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DKL D2-SOLO Operating Instructions Manual

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Operating Instructions
D2-SOLO
D2-SOLO-S
Manufacturer:
DKL CHAIRS GmbH
An der Ziegelei 3
D-37124 Rosdorf
Germany
+49 (0)551-50060
info@dkl.de
www.dkl.de
Form-Nr. GEN-D2SOLO
Rev. 06 / 01.04.2024
Subject to change without notice

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  • Page 1 Operating Instructions D2-SOLO Manufacturer: DKL CHAIRS GmbH An der Ziegelei 3 D-37124 Rosdorf Germany +49 (0)551-50060 info@dkl.de www.dkl.de D2-SOLO-S Form-Nr. GEN-D2SOLO Rev. 06 / 01.04.2024 Subject to change without notice...
  • Page 2 Contents Symbols in the Operating Instructions Symbols inside the Unit Introduction Electromagnetic Compatibility (EMC) Safety Notes – General Technical Specifi cations Media Requirements Dimensions in Millimetres Product Description Moving the Treatment Chair Putting the Treatment Unit into Operation Operating Lamp LED.light EVA Tray Cuspidor Suction System...
  • Page 3 Symbols in the Operating Instructions WARNING! CAUTION! General explanations, (risk of injury) (to prevent without risk to damage occurring) persons or objects Sterilisable up to the Thermodisinfectable Call customer service! specifi ed temperature Symbols on the unit Consult instructions for ON / OFF Do not dispose of with use or consult electronic...
  • Page 4 Symbols inside the Unit Functional Earth conductor connection - Connection point for earth Protective earth neutral conductor Symbols on the packaging Air humidity, limitation Atmospheric pressure limitation Permissible temperature range Transport upright; top Protect from moisture! Do not stack! Fragile...
  • Page 5 Qualifi cation of the user The DKL treatment unit may only be used after medically, professionally and practically trained personnel have been instructed. The development and design of the treatment unit were geared towards the target group of dentists, dental hygienists, qualifi...
  • Page 6 EMC instructions. DKL guarantees that the dental unit complies with the EMC guidelines only if original DKL accessories and spare parts are used. The use of accessories and spare parts not approved by DKL may lead to an increased emission of electromagnetic interference or to a reduced resistance to electromagnetic interference.
  • Page 7 > Make sure that in the event of a device or instrument failure, the treatment can be completed safely. > Use only original DKL fuses. > Never touch the patient and the electrical connection at the treatment unit at the same time.
  • Page 8 Ordinary device (without protection against water ingress). Permanently connected device. In order to avoid the risk of electric shock, this device may only be connected to a power supply with an earth conductor. Weight D2-SOLO max. 165 kg D2-SOLO-S max. 210 kg...
  • Page 9 Media Requirements Media water Water hardness 1.5 to 2.14 mmol/l = 8,4-12 dH ph-value 6,5 to 8,5 Water fi ltration on site ≤ 100 µm Water infl ow Pipe 10x1mm, angle valve outlet 3/8“ Water connection above fl oor min. 40 mm, max. 60 mm Water inlet pressure 2.0 to max.
  • Page 10 Control line to suction device 5x1.5 mm 2 Water: pipe min. 10x1 mm, angle valve outlet 3/8“ (2 outlets with 2 stopcocks) With the D2-SOLO the connections 1, 2, 3, 5 and the control line to the suction device are not needed.
  • Page 11 Dimensions in Millimetres D2-SOLO-S D2-SOLO Treatment chair: lowest position 395 mm highest position 730 mm...
  • Page 12 Product Description Identifi cation label D2-SOLO D2-SOLO-S Treatment chair, seat Treatment chair, back rest Treatment chair, double-jointed headrest Treatment chair, joystick Treatment chair, arm rest Tray Operating Lamp LED.light EVA Cuspidor...
  • Page 13 Moving the Treatment Chair Joystick at the chair base Move the joystick downwards > Treatment chair moves downwards. Move the joystick upwards > Treatment chair moves upwards. Move the joystick to the left > Back rest tilts backwards. Move the joystick to the right >...
  • Page 14 The treatment chair then moves the seat and the back rest into the lowest position. The motion sequence has been reset now. You can fi nd an application fi lm at www.youtube DKL Germany. Video: DKL CHAIRS D2 SERIES FUNKTIONEN UPHOLSTERY POSITIONS LINK: https://youtu.be/o307-rWGp5A...
  • Page 15 Putting the Treatment Unit into Operation > Before putting the device into initial operation and after downtimes (weekends, (public) holidays etc.), fl ush the water lines intensively. > Press the cup fi ll button several times before starting work. Activating / Deactivating the Treatment Unit T 6,3A H 250V The treatment unit is equipped with a power switch on the chair base.
  • Page 16 Operating Lamp LED.light EVA For the intended use, please observe the operating instructions issued by FARO: USER MANUAL EVA Indicator light Handles When swivelling and moving the operating lamp, always make sure Mirror that no objects or persons are in the swivelling range of the arm system.
  • Page 17 On the back of the cover there is a mirror. At- tach the mirror to the plastic cover. You can fi nd an application fi lm at www.youtube DKL Germany. Video: DKL CHAIRS L2-D2 SERIES FUNCTIONS LED.LIGHT OPERATING LAMP EVA LINK: https://youtu.be/vaKW9RdjtLM...
  • Page 18 Cleaning and disinfection of the Operating Lamp LED.light EVA Pull the protective cap towards you to remove it for cleaning. Cleaning and care The refl ectors must be cleaned with cotton wool and ethyl alcohol. Do not use detergents that contain surfac- tants or water-repellent substances (staining).
  • Page 19 Move the tray into a horizontal position. Secure the adjusting screw (1) for the inclina- tion with thread locking fl uid (blue). You can fi nd an application fi lm at www.youtube DKL Germany. Video: DKL CHAIRS L2-D2-RANGE TRAY SETTINGS LINK:...
  • Page 20 After switching on the treatment unit, the bowl rinsing process starts automatically for the saved duration and rinses the bowl. You can fi nd an application fi lm at www.youtube DKL Germany. Video: DKL CHAIRS L2-D2 SERIES FUNCTIONS CUSPIDOR CUP FILLER & BOWL RINSER LINK: https://youtu.be/SsFSKDpJI_I...
  • Page 21 Suction System For the intended use, please observe the operating instructions issued by DÜRR Dental: > Cuspidor valve, Version 3 > CAS 1 operating instructions issued by DÜRR Dental > CS 1 operating instructions issued by DÜRR Dental, depending on the equipment and design of the suction system. Open the door of the cuspidor fountain by pulling the handle.
  • Page 22 Cleaning and Disinfection of the Surfaces Hygiene and Care of the Stainless-Steel Surfaces The regular cleaning of stainless-steel surfaces is recommended for hygienic as well as aesthetic reasons and serves to remove grease stains or fi nger marks. These can be easily removed with commercially available chlorine- and acid-free stainless-steel cleaners.
  • Page 23 Cleaning and Disinfection of the Surfaces DentaClean: cleaning agent for imitation leather and plastic surfaces Properties DentaClean gently and easily cleans soiled imitation leather and plastic surfaces. Test on a hidden area fi rst. We recommend cleaning the chair upholstery at the end of every treatment day.
  • Page 24 6 wipe dispenser boxes with 100 wipes each in a disposable sealing bag Cleaning brush set, 4 pieces Article number RB4 Cleaning sponge set, 8 pieces Article number RS8 You can fi nd an application fi lm at www.youtube DKL Germany. Video: MEDICAL UPHOLSTERY – CLEANING DISINFECTION PROTECTION LINK: https://youtu.be/kM2E0kM6J1M...
  • Page 25 (e.g. faulty electrical insulation). These checks are carried out by an authorised technician of your specialist dealer or a DKL CHAIRS technician. The work steps to be performed are specifi ed in the document “Safety Inspections“. The measured values have to be documented.
  • Page 26 DKL! Any warranty claims must be fi led with the supplier or an authorised DKL service partner and the sales slip must be enclosed. Any performance of this warranty does not extend the warranty period.
  • Page 27 EMC - Manufacturer‘s Declaration for the Model D2-SOLO • WARNING: The use of accessories that do not conform to the manufacturer‘s specifi cations may result in higher interference levels and/or lower interference immunity. • Operate the equipment in a location as far away as possible from equipment that emits electrical and magnetic disturbances.
  • Page 28 IEC STANDARD 60601-1-2:2014, 4 Edition This device is approved for use in a specifi c electromagnetic environment. The customer or user of the device must ensure that it is used in an electromagnetic environment in accordance with the description given below. Emission Measurement Agreement Guidelines Regarding the Electromagnetic...
  • Page 29 Specifi cations for Enclosure Port Immunity Electromagnetic Environmental Immunity Test Test condition IEC 60601 level of Recommendation conformity 10 V/m 10 V/m The quality of the main power supply should Radiated electromagnetic 80 MHz – 2,7 GHz 80 MHz – 2,7 GHz correspond to the one for a professional fi...
  • Page 30 30 cm to the ME-equipment or ME-system, including those cables specifi ed by the manufacturer. Otherwise, a power limitation of the device could be caused. Manufacturer: DKL CHAIRS GmbH, An der Ziegelei 3, D-37124 Rosdorf, Germany Tel. +49 (0)551-50060 info@dkl.de...
  • Page 31 Spittoon valve 3 Installation and operating instructions 7560100003L02...
  • Page 33 Contents Contents Information about electrical con- nections ....Installation ..... . . Important information Installation overview .
  • Page 34 Important information The signal word differentiates between four levels Important information of danger: DANGER Immediate danger of severe injury or death About this document WARNING Possible danger of severe injury or death These installation and operating instructions rep- CAUTION resent part of the unit. Risk of minor injuries If the instructions and information in these NOTICE...
  • Page 35 Important information Copyright information Safety All circuits, processes, names, software pro- Dürr Dental has designed and constructed this grams and units mentioned in this document are unit so that when used properly and for the inten- protected by copyright. ded purpose it does not pose any danger to The Installation and Operating Instructions must people or property.
  • Page 36 Important information General safety information Only use original parts Always comply with the specifications of all Only use accessories and optional items that guidelines, laws, and other rules and regula- have been recommended or specifically tions applicable at the site of operation for the approved by Dürr Dental.
  • Page 37 Product description Product description Overview Spittoon valve Scope of delivery The following items are included in the scope of delivery (possible variations due to country-spe- cific requirements and/or import regulations): Spittoon valve 3 ....7560700xxx Spittoon valve Optional items The following optional items can be used with the...

  • Page 38: Table Of Contents

    Product description Technical data Electrical data Safety low voltage 24 AC/DC Frequency 50/60 Nominal current Rated power Type of protection IP 21 Electrical data, suction unit relay Switching voltage min. 0.03 DC max. 30 DC Switching current min. max. Connections Supply and waste water connection DürrConnect Collection vessel vent connection...
  • Page 39 Product description Ambient conditions during operation Air pressure 700 - 1060 Electromagnetic compatibility (EMC) Interference emission measurements High-frequency emissions in accordance with CISPR 11 Group 1 Class B Interference voltage at the power supply connection Compliant CISPR 11:2009+A1:2010 Electromagnetic interference radiation Compliant CISPR 11:2009+A1:2010 Emission of harmonics...
  • Page 40 Product description Electromagnetic compatibility (EMC) Interference immunity measurements SIP/SOP Immunity to electrical fast transients/bursts – I/O, SIP/SOP ports IEC 61000-4-4:2012 Compliant ± 1 kV 100 kHz repetition rate Immunity to impulse voltages, conductor to earth IEC 61000-4-5:2005 ± 2 kV Immunity to conducted disturbances, induced by radio- frequency fields –...
  • Page 41 Product description Immunity to interference table, near fields of wireless HF communication devices Radio service Frequency band Test level LTE band 13, 17 704 - 787 GSM 800/900 TETRA 800 iDEN 820 800 - 960 CDMA 850 LTE band 5 GSM 1800 CDMA 1900 GSM 1900...
  • Page 42 Product description Type plate The type plates are located on the side of the fluid collector. Type plate Evaluation of conformity This device has been subjected to conformity acceptance testing in accordance with the cur- rent relevant European Union guidelines. This equipment conforms to all relevant requirements.
  • Page 43 Product description Air extraction seal Operation Vent Protective strainer Exhaust air damper Solenoid valve Compressed air connection Shut-off valve Float sensor Magnet in float sensor Float sensor detection Magnet in cleaning button Cleaning button detection sensor Operating function The waste water from the spittoon flows through the coarse filter into the collector vessel.
  • Page 44 Assembly Assembly Requirements Setup options Installation in treatment units in dental surger- ies or dental clinics. Preparing for the installation Prior to installation of the spittoon valve the fol- lowing media should be checked and if neces- sary adjusted; refer also to "4 Technical data": Vacuum of the suction system Compressed air supply Water amount from the spittoon...
  • Page 45 Assembly Installation Installation overview Spittoon valve Station selection valve Pressure reducer Suction pipe connection Rinsing unit Auxiliary air nozzle Hose manifold Switch control panel Spittoon outlet 7560100003L02 2102V003...
  • Page 46 Assembly Route the compressed air hose to the spittoon Installation of the spittoon valve, cut it off straight and insert it. valve The cleaning function can be activated via the yellow button. For this reason the spittoon valve should be positioned in an easily accessible location.
  • Page 47 Assembly Secure the connection lines with cable ties to the housing. X5 X1 24 V Cleaning button for switch control panel Solenoid valve Control line for suction unit Power supply Suction unit relay Float sensor detection Cleaning button detection sensor 7560100003L02 2102V003...
  • Page 48 Assembly Circuit diagram 24 V AC/DC Hose manifold Station selection valve Rinsing unit Spittoon valve Cleaning button for switch control panel Solenoid valve Control line for suction unit Power supply Suction unit relay Float sensor detection Cleaning button detection sensor Suction machine relay in the treatment unit 7560100003L02 2102V003...
  • Page 49 Assembly Commissioning Turn on the unit power switch or the main sur- gery switch. Carry out a function check of the system. Check all connections for leak tightness. Carry out an electrical safety check in accord- ance with applicable regulations (e.g. regula- tions concerning set up, operation and applica- tion of medical devices) and record the results as appropriate, e.g.
  • Page 50 Usage Suction system Usage After every treatment Aspirate a glass of cold water through the large Disinfection and cleaning and the small suction hoses. Do this even if only the small suction hose was actually used during treatment. NOTICE Device malfunctions or damage due to use of incorrect media Guarantee claims may become invalid as a result.
  • Page 51 Usage 10 Maintenance All maintenance work must be performed by a qualified expert or by one of our Service Techni- cians. WARNING Infection due to contaminated unit Clean and disinfect the suction before working on the unit. Wear protective equipment when working (e. g. impermeable gloves, protective goggles and mouth and nose protection).
  • Page 52 Troubleshooting Troubleshooting 11 Tips for operators and service technicians Any repairs exceeding routine maintenance may only be carried out by qualified personnel or our service. WARNING Infection due to contaminated unit Clean and disinfect the suction before working on the unit. Wear protective equipment when working (e.
  • Page 53 Troubleshooting 12 Transporting the unit WARNING Infection due to contaminated unit Disinfect the unit before transport. Close all media connections. Wear protective equipment to avoid any risk of infection (e.g. liquid-tight protective gloves, protective goggles, face mask). Before disassembly, clean and disinfect the suction unit and the unit using a suitable disin- fectant approved by Dürr Dental.
  • Page 58 Hersteller / Manufacturer: DÜRR DENTAL SE Höpfigheimer Str. 17 74321 Bietigheim-Bissingen Germany Fon: +49 7142 705-0 www.duerrdental.com info@duerrdental.com...
  • Page 59 CAS 1 Combi-Separator Installation and operating instructions 7117100018L30...
  • Page 61 Contents Contents Amalgam separation ..Sediment level measurement ..Operating problems ... Important information Service key ....About this document .
  • Page 62 Contents 11.4 Amalgam collector vessel not in position ....11.5 Motor fault ....23 12 Disinfection and cleaning .
  • Page 63 Important information The signal word differentiates between four levels Important information of danger: – DANGER Immediate danger of severe injury or death About this document – WARNING Possible danger of severe injury or death These installation and operating instructions rep- resent part of the unit.
  • Page 64 Important information Safety Order number Dürr Dental has designed and constructed this unit so that when used properly and for the inten- Serial number ded purpose it does not pose any danger to people or property. Medical device Despite this, the following residual risks can remain: Health Industry Bar Code (HIBC) –...
  • Page 65 Important information – Use for separation of dust, sludge, plaster or Installation and repairs similar. Installation, readjustments, alterations, – Use in conjunction with flammable or explosive upgrades and repairs must be carried out by mixtures. Dürr Dental or by qualified personnel specifi- cally approved and authorized by Dürr Dental.
  • Page 66 Important information Uncontaminated parts (e.g. electronics, plastic NOTICE and metal parts etc.) should be disposed of in Erroneous operation mode due to use accordance with the local waste disposal regu- lations. immediately adjacent to other devices or with other stacked devices If you have any questions about the correct disposal of parts, please contact your dental Do not stack the unit together with...
  • Page 67 Product description Station selection valve ... 7560-500-60 Product description Station selection valve for CAS 1 / CS 1 ......7560-500-80 Vario rinsing unit .

  • Page 68: Type Of Protection Ip

    Product description Technical data CAS 1 Combi-Separator Electrical data – centrifuge motor Rated voltage 24 AC Frequency 50 / 60 Rated power Current consumption in stand-by Signal input from hose manifold 24 AC 50/60 Signal output 24 DC Media Air flow volume l/min Flow rate high...

  • Page 69: Ambient Conditions During Operation Temperature

    Product description Ambient conditions during operation Temperature °C +10 to +40 Relative humidity < 70 Classification Medical Device Class Electromagnetic compatibility (EMC) Interference emission measurements High-frequency emissions in accordance with CISPR 11 Group 1 Class B Interference voltage at the power supply connection Compliant CISPR 11:2009+A1:2010 Electromagnetic interference radiation...
  • Page 70 Product description Electromagnetic compatibility (EMC) Interference immunity measurements Immunity to voltage dips, short interruptions and voltage variations Compliant IEC 61000-4-11:2004 Immunity to interference levels, near fields of wireless HF communication devices Radio service Frequency band Test level TETRA 400 380 - 390 GMRS 460 430 - 470 FRS 460...
  • Page 71 Product description Electromagnetic compatibility (EMC) Interference immunity measurements on the supply input Immunity to conducted disturbances, induced by radio- frequency fields – AC mains voltage IEC 61000-4-6:2013 0.15–80 MHz Compliant ISM frequency bands 0.15–80 MHz 80% AM at 1 kHz Immunity to voltage dips, short interruptions and voltage variations Compliant...
  • Page 72 Product description Type plate The type plates are located on the cover of the motor. Type plate Evaluation of conformity This device has been subjected to conformity acceptance testing in accordance with the cur- rent relevant European Union guidelines. This equipment conforms to all relevant requirements.
  • Page 73 Product description Operation CAS 1 Fluid intake Vacuum, to suction unit Aspiration input Fluid output Motor Separation Separation rotor Centrifuge Light barriers (3x) Sensor enclosure Cone pump Amalgam collector vessel Float sensor Fluids Amalgam particles 7117100018L30 2011V003...
  • Page 74 Product description An external station selection valve connects the Operation CAS 1 with the suction unit via the vacuum con- CAS 1 Combi-Separator nection (2). The task of the CAS 1 combi-separator is to pro- Spittoon connections vide continuous separation of secretions and air as well as the amalgam separation of all the The waste water from the spittoon flows through waste water from the treatment unit.
  • Page 75 Product description off brakes the motor, as a result of which the ring of water, which continues to rotate due to inertia, rinses the separated particles out of the centri- fuge (8) downwards into the collector vessel. The separated amalgam particles form a sedi- ment in the replaceable collector vessel.
  • Page 76 Assembly Lay the hose installation of the drains to or Assembly from the unit at a sufficient incline. If incorrectly laid, the hoses can become blocked with sedimentation. Requirements Installation/setup room Information about electrical The room chosen for set up must fulfil the follow- connections ing requirements: Ensure that electrical connections to the mains...
  • Page 77 Assembly Installation Installation type Line layout (minimum requirements) Prior to working on the unit or in case of Flexible – PVC data cable with danger, disconnect it from the mains. shielded cable sheath- ing, as used for tele- Combining devices safely communications and IT processing systems Take care when connecting units together or to...
  • Page 78 Assembly device is running. Vibrations may occur if the unit is not positioned vertically. A minimum distance of 3 mm must be maintained to the surround- ings. Hose manifold Spittoon Outlet Suction unit Station selection valve In various types, the station selection valve is Spittoon connections directly mounted on the CAS 1.
  • Page 79 Assembly Rinsing unit Connect the rinsing unit using a 2-core wire with connector to the X3 connection of the control. At the connection for the rinsing unit, a suction unit relay, for example, can be 230V 24V connected if there is no isolation present between the suction unit signal and sta- tion selection valve in the treatment unit.
  • Page 80 Assembly Commissioning In many countries technical medical prod- ucts and electrical devices are subject to regular checks at set intervals. The owner must be instructed accordingly. Turn on the unit power switch or the main sur- gery switch. Carry out an electrical safety check in accord- ance with applicable local regulations (e.g.
  • Page 81 Assembly Service program 7117100018L30 2011V003...
  • Page 82 Assembly Every time the service key is pressed, the sedi- 10 Description of the service ment level is checked. If a test collector vessel is used for this, the different levels can be scanned program and made visible on the display panel. While changing the collectors (collector vessel - Wear protective equipment to avoid any risk of infection (e.g.

  • Page 83: Amalgam Collector Vessel Not In Position

    Usage 11.3 Amalgam collector vessel is Usage 100% full Yellow LED is on 11 Display/handling Red display flashes Audible signal melody sounds – At a fill level of 100% the signal melody can no longer be switched off by pressing the reset button.

  • Page 84: Disinfection And Cleaning

    Usage 12 Disinfection and cleaning If, after pressing the reset button repeat- edly, the fault report reappears again each time, this indicates a technical NOTICE defect – inform your Service Technician. Device malfunctions or damage due to use of incorrect media Guarantee claims may become invalid as a result.

  • Page 85: Once Or Twice A Week Before The Midday Break

    Usage The following are required for disinfection/clean- 13 Replace the amalgam col- ing: lector vessel Non-foaming disinfectant/cleaning agent that is compatible with the materials. NOTICE Unit care system, e.g. OroCup Risk of contamination if the amalgam To pre-clean, suck up 2 litres of water with the collector vessel is reused since the care system.
  • Page 86 Usage Arrange to have filled amalgam collector ves- sels collected from the surgery by a local waste management company. New amalgam collector vessels should be ordered from your specialist dental equipment retailer. Document the replacement and legally compli- ant disposal of the filled waste amalgam collec- tor vessel in the Operating Handbook.

  • Page 87: Maintenance

    Usage 14 Maintenance All maintenance work must be performed by a qualified expert or by one of our Service Techni- cians. WARNING Infection due to contaminated unit Clean and disinfect the suction before working on the unit. Wear protective equipment when working (e. g. impermeable gloves, protective goggles and mouth and nose protection).

  • Page 88: Tests

    Usage Once the device has switched off, remove 14.1 Tests the test vessel and measure the remaining amount of water. WARNING The unit is working correctly if: – there is at minimum content of 140 ml in the Infection due to contaminated unit test vessel.

  • Page 89: Troubleshooting

    Troubleshooting Troubleshooting 15 Tips for operators and service technicians Any repairs exceeding routine maintenance may only be carried out by qualified personnel or our service. WARNING Infection due to contaminated unit Clean and disinfect the suction before working on the unit. Wear protective equipment when working (e.
  • Page 90 Troubleshooting Error Possible cause Remedy Yellow display is on Amalgam collecting container is Change the amalgam collect- GREEN LED illuminates 95% full ing container. Audible signal melody sounds Float sensor dirty or blocked If this display occurs repeat- edly even when the collecting container is empty, check that the float sensor can move freely.
  • Page 91 Troubleshooting Error Possible cause Remedy Device running continuously Float sensor blocked in water Clean the float. * start position Free up the float sensor link- age so that it can move freely. Start signal at the signal input Check the control voltage. * (X2) Waster water line/siphon trap Clean the waste water line/...

  • Page 92: Transporting The Unit

    Troubleshooting 16 Transporting the unit WARNING Infection due to contaminated unit Disinfect the unit before transport. Close all media connections. Wear protective equipment to avoid any risk of infection (e.g. liquid-tight protective gloves, protective goggles, face mask). Before disassembly, clean and disinfect the suction unit and the unit using a suitable disin- fectant approved by Dürr Dental.

  • Page 93: Appendix

    Appendix Appendix 17 Handover record This document confirms that a qualified handover of the medical device has taken place and that appropriate instructions have been provided for it. This must be carried out by a qualified adviser for the medical device, who will instruct you in the proper handling and operation of the medical device. Product name Order number (REF) Serial number (SN)
  • Page 98 Hersteller/Manufacturer: DÜRR DENTAL SE Höpfigheimer Str. 17 74321 Bietigheim-Bissingen Germany Fon: +49 7142 705-0 www.duerrdental.com info@duerrdental.com...
  • Page 99 CS 1 Combi-Sepamatic 24 V AC Installation and operating instructions 9000-606-39/30...
  • Page 101 Contents Contents Hose materials ....Installation and routeing of hoses and pipes ....Important information Information about electrical con- About this document .

  • Page 102: Important Information

    Important information The signal word differentiates between four levels Important information of danger: – DANGER Immediate danger of severe injury or death About this document – WARNING Possible danger of severe injury or death These installation and operating instructions rep- –...

  • Page 103: Copyright Information

    Important information Copyright information Safety All circuits, processes, names, software pro- Dürr Dental has designed and constructed this grams and units mentioned in this document are unit so that when used properly and for the inten- protected by copyright. ded purpose it does not pose any danger to The Installation and Operating Instructions must people or property.

  • Page 104: General Safety Information

    Important information – Use for separation of dust, sludge, plaster or Specialist personnel similar. Operation – Use in conjunction with flammable or explosive Unit operating personnel must ensure safe and mixtures. correct handling based on their training and – Installation in a manner that does not comply knowledge.

  • Page 105: Only Use Original Parts

    Important information 2.10 Transport NOTICE The original packaging provides optimum protec- Negative effects on the EMC due to tion for the unit during transport. non-authorised accessories If required, original packaging for the unit can be Use only Dürr Dental parts or accesso- ordered from Dürr Dental.

  • Page 106: Product Description

    Product description Optional items Product description The following optional items can be used with the device: Various installation sets are available on request Overview Safety transformer 24 V, 100 VA . . . 9000-150-46 Station selection valve for CAS 1 / CS 1 .

  • Page 107: Technical Data

    Product description Technical data Electrical data – centrifuge motor 7117-100-7x 7117-100-8x Rated voltage 24 AC Frequency 50 / 60 Rated power Nominal current in standby Signal input from the hose manifold 24 AC 50/60 Signal output 24 DC Media Fluid volume min.
  • Page 108 Product description Electromagnetic compatibility (EMC) Interference emission measurements High-frequency emissions in accordance with CISPR 11 Group 1 Class B Interference voltage at the power supply connection Compliant CISPR 11:2009+A1:2010 Electromagnetic interference radiation Compliant CISPR 11:2009+A1:2010 Emission of harmonics IEC 61000-3-2:2005+A1:2008+A2:2009 Voltage changes, voltage fluctuations and flicker emis- sions IEC 61000-3-3:2013...
  • Page 109 Product description Electromagnetic compatibility (EMC) Interference immunity measurements on the supply input Immunity to fast electrical transients/bursts – AC mains voltage IEC 61000-4-4:2012 Compliant ± 2 kV 100 kHz repetition rate Immunity to surges, line-to-line IEC 61000-4-5:2005 Compliant ± 0.5 kV, ± 1 kV Immunity to conducted disturbances, induced by radio- frequency fields –...
  • Page 110 Product description Immunity to interference table, near fields of wireless HF communication devices Radio service Frequency band Test level GSM 800/900 TETRA 800 iDEN 820 800 - 960 CDMA 850 LTE band 5 GSM 1800 CDMA 1900 GSM 1900 1700 - 1990 DECT LTE band 1, 3, 4, 25 UMTS...

  • Page 111: Type Plate

    Product description Type plate The type plates are on the motor cover and on the motor flange. Type plate Evaluation of conformity This device has been subjected to conformity acceptance testing in accordance with the cur- rent relevant European Union guidelines. This equipment conforms to all relevant requirements.

  • Page 112: Operation

    Product description Operation Motor Vacuum, to suction unit Separation Aspiration input Pump wheel Separation rotor Fluid output Waste valve Relief valve Separation Every time the suction hose is taken out of the hose manifold, the CS 1 Combi-Sepamatic and the suc- tion unit are started.

  • Page 113: Assembly 6 Requirements

    Assembly Install an all-pole disconnect switch with a con- Assembly tact opening width of at least 3 mm in the elec- trical connection to the mains power supply. It must be possible to secure the disconnect Requirements switch so that it cannot be inadvertently switched back on again.

  • Page 114: Installation

    Assembly Inlet and outlet hoses Installation Connect and attach the inlet and outlet hoses with DürrConnect connectors to the relevant WARNING connections on the unit. Route the hoses at an Infection due to contaminated unit incline. Clean and disinfect the suction before Recommended diameter of the connection working on the unit.

  • Page 115: Power Supply

    Assembly Power supply Electrical connections – Safety transformer order number: 9000 150 46 – Safety transformer 24 V AC with an isolator consisting of two means of patient protection (MOPP) between the mains circuit and secon- dary circuit, min. 100 VA, secondary fuse T 4 AH (or IEC 60127 2/V T 4 AH, 250 V) Electrical connections, con- troller...

  • Page 116: Commissioning

    Assembly Commissioning In many countries technical medical prod- ucts and electrical devices are subject to regular checks at set intervals. The owner must be instructed accordingly. Turn on the unit power switch or the main sur- gery switch. Carry out an electrical safety check in accord- ance with applicable local regulations (e.g.

  • Page 117: Usage

    Usage The following are required for disinfection/clean- Usage ing: Non-foaming disinfectant/cleaning agent that is compatible with the materials. Disinfection and cleaning Unit care system, e.g. OroCup To pre-clean, suck up 2 litres of water with the NOTICE care system. Aspirate the disinfection/cleaning agent with Device malfunctions or damage due the care system.

  • Page 118: Maintenance

    Usage 10 Maintenance All maintenance work must be performed by a qualified expert or by one of our Service Techni- cians. WARNING Infection due to contaminated unit Clean and disinfect the suction before working on the unit. Wear protective equipment when working (e. g. impermeable gloves, protective goggles and mouth and nose protection).

  • Page 119: Troubleshooting

    Troubleshooting Troubleshooting 11 Tips for operators and service technicians Any repairs exceeding routine maintenance may only be carried out by qualified personnel or our service. WARNING Infection due to contaminated unit Clean and disinfect the suction before working on the unit. Wear protective equipment when working (e.

  • Page 120: Replacing The Fuse

    Troubleshooting 12 Transporting the unit 11.1 Replacing the fuse WARNING Prior to working on the unit or in case of danger, disconnect it from the mains. Infection due to contaminated unit Disinfect the unit before transport. Transformer Close all media connections. Unscrew and remove the safety cover.

  • Page 121: Appendix

    Appendix Appendix 13 Handover record This document confirms that a qualified handover of the medical device has taken place and that appropriate instructions have been provided for it. This must be carried out by a qualified adviser for the medical device, who will instruct you in the proper handling and operation of the medical device. Product name Order number (REF) Serial number (SN)
  • Page 122 Appendix 9000-606-39/30 2103V007...
  • Page 126 Hersteller / Manufacturer: DÜRR DENTAL SE Höpfigheimer Str. 17 74321 Bietigheim-Bissingen Germany Fon: +49 7142 705-0 www.duerrdental.com info@duerrdental.com...
  • Page 128 USER MANUAL - EN TABLE OF CONTENTS SYMBOLS USED ..................................................3 SYMBOLS USED IN THIS MANUAL ........................................3 SYMBOLS USED IN THE LABELLING AND ON THE PACKAGING ..........................3 INTENDED USE..................................................4 INTENDED USER ............................................... 4 2.1.1 Professional qualification:..........................................4 2.1.2 Minimum skills ..............................................4 2.1.3 Experience .................................................

  • Page 129: Symbols Used

    USER MANUAL - EN Dear Customer, FARO hopes you enjoy your work with the new high quality light. For safe work and to take full advantage of the performance of the product, read carefully this manual before using the device. In particular, follow all the warnings and the notes described into the Safety Recommendations included in the Packaging.

  • Page 130: Intended Use

    USER MANUAL - EN Symbol Description Serial Number Can be sterilized with heat at 134°C Use the device at a temperature between 10°C and 40°C Use the device at pressure between 80 kPa and 106 kPa Use the device at relative humidity between 30 RH and 75RH Symbol to adjust light intensity Symbol to switch on/off the light Symbol to switch on/off the light on the rear arm (Alya with Theia Tech)

  • Page 131: Description Of The Product

    USER MANUAL - EN DESCRIPTION OF THE PRODUCT Picture 1 –Dental Light – Unit Mount Picture 2 –Dental Light – Ceiling Mount The device is available in two main product variants: EVA with light source at 5000 K with “Sunlight” Spectrum EVA with Tunable White light source (4000 K, 5000 K, 5700 K, Composave setting (2700 K)) selectable by the operator.

  • Page 132: Description Of Common User's Interface

    USER MANUAL - EN DESCRIPTION OF COMMON USER’S INTERFACE Knob of the handle Joystick Indicator Strip Button for pairing and Tk change Sensor (alternative to Joystick) Sterilizable Handle Button for Theia Tech INSTRUCTION FOR USE The device must be cleaned before use (see Device Cleaning paragraph). Caution Do not use the device in flammable or explosive environments Simultaneous use of the light with electro-surgical devices can cause malfunctioning (flickering, no command, etc)

  • Page 133: Changing Color Temperature On Tunable White Version

    USER MANUAL - EN Sensor - Increase and decrease light intensity Bring the hand towards the sensor up to 2 cm and keep this distance until the desired light intensity is reached Acoustic signal: 1 beep at command Maximum intensity reached: 2 beeps Minimum intensity reached: 1 beep in sensor version the light intensity changes continuously decreasing until minimum and...

  • Page 134: Composave Setting On Tunable White Version

    USER MANUAL - EN COMPOSAVE SETTING ON TUNABLE WHITE VERSION Composave setting allow the user to work with restorative material avoiding their polymerization. Select the composave setting as described below: Joystick version option 1 Joystick version option 2 Visual information At the command selection of compo save a wigwag beep will be heard.

  • Page 135: Syncro Mode With Faro Room Light

    USER MANUAL - EN SYNCRO MODE WITH FARO ROOM LIGHT When present, the device can be connected by Radio Frequency (RF) connection to the Faro Room Light to create a synchronized lighting system. The procedure to create this connection is called “pairing”. If more than one Room Lights are installed in the cabinet, take care that the other Room Lights are turned off or are turned on for more than 60 seconds.

  • Page 136: Preventive Maintenance And Routine Checks

    USER MANUAL - EN PREVENTIVE MAINTENANCE AND ROUTINE CHECKS Only Service Engineer are allowed to perform corrective Maintenance and replacement of any part of the device, according to Manufacturer’s Service Manual. Checks Frequency Procedure Responsible No plays or space gaps between the Yearly Service junction points (points 1, 2, 3, 4)

  • Page 137: Cleaning And Disinfection

    USER MANUAL - EN CLEANING AND DISINFECTION Warning against danger of wear and corrosion and falling suspended mass For all metal or plastic parts it is strictly forbidden to use substances that are abrasive, corrosive, acids, substances containing chlorine or chloride ions, phosphorous or phosphorous ions, detergents with Trilene base, petrol, white spirit, chlorine or similar.

  • Page 138: Troubleshooting

    USER MANUAL - EN TROUBLESHOOTING ERROR LIST Error Description Indicator Strip Acoustic indication First sector blinking. Open Led channel 1 Colour set-up: RED 3 short beeps repeated 3 times First and second sectors blinking OPL Open Led channel 2 Colour set-up: RED High temperature on the Led group All sectors blinking together.

  • Page 139: Storage And Transportation: Environmental Conditions

    USER MANUAL - EN (*) Typical optical values subjected to tolerances Measurement performed at 700 mm distance. Contact Faro for the correct procedure for the measurement. STORAGE AND TRANSPORTATION: ENVIRONMENTAL CONDITIONS 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 Relative humidity from 10% to 90% Atmospheric pressure from 50 kPa to 106 kPa...
  • Page 140 USER MANUAL - EN Edition 1.0 April 2020 Pag. 14 di 14...

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