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DKL CHAIRS D2-SAE Operating Instructions Manual

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Operating Instructions
D2-SAE
Form no. GEN-D2SAE
Rev. 03 / 21.01.2022
Subject to change without
notice.
Manufacturer:
DKL CHAIRS GmbH
An der Ziegelei 3
D-37124 Rosdorf
+49 (0)551-50060
info@dkl.de
www.dkl.de

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  • Page 1 Operating Instructions Manufacturer: DKL CHAIRS GmbH An der Ziegelei 3 D-37124 Rosdorf +49 (0)551-50060 info@dkl.de www.dkl.de D2-SAE Form no. GEN-D2SAE Rev. 03 / 21.01.2022 Subject to change without notice.
  • Page 2 Contents Symbols in the Operating Instructions Symbols inside the Unit Introduction Electromagnetic Compatibility (EMC) Safety Instructions - General Safety Notes – Cuspidor with Assistant’s Device Technical Specifi cations Media Requirements Product Description Moving the Treatment Chair Putting the Treatment Unit into Operation Function Syringe LED.light Operating Lamp LED.light EVA Operating Lamp...
  • 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 Observe the operating ON / OFF Do not dispose of with instructions!
  • Page 4 Symbols inside the Unit Earth conductor Functional Connection point for neutral connection - Protective earth conductor earth Symbols on the packaging Air humidity, limitation Permissible temperature range Transport upright; top Protect from moisture! Do not stack! Fragile...
  • Page 5 Introduction For your safety and the safety of your patients These operating instructions are intended to explain how to use your product. However, we must also warn of possible dangerous situations. Your safety, the safety of your team and, of course, the safety of your patients are very important to us. Please observe the safety instructions! Intended purpose This treatment unit is used for the diagnosis and therapy of children and adults in the fi...
  • Page 6 Electromagnetic Compatibility (EMC) Medical electrical equipment is subject to special precautions with regard to EMC and must be installed and commissioned in accordance with the EMC instructions. DKL guarantees that the dental unit complies with the EMC guidelines only if original DKL accessories and spare parts are used.
  • Page 7 Safety Instructions - General > Before being put into initial operation, the treatment unit must be kept at room temperature for 24 hours. > Before each application, check the treatment unit and the instruments with cables for damage and loose parts. >...
  • Page 8 Safety Notes – Cuspidor with Assistant’s Device >Before putting the device into initial operation and after downtimes (weekends, (public) holidays etc.), fl ush the water lines intensively. > Flush all instrument connections for 2 minutes before starting work. > Press the cup fi ll button several times before starting work. >...
  • Page 9 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-SAE max. 225 kg Transport and storage conditions Ambient temperature 30 to +70 °C...
  • Page 10 Media Requirements Media water Water hardness 1.5 to 2.14 mmol/l 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 11 Requirements for the suction system Vacuum at supply connection min. 0,12 bar, max. 0,18 bar Minimum suction power at supply connection ≥750Nl/min Suction system Type 1: high fl ow rate wet or dry suction Diameter of suction handpieces: small suction handpiece: 6 mm large suction handpiece: 16 mm Suction pipe DN40 HT-PP (polypropylene, inside diameter approx.
  • Page 12 Dimensions in Millimetres Treatment chair: lowest position 395 mm highest position 730 mm...
  • Page 13 Product Description Identifi cation label Treatment chair,seat Treatment chair, back rest Treatment chair, double-jointed head rest Treatment chair, joystick Treatment chair, arm rest Assistant’s device Cuspidor Operating lamp LED.light Tray...
  • Page 14 Product Description Spray mist suction Saliva ejector Syringe Connecting the instrument hoses and suction tubes. The instrument hoses can be connected or disconnected via a plug connection under the assistant’s device. Depending on the equipment of the model, the assistant’s device is equipped with the following instruments (from the left): the syringe, Spray mist suction and fi...
  • Page 15 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 >Back rest moves to an upright position.
  • Page 16 The release lever must always be pulled up completely to move the head rest. 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 17 Putting the Treatment Unit into Operation Putting the Unit into Operation Before putting your treatment unit into initial operation, an intensive fl ushing must be carried out [→page 37 or page 40]. Activating / Deactivating the Treatment Unit T 6,3A H 250V The treatment unit is equipped with a power switch on the chair base.
  • Page 18 Function FARO Syringe SYR3 See also operating instructions of the FARO company for their SYR3 dental syringe! Press the green button to release water. Press the light blue button to release air. Press both buttons simultaneously to release spray. To remove the sleeve, press button „A“.
  • Page 19 Function Luzzani Syringe Minilight See also operating instructions of the Luzzani company for their Minilight syringe! Nozzle retainer Water Nozzle Symbol: Air To blow water into the operating fi eld, just press the left button on Symbol: Water Handpiece the handpiece, symbol: water.To insuffl...
  • Page 20 : 8,000 to 50,000 lux at a distance of 700 mm Colour temperature : 5,000 K CRI (colour rendering index) : > 85 You can fi nd an application fi lm at www.youtube DKL Germany. Video: DKL CHAIRS L2-D2 SERIES FUNCTIONS LED.LIGHT OPERATING LAMP LINK: https://youtu.be/OXSchFNIFXM...
  • Page 21 Cleaning and Disinfection of the LED.light Operating Lamp 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 surfactants or water-repellent substances (staining). Sterilisation of the handles To remove the handles, turn the handle lock on the handles and pull off...
  • Page 22 LED.light EVA Operating Lamp When swivelling and moving the operating lamp, always make sure that no objects or persons are in the swivelling range of the arm system. Otherwise, personal injury or property damage may occur. In order to move the operating lamp only touch its handles! For the intended use, please observe the operating instructions issued by FARO: USER MANUAL EVA...
  • Page 23 LED.light EVA Operating Lamp Every time a double click is performed, the colour temperature in Kelvin (Tk) of the light changes. Repeat the procedure until the desired colour temperature is shown on the indicator light. 2 beeps will inform the user that Tk is changing. Indicator light Indicator light Indicator light...
  • Page 24 Move the tray into a horizontal position. Secure the adjusting screw (1) for the inclination 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: https://youtu.be/r-Y14eEYtqI...
  • Page 25 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 26 Suction System Refl ux Eff ect When the suction cannula adheres to the mucous membrane of the oral cavity or to the tongue, a so-called refl ux eff ect may occur. To prevent cross-infection among patients we recommend using suction cannulas with air-bleed openings. Here a defi ned bypass airstream is introduced into the suction handpiece via lateral recesses.
  • Page 27 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 28 Cleaning and Disinfection of the Suction Handpieces...
  • Page 29 Cleaning and Disinfection of the Suction Handpieces...
  • Page 30 Cleaning and Disinfection of the Suction System We recommend using the OroCup system of the DÜRR company for cleaning and disinfection. Scope of delivery 1. OroCup, order no. 0780-350-00 2. 2 x Ø 16 mm insert (for large suction tube), (1x loose, 1x fi...
  • Page 31 •After the exposure time has elapsed, aspirate 2 litres of water, see 2.1 (Pre-cleaning with water). You can fi nd an application fi lm at www.youtube DKL Germany. Video: DKL CHAIRS L2-D2 SERIES CLEANING AND DISINFECTION OF THE SUCTION SYSTEM LINK:...
  • Page 32 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 33 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 34 Cleaning and Disinfection of the Surfaces Disinfection proPad dispenser box incl. XL disinfectant wipes Article number PP100 100 wipes proPad XL Refi ll 300 disinfectant wipes Article number PP300 3 x 100 wipes Cleaning and Care Care set Article number PSET 1 x DentaClean 200 ml spray foam cleaner (article DC200) 1 x DentaProtect wipe dispenser box (article DP100) 1 x cleaning brush, 3 x cleaning sponges...
  • Page 35 Cleaning and Disinfection of the Instrument Holders • Pull out the instrument holder • Rinse off any soiling with water • Remove any residual liquid (absorbent cloth; blow dry with compressed air) • Disinfection with disinfectants; wipe disinfection is recommended. •...
  • Page 36 Bottle Care System The Bottle Care System is a treatment water system for the self-suffi cient water supply for all the instruments and the glass fi ller. There is also the possibility of intensive decontamination of the service water lines in the treatment unit. Changing the treatment water bottle on the outside of the cuspidor: 1.
  • Page 37 LINK: https://youtu.be/1ySjnPDyuBQ Test water quality with Bottle Care System or Water Separation Unit (WTE) You can fi nd an application fi lm at www.youtube DKL Germany. Video: DKL CHAIRS L2-D2 TEST STRIPS FOR THE DK-DOX-150 DETECTION IN THE TREATMENT WATER LINK: https://youtu.be/3JUx-PY1xHo...
  • Page 38 Water Separation Unit (WSU) The water separation unit meets the requirements of ISO 7494-2 and EN 1717 (free outlet with separation distance ≥ 20 mm). It is intrinsically safe in accordance with DVGW (GermanTechnical and Scientifi c Association for Gas and Water) worksheet 540 and also meets the requirements of W270 and KTW (guideline for hygienic assessment of organic materials in contact with drinking water).
  • Page 39 Error Messages and Service Mode WARNING! Push-button of the water separation unit (WSU) is fl ashing yellow-red. Fault in the dosing unit. WSU continues to work. Call customer service! Push-button of the WSU is fl ashing red. Call customer service immediately! Push-button of the WSU lights up permanently red.
  • Page 40 Flushing Function with the Water Separation Unit (WSU) If the treatment unit is equipped with a water separation unit, make sure that the LED button on the cuspidor lights up green. Remove the fi rst instrument. Activate the instrument with the setting “Spray active” for 120 seconds.
  • Page 41 Open the cover of the storage container for the water separation unit at the base of the cuspidor. You can fi nd an application fi lm at www.youtube DKL Germany. Video: DKL CHAIRS L2-D2 SERIES FILLING DK-DOX 150 WATER SEPARATION UNIT (WSU) LINK: https://youtu.be/CObiIs6gklQ...
  • Page 42 (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 43 Warrantee Declaration 12 Months Warranty This DKL medical product has been manufactured with the utmost care by highly qualifi ed specialists. Multifarious checks and inspections ensure faultless perfor- mance. Please note that warranty claims will only be accepted if all the instructions in this operating manual have been observed.
  • Page 44 EMC - Manufacturer‘s Declaration for the Model D2-SAE • 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 45 IEC STANDARD 60601-1-2:2014, 4th 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 46 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 47 Manufacturer‘s Declaration - Electromagnetic Interference Immunity III The 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 as described below Electromagnetic environment – Interference Immunity IEC 60601- Compliance level...
  • Page 48 Minilight Installation and use manual...
  • Page 49 LUZZANI DENTAL S.R.L. 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 MADE IN ITALY 1 3 7 0...
  • Page 50 CONTENTS SYRINGE LEGEND CLEANING AND STERILIZATION — — MAINTENANCE WARNINGS — — DISPOSAL AND SCRAPPING PRODUCT DESCRIPTION — — GENERAL INFORMATION FOR THE DENTIST — — GENERAL CHARACTERISTICS — FAULT REPORT FORM — MODELS — CONTROLS — SYMBOLS — CE MARKING —...
  • Page 51 0 —— SYRINGE LEGEND Air button (6F, G6F and L) Tip retainer Water button Handpiece line Selector switch Water line Power cables Pawl (6F, G6F, and L) Stress absorber cord...
  • Page 52 1 —— WARNINGS 1.1 — Any unauthorised tampering, modification or 1.14 — Do not use the device in close contact with improper use immediately terminates the warranty and anaesthetic gases or in highly oxygenated environments (with exonerates our company from all liability for injury or damage an oxygen content >25%) or in areas where there is a risk of to persons, animals or property that may be caused by such explosion.
  • Page 53 This difference lets the dentist choose the tool ergonomically number of functions provided: best suited for the purpose. To guarantee maximum hygiene • 3F: cold water/air/spray and atoxicity, the handpieces are made of stainless steel. The devices are produced entirely in our workshop, with a tested, •...
  • Page 54 IMPORTANT NOTE: 5.2 — TRANSPORT AND STORAGE CONDITIONS With each syringe, the package also includes a User’s manual which also includes a “Fault Report Form”. Since this is Temperature -20°C / +60°C required by law, the user must receive this User’s manual. Therefore, the syringe installer is responsible for delivering these forms to the dentist.
  • Page 55 LED lights up) unit. This cord is designed to absorb any strains, thus preventing abnormal traction on the electrical or air/water line connections. The manufacturer cannot be held liable for malfunctions caused by failure to anchor the stress absorber cord. 6.5 —...
  • Page 56 and press both buttons on the handpiece at the same time: Check the tip for any obstructions or deposits. Clean if necessary. NOTE • Flush out the syringe at the beginning of each work day (minimum flushing time: 2 minutes) and before each patient (minimum flushing time: 20-30 sec.).
  • Page 57 or remove the entire handpiece by pressing the button on Not envisaged the lower part of the handpiece and pulling upwards. E — MANUAL DISINFECTION press the pawl to release the handpiece Disinfect only with a disposable cloth and the permitted disinfectant (following the instructions on the label and product technical data sheet).
  • Page 58 10 —— DISPOSAL AND SCRAPPING The product does not contain dangerous or toxic- hazardous components. Separate waste collection is required for electrical equipment. Follow the regulations in force in your country. 11 —— INFORMATION FOR THE DENTIST The dental unit manufacturer is required to deliver the Luzzani Dental syringe User’s manual to the end user.
  • Page 59 14 —— WIRING DIAGRAM 14.1 – VERSION 6F 14.2 – VERSION L...
  • Page 60 INSTRUCTIONS FOR CLEANING AND STERILIZATION OF MINILIGHT, MINIMATE, MINIBRIGHT SYRINGES IN ACCORDANCE WITH UNI EN ISO 17665 REQUIREMENTS Warning • Sterilization must be performed even when using the syringe for the first time. • Inappropriate sterilization is dangerous for patients and operators. •...
  • Page 61 FAULT REPORT FORM PRODUCT _______________________________________________________________________________________________________ TYPE _________________________________________________ BATCH ___________________________________________________ REPORTED BY ___________________________________________________________________________________________________ COMPANY ______________________________________________________________________________________________________ _________________________________________________________________________________________________________________ _________________________________________________________________________________________________________________ TYPE OF REPORT ANOMALY SUGGESTIONS __________________ DESCRIPTION NOTES DATE _____________________ SIGNATURE _____________________ SEND TO: LUZZANI DENTAL SRL Via Torino 3 - Senago (MI) - ITALY Tel.
  • Page 62 SYR3 S I R I N G A D E N TA L E DENTAL SYRINGE M A N UA L E D ’ U S O I N ST R U C T I O N M A N UA L M O D E D ’...
  • Page 63 DICHIARAZIONE DI CONFORMITÀ CE CE DECLARATION OF CONFORMITY Il fabbricante FARO S.p.A.Via Faro n°15 The manufacture 20060 Ornago ( Milano ) ITALY dichiara sotto la propria responsabilità, che il prodotto: declares under it’s own responsibility that the product: Designazione del prodotto: Siringa dentale Product’s designation: Dental syringe Modello: SYR3 Model:: SYR3...
  • Page 64 ISTRUZIONI D’USO - Per erogare l’acqua premere il pulsante di colore verde. - Per erogare l’aria premere il pulsante di colore azzurro. - Per ottenere lo spray premere contemporaneamente i due pulsanti Smontaggio del guscio e del beccuccio Per togliere il beccuc- - P e r t o g l i e r e i l guscio, premere il cio, svitare la ghiera...
  • Page 65 SAFETY RULES The SYR3 dental syringe is designed exclusively for use in dentistry, by dental professionals or an assistant under a dentist’s supervision, in order to perform specific cleaning and drying operations on the operating area. The device must be installed on a specific supply system (dental unit) and be connected to a dedicated FARO hose.
  • Page 66 TECHNICAL SPECIFICATIONS Three-function syringe SYR3 :4 bar - Air pressure - Water pressure :2 bar - Air flow :10 l/min :80-100 ml/min - Water flow :AIR - Blue tube for passage of - Green tube for passage of :WATER - Weight :100 g - WATER-AIR temperature system temperature...
  • Page 67 MODE D’EMPLOI - Pour actionner l’arrivée d’eau, appuyer sur le bouton vert. - Pour actionner l’arrivée d’air, appuyer sur le bouton bleu. - Pour obtenir le jet, appuyer simultanément sur les deux boutons. Démontage de la coque et de l’embout - Pour retirer la - Pour retirer l’em- coque, appuyer sur...
  • Page 68 SICHERHEITSNORMEN Die Dentalspritze ist ausschließlich für den Einsatz in einer Zahnarztpraxis und durch ärztliches Personal bzw. durch den zahnärztlichen Assistenten und unter der Verantwortung des Arztes vorgesehen und darf nur für spezifische Reinigungsarbeiten und das Trocknen während der Behandlungen eingesetzt werden. Die Vorrichtung muss auf einem spezifischen Versorgungssystem (Dentaleinheit) installiert und an ein eigenes FARO-Kabel angeschlossen werden.
  • Page 69 TECHNISCHE SPEZIFIKATIONEN 3-Funktions-Spritze SYR3 : 4 bar - Betriebsdruck Luft - Betriebsdruck Wasser : 2 bar - Luft-Fördermenge : 10 l/min : 80-100 ml/min - Wasserdurchfluss : LUFT - Hellblauer Schlauch für - Grüner Schlauch für : WASSER - Gewicht : 100 g : wie aus der Leitung - Temperatur WASSER/LUFT...
  • Page 70 INSTRUCCIONES DE USO - Para erogar el agua pulsar el interruptor de color verde. - Para erogar el aire pulsar el interruptor de color azul. - Para obtener el espray pulsar al mismo tiempo los dos interruptores Desmontaje de la cubierta y la embocadura - Para sacar la cubierta Para sacar la embo- pulsar el interruptor...
  • Page 71 CERTIFICATO DI GARANZIA La Faro concede al cliente finale una garanzia di 12 mesi, dalla data della fattura di acquisto. La riparazione in garan- zia dovrà essere effettuata presso la FARO o presso un riparatore autorizzato FARO; spese e rischi di trasporto sono a carico dell’acquirente.
  • Page 72 12 mesi-months-mois-monaten-meses nome-name-nom-vorname-nombre cognome-surname-prenom-nachname-apellido indirizzo-address-adresse-auschrift-direccion città-town-ville-ort-ciudad data d’acquisto-purchase date-date d’achat einkaufdatum-fecha de compra Siringa dentale SYR 3 versione-version-version-modell-versión Timbro del rivenditore-Dealer’s stamp-Cachet d’achat Stempel der Fachhändlers-Sello del revendedor...
  • Page 73 Azienda FARO S.p.A. Certificata via Faro, 15 - 20876 Ornago (MB) - Italy Tel. +39 039.68781 - Fax +39 039.6010540 www.faro.it - comm.italia@faro.it - @faro.it x� FARO FRANCE Za Tgv Coriolis - 71210 Monchanin - France Tel. +33 385.779680 - Fax +33 385.779688 CERT.
  • Page 74 Spittoon valve 3 Installation and Operating Instructions 7560100003L02 ...
  • Page 76 Contents Important information Installation 1 About this document                2 6 Requirements                      9 Warnings and symbols           2 Setup options                  9 Copyright information            2...
  • Page 77 Important information About this document Other symbols These symbols are used in the document and These installation and operating instructions on or in the unit: form part of the unit Note, eg specific instructions regarding If the instructions and information in efficient and cost-effective use of the unit these installation and operating instruc- tions are not followed, Dürr Dental will Comply with the Operating Instructions...
  • Page 78 Important information Safety Whoever connects additional devices to medical electrical devices automatically becomes the Dürr Dental has designed and constructed this system configurator and is responsible for en- device so that when used properly and for the suring that the system corresponds with the intended purpose there is no danger to people standard requirements for systems Local laws or property Nevertheless, residual risks can re-...
  • Page 79 Important information 2.9 Transport The original packaging provides optimum pro- tection for the device during transport If required, original packaging for the unit can be ordered from Dürr Dental Dürr Dental does not accept any respon- sibility or liability for damage occurring during transport due to the use of incor- rect packaging, even where the unit is still under guarantee...
  • Page 80 Product description Overview Spittoon valve 3.1 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 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...
  • Page 81 Product description Technical data Electrical data Safety low voltage (AC/DC) Frequency 50 - 60 Nominal current Rated power Type of protection IP 21 Electrical data, suction unit relay Switching voltage (AC/DC) min max Switching current min max Connections Supply and waste water connection ∅ 20 DürrConnect ∅...
  • Page 82 Product description 4.1 Type plate The type plates are located on the side of the fluid collector Type plate 4.2 Conformity assessment 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 require- ments 7560100003L02 1801V002...
  • Page 83 Product description Operation Fluid collector Air extraction seal Vent Protective strainer Exhaust air damper Solenoid valve Compressed air connection Shut-off valve Float sensor 10 Magnet in float sensor 11 Float sensor detection 12 Magnet in cleaning button 13 Cleaning button detection sensor 5.1 Operating function The waste water from the spittoon flows through the coarse filter into the collector vessel If...
  • Page 84 Installation Requirements 6.1 Setup options – Installation in treatment units in dental surger- ies or dental clinics 6.2 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": –...
  • Page 85 Installation Installation 7.1 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 1801V002...
  • Page 86 Installation 7.2 Installation of the spittoon valve 7.3 Establishing the compressed air connection The cleaning function can be activated Disconnect a suitable compressed air line via the yellow button For this reason the from the treatment unit spittoon valve should be positioned in an easily accessible location If this is not Install a T-piece with 4 mm branch in the com- possible, a separate switch control panel pressed air line...
  • Page 87 Installation 7.4 Electrical connections Prior to working on the device or in case of danger, disconnect it from the mains (e g pull the mains plug) The requirements of IEC 60601-1 must be satisfied during installation Open the cover of the control electronics Route the power supply and control line to the spittoon valve Attach the connector to the connection lines...
  • Page 88 Installation 7.5 Circuit diagram 24 V AC/DC Hose manifold Station selection valve Rinsing unit Spittoon valve X1 Cleaning button for switch control panel X3 Solenoid valve X4 Control line for suction unit X5 Power supply K1 Suction unit relay N2 Float sensor detection N3 Cleaning button detection sensor Suction machine relay in the treatment unit 7560100003L02 1801V002...
  • Page 89 Installation Commissioning and first start-up In many countries technical medical products and electrical devices are sub- ject 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 (eg the German Ordinance on the Installation, Opera- tion and Use of Medical Devices / Medizin-...
  • Page 90 Operation Disinfection and cleaning 9.2 Suction system After every treatment NOTICE Aspirate a glass of cold water through the Device malfunctions or damage due large and the small suction hoses Do this to use of incorrect media even if only the small suction hose was actual- Guarantee claims may become invalid ly used during treatment as a result Do not use any foaming agents, eg household cleaning agents or instru-...
  • Page 91 Operation 10 Maintenance All maintenance work must be performed by a qualified expert or by one of our Service Technicians Prior to working on the device or in case of danger, disconnect it from the mains (e g pull the mains plug) WARNING Infection due to contaminated unit Clean and disinfect the suction before...
  • Page 92 Troubleshooting 11 Tips for operators and service technicians Any repairs above and beyond routine maintenance must only be carried out by suitably quali- fied personnel or by one of our service technicians 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) Prior to working on the device or in case of danger, disconnect it from the mains (e g pull the mains plug)...
  • Page 93 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 (eg liquid-tight protec- tive 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 Disinfect a defective unit using a suitable sur- face disinfection agent...
  • Page 94 Appendix 13 Information about EMC in accordance with EN 60601-1-2 13.1 General information The information in this leaflet includes excerpts from the relevant European standards for electrical, medical devices It must be observed when installing Dürr Dental devices or combining them with products of other manufacturers If you are uncertain about anything, please refer to the complete standard 13.2 Abbreviations Electromagnetic compatibility...
  • Page 95 Appendix Resistance to electromagnetic interference (immunity) for all devices and systems The device is designed for use in electromagnetic environments specified below The customer or op- erator of the device should ensure that the device is operated such an environment Interference im- IEC 60601 - test Compliance level Electromagnetic environment munity tests level - guidelines Electrostatic dis- ±8 kV contact dis- ±8 kV contact dis- Floors should be made of wood...
  • Page 96 Appendix Electromagnetic interference immunity for devices or systems that are not life-sustaining Portable and mobile communication devices should not be used any closer to the unit (including ca- bles) than the recommended safety distance, which is calculated based on the applicable formula for the transmission frequency Interference im- IEC 60601 - test Compliance Recommended safety distance munity tests level level...
  • Page 97 Appendix Recommended safety distance between portable and mobile HF communication devices and the unit The device is designed for use in the electromagnetic environments specified below, in which the HF disturbance variables are controlled The customer or the operator of the device can help to prevent electromagnetic interference by maintaining the minimum distances between mobile HF communica- tion equipment (transmitters) and the device as recommended below in accordance with the maxi- mum output line of the communication equipment Keep a minimum distance of 30 cm between the device and mobile communication devices...
  • Page 101 Hersteller/Manufacturer: DÜRR DENTAL SE Höpfigheimer Str. 17 74321 Bietigheim-Bissingen Germany Fon: +49 7142 705-0 www.duerrdental.com info@duerrdental.com...
  • Page 102 CAS 1 Combi-Separator Installation and Operating Instructions 7117100018L30 ...
  • Page 104 Contents Important information Installation About this document � � � � � � � � � � � � � � � 3 Requirements � � � � � � � � � � � � � � � � � � � � 12 1�1 Warnings and symbols �...

  • Page 105: Table Of Contents

    Contents Operation 11 Display/handling� � � � � � � � � � � � � � � � � � 19 11�1 Ready for operation � � � � � � � � � � � 19 11�2 Amalgam collector vessel is 95% full �...
  • Page 106 Important information About this document Note, e�g� specific instructions regarding efficient and cost-effective use of the unit� These installation and operating instructions form part of the unit� Comply with the Operating Instructions� If the instructions and information in these installation and operating instruc- tions are not followed, Dürr Dental will Wear hand protection�...
  • Page 107 Important information Safety The CAS 1 Combi Separator for KaVo treatment units must be set up in a defined installation Dürr Dental has designed and constructed this setup in order to meet the relevant safety stand- device so that when used properly and for the ards�...
  • Page 108 Important information 2.8 Only use genuine parts Whoever connects additional devices to med- ical electrical devices automatically becomes Only use Dürr Dental parts or accessories and the system configurator and is responsible for special accessories specifically approved by ensuring that the system corresponds with the Dürr Dental�...
  • Page 109 Product description Overview 3.3 Disposable materials The following materials are consumed during operation of the device and must be ordered separately: Disposable amalgam container � � � 7117-033-00 DürrConnect protective strainer, 5 pieces � � � � � � � � � � � � � � � � � � � 0700-700-18E DürrConnect protective strainer, 5 pieces �...
  • Page 110 Product description Technical data 4.1 CAS 1 Combi-Separator Electrical data – centrifuge motor Nominal voltage 24 AC Frequency 50 / 60 Rated power Electrical data – electronics Nominal voltage 24 AC Nominal current 0�2 Signal input from the hose manifold 24 AC/DC Media ≤...
  • Page 111 Product description 4.2 Type plate The type plates are located on the cover of the motor� Type plate 4.3 Conformity 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�...
  • Page 112 Product description Operation CAS 1 Fluid intake Vacuum, to suction unit Aspiration input Fluid output Motor Separation Separation rotor Centrifuge Light barriers (3x) 10 Sensor enclosure 11 Cone pump 12 Amalgam collector vessel 13 Float sensor 14 Fluids 15 Amalgam particles 7117100018L30 1712V002...
  • Page 113 Product description 5.1 Operation The spiral motion feeds the separated fluid con- tinuously to the pump wheel, which transports CAS 1 Combi-Separator the fluid into the collector vessel� The fluid is The task of the CAS 1 combi-separator is to transported to the centrifuge (8) via a pump provide continuous separation of secretions and cone (11)�...
  • Page 114 Product description As soon as no further fluid is fed to the amal- gam separator, e�g� when the suction hose is placed back in the hose manifold, the centrifuge drum is switched off after a short delay time� This switch-off brakes the motor, as a result of which the ring of water, which continues to rotate due to inertia, rinses the separated parti- cles out of the centrifuge (8) downwards into the...
  • Page 115 Installation Requirements 6.5 Information about electrical connections 6.1 Installation/setup room Ensure that electrical connections to the The room chosen for set up must fulfil the fol- mains power supply are carried out in accord- lowing requirements: ance with current valid national and local reg- –...
  • Page 116 Installation Installation Control cable Installation type Line layout (minimum Prior to working on the device or in case requirements) of danger, disconnect it from the mains (e� g� pull the mains plug)� Fixed installation – Shielded sheathed cable (e�g�  (N)YM (St)-J) 7.1 Combining devices safely Flexible –...
  • Page 117 Installation 7.2 Installation of the CAS 1 in Inlet and outlet hoses Connect and attach the inlet and outlet hoses treatment units with DürrConnect connectors to the relevant connections on the unit�Route the hoses at an WARNING incline� Infection due to contaminated unit Recommended diameter of the connection Clean and disinfect the suction before hoses: ∅ 25 mm�...
  • Page 118 Installation 7.3 Electrical connections, Place selection valve Rinsing unit controller Suction unit relay (alternative) Power supply: Display panel, external – Safety transformer order number: 9000-150-46 7.4 Electrical connections – Safety transformer 24 V AC with a with an Station selection valve / safety valve isolator consisting of two means of patient Connect the station selection valve / safety protection (MOPP) between the mains circuit...
  • Page 119 Installation Commissioning and first start-up In many countries technical medical products and electrical devices are sub- ject to regular checks at set intervals� The owner must be instructed accordingly� Turn on the unit power switch or the main surgery switch� Carry out an electrical safety check in accord- ance with applicable local regulations (e�g�...
  • Page 120 Installation Service program 7117100018L30 1712V002...
  • Page 121 Installation 10 Description of the service 10.3 Sediment level measurement program While the service program is activated, the safety check for the collector vessel Wear protective equipment to avoid any is deactivated� risk of infection (e�g� liquid-tight pro- The sediment level measurement can be used tective gloves, protective goggles, face to check the function of the sediment sensor mask)�...

  • Page 122: Display/Handling

    Operation 11 Display/handling 11.3 Amalgam collector vessel is 100% full Yellow LED is on 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 123: 11�5 Motor Fault

    Operation 12 Disinfection and cleaning 11.5 Motor fault Red display and NOTICE green LED flash alternately Device malfunctions or damage due to use of incorrect media Audible signal Guarantee claims may become invalid as a result� – Press the reset button briefly to switch off the Do not use any foaming agents, e�g�...

  • Page 124: 12�3 Once Or Twice A Week Before The

    Operation 13 Replace the amalgam 12.3 Once or twice a week before the midday break collector vessel Under harsher conditions (e�g� hard water or frequent use of prophylaxis powders) WARNING 1x daily before the midday break Risk of contamination if the amalgam collector vessel is reused since the The following are required for cleaning: collector vessel is not water-tight.

  • Page 125: 13�1 Disposal Of The Collector Vessel

    Operation 13.1 Disposal of the collector vessel Used amalgam collector vessels must not be sent in the post! Dürr Dental is not a waste management company and is not allowed by law to accept any filled amalgam collector ves- sels� Arrange to have filled amalgam collector vessels collected from the surgery by a local waste management company�...

  • Page 126: Maintenance

    Operation 14 Maintenance All maintenance work must be performed by a qualified expert or by one of our Service Tech- nicians� Prior to working on the device or in case of danger, disconnect it from the mains (e� g� pull the mains plug)�...
  • Page 127 Operation 14.1 Tests Work steps to be performed: Fill the test vessel with water and insert it into the unit� WARNING Infection due to contaminated unit Start the device and wait until it switches off again� Clean and disinfect the suction before working on the unit�...

  • Page 128: Troubleshooting

    Troubleshooting 15 Tips for operators and service technicians Any repairs above and beyond routine maintenance must only be carried out by suitably quali- fied personnel or by one of our service technicians� WARNING Infection due to contaminated unit Clean and disinfect the suction before working on the unit� Wear protective equipment when working (e� g�...
  • Page 129 Troubleshooting Fault Probable cause Solution Yellow display is on Amalgam collecting container is Change the amalgam collecting 95% full container� GREEN LED illuminates Audible signal melody Float sensor dirty or blocked If this display occurs repeatedly sounds even when the collecting con- tainer is empty, check that the float sensor can move freely�...
  • Page 130 Troubleshooting Fault Probable cause Solution Increased vibration of the Pump cone dirty Clean or replace the pump cone� * device Centrifuge dirty Clean or replace the centrifuge� * Water supply too low Introduce water into the suction pipe� Retrofit the rinsing unit� * Check the rinsing unit for its correct installation position�...

  • Page 131: 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 pro- tective 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 132: Appendix

    Appendix 17 Information about EMC in accordance with EN 60601-1-2 17.1 General information The information in this leaflet includes excerpts from the relevant European standards for electrical, medical devices� It must be observed when installing Dürr Dental devices or combining them with products of other manufacturers�...
  • Page 133 Appendix Resistance to electromagnetic interference (immunity) for all devices and systems The device is designed for use in electromagnetic environments specified below� The customer or operator of the device should ensure that the device is operated such an environment� Interference immu- IEC 60601 - test Compliance level Electromagnetic environment...
  • Page 134 Appendix Electromagnetic interference immunity for devices or systems that are not life-sustaining Portable and mobile communication devices should not be used any closer to the unit (including cables) than the recommended safety distance, which is calculated based on the applicable formula for the transmission frequency�...
  • Page 135 Appendix Recommended safety distance between portable and mobile HF communication devices and the unit The device is designed for use in the electromagnetic environments specified below, in which the HF disturbance variables are controlled� The customer or the operator of the device can help to prevent electromagnetic interference by maintaining the minimum distances between mobile HF communica- tion equipment (transmitters) and the device as recommended below in accordance with the maxi- mum output line of the communication equipment�...
  • Page 137 Hersteller/Manufacturer: DÜRR DENTAL SE Höpfigheimer Str. 17 74321 Bietigheim-Bissingen Germany Fon: +49 7142 705-0 www.duerrdental.com info@duerrdental.com...
  • Page 138 CS 1 Combi-Sepamatic Installation and Operating Instructions 9000-606-39/30 ...

  • Page 140: Information

    Contents Important information Installation About this document � � � � � � � � � � � � � � � 2 Requirements � � � � � � � � � � � � � � � � � � � � � 9 1�1 Warnings and symbols �...

  • Page 141: Important Information

    Important information About this document Other symbols These symbols are used in the document and These installation and operating instructions on or in the unit: form part of the unit� Note, e�g� specific instructions regarding If the instructions and information in efficient and cost-effective use of the unit�...

  • Page 142: Safety

    Important information Safety 2.3 Improper use Any other usage or usage beyond this scope is Dürr Dental has designed and constructed this deemed to be improper� The manufacturer ac- device so that when used properly and for the cepts no liability for damages resulting from this� intended purpose there is no danger to people In these cases the user/operator will bear the or property�...

  • Page 143: General Safety Information

    Important information 2.5 General safety information 2.8 Only use genuine parts When operating this device always observe all Only use Dürr Dental parts or accessories and guidelines, laws, and other rules and regula- special accessories specifically approved by tions that are applicable at the site of opera- Dürr Dental�...

  • Page 144: Product Description

    Product description Overview 3.3 Special accessories The following optional items can be used with the device: Station selection valve � � � � � � � � � � 7560-500-60 Rinsing unit II � � � � � � � � � � � � � � � � 7100-250-50 OroCup care system �...

  • Page 145: Technical Data

    Product description Technical data 4.1 CS 1 Combi-Sepamatic Electrical data – centrifuge motor Nominal voltage 24 AC Frequency 50 / 60 Rated power Media Fluid volume min� l/min ≥ 0�1 max� l/min ≤ 2�0 Air flow volume l/min ≤ 350 Flow rate high The suction system must be suitable for a high flow rate in accordance with EN ISO 10637�...

  • Page 146: Type Plate

    Product description 4.2 Type plate The type plates are on the motor cover and on the motor flange� Type plate 4.3 Conformity assessment 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 require- ments�...

  • Page 147: Operation

    Product description Operation Motor Vacuum, to suction unit Separation Aspiration input Pump wheel Separation rotor Fluid output Waste valve Relief valve 5.1 Separation Every time the suction hose is taken out of the hose manifold, the CS 1 Combi-Sepamatic and the suction unit are started� The mixture of liquid and air drawn up is accelerated in the intake connection and then set in spiral motion in the separation�...

  • Page 148: Requirements

    Installation Requirements Install an all-pole disconnect switch with a contact opening width of at least 3 mm in the 6.1 Setup options electrical connection to the mains power sup- ply� It must be possible to secure the discon- CS 1 Combi-Sepamatic nect switch so that it cannot be inadvertently –...

  • Page 149: Installation Of The Cs 1 In

    Installation Installation Inlet and outlet hoses Connect and attach the inlet and outlet hoses Prior to working on the device or in case with DürrConnect connectors to the relevant of danger, disconnect it from the mains connections on the unit�Route the hoses at an (e� g�...

  • Page 150: Electrical Connections, Controller

    Installation 7.2 Electrical connections, 7.3 Electrical connections controller Power supply: – Safety transformer order number: 9000-150-46 – Safety transformer 24 V AC with a with an isolator consisting of two means of patient protection (MOPP) between the mains circuit and secondary circuit, min� 100 VA, second- ary fuse T 4 AH (or IEC 60127-2/V T 4 AH, 250 V) X1 Power supply...

  • Page 151: Commissioning And First Start-Up

    Installation Commissioning and first start-up In many countries technical medical products and electrical devices are sub- ject 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 152: Operation

    Operation Disinfection and cleaning 9.3 Once or twice a week before the midday break NOTICE Under harsher conditions (e�g� hard water Device malfunctions or damage due or frequent use of prophylaxis powders) to use of incorrect media 1x daily before the midday break Guarantee claims may become invalid The following are required for cleaning: as a result�...

  • Page 153: Maintenance

    Operation 10 Maintenance All maintenance work must be performed by a qualified expert or by one of our Service Techni- cians� Prior to working on the device or in case of danger, disconnect it from the mains (e� g� pull the mains plug)�...

  • Page 154: Troubleshooting

    Troubleshooting 11 Tips for operators and service technicians Any repairs above and beyond routine maintenance must only be carried out by suitably quali- fied personnel or by one of our service technicians� Prior to working on the device or in case of danger, disconnect it from the mains (e� g� pull the mains plug)�...

  • Page 155: 11�1 Replacing The Fuse

    Troubleshooting 12 Transporting the unit 11.1 Replacing the fuse Prior to working on the device or in case of danger, disconnect it from the mains WARNING (e� g� pull the mains plug)� Infection due to contaminated unit Disinfect the unit before transport� Transformer Close all media connections�...

  • Page 156: Appendix

    Appendix 13 Information about EMC in accordance with EN 60601-1-2 13.1 General information The information in this leaflet includes excerpts from the relevant European standards for electrical, medical devices� It must be observed when installing Dürr Dental devices or combining them with products of other manufacturers�...
  • Page 157 Appendix Resistance to electromagnetic interference (immunity) for all devices and systems The device is designed for use in electromagnetic environments specified below� The customer or op- erator of the device should ensure that the device is operated such an environment� Interference immu- IEC 60601 - test Compliance level...
  • Page 158 Appendix Electromagnetic interference immunity for devices or systems that are not life-sustaining Portable and mobile communication devices should not be used any closer to the unit (including ca- bles) than the recommended safety distance, which is calculated based on the applicable formula for the transmission frequency�...
  • Page 159 Appendix Recommended safety distance between portable and mobile HF communication devices and the unit The device is designed for use in the electromagnetic environments specified below, in which the HF disturbance variables are controlled� The customer or the operator of the device can help to prevent electromagnetic interference by maintaining the minimum distances between mobile HF communica- tion equipment (transmitters) and the device as recommended below in accordance with the maxi- mum output line of the communication equipment�...
  • Page 160 Appendix 13.4 Calculation table If the measured values deviate from the standard, the values are specified in chapter "4 Technical data"� The safety distances can then be calculated in the tables shown below� ���������� ���������� ���������� Rated power of the transmitter in Watts (W) in accordance with the specifications of the transmitter manufacturer Compliance level for the test in acc�...
  • Page 165 Hersteller/Manufacturer: DÜRR DENTAL SE Höpfigheimer Str. 17 74321 Bietigheim-Bissingen Germany Fon: +49 7142 705-0 www.duerrdental.com info@duerrdental.com...
  • Page 167 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 168: 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 169: 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 170: 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 171: 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 172: 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 173: 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 174: 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 175: 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 176: 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 177: 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 178: 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 179 USER MANUAL - EN Edition 1.0 April 2020 Pag. 14 di 14...

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