpiece symbo...

Page 32: ...ding speed and torque when positioning superstructure screws Please note that as described above positioning these screws mechanically presents a potential risk which needs to be assessed Always ensur...

Page 33: ...g function Programme 5 P5 Implant placement Icons Implantmed Odontogram UNS Universal Numbering System American odontogram FDI F deration Dentaire Internationale International odontogram Torque curve...

Page 34: ...y in place Do not attach or remove during operation Hook in the holder for the motor and fasten it Insert the irrigation tube and close the pump cover We recommend that you remove the pump cover befor...

Page 35: ...e accuracy of the set torque with the W H WI 75 and WS 75 contra angle handpieces is 10 at a torque of 20 50 Ncm Larger deviations are possible with di erent contra angle handpieces Documentation DOCU...

Page 36: ...l surgery P1 P2 P3 Transmission 1 1 1 1 1 2 7 Speed rpm 35 000 10 000 108 000 Setting range rpm 200 40 000 200 40 000 540 108 000 Motor rotation direction right right right Pump on on on Torque Ncm 10...

Page 37: ...rt of the motor Further documentation Add new position Start new documentation Exit documentation After the motor has stopped a diagram appears which is automatically saved on the USB stick Processing...

Page 38: ...ating lamp dims to 8 000 LUX When the switch is pressed again the light intensity set last is selected In addition the operating lamp can be dimmed via the foot controller By keeping the button 4 on t...

Page 39: ...isation of the handles To remove the handles turn the handle lock on the handles and pull o the handles To mount the handles reattach them and push them to the limit Then lock the handle lock The hand...

Page 40: ...the intended use please observe the operating instructions issued by FARO USER MANUAL EVA Switching on o on the joystick Push right or left Increase the light intensity on the joystick Push left and...

Page 41: ...droxide Hydrogen peroxide Ammonium Chloride Methylene chloride Methyl alcohol Acids and corrosive substances of all kinds It is forbidden to directly spray any chemical substance on the device LED lig...

Page 42: ...position with a slight upward tendency Turn the adjusting screw in the direction high weight Turn the adjusting screw in the direction low weight Secure the 3 grub screws 2 with safety lacquer blue Wi...

Page 43: ...s con rmed with another signal tone Maximum lling time 10 seconds Activate the bowl rinser at the display of the doctor s device or at the cuspidor Activate the cup ller at the display of the doctor s...

Page 44: ...irstream from the patient to the suction system and not the other way round is maintained Control knob Slider Remove the suction tube from the suction tube retainer By opening the slider or turning th...

Page 45: ...et suction CAS 1 operating instructions issued by D RR Dental dry suction CS 1 operating instructions issued by D RR Dental dry suction For the intended use please observe the operating instructions i...

Page 46: ...46 Cleaning and Disinfection of the Suction Handpieces...

Page 47: ...Cleaning and Disinfection of the Suction Handpieces 47...

Page 48: ...pped with all the components and the cuspidor can be cleaned and disinfected The OroCup is suitable for standard suction tubes with di erent diameters In the lid of the OroCup there is one xed insert...

Page 49: ...use Up to 2 litres of ready to use solution can be prepared in the OroCup Position the OroCup for aspirating the ready to use solutionas follows When aspirating the liquid place the OroCup in a vertic...

Page 50: ...ing stainless steel surfaces dry with a lint free cloth to remove water stains or residual cleaning agent Disinfection of Stainless Steel Surfaces Do you put emphasis on a germ free surface Here too s...

Page 51: ...s particularly important with light colours any visible soiling must be removed immediately Use the provided sponge to apply DentaClean in circular motions to the surfaces to be cleaned Then remove mo...

Page 52: ...ttle for spray foam cleaner DentaClean 200ml Article number DC200 Spray foam cleaner incl 2 x cleaning sponges DentaProtect wipe dispenser box Article number DP100 100 wipes in a disposable sealing ba...

Page 53: ...ompressed air Disinfection of the instrument panel with disinfectants wipe disinfection is recommended Observe the disinfectant manufacturer s instructions for use Put the instrument holders back into...

Page 54: ...thetreatment unit DK DOX 150 must be re lled Caution Continued operation without DK DOX 150 only possible after con rmationby brie y pressing the button If DK DOX 150 is not re lled the button of the...

Page 55: ...too slow Reset the WSU by keeping the button pressed for 8 seconds and restart it by pressing the button brie y If the magenta ashes continue call customer service WARNING Push button of the water sep...

Page 56: ...water separation unit make sure that the LED button on the cuspidor lights up green Put the hygiene cover into the cuspidor bowl Remove all the instruments from their holders and insert them into the...

Page 57: ...ights up blue do not work on the patient The push button lights up blue intensive ushing has started Double click on the button of the cuspidor to activate intensive ushing Intensive ushing is carried...

Page 58: ...aration unit Only re ll with DK DOX150 Open the cover of the storage container for the water separation unit at the base of the cuspidor DK DOX 150 bottle Content 250 ml Order number 590007 Open the c...

Page 59: ...ccording to the order of the instruments in the instrument holders The spray intensity can be adjusted with the control knobs The operating air for the turbine or the cooling air for the motor can be...

Page 60: ...ts operators or third parties Therefore it is important to detect such faults before a second fault occurs which may result in a hazard For this reason safety inspections should be carried out every 3...

Page 61: ...automatically to the coolant water With the option ImplantMed motor the pump is obligatory Otherwise the ImplantMed motor cannot be used Call customer service Temperature of the drive motor for the t...

Page 62: ...ug in USB stick with su cient memory Warning overheating Switch o the treatment unit Let the treatment unit cool down for at least 10 minutes Switch on the treatment unit If the error message appears...

Page 63: ...anty claims will only be accepted if all the instructions in this operating manual have been observed DKL as the manufacturer shall be liable for material and manufacturing faults within a warranty pe...

Page 64: ...ng criteria This is considered in the risk analysis of the system Criterion A The dental unit will withstand the test without damage or other interference During and after the test the device will ope...

Page 65: ...600 2 kV for mains 100 kHz repeat rate 2 kV for mains 100 kHz repeat rate The quality of the mains power supply should meet the requirements for a normal commercial or clinical environment Criterion B...

Page 66: ...ce calculated with the equation applicable to the transmission frequency Recommended protective distance d 1 2 P d 1 2 P for 80 MHz to 800MHz d 2 3 P for 800 MHz to 2 7 GHz Here P is the maximum nomin...

Page 67: ...h are based on the maximum output power and frequency of the communication device Interference Immunity Test IEC 60601 test level Compliance level Electromagnetic environment guidelines Fluctuations i...

Page 68: ...Instructions for use Electric motor EM 12 L Supply hose VE 10...

Page 69: ...ription 14 4 Operation 16 Screw on the medical device 16 Unscrew the medical device 17 Test run 19 5 Hygiene and maintenance 20 General notes 20 Limitations on processing 22 Initial treatment at the p...

Page 70: ...Maintenance and Testing 28 Packaging 29 Sterilization 30 Storage 32 6 Maintenance 33 7 Servicing 36 8 W H Accessories and spare parts 38 9 Technical data 39 10 Disposal 42 Explanation of warranty ter...

Page 71: ...TENTION to prevent damage occurring WARNING risk of injury Caution According to Federal law this medical device may only be sold by or on the order of a dentist physician or any other medical practiti...

Page 72: ...Body UL Component Recognition Mark indicates compliance with Canadian and U S requirements DataMatrix Code for product information including UDI Unique Device Identification Data structure in accorda...

Page 73: ...on the supply hose Symbols Catalogue number Type B applied part not suitable for intracardiac application Serial number 6...

Page 74: ...use please read the Instructions for use These explain how to use your medical device and guarantee a smooth and efficient operation Observe the safety notes Intended use The electrical drive EM 12L...

Page 75: ...ibility of the manufacturer The manufacturer can only accept responsibility for the safety reliability and performance of the medical device when it is used in compliance with the following directions...

Page 76: ...lid health and safety at work regulations the valid accident prevention regulations and in compliance with these Instructions for use The medical device should be prepared for use and maintained by st...

Page 77: ...upply failure the medical device must be stopped immediately Check the medical device for damage and loose parts each time before using Do not operate the medical device if it is damaged Use only filt...

Page 78: ...al device may cause a malfunction Risk of short circuit The medical device must not be oiled pre oiled for entire service life Do not twist kink or squeeze the supply hose risk of damage Replace fault...

Page 79: ...the risks and benefits Keep the medical device away from implanted systems Make appropriate emergency provisions and take immediate action on any signs of ill health Symptoms such as raised heartbeat...

Page 80: ...nd manufacturer approved transmission instruments Follow the directions of the manufacturer of dental handpieces with reference to transmission ratio maximum speed and maximum torque Hygiene and maint...

Page 81: ...3 Product description Motor EM 12 L Motor shealt LED Connection for instruments as per ISO 3964 O rings Seal 14...

Page 82: ...Supply hose VE 10 Connection sheat Connection quick release coupling 15...

Page 83: ...on the medical device Do not assemble remove during operation Align the connection tubes of the medical device with the connection openings of the supply hose Screw the medical device and the supply...

Page 84: ...rry out a visual inspection The medical device and supply hose coupling must sit flush to one another Verify full engagement Unscrew the medical device Unscrew the supply hose from the medical device...

Page 85: ...on instruments Do not assemble remove during operation Push the transmission instrument onto the medical device and turn it until it engages audibly Verify full engagement Remove the transmission inst...

Page 86: ...rt the medical device using the attached transmission instrument In the event of operating malfunctions e g vibrations unusual noise overheating coolant failure or leakage stop the medical device imme...

Page 87: ...ctive clothing safety glasses face mask and gloves Remove the transmission instrument from the medical device Use only oil free filtered compressed air with a maximum operating pressure of 3 bar for m...

Page 88: ...and exposure times specified by the manufacturer of the disinfectant Use disinfectants which have been tested and found effective by the Verbund f r Angewandte Hygiene e V VAH Association for Applied...

Page 89: ...use and chemical influences due to processing Send worn or damaged medical devices and or medical devices with material changes to an authorized W H service partner Processing cycles We recommend a re...

Page 90: ...ical device immediately after every treatment Note that the disinfectant used during pre treatment is only for personal protection and cannot replace the disinfectant step after cleaning Hygiene and m...

Page 91: ...in liquid disinfectant or in an ultrasonic bath Clean the medical device under running tap water 35 C 95 F Rinse and brush off all surfaces Remove any liquid residues using compressed air Hygiene and...

Page 92: ...with cleaning fluid and a soft cloth Blow the optic outlet dry with compressed air or dry it carefully with a soft cloth Carry out a visual inspection after each cleaning process Do not use the medica...

Page 93: ...recommends wiping down with disinfectant Evidence of the medical device s basic suitability for effective manual disinfection was provided by an independent test laboratory using the mikrozid AF wipe...

Page 94: ...Hygiene and maintenance Drying Ensure that the medical device is completely dry internally and externally after cleaning and disinfection Remove any liquid residues using compressed air 27...

Page 95: ...sting Inspection Check the medical device after cleaning and disinfection for damage visible residual soiling and surface changes Reprocess any medical devices that are still soiled Sterilize the moto...

Page 96: ...ollowing requirements The sterilization package must meet the applicable standards in respect of quality and use and must be suitable for the sterilization method The sterilization package must be lar...

Page 97: ...H recommends sterilization according to EN 13060 EN 285 or ANSI AAMI ST79 Read the notes follow the instructions and heed the warnings provided by the manufacturers of steam sterilizers The program se...

Page 98: ...ic suitability for effective sterilization was provided by an independent test laboratory using the LISA 517 B17L steam sterilizer W H Sterilization S r l Brusaporto BG and the CertoClav MultiControl...

Page 99: ...Store sterile goods dust free and dry The shelf life of the sterile goods depends on the storage conditions and type of packaging Hygiene and maintenance Storage 32...

Page 100: ...use sharp instruments Squeeze the O ring together between thumb and forefinger to form a loop Pull off the O rings Slide on the new O rings Always change all three O rings at the same time in order t...

Page 101: ...Maintenance Lift up the seal with the tip of a pair of tweezers Remove the seal Carefully insert the new seal Pay attention to the positioning of the seal Replacing the seal 34...

Page 102: ...Maintenance Exchange damaged or leaking O rings immediately Do not use sharp instruments Pull off the O ring Slide on the new O ring Exchanging the supply hose O ring 35...

Page 103: ...horter intervals are prescribed by law The inspection must be undertaken by a qualified organisation and must include the following procedures External visual inspection and a check for any changes wh...

Page 104: ...ng malfunctions immediately contact an authorized W H service partner Repairs and maintenance work must only be undertaken by an authorized W H service partner Ensure that the medical device has been...

Page 105: ...ries and spare parts Use only original W H accessories and spare parts or accessories approved by W H Suppliers W H service partners 01862300 Motor O rings 3 pcs 06893400 Seal 1 pcs 07072400 Supply ho...

Page 106: ...standard VE 10 ISO 3964 Direction of rotation forward reverse Speed range 100 40 000 rpm Maximum torque at the motor 3 Ncm Adjustment cooling air 6 8 Nl min Air coolant pressure The air coolant pressu...

Page 107: ...roved electric motor EM 12 L Drive air respective cooling air at 250 kPa 2 5 bar 8 Nl min Spray air at 250 kPa 2 5 bar 8 Nl min Spray water at 200 kPa 2 0 bar 200 ml min Maximum pressure 400 kPa 4 0 b...

Page 108: ...conditions Temperature during storage and transport 40 C to 70 C 40 F to 158 F Humidity during storage and transport 8 to 80 relative non condensing Temperature during operation 10 C to 35 C 50 F to...

Page 109: ...Disposal Ensure that the parts are not contaminated on disposal Follow your local and national laws directives standards and guidelines for disposal Medical device Waste electrical equipment Packaging...

Page 110: ...cturing defects within a warranty period of 24 months from the date of purchase 24 months for the motor EM 12 L 12 months for the supply hose VE 10 Accessories and consumables are excluded from the wa...

Page 111: ...2NJ Hertfordshire t 44 1727 874990 f 44 1727 872254 E Mail technical uk wh com W H Impex Inc 6490 Hawthorne Drive Windsor Ontario N8T 1J9 Canada t 1 519 944 6739 f 1 519 974 6121 E Mail service ca wh...

Page 112: ......

Page 113: ...Form Nr 50797 AEN Rev 002 26 09 2018 Subject to alterations Manufacturer W H Dentalwerk B rmoos GmbH Ignaz Glaser Stra e 53 5111 B rmoos Austria t 43 6274 6236 0 f 43 6274 6236 55 office wh com wh com...

Page 114: ...Instructions for use Handpiece PB 5 L PB 5 L S PB 5 L Q...

Page 115: ...use 4 on the medical device 5 packaging 6 1 Introduction 7 2 Safety notes 10 3 Product description 15 4 Operation 16 Assembly Removal 16 Changing the tip 17 Test run 20 5 Hygiene and maintenance 21 G...

Page 116: ...and disinfection 30 Drying 31 Inspection Maintenance and Testing 32 Packaging 34 Sterilization 35 Storage 38 6 Exchanging the supply hose O rings 39 7 Servicing 40 8 W H Accessories and spare parts 41...

Page 117: ...k of injury ATTENTION to prevent damage occurring General explanations without risk to persons or objects Symbols Do not dispose of with domestic waste Type B applied part not suitable for intracardia...

Page 118: ...ucture in accordance with Health Industry Bar Code DataMatrix Code for product information including UDI Unique Device Identification Date of manufacture Serial number Catalogue number CE marking with...

Page 119: ...ation Data structure in accordance with Health Industry Bar Code XXXX packaging Caution According to Federal law this medical device may only be sold by or on the order of a dentist physician or any o...

Page 120: ...d the Instructions for use These explain how to use your medical device and guarantee a smooth and efficient operation Observe the safety notes Intended use Drive unit with a piezoceramic oscillating...

Page 121: ...er The manufacturer can only accept responsibility for the safety reliability and performance of the medical device when it is used in compliance with the following directions The medical device must...

Page 122: ...nce with these Instructions for use The medical device should be prepared for use and maintained by staff who have been trained in procedures for infection control personal safety and patient safety I...

Page 123: ...mediately maximum operating time without coolant is 30 seconds The exception are applications where no coolant is used e g endodontics Maximum operating time without coolant is 2 minutes Check the med...

Page 124: ...tment Ensure that the original shape of the tips is not affected e g by being dropped The tips must not be bent back into shape or resharpened Locate and secure the tip only with the medical device sw...

Page 125: ...12 Approved coolants and rinsing liquids Physiological saline solution NaCl 0 9 Hydrogen peroxide H2O2 1 3 Liquids with the active substance chlorhexidine CHX 0 2 Tap water...

Page 126: ...ponents could lead to deviating parameters or even the destruction of the system Risks due to electromagnetic fields This medical device complies with the reference values defined in EN 50527 2 1 2016...

Page 127: ...or to initial use The medical device is not sterilized when delivered The packaging is non sterilizable Clean and disinfect the medical device the tips and the tip changer Sterilize the medical device...

Page 128: ...15 3 Product description Thread Connection for supply hose Handpiece cap Optical fibre Optic outlet Nozzle cleaner...

Page 129: ...16 4 Operation Assembly Removal Push the medical device onto the supply hose Note the positioning w Remove the medical device...

Page 130: ...at the handpiece tip changer tip Position the tip on the thread of the medical device w Turn the tip changer until it audibly engages e Withdraw the tip changer Verify full engagement Press the tip w...

Page 131: ...18 Remove tip with tip changer Place the tip changer onto the tip w Unscrew the tip with the tip changer Leave the tip in the tip changer until the hygienic maintenance process w...

Page 132: ...19 Insert remove tip with spanner Position the tip on the thread of the medical device w Screw the tip down Verify full engagement e Unscrew the tip w...

Page 133: ...device to the supply hose Insert the tip Put the medical device into operation In the event of operating malfunctions e g vibrations unusual noise overheating coolant supply failure or leakage stop th...

Page 134: ...and national laws directives standards and guidelines for cleaning disinfection and sterilization Wear protective clothing safety glasses face mask and gloves Use only oil free filtered compressed air...

Page 135: ...mes specified by the manufacturer of the disinfectant Use disinfectants which have been tested and found effective by the Verbund f r Angewandte Hygiene e V VAH Association for Applied Hygiene the ste...

Page 136: ...chemical influences due to processing Send worn or damaged medical devices and or medical devices with material changes to an authorized W H service partner Processing cycles We recommend a regular se...

Page 137: ...ternal parts Operate the medical device for at least 10 seconds at idle speed Ensure that all coolant outlets are rinsed out Wipe the entire surface of the medical device the tip and the tip changer w...

Page 138: ...25 Hygiene and maintenance Manual cleaning Disassembling the medical device Unscrew the handpiece cap w Remove the optical fibre w...

Page 139: ...dence of the tips basic suitability for effective manual cleaning and disinfection was provided by an independent test laboratory using the Bandelin Type RK 100 CC ultrasonic bath and the cleaning age...

Page 140: ...move dirt and deposits The nozzle cleaner can be cleaned in an ultrasonic bath and or in the washerdisinfector Cleaning the coolant tube Blow through the coolant tube using compressed air In the case...

Page 141: ...l fibre with cleaning fluid and a soft cloth w Blow the optic outlet and the optical fibre dry using compressed air or dry it carefully with a soft cloth Carry out a visual inspection after each clean...

Page 142: ...iping down with disinfectant Evidence of the medical device s the tips and the tip changer s basic suitability for effective manual disinfection was provided by an independent test laboratory using th...

Page 143: ...ved for automated processing in a washer disinfector Evidence of the tips and the tip changer s basic suitability for effective automated disinfection was provided by an independent test laboratory us...

Page 144: ...ene and maintenance Drying Ensure that the medical device the tip and the tip changer are completely dry internally and externally after cleaning and disinfection Remove liquid residues using compress...

Page 145: ...nd maintenance Inspection Check the medical device the tip and the tip changer after cleaning and disinfection for damage visible residual soiling and surface changes Reprocess any medical devices the...

Page 146: ...vice Reassemble the medical device following cleaning and disinfection Fit optic fibre onto medical device w Screw on the handpiece cap Sterilize the medical device the tip and the tip changer followi...

Page 147: ...s that meet the following requirements The sterilization package must meet the applicable standards in respect of quality and use and must be suitable for the sterilization method The sterilization pa...

Page 148: ...ow the instructions and heed the warnings provided by the manufacturers of steam sterilizers The program selected must be suitable for the medical device Only sterilize the tip in the tip changer This...

Page 149: ...e sterilization was provided by an independent test laboratory using the LISA 517 B17L steam sterilizer W H Sterilization S r l Brusaporto BG and the CertoClav MultiControl MC2 S09S273 steam sterilize...

Page 150: ...again Wait until the medical device is completely dry Moisture in the medical device can lead to a malfunction Risk of short circuit Wait until the tip the tip changer and the spanner have completely...

Page 151: ...38 Hygiene and maintenance Storage Store sterile goods dust free and dry The shelf life of the sterile goods depends on the storage conditions and type of packaging...

Page 152: ...39 6 Exchanging the supply hose O rings Remove O rings Slide on the new O rings with a pair of tweezers Always change all O rings to ensure tightness...

Page 153: ...f operating malfunctions immediately contact an authorized W H service partner Repairs and maintenance work must only be undertaken by an authorized W H service partner Ensure that the medical device...

Page 154: ...spare parts Use only original W H accessories and spare parts or accessories approved by W H Suppliers W H partners 08025210 Handpiece cap and 3 optical fibres 00636901 Nozzle cleaner 02060203 O ring...

Page 155: ...ml min 0 20 Maximum coolant supply volume ml min 50 Water pressure bar 1 6 Max oscillating amplitude Tip 1U mm 0 2 for tips where no coolant is used Classification according to 6 of the General Speci...

Page 156: ...ient side optical fibre maximum 48 C 118 4 F Temperature of the working part tip maximum 41 C 105 8 F Ambient conditions Temperature during storage and transport 40 C to 70 C 40 F to 158 F Humidity du...

Page 157: ...Disposal Ensure that the parts are not contaminated on disposal Follow your local and national laws directives standards and guidelines for disposal Medical device Waste electrical equipment Packaging...

Page 158: ...in a warranty period of 24 months from the date of purchase Accessories and consumables tips tip changer nozzle cleaner are excluded from the warranty We accept no responsibility for damage caused by...

Page 159: ......

Page 160: ...h com W H Impex Inc 6490 Hawthorne Drive Windsor Ontario N8T 1J9 Canada t 1 519 9446739 f 1 519 9746121 E Mail service ca wh com W H Impex Inc 33091 W Jefferson Ave Brownstown MI 48173 USA t 1 800 265...

Page 161: ...Form Nr 51005 AEN Rev 001 01 03 2019 Subject to alterations Manufacturer W H Dentalwerk B rmoos GmbH Ignaz Glaser Stra e 53 5111 B rmoos Austria t 43 6274 6236 0 f 43 6274 6236 55 office wh com wh com...

Page 162: ...Instructions for Use Foot control S NW S N2 S N1...

Page 163: ...17 Connecting and disconnecting the CAN dongle 18 Description of CAN dongle 19 Connecting and disconnecting the SPI dongle 20 Description of SPI dongle 21 Assistance with pairing problems 22 7 Foot c...

Page 164: ...3 Symbols WARNING if persons could be injured ATTENTION if property could be damaged General explanations without risk to persons or property in the Instructions for Use Foot control...

Page 165: ...radiation Battery compartment closed Do not dispose of with domestic waste Battery compartment open Catalogue number Serial number Date of manufacture DataMatrix code for product information including...

Page 166: ...ence 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 recept...

Page 167: ...ose of with domestic waste Catalogue number Serial number Date of manufacture DataMatrix code for product information including UDI Unique Device Identification CE marking with identification number o...

Page 168: ...e handle with care Keep dry Temperature limitation Humidity limitation Der Gr ne Punkt The Green Dot trademark of Duales System Deutschland GmbH Trademark of RESY OfW GmbH for identification of recycl...

Page 169: ...patients are of paramount importance to us Observe the safety notes Intended use Foot control for operation of medical electrical equipment Misuse may damage the foot control and hence cause risks and...

Page 170: ...he foot control has no components that can be repaired by the user Modifications or repairs must only be undertaken by an authorized W H service partner see page 31 Unauthorized opening of the foot co...

Page 171: ...HF communications equipment including peripherals such as antenna cables and external antennas should be used no closer than 30 cm 12 inches to the medical device Otherwise degradation of the performa...

Page 172: ...23 REF 16929000 16929001 S N2 REF 30285000 S N2 REF 30285002 SI 1010 SI 1015 SI 1023 SI 915 SI 923 REF 30286xxx 30287xxx M UK1010 M UK1015 M UK1023 SA 430 M SA 435 M Built In Solution to be agreed wit...

Page 173: ...rol if it is damaged Replace the foot control as soon as the resistance is noticeably reduced Never touch the patient and the electrical contacts on the medical device simultaneously The ESD spring co...

Page 174: ...out if patient or user have implanted systems before using the medical device and consider the application Weigh the risks and benefits Keep the medical device away from implanted systems Make appropr...

Page 175: ...waste Use only high quality disposable alkaline AA Mignon LR6 1 5 V batteries Risk of explosion if the wrong type of battery is used Do not mix new old or different types of disposable batteries Do n...

Page 176: ...15 5 Attaching detaching the locator Attaching and detaching the locator Push it right in until the locator reaches the stop Pull the locator out...

Page 177: ...hread to remove the batteries Open battery compartment Remove batteries Inserting and replacing batteries Lock the battery compartment Insert batteries Reposition the red thread before inserting batte...

Page 178: ...Foot control S NW Do not use sharp tools Firmly squeeze the O ring between your thumb and index finger so that it forms a loop Pull off the O ring Push the new O ring on in its place Replacing the O r...

Page 179: ...lug in the CAN dongle Pay attention to the positioning Press the side lock and remove the CAN dongle Foot control S NW Connecting CAN dongle Removing CAN dongle Connecting and disconnecting the CAN do...

Page 180: ...Implantmed system assembler and follow the directions Press and hold the green left and orange middle buttons simultaneously on the S NW foot control for at least 3 seconds Disable pairing Press and h...

Page 181: ...I dongle Pay attention to the positioning Plug in the SPI dongle or disconnect the SPI dongle from the control unit Attach the SPI dongle to the irrigant support or remove the SPI dongle from the irri...

Page 182: ...s If pairing is inactive Press and hold the button on the SPI dongle for 4 seconds LED indicator flashes SPI dongle is in pairing mode for 30 seconds Press and hold the green and orange buttons simult...

Page 183: ...foot control Eliminate any sources of interference e g brush motors mobile telephones radios WLAN Replace the pairing and repeat the pairing process Remove and replace the batteries If the pairing pro...

Page 184: ...23 7 Foot control S N2 S N1 Pay attention to the positioning Plug in the foot control S N2 S N1 or disconnect the foot control from the control unit Connecting disconnecting...

Page 185: ...nes for cleaning Wear protective clothing safety glasses face mask and gloves The foot control is sealed and may be wiped clean The foot control is not approved for automated processing in a washer di...

Page 186: ...by law The periodic inspection covers the complete medical device and must only be performed by an authorized service partner Repairs and returns In the event of operating malfunctions immediately con...

Page 187: ...pare parts Use only original W H accessories and spare parts or accessories approved by W H Suppliers W H partners Link https www wh com 07759700 CAN dongle 07795800 SPI dongle 04653500 Locator for fo...

Page 188: ...10 C to 40 C 50 F to 104 F Humidity during operation 15 to 80 relative non condensing Foot control S NW S N2 S N1 Power supply 3 disposable batteries AA Mignon LR6 1 5V Dimensions in mm height x widt...

Page 189: ...trical Device according to IEC 60601 1 ANSI AAMI ES 60601 1 S NW S N2 S N1 are waterproof according to IPX8 1 m depth of immersion 1 hour water tight in accordance with IEC 60529 Pollution level 2 Alt...

Page 190: ...9 12 Disposal Ensure that the parts are not contaminated on disposal Follow your local and national directives standards and guidelines for disposal Medical device Waste electrical equipment Packaging...

Page 191: ...anufacturing defects within a warranty period of twenty four months from the date of purchase Accessories and consumables batteries O ring locator for foot control are not covered by the warranty We a...

Page 192: ...31 Find your nearest authorized W H service partner at http wh com Simply go to the menu option Service for full details Or simply scan the QR code Authorized W H service partners...

Page 193: ...32 Manufacturer s declaration...

Page 194: ...33 Manufacturer s declaration...

Page 195: ...34 Manufacturer s declaration...

Page 196: ...35 Manufacturer s declaration...

Page 197: ...Form Nr 50882 AEN Rev 006 04 06 2021 Subject to alterations Manufacturer W H Dentalwerk B rmoos GmbH Ignaz Glaser Stra e 53 5111 B rmoos Austria t 43 6274 6236 0 f 43 6274 6236 55 office wh com wh com...

Page 198: ...Instructions for use Electric motor EM 19 EM 19 LC...

Page 199: ...ce packaging 5 1 Introduction 6 2 Safety notes 9 3 Product description 12 4 Operation Assembly Removal 14 Test run 15 5 Hygiene and maintenance General notes 16 Limitations on processing 18 Initial tr...

Page 200: ...fection 22 Drying 23 Inspection Maintenance and Testing 24 Packaging 25 Sterilization 26 Storage 28 6 Servicing 29 7 W H Accessories and spare parts 31 8 Technical data 32 9 Disposal 34 Explanation of...

Page 201: ...g WARNING risk of injury Symbols in the Instructions for use Caution According to Federal law this medical device may only be sold by or on the order of a dentist physician or any other medical practi...

Page 202: ...cates compliance with Canadian and U S requirements DataMatrix Code for product information including UDI Unique Device Identification Datastructurein accordancewith HealthIndustryBarCode Symbols on t...

Page 203: ...or to initial use please read the Instructions for use These explain how to use your medical device and guarantee a smooth and efficient operation Observe the safety notes Intended use Electrical driv...

Page 204: ...rements of Directive 93 42 EEC Responsibility of the manufacturer The manufacturer can only accept responsibility for the safety reliability and performance of the medical device when it is used in co...

Page 205: ...valid health and safety at work regulations the valid accident prevention regulations and in compliance with these Instructions for use The medical device should be prepared for use and maintained by...

Page 206: ...vice is restarted Perform a test run each time before using Ensure that it is possible to complete the operation safely should the units or instruments fail Do not twist or kink the motor cable Do not...

Page 207: ...the application Weigh the risks and benefits Keep the medical device away from implanted systems Make appropriate emergency provisions and take immediate action on any signs of ill health Symptoms su...

Page 208: ...nufacturerapproved transmission instruments Follow the directions of the manufacturer of transmission instruments with reference to transmission ratio maximum speed and maximum torque Hygiene and main...

Page 209: ...12 Motor sheath Electrical contacts O Ring Motor cable only EM 19 LC 3 Product description...

Page 210: ...13 4 Operation Do not assemble or remove the medical device during operation Connect motor cable Pay attetion to the positioning Verify full engagement...

Page 211: ...emove the medical device during operation Push the transmission instrument onto the medical device and turn it until it engages audibly Verify full engagement Remove the transmission instrument from t...

Page 212: ...at eye level Start the medical device using the attached transmission instrument In the event of operating malfunctions e g vibrations unusual noise overheating stop the medical device immediately and...

Page 213: ...infection and sterilization Wear protective clothing safety glasses face mask and gloves Remove the transmission instrument from the medical device Use only oil free filtered compressed air with a max...

Page 214: ...mes specified by the manufacturer of the disinfectant Use disinfectants which have been tested and found effective by the Verbund f r Angewandte Hygiene e V VAH Association for Applied Hygiene the ste...

Page 215: ...se and chemical influences due to processing Send worn or damaged medical devices and or medical devices with material changes to an authorized W H service partner Processing cycles We recommend a reg...

Page 216: ...ment Wipe the entire surface of the meeical device with disinfectant Note that the disinfectant used during pre treatment is only for personal protection and cannot replace the disinfectant step after...

Page 217: ...Manual cleaning Do not place the medical device in liquid disinfectant or in an ultrasonic bath Clean the medical device under running tap water 35 C 95 F Rinse off all surfaces Remove any liquid res...

Page 218: ...W H recommends wiping down with disinfectant Evidence of the medical device s basic suitability for effective manual disinfection was provided by an independent test laboratory using the mikrozid AF w...

Page 219: ...urers of washer disinfectors cleaning agents and or disinfectants Evidence of the medical device s basic suitability for effective automated disinfection was provided by an independent test laboratory...

Page 220: ...23 Ensure that the medical device is completely dry internally and externally after cleaning and disinfection Remove any liquid residues using compressed air Hygiene and maintenance Drying...

Page 221: ...disinfection for damage visible residual soiling and surface changes Reprocess any medical devices that are still soiled Sterilize the reassembled medical device following cleaning and disinfection I...

Page 222: ...The sterilization package must meet the applicable standards in respect of quality and use and must be suitable for the sterilization method The sterilization package must be large enough for the ste...

Page 223: ...N 13060 EN 285 oder ANSI AAMI ST79 Read the notes follow the instructions and heed the warnings provided by the manufacturers of steam sterilizers The program selected must be suitable for the medical...

Page 224: ...sic suitability for effective sterilization was provided by an independent test laboratory using the LISA 517 B17L steam sterilizer Firma W H Sterilization S r l Brusaporto BG and the CertoClav MultiC...

Page 225: ...28 Store sterile goods dust free and dry The shelf life of the sterile goods depends on the storage conditions and type of packaging Hygiene and maintenance Storage...

Page 226: ...hree years unless shorter intervals are prescribed by law The inspection must be undertaken by a qualified organization and must include the following procedures Visual inspection of internal componen...

Page 227: ...ating malfunctions immediately contact an authorized W H service partner Repairs and maintenance work must only be undertaken by an authorized W H service partner Ensure that the medical device has be...

Page 228: ...ccessories and spare parts 04363600 Disposable irrigation tubing set 2 2 m 6 pcs 06290600 Hose clips 5 pcs Use only original W H accessories and spare parts or accessories approved by W H Suppliers W...

Page 229: ...Technical data Motor EM 19 EM 19 LC Direction of rotation forward reverse Speed range 200 40 000 rpm Maximum torque at the motor 6 2 Ncm Coolant volume flow at 100 min 90 ml min Maximum power output...

Page 230: ...ient conditions Temperature during storage and transport 40 C to 70 C 40 F to 158 F Humidity during storage and transport 8 to 80 relativ non condensing Temperature during operation 10 C to 35 C 50 F...

Page 231: ...sposal Ensure that the parts are not contaminated on disposal Follow your local and country specific laws directives standards and guidelines for disposal Medical device Waste electrical equipment Pac...

Page 232: ...or material or manufacturing defects within a warranty period of 24 months from the date of purchase Accessories and consumables are not covered by the warranty We accept no responsibility for damage...

Page 233: ...AL2 2NJ Hertfordshire t 44 1727 874990 f 44 1727 872254 E Mail technical uk wh com W H Impex Inc 6490 Hawthorne Drive Windsor Ontario N8T 1J9 Canada t 1 519 944 6739 f 1 519 974 6121 E Mail service ca...

Page 234: ......

Page 235: ...Manufacturer Form Nr 50983 AEN Rev 000 23 08 2018 Subject to alterations W H Dentalwerk B rmoos GmbH Ignaz Glaser Stra e 53 5111 B rmoos Austria t 43 6274 6236 0 f 43 6274 6236 55 office wh com wh com...

Page 236: ...Instructions for Use Peristaltic pump...

Page 237: ...2...

Page 238: ...mpatibility EMC 8 3 Unpacking 9 4 Scope of delivery 10 5 Safety notes 11 6 Description 13 7 Handling 14 Changing the irrigation tubing set 14 8 Hygiene and maintenance 19 9 Servicing 20 10 W H accesso...

Page 239: ...4 Symbols in the Instructions for Use ATTENTION in cases where something could be damaged ATTENTION in cases where something could be damaged WARNING risk of injury...

Page 240: ...ical device Catalogue number Serial number DataMatrix Code for product information including UDI Unique Device Identification UL Component Recognition Mark indicates compliance with Canadian and U S r...

Page 241: ...our team and of course the safety of your patients are of paramount importance to us The peristaltic pump is defined as medical device Observe the safety notes Intended use The pump is a peristaltic p...

Page 242: ...er Modifications or repairs must only be undertaken by an authorised W H service partner page 25 The electrical installation at the premises must comply with the regulations laid out in IEC 60364 7 71...

Page 243: ...and spare parts The use of accessories and spare parts not approved by W H can lead to an increased emission of electromagnetic interference or to a reduced resistance against electromagnetic interfe...

Page 244: ...aging is environmentally friendly and can be disposed of by industrial recycling companies However we recommend that you keep the original packaging Open the packaging Remove the foil Remove the peris...

Page 245: ...10 4 Scope of delivery REF 30358000 Peristaltic pump REF 774010 Screw kit M3...

Page 246: ...overheating stop the medical device immediately and contact an authorized W H service partner The responsibility for the use and timely shutdown of the system lies with the user Ensure that it is pos...

Page 247: ...magnetic and electromagnetic fields Find out if patient and user have implanted systems before using the medical device and consider the application Weigh the risks and benefits Keep the medical devi...

Page 248: ...13 6 Description Peristaltic pump at the dental unit...

Page 249: ...14 7 Handling Changing the irrigation tubing set Unlocking of the coverl Fold up lever w Remove cover...

Page 250: ...15 Handling Changing the irrigation tubing set Placement of the irrigation tubing set Place the tubing a into the guide until the prominent part snaps into the groove w Place the tubing b into guide b...

Page 251: ...16 Handling Changing the irrigation tubing set Irrigation tubing set in place...

Page 252: ...17 Closing the cover Align the cover grooves a with the lever pins b w Move the cover onto the pins until it is seated on the pump Handling Changing the irrigation tubing set...

Page 253: ...18 Handling Exchanging the irrigation tubing set Lock the cover Fold down lever w Cover is locked...

Page 254: ...ines for cleaning Wear protective clothing safety glasses face mask and gloves The medical device may be wiped clean The medical device is not approved for mechanical cleaning thermo washer disinfecto...

Page 255: ...isation and must include the following procedures Visual inspection for external damage Visual inspection of internal components on suspicion of safety interference The regular service must only be pe...

Page 256: ...21 10 W H accessories Use only original W H accessories and spare parts or accessories approved by W H Suppliers W H partners 06290600 Hose clips 5 pcs 04363600 Irrigation tubing set 2 2 m 6 pcs...

Page 257: ...and transport 40 C to 70 C 40 F to 158 F Humidity during storage and transport 8 to 80 relative non condensing Temperature during operation 10 C to 40 C 50 F to 104 F Humidity during operation 15 to 8...

Page 258: ...12 Disposal Ensure that the parts are not contaminated on disposal Follow your local and national laws directives standards and guidelines for disposal Medical device Waste electrical equipment Packag...

Page 259: ...ufacturer W H is liable for material or manufacturing defects within a warranty period of 12 months from the date of purchase Accessories and consumables are excluded from the warranty We accept no re...

Page 260: ...H Austria GmbH Ignaz Glaser Stra e 53 5111 B rmoos Austria t 43 6274 6236 239 f 43 6274 6236 890 E Mail office at wh com W H CH AG Industriepark 9 8610 Uster ZH Schweiz t 41 43 4978484 f 41 43 4978488...

Page 261: ...Form No 50993 AEN Rev 000 15 10 2018 Subject to alterations Manufacturer W H Dentalwerk B rmoos GmbH Ignaz Glaser Stra e 53 5111 B rmoos Austria t 43 6274 6236 0 f 43 6274 6236 55 office wh com wh com...

Page 262: ...1 Minilight Installation and use manual...

Page 263: ...LUZZANI DENTAL S R L MADE IN ITALY Via Torino 3 20030 Senago MI Italy www luzzani it E mail info luzzani it Tel 39 029988433 Fax 39 0299010379 ED 5 REV 0 1 3 7 0...

Page 264: ...ESSED AIR SYSTEM 6 4 CONNECTION OF STRESS ABSORBER CORD 6 5 NOTES FOR CORRECT CONNECTION 7 NORMAL USE 7 1 INSUFFLATION OF COLD WATER 7 2 INSUFFLATION OF COLD AIR 7 3 COMBINED INSUFFLATION OF COLD WATE...

Page 265: ...4 0 SYRINGE LEGEND Tip Air button Water button Tip retainer Handpiece Selector switch LED 6F G6F and L Water line Air line Pawl Stress absorber cord Power cables 6F G6F and L...

Page 266: ...y the manufacturer If non OEM accessories or consumables are used the company cannot guarantee safe operation and function No claims can be made for damages resulting from improper use 1 13 Disposable...

Page 267: ...The shape of the handpiece can be STYLET 3 IDENTIFICATION DATA AND WARRANTY ANGLED This difference lets the dentist choose the tool ergonomically best suited for the purpose To guarantee maximum hygie...

Page 268: ...ing the Minilight syringe national regulations regarding water and air quality must also be met The air must be medical grade dry and free of oil and bacteria a 5 m air filter is recommended 6 4 CONNE...

Page 269: ...ld air into the operating field just press the right button on the handpiece symbol 7 3 COMBINED INSUFFLATION OF COLD WATER AND AIR SPRAY To blow a combination of cold air and water spray press both b...

Page 270: ...d tip of the syringe MUST be cleaned and sterilised to guarantee maximum hygiene Sterilisation symbol on the handpiece To do this proceed as follows Disconnect the tip by unscrewing the tip retainer 1...

Page 271: ...rities or dirt that may be present D AUTOMATIC CLEANING Not envisaged E MANUAL DISINFECTION Disinfect only with a disposable cloth and the permitted disinfectant following the instructions on the labe...

Page 272: ...to patient or user by malfunction or deterioration in the characteristics and or performance of a device as well as any inadequacy in the instructions for use We kindly ask you to inform us of any an...

Page 273: ...12 14 WIRING DIAGRAM 14 1 VERSION 6F 14 2 VERSION L...

Page 274: ...Automatic cleansing Not available Manual disinfection Perform disinfection only with a disposable tissue and with compatible disinfectants in accordance with the instructions included in the product...

Page 275: ...____ COMPANY ______________________________________________________________________________________________________ ____________________________________________________________________________________...

Page 276: ...SYR3 04 MANUALE D USO INSTRUCTION MANUAL MODE D EMPLOI GEBRAUCHSANLEITUNG MANUAL DE USO SIRINGA DENTALE DENTAL SYRINGE Dispositivo Medico conforme alla direttiva 93 42 CE FARO SPA Ornago Italy 0051...

Page 277: ...is placed on manufacturer s files with the relative serial numbers NORME DI SICUREZZA La siringa dentale destinata esclusivamente ad essere utilizzata in uno studio dentistico solo da personale medic...

Page 278: ...la che impedisce la contaminazione del corpo della siringa Pulizia degli ugelli Qualora i piccoli fori del beccuccio da cui fuoriescono acqua e aria fossero ostruiti liberare il passag gio utilizzando...

Page 279: ...n the safety cord Connect the hose to the syringe by tightening the ring nut Check the water and air pressure va lues and make sure the fluids are at ambient temperature Tmax 41 C INSTRUCTIONS FOR USE...

Page 280: ...all sur un syst me d alimentation sp cifique groupe dentaire et devra tre branch un cordon d di FARO Le dispositif doit tre st rilis dans un autoclave avant d tre utilis sur un nouveau patient Le disp...

Page 281: ...alcool St rilisation Retirer la coque et l embout du corps de la seringue en les faisant glisser Nettoyer la coque e l embout St riliser la coque et l embout dans un autoclave La coque est dot e d un...

Page 282: ...O Eingang anschlie en und das Sicherheitskabel fixieren Das Kabel durch Einschrauben des dementsprechenden Rings an die Spritze anschlie en Die Wasser und Luftdruckwerte pr fen und sicherstellen dass...

Page 283: ...un sistema de alimentaci n espec fico asociado al dental y tendr que ser conectado a un cable especial FARO El aparato tiene que ser esterilizado en autoclave antes de utilizarlo para un nuevo pacient...

Page 284: ...ncluyendo la embocadura del cuerpo de la jeringa Limpiar la cubierta y la embocadura Esterilizar en autoclave la cubierta incluyendo la embocadura La cubierta incorpora una v lvula qu impide la contam...

Page 285: ...imbre du revendeur Les r parations sous garantie pendant la p riode de validit seront effec tu es seulement si l article reparer est accompagn du bulletin ou de la facture d achat La garantie r pond d...

Page 286: ...rizzo address adresse auschrift direccion citt town ville ort ciudad SN SD data d acquisto purchase date date d achat einkaufdatum fecha de compra versione version version modell versi n Timbro del ri...

Page 287: ...che oder bauliche nderung worzunehmen FARO SpA se reserva el derecho de modificar sin aviso previo la caracteristicas incluidas en el presente manual de uso ED 1 COD 988 _REV 00 FARO S p A via Faro 15...

Page 288: ...EN 1801V002 7560100003L02 Installation and Operating Instructions Spittoon valve 3...

Page 289: ......

Page 290: ...18 Appendix 13 Information about EMC in accord ance with EN 60601 1 2 19 13 1 General information 19 13 2 Abbreviations 19 13 3 Guidelines and manufacturer s in formation 19 EN Contents Important inf...

Page 291: ...If the instructions and information in these installation and operating instruc tions are not followed D rr Dental will not be able to offer any warranty or as sume any liability for the safe operati...

Page 292: ...Dental parts or accessories and special accessories specifically approved by D rr Dental i i Only use only genuine working parts and spare parts 2 Safety D rr Dental has designed and constructed this...

Page 293: ...der guarantee i i Only transport the device in its original pack aging i i Keep the packing materials out of the reach of children 2 10 Disposal The unit may be contaminated Instruct the company dispo...

Page 294: ...xxx Spittoon valve 3 2 Special accessories The following optional items can be used with the device Switch control panel 7560 520 00 3 3 Wear parts and spare parts The following working parts need to...

Page 295: ...ct mm 20 Collection vessel vent connection mm 9 Compressed air connection mm 4 Media Compressed air min max bar MPa bar MPa 3 0 3 5 0 5 Fluid flow rate max l min 3 5 Fluid temperature max C 35 Suction...

Page 296: ...are located on the side of the fluid collector 1 1 Type plate 4 2 Conformity assessment This device has been subjected to conformity acceptance testing in accordance with the cur rent relevant Europea...

Page 297: ...en sucked into the suction pipe As soon as the fill level in the collector vessel has dropped this is detected by the control elec tronics and the solenoid valve is switched off While waste water cont...

Page 298: ...types Flexible spiral hoses made of PVC with inte grated spiral or equivalent hoses Hoses that are resistant to dental disinfectants and chemicals Plastic hoses will display signs of ageing over time...

Page 299: ...nstallation 7 1 Installation overview 1 9 2 3 5 4 6 7 8 1 Spittoon valve 2 Station selection valve 3 Pressure reducer 4 Suction pipe connection 5 Rinsing unit 6 Auxiliary air nozzle 7 Hose manifold 8...

Page 300: ...pressed air connection in wards 7 2 Installation of the spittoon valve The cleaning function can be activated via the yellow button For this reason the spittoon valve should be positioned in an easily...

Page 301: ...Route the power supply and control line to the spittoon valve i i Attach the connector to the connection lines i i Plug in the connector at the corresponding positions on the control electronics i i S...

Page 302: ...V AC DC 1 Hose manifold 2 Station selection valve 3 Rinsing unit 4 Spittoon valve X1 Cleaning button for switch control panel X3 Solenoid valve X4 Control line for suction unit X5 Power supply K1 Suc...

Page 303: ...nit power switch or the main sur gery switch i i Carry out an electrical safety check in accord ance with applicable local regulations e g the German Ordinance on the Installation Opera tion and Use o...

Page 304: ...cleaning Material compatible non foaming special cleaning agents that have been approved by D rr Dental e g MD 555 Cleaner Unit care system e g OroCup i i To pre clean suck up 2 litres of water with t...

Page 305: ...t i i Wear protective equipment when working e g impermeable gloves protective goggles and mouth and nose protection Mainte nance interval Maintenance work Monthly i i Press the yellow cleaning button...

Page 306: ...ttoon valve not working No power supply i i Check power supply and restore Faulty connections i i Check the plug connections Relay not switching i i Check the switching function of the relay No compre...

Page 307: ...bly clean and disinfect the suction unit and the unit using a suitable disin fectant approved by D rr Dental i i Disinfect a defective unit using a suitable sur face disinfection agent i i Seal all co...

Page 308: ...anufacturer s information Electromagnetic emissions for all devices and systems The device is designed for operation in an electromagnetic environment as specified below The cus tomer or operator of t...

Page 309: ...30 Electrical fast tran sient burst immunity test in accordance with IEC 61000 4 4 2 kV for mains ca bles 1 kV for input and output cables 2 kV for mains ca bles 1 kV for input and output cables The q...

Page 310: ...lower than the compli ance level for all frequencies based on inspections on sitea b Interference is possible in the environment of units that have the following symbols Comment 1 The higher frequenc...

Page 311: ...ty distance based on the transmission frequency m 150 kHz to 80 MHz d 0 35 P 80 MHz to 800 MHz d 0 35 P 800 MHz to 2 5 GHz d 0 7 P 0 1 0 11 0 11 0 22 1 0 35 0 35 0 7 10 1 11 1 11 2 21 100 3 5 3 5 7 Ta...

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Page 313: ......

Page 314: ......

Page 315: ...Hersteller Manufacturer D RR DENTAL SE H pfigheimer Str 17 74321 Bietigheim Bissingen Germany Fon 49 7142 705 0 www duerrdental com info duerrdental com...

Page 316: ...EN 1712V002 7117100018L30 Installation and Operating Instructions CAS 1 Combi Separator...

Page 317: ......

Page 318: ...output signals 18 EN Contents Important information 1 About this document 3 1 1 Warnings and symbols 3 1 2 Copyright information 3 2 Safety 4 2 1 Intended purpose 4 2 2 Intended use 4 2 3 Improper us...

Page 319: ...atment 20 12 2 Daily after the end of treatment 20 12 3 Once or twice a week before the midday break 21 13 Replace the amalgam collector vessel 21 13 1 Disposal of the collector vessel 22 14 Maintenan...

Page 320: ...e unit If the instructions and information in these installation and operating instruc tions are not followed D rr Dental will not be able to offer any warranty or assume any liability for the safe op...

Page 321: ...eir corresponding IEC or ISO standards All configurations must continue to comply with the standard requirements for medical systems see IEC 60601 1 1 or section 16 of the 3rd edition of IEC 60601 1 r...

Page 322: ...ease contact your dental trade supplier Whoever connects additional devices to med ical electrical devices automatically becomes the system configurator and is responsible for ensuring that the system...

Page 323: ...formation on spare parts can be found on the website portal for authorised spe cialist dealers under www duerrdental net 3 Overview 1 1 CAS 1 Combi Separator 3 1 Scope of delivery The scope of deliver...

Page 324: ...iquids l min 4 Usable volume in amalgam collecting container ccm c 90 Replacement interval 4 6 months General data Drive motor nominal speed rpm 2800 Operating mode S5 95 DC Type of protection IP 20 P...

Page 325: ...assessment This device has been subjected to conformity acceptance testing in accordance with the current relevant European Union guidelines This equipment conforms to all relevant require ments 4 4...

Page 326: ...1 12 13 14 15 1 6 CAS 1 1 Fluid intake 2 Vacuum to suction unit 3 Aspiration input 4 Fluid output 5 Motor 6 Separation 7 Separation rotor 8 Centrifuge 9 Light barriers 3x 10 Sensor enclosure 11 Cone p...

Page 327: ...e pumped through the fluid output 4 to the central waste water system 5 1 Operation CAS 1 Combi Separator The task of the CAS 1 combi separator is to provide continuous separation of secretions and ai...

Page 328: ...r vessel 12 is checked by a float sensor 13 every time the main power switch is switched on The centrifuge motor starts fluid is transported via the pump cone to the centrifuge drum 8 and provides a c...

Page 329: ...6 Requirements 6 1 Installation setup room The room chosen for set up must fulfil the fol lowing requirements Closed dry well ventilated room Should not be a room made for another pur pose e g boiler...

Page 330: ...unit data sheet that such connections can be safely made or if you are in any doubt always get a suitably qualified person e g the manufacturer to verify that the setup is safe A copy of the system m...

Page 331: ...g unit installation and operating instructions 7 2 Installation of the CAS 1 in treatment units WARNING Infection due to contaminated unit i i Clean and disinfect the suction before working on the uni...

Page 332: ...s connected to the X6 socket RJ 45 socket An existing D rr Dental display panel with a 6 pin connector can be connected to the X6A connector when replacing an older device If the installation of the a...

Page 333: ...ower switch or the main surgery switch i i Carry out an electrical safety check in accord ance with applicable local regulations e g the German Ordinance on the Installation Oper ation and Use of Medi...

Page 334: ...7117100018L30 1712V002 17 Installation 9 Service program EN...

Page 335: ...nal for the rinsing unit If the suction hose is lifted off the hose mani fold the green LED will also come on Removal of the collecting container causes the red LED to illuminate 10 Description of the...

Page 336: ...ainer Switch on the unit Green LED lights up Ready for operation If this error message occurs when the collecting container is correctly inserted this indicates that there is a technical defect inform...

Page 337: ...derably increasing the cleaning effect 12 2 Daily after the end of treatment After higher workloads before the midday break and in the evening The following are required for disinfection clean ing Mat...

Page 338: ...full amalgam collector vessel i i Close and secure the full amalgam collector vessel using the cap Observe the markings on the cap and on the collector vessel i i Place the securely closed amalgam co...

Page 339: ...m collector vessels collected from the surgery by a local waste management company i i New amalgam collector vessels should be ordered from your specialist dental equipment retailer i i Document the r...

Page 340: ...evice i i Replace the amalgam collecting container when a fill level of 95 or 100 is indicated on the display panel i i Clean or replace protective sieves during replacement of the amalgam collecting...

Page 341: ...dbook must document all maintenance work service work checks and amalgam disposal Annual inspection This inspection should only be carried out by suitably trained staff For inspection the following ar...

Page 342: ...gloves protective goggles and mouth and nose protection Prior to working on the device or in case of danger disconnect it from the mains e g pull the mains plug 2 3 4 5 6 1 1 Display panel 2 RED displ...

Page 343: ...t X9 i i Plug in the connector correctly i i Replace the PCB main board and connector on the motor Orange LED flashes Audible signal Press the service key briefly to switch off the audible signal Amal...

Page 344: ...y too low i i Introduce water into the suction pipe i i Retrofit the rinsing unit i i Check the rinsing unit for its correct installation position i i Check the function of the rinsing unit Water cann...

Page 345: ...ection e g liquid tight pro tective gloves protective goggles face mask i i Before disassembly clean and disinfect the suction unit and the unit using a suitable disin fectant approved by D rr Dental...

Page 346: ...delines and manufacturer s information Electromagnetic emissions for all devices and systems The device is designed for operation in an electromagnetic environment as specified below The cus tomer or...

Page 347: ...hospital environ ment Voltage surge in accordance with IEC 61000 4 5 0 5 1 kV voltage outer conduc tor outer conductor 0 5 1 kV symmetri cal voltage The quality of the supply voltage should correspon...

Page 348: ...on inspections on sitea b Interference is possible in the environment of units that have the following symbols Comment 1 The higher frequency range applies for 80 MHz and 800 MHz Comment 2 These guide...

Page 349: ...Safety distance based on the transmission frequency m 150 kHz to 80 MHz d 1 2 P 80 MHz to 800 MHz d 1 2 P 800 MHz to 2 7 GHz d 2 3 P 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 10 3 8 3 8 7 3 100 12 12 23 Table...

Page 350: ......

Page 351: ...Hersteller Manufacturer D RR DENTAL SE H pfigheimer Str 17 74321 Bietigheim Bissingen Germany Fon 49 7142 705 0 www duerrdental com info duerrdental com...

Page 352: ...EN 1709V004 9000 606 39 30 Installation and Operating Instructions CS 1 Combi Sepamatic...

Page 353: ......

Page 354: ...2 1 Close the CS 1 16 Appendix 13 Information about EMC in accordance with EN 60601 1 2 17 13 1 General information 17 13 2 Abbreviations 17 13 3 Guidelines and manufacturer s information 17 13 4 Calc...

Page 355: ...tions form part of the unit If the instructions and information in these installation and operating instruc tions are not followed D rr Dental will not be able to offer any warranty or as sume any lia...

Page 356: ...equirements outlined above 2 Safety D rr Dental has designed and constructed this device so that when used properly and for the intended purpose there is no danger to people or property Nevertheless r...

Page 357: ...isposed of in accordance with the local waste disposal reg ulations i i If you have any questions about the correct disposal of parts please contact your dental trade supplier 2 5 General safety infor...

Page 358: ...regular intervals refer to the Maintenance section Protective strainer Rubber grommets O rings Information on spare parts can be found on the website portal for authorised spe cialist dealers under w...

Page 359: ...peed min 1 2800 Operating mode S1 100 DC Type of protection IP 20 Protection class II Noise level approx dB A 49 Dimensions H x W x D cm 12 5 x 15 x 12 Weight approx kg 1 4 Medical device class I DC d...

Page 360: ...are on the motor cover and on the motor flange 1 1 Type plate 4 3 Conformity assessment This device has been subjected to conformity acceptance testing in accordance with the cur rent relevant Europe...

Page 361: ...ect to high centrifugal forces by the separation rotor which ensures that no fluid or blood foam can be carried into the suction unit The spiral motion serves to continuously transport the separated l...

Page 362: ...ction external valves units 0 5 mm 6 Requirements 6 1 Setup options CS 1 Combi Sepamatic Directly in the treatment unit In a special housing in an extension of the treatment unit 6 2 Hose materials Fo...

Page 363: ...Prior to working on the device or in case of danger disconnect it from the mains e g pull the mains plug 7 1 Installation of the CS 1 in treatment units WARNING Infection due to contaminated unit i i...

Page 364: ...the control i i Put the motor cover on 7 2 Electrical connections controller Power supply Safety transformer order number 9000 150 46 or Safety transformer 24 V AC with a with an isolator consisting o...

Page 365: ...i i Turn on the unit power switch or the main sur gery switch i i Carry out an electrical safety check in accord ance with applicable local regulations e g the German Ordinance on the Installation Op...

Page 366: ...ehold cleaning agents or instru ment disinfection agents i i Do not use abrasive cleaners i i Do not use agents containing chlo rine i i Do not use any solvents like acetone 9 1 After every treatment...

Page 367: ...erval Maintenance work Dependent upon the level of usage of the device i i Clean or replace the protective sieves at the aspiration inlet At the lat est however when the suction power of the unit dimi...

Page 368: ...unit i i Wear protective equipment when working e g impermeable gloves protective goggles and mouth and nose protection Fault Probable cause Solution Device does not start No power supply i i Check p...

Page 369: ...suitable disin fectant approved by D rr Dental i i Disinfect a defective unit using a suitable sur face disinfection agent i i Seal all connections with sealing caps i i Pack the unit securely in prep...

Page 370: ...of the transmitter manufacturer d Recommended safety distance in metres m 13 3 Guidelines and manufacturer s information Electromagnetic emissions for all devices and systems Interference emission mea...

Page 371: ...1000 4 5 1 kV voltage outer conductor outer conductor 2 kV voltage outer conductor earth 1 kV push pull voltage 2 kV common mode voltage The quality of the supply voltage should correspond to a typica...

Page 372: ...ary communication devices should be lower than the compli ance level for all frequencies based on inspections on sitea b Interference is possible in the environment of units that have the following sy...

Page 373: ...m 150 kHz to 80 MHz d 1 2 P 80 MHz to 800 MHz d 1 2 P 800 MHz to 2 5 GHz d 2 3 P 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 10 3 8 3 8 7 3 100 12 12 23 Table 3 Recommended safety distance be...

Page 374: ...mpliance level for the test in acc with IEC61000 4 3 Interference immu nity tests IEC 60601 test level Compliance level Recommended safety dis tances Conducted HF dis turbance variables in accordance...

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Page 379: ...Hersteller Manufacturer D RR DENTAL SE H pfigheimer Str 17 74321 Bietigheim Bissingen Germany Fon 49 7142 705 0 www duerrdental com info duerrdental com...

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Page 381: ...LE WHITE VERSION 7 4 4 COMPOSAVE SETTING ON TUNABLE WHITE VERSION 8 4 5 MINIMUM INTENSITY SETTING ON SOLAR VERSION 8 4 6 AUTO ON SETTING 8 4 7 SWITCHING ON OFF THEIA 8 4 8 REMOTE CONTROL 8 4 9 SYNCRO...

Page 382: ...nd the competent authority of the Member State in which the user and or patient is established 1 SYMBOLS USED 1 1 SYMBOLS USED IN THIS MANUAL WARNING The paragraphs marked with this symbol contain ins...

Page 383: ...ce and is intended for illuminating the oral cavity and oral structures of patients in dentistry In the normal use the device is positioned distance of 700mm from the operative area the distance for w...

Page 384: ...DIGIT Fixed Arm 4 DIGIT Light Source Integrated Camera 5 DIGIT Command radiofrequency RF 6 DIGIT Cables 7 DIGIT Custom 1 8 9 DIGIT 5 U 0 Only Head No arms 0 Only Head No arms 0 Tunable White 0 Joystic...

Page 385: ...eters are memorized by the lamp and made available at every switching on Last light intensity setting light colour temperature Setting for Tunable White variant Warning Do not use the device if parts...

Page 386: ...or light changes according to the illuminance level according to the images below Light Intensity Minimum Light Intensity Medium Minimum Light Intensity Medium Maximum Light Intensity Maximum 4 3 CHAN...

Page 387: ...hen the on mode in set in on position the lamps turn on automatically without a specific command from the user when there is power supply 4 7 SWITCHING ON OFF THEIA The light on the fixed arm secondar...

Page 388: ...Light it is necessary to repeat the procedure from point 1 3 After the blue LED switches on the room light there are 60 seconds to confirm the Pairing by pressing the programming button placed on the...

Page 389: ...arter 1 2 must be well secured and safety screws intact The screws under carter 3 must be well secured Yearly Carter 3 Carter 2 Carter 1 Service Engineer Check the absence of any oxidation into joints...

Page 390: ...es Never use detergents containing surfactants or water repellents that depositing can leave streaks Slight streaking will not prejudice the quality of the light Products differing from those suggeste...

Page 391: ...0 60 Hz 32 V dc 10 Max Power 24 V ac 26 VA 32 V dc 14 VA 24 V ac 40 VA 32 V dc 28 VA Recommended fuses for installation not supplied in charge to installation 24 V ac T1 6AL 250V 32 V dc T1 25AL 250V...

Page 392: ...IONS The device in the original packaging can be transported and stored for a maximum period of 15 weeks if the following environmental conditions are met Environmental temperature from 20 C to 70 C R...

Page 393: ...EVA USER MANUAL EN Edition 1 0 April 2020 Pag 14 di 14...

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DKL CHAIRS D2-AVEO, Operating Instructions Manual, Page: 1 / 393

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