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DKL L2-S300, Operating Instructions Manual, Page: 303 / 327

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DKL L2-S300 Operating Instructions Manual Download Page 303

16 

9000-606-39/30  1709V004 

Troubleshooting

12  Transporting the unit

WARNING
Infection due to contaminated unit

 

i

Disinfect the unit before transport�

 

i

Close all media connections�

Wear protective equipment to avoid any 
risk of infection (e�g� liquid-tight protec-
tive gloves, protective goggles, face 
mask)�

 

i

Before disassembly, clean and disinfect the 
suction unit and the unit using a suitable disin-
fectant approved by Dürr Dental�

 

i

Disinfect a defective unit using a suitable sur-
face disinfection agent�

 

i

Seal all connections with sealing caps�

 

i

Pack the unit securely in preparation for trans-
port�

12.1 Close the CS 1

1

2

2

1

2

1

1  Dummy bushing
2  Ring clamp

11.1 Replacing the fuse

Prior to working on the device or in case 
of danger, disconnect it from the mains 
(e� g� pull the mains plug)�

Transformer

 

i

Unscrew and remove the safety cover�

 

i

Replace the fuse�

Fuse housing

 

i

Turn the fuse housing to open it�

 

i

Replace the fuse�

1

2

1  Fuse housing
2 Fuses

EN

Summary of Contents for L2-S300

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 Form no GEN L2S300 Rev 05 21 01 2022 Subject to change without notice L2 S300...

Page 2: ...uction System 43 Cleaning and Disinfection of the Surfaces 45 Cleaning and Disinfection of the Instrument Holders 48 Cleaning the Turbine Return Air Filter 48 Bottle Care System 49 Flushing Function w...

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: ...ruments only use coupling systems according to ISO 9168 For air powered instruments only use coupling systems with anti retraction stop for contaminated cooling water Observe the information provided...

Page 9: ...according to protection class IPX8 The motors of the treatment unit are designed for intermittent operation in accordance with the dental treatment method Driving motors for patient chair and backres...

Page 10: ...ets and 2 stop cocks The second outlet allows easy sampling of water for microbiological analysis Clean air and water pipes before installing the unit Chips and other foreign substances could be ushed...

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 Treatment chair lowest position 570 mm highest position 800 mm L2 S300 Version with short back rest L2 S300 Version with long back rest Dimensions in Millimetres...

Page 13: ...nt chair back rest 3 Treatment chair double jointed head rest 4 Treatment chair joystick 5 Treatment chair arm rest 6 Doctor s device 7 Tray 8 Cuspidor 9 Operating lamp LED light 10 Foot controller do...

Page 14: ...rbine 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 Depending o...

Page 15: ...treatments in the upper jaw region the patient s head is slightly overstretched backwards The double jointed headrest o ers stable support for the patient s head at the starting point of the neck musc...

Page 16: ...Stop abortion of programme run 2 Press brie y coolant 2 Press long chipblower 3 Programmes to activate instruments 4 Press brie y left right hand rotation micro motor 4 Press long dim operating lamp 5...

Page 17: ...ir activate programme run Display lock Bell Glass ller Bowl rinser 17 Touch Screen You can nd application lms at www youtube DKL Germany Playlist DKL CHAIRS L2 D2 SERIES DOCTOR S DEVICE WITH TOUCH SCR...

Page 18: ...tion red 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 us...

Page 19: ...19 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 20: ...Treatment chair moves to treatment position p2 Press p3 Treatment chair moves to treatment position p3 Brie y press lp Treatment chair moves to the rinsing position and after renewed pressing back to...

Page 21: ...has been reset now Once an instrument has been activated the treatment chair cannot be moved any more The treatment chair can optionally be equipped with arm rests The arm rest on the assistant s sid...

Page 22: ...een Operating the touchscreen with hard objects can scratch or damage the surface 1 2 Activating Deactivating the Treatment Unit T 6 3A H 250V The treatment unit is equipped with a power switch 1 on t...

Page 23: ...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 24: ...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 25: ...l substance can be damaged by frictional heat Make sure that thetreatment point is not overheated when you have switched o the coolant Adjusting the Coolant Spray on water Spray o Air only adjustment...

Page 26: ...Activate the work display mode 7 on the touchscreen Display speed intensity of the instrument while activated in bar structure Display speed intensity of the instrument while activated in Display of...

Page 27: ...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 28: ...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 29: ...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 30: ...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 31: ...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 32: ...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 33: ...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 34: ...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 35: ...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 36: ...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 37: ...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 38: ...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 devic...

Page 39: ...airstream from the patient to the suction system and not the other way round is maintained To reduce the risk of infection liquid tight gloves must be worn during maintenance work Control knob Slider...

Page 40: ...issued by D RR Dental depending on the equipment and design of the suction system Open the door of the cuspidor fountain by pulling the handle Depending on the equipment and design of the suction syst...

Page 41: ...41 Cleaning and Disinfection of the Suction Handpieces...

Page 42: ...42 Cleaning and Disinfection of the Suction Handpieces...

Page 43: ...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 44: ...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 45: ...ping 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...

Page 46: ...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 47: ...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 48: ...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 49: ...rn it clockwise into the bottle holder 3 Set the ip switch 1 on the bottle holder to on The water supply is ready for operation Empty the treatment water bottle at the end of a working day and re ll t...

Page 50: ...iene cover it is possible to ush all the instruments rapidly or intensively Put the hygiene cover into the cuspidor bowl Remove all the instruments from their holders and insert them into the hygiene...

Page 51: ...y Flushing Function with the Bottle Care System Flushing times can be adjusted by the customer service in the setup The standard ushing time is set to 120 seconds If the device is equipped with a bott...

Page 52: ...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 53: ...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 54: ...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 55: ...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 56: ...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 57: ...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 58: ...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 59: ...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 60: ...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 61: ...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 62: ...ing 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 op...

Page 63: ...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...

Page 64: ...nce 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 nomi...

Page 65: ...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 66: ...Instructions for use Electric motor EM 12 L Supply hose VE 10...

Page 67: ...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 68: ...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 69: ...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 70: ...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 71: ...on the supply hose Symbols Catalogue number Type B applied part not suitable for intracardiac application Serial number 6...

Page 72: ...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 73: ...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 74: ...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 75: ...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 76: ...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 77: ...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 78: ...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 79: ...3 Product description Motor EM 12 L Motor shealt LED Connection for instruments as per ISO 3964 O rings Seal 14...

Page 80: ...Supply hose VE 10 Connection sheat Connection quick release coupling 15...

Page 81: ...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 82: ...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 83: ...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 84: ...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 85: ...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 86: ...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 87: ...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 88: ...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 89: ...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 90: ...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 91: ...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 92: ...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 93: ...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 94: ...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 95: ...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 96: ...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 97: ...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 98: ...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 99: ...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 100: ...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 101: ...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 102: ...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 103: ...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 104: ...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 105: ...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 106: ...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 107: ...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 108: ...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 109: ...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 110: ......

Page 111: ...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 112: ...Instructions for use Handpiece PB 5 L PB 5 L S PB 5 L Q...

Page 113: ...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 114: ...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 115: ...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 116: ...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 117: ...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 118: ...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 119: ...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 120: ...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 121: ...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 122: ...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 123: ...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 124: ...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 125: ...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 126: ...15 3 Product description Thread Connection for supply hose Handpiece cap Optical fibre Optic outlet Nozzle cleaner...

Page 127: ...16 4 Operation Assembly Removal Push the medical device onto the supply hose Note the positioning w Remove the medical device...

Page 128: ...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 129: ...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 130: ...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 131: ...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 132: ...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 133: ...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 134: ...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 135: ...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 136: ...25 Hygiene and maintenance Manual cleaning Disassembling the medical device Unscrew the handpiece cap w Remove the optical fibre w...

Page 137: ...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 138: ...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 139: ...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 140: ...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 141: ...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 142: ...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 143: ...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 144: ...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 145: ...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 146: ...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 147: ...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 148: ...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 149: ...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 150: ...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 151: ...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 152: ...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 153: ...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 154: ...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 155: ...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 156: ...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 157: ......

Page 158: ...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 159: ...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 160: ...Instructions for Use Foot control S NW S N2 S N1...

Page 161: ...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 162: ...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 163: ...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 164: ...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 165: ...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 166: ...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 167: ...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 168: ...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 169: ...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 170: ...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 171: ...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 172: ...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 173: ...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 174: ...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 175: ...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 176: ...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 177: ...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 178: ...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 179: ...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 180: ...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 181: ...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 182: ...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 183: ...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 184: ...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 185: ...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 186: ...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 187: ...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 188: ...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 189: ...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 190: ...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 191: ...32 Manufacturer s declaration...

Page 192: ...33 Manufacturer s declaration...

Page 193: ...34 Manufacturer s declaration...

Page 194: ...35 Manufacturer s declaration...

Page 195: ...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 196: ...1 Minilight Installation and use manual...

Page 197: ...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 198: ...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 199: ...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 200: ...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 201: ...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 202: ...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 203: ...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 204: ...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 205: ...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 206: ...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 207: ...12 14 WIRING DIAGRAM 14 1 VERSION 6F 14 2 VERSION L...

Page 208: ...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 209: ...____ COMPANY ______________________________________________________________________________________________________ ____________________________________________________________________________________...

Page 210: ...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 211: ...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 212: ...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 213: ...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 214: ...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 215: ...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 216: ...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 217: ...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 218: ...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 219: ...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 220: ...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 221: ...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 222: ...EN 1801V002 7560100003L02 Installation and Operating Instructions Spittoon valve 3...

Page 223: ......

Page 224: ...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 225: ...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 226: ...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 227: ...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 228: ...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 229: ...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 230: ...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 231: ...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 232: ...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 233: ...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 234: ...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 235: ...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 236: ...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 237: ...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 238: ...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 239: ...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 240: ...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 241: ...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 242: ...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 243: ...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 244: ...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 245: ...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 249: ...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 250: ...EN 1712V002 7117100018L30 Installation and Operating Instructions CAS 1 Combi Separator...

Page 251: ......

Page 252: ...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 253: ...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 254: ...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 255: ...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 256: ...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 257: ...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 258: ...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 259: ...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 260: ...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 261: ...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 262: ...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 263: ...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 264: ...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 265: ...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 266: ...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 267: ...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 268: ...7117100018L30 1712V002 17 Installation 9 Service program EN...

Page 269: ...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 270: ...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 271: ...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 272: ...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 273: ...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 274: ...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 275: ...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 276: ...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 277: ...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 278: ...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 279: ...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 280: ...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 281: ...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 282: ...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 283: ...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 284: ......

Page 285: ...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 286: ...EN 1709V004 9000 606 39 30 Installation and Operating Instructions CS 1 Combi Sepamatic...

Page 287: ......

Page 288: ...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 289: ...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 290: ...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 291: ...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 292: ...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 293: ...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 294: ...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 295: ...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 296: ...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 297: ...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 298: ...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 299: ...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 300: ...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 301: ...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 302: ...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 303: ...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 304: ...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 305: ...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 306: ...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 307: ...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 308: ...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 313: ...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 315: ...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 316: ...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 317: ...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 318: ...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 319: ...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 320: ...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 321: ...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 322: ...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 323: ...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 324: ...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 325: ...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 326: ...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 327: ...EVA USER MANUAL EN Edition 1 0 April 2020 Pag 14 di 14...

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