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Instructions for use
MASTERmatic LUX M07 L - 1.009.3610
MASTERmatic LUX M20 L - 1.009.3620
MASTERmatic LUX M29 L - 1.009.3580

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Summary of Contents for KaVo MASTERmatic LUX M07 L - 1.009.3610

  • Page 1 Instructions for use MASTERmatic LUX M07 L - 1.009.3610 MASTERmatic LUX M20 L - 1.009.3620 MASTERmatic LUX M29 L - 1.009.3580...
  • Page 2 Distributed by: Manufacturer: KaVo Dental GmbH Kaltenbach & Voigt GmbH Bismarckring 39 Bismarckring 39 D-88400 Biberach D-88400 Biberach Phone +49 7351 56-0 www.kavo.com Fax +49 7351 56-1488...
  • Page 3: Table Of Contents

    Contents 3 / 74 Table of contents 1 User instructions............................6 2 Safety................................ 8 2.1 Description of safety instructions....................... 8 2.2 Safety instructions........................... 11 3 Product description..........................16 3.1 Purpose – Intended use........................19 3.2 Technical Specifications M07 L....................... 21 3.3 Technical Specifications M20 L.......................
  • Page 4 Contents 4 / 74 5.3 Insert the INTRA LUX ........................33 5.4 Remove the INTRA LUX ........................ 34 6 Troubleshooting............................35 6.1 Check for malfunctions........................35 6.2 Troubleshooting..........................38 6.2.1 Replacing the O-rings......................38 6.2.2 Cleaning the spray nozzle....................39 6.2.3 Changing the water filter.....................
  • Page 5 7.5.1 Care with KaVo Spray......................57 7.5.2 Care with the KaVo SPRAYrotor..................58 7.5.3 Servicing with KaVo QUATTROcare 2104 / 2104A............59 7.5.4 Servicing with KaVo QUATTROcare PLUS 2124 A............62 7.5.5 Servicing with KaVo QUATTROcare 2140 A..............63 7.6 Packaging............................64 7.7 Sterilisation............................
  • Page 6: User Instructions

    1 User instructions 6 / 74 1 User instructions Dear User Congratulations on purchasing this KaVo quality product. By following the instructions below you will be able to work smoothly, economically and safely. © Copyright by KaVo Dental GmbH Symbols...
  • Page 7 1 User instructions 7 / 74 Can be steam-sterilised at 134 C -1 C / +4 C (273 F -1.6 +7.4 Thermodisinfectable CE-Zeichen (Communauté Européenne). Ein Produkt mit diesem Zeichen entspricht den Anforderungen der anwendbaren EG- Richtlinie. Action request Target group This document is intended for dentists and their assistants.
  • Page 8: Safety

    2 Safety 8 / 74 2 Safety 2.1 Description of safety instructions Warning symbol Structure DANGER The introduction describes the type and source of the haz‐ ard. This section describes potential consequences of non-compliance. ▶ The optional step includes necessary measures for hazard prevention.
  • Page 9 2 Safety 9 / 74 Description of hazard levels The safety instructions listed here, together with the three levels of danger will help avert property damage and injury. CAUTION CAUTION indicates a hazardous situation that can cause damage to property or mild to moderate injuries.
  • Page 10 2 Safety 10 / 74 WARNING WARNING indicates a hazardous situation that can lead to serious or fatal injury. DANGER DANGER indicates a maximal hazard due to a situation that can directly cause death or fatal injury.
  • Page 11: Safety Instructions

    2 Safety 11 / 74 2.2 Safety instructions WARNING Hazard from incorrectly reconditioned products. An infection hazard exists from contaminated products. ▶ Take suitable personal protective measures.
  • Page 12 2 Safety 12 / 74 WARNING Hazards for the care provider and the patient. In the case of damage, irregular running noise, excessive vibration, un- typical warming or when the cutter or grinder cannot be held. ▶ Do not use further and notify Service.
  • Page 13 2 Safety 13 / 74 CAUTION Hazard from use as a light probe. Do not use the device as a light probe since the rotating cutters or grind‐ ers can cause injury. ▶ Use an appropriate light probe for additional illumination of the oral cavity or site of preparation.
  • Page 14 ▶ The medical device should be cleaned, serviced and stored in a dry lo‐ cation, according to instructions, before long periods of nonuse. The following individuals are authorized to repair and service KaVo prod‐ ucts: ▪ Technicians at KaVo branches throughout the world...
  • Page 15 To ensure proper function, the medical device must be set up according to the reprocessing methods described in the KaVo Instructions for Use, and the care products and care systems described therein must be used. KaVo recommends specifying a service interval at the dental office for a licensed shop to clean, service and check the functioning of the medical device.
  • Page 16: Product Description

    3 Product description 16 / 74 3 Product description MASTERmatic LUX M07 L (Mat. no. 1.009.3610)
  • Page 17 3 Product description 17 / 74 MASTERmatic LUX M20 L (Mat. no. 1.009.3620)
  • Page 18 3 Product description 18 / 74 MASTERmatic LUX M29 L (Mat. no. 1.009.3580)
  • Page 19: Purpose - Intended Use

    3 Product description 19 / 74 3.1 Purpose – Intended use Indications for use: This medical device is ▪ intended for dental treatment only. All other types of use or modifica‐ tions of the product are not permitted and can be hazardous. The medical device, used in combination with the respective handpiece heads, is intended for the following applications: Removal of carious material, cavity and crown preparations, removal of fillings, processing...
  • Page 20 3 Product description 20 / 74 Proper use: According to these regulations, this medical device may only be used for the described application by a knowledgeable user. You need to comply with the following: ▪ the applicable health and safety regulations ▪...
  • Page 21: Technical Specifications M07 L

    3 Product description 21 / 74 ▪ avoid contamination from the product. 3.2 Technical Specifications M07 L Drive speed max. 40,000 rpm Step-down ratio 2.7 : 1 Maximum speed: max. 15,000 rpm identification 1 green ring Spray water pressure 0.8 to 2.0 bar (12 to 29 psi) Spray air pressure 1.0 to 2.0 bar (15 to 29 psi) Spray air quantity...
  • Page 22: Technical Specifications M20 L

    3 Product description 22 / 74 The shank can be mounted on all INTRAmatic motors and motors fitted with a connection in accordance with ISO 3964 / DIN 13940. 3.3 Technical Specifications M20 L Drive speed max. 40,000 rpm Step-down ratio 1 : 1 Maximum speed: max.
  • Page 23: Technical Specifications M29 L

    3 Product description 23 / 74 The shank can be mounted on all INTRAmatic motors and motors fitted with a connection in accordance with ISO 3964 / DIN 13940. 3.4 Technical Specifications M29 L Drive speed max. 40,000 rpm Step-down ratio 7.4 : 1 Maximum speed: max.
  • Page 24: Transportation And Storage Conditions

    3 Product description 24 / 74 The shank can be mounted on all INTRAmatic motors and motors fitted with a connection in accordance with ISO 3964 / DIN 13940. 3.5 Transportation and storage conditions CAUTION It is hazardous to start up the medical device after it has been stored strongly refrigerated.
  • Page 25 3 Product description 25 / 74 Relative humidity: 5% RH to 95% RH absence of condensation Air pressure: 700 hPa to 1060 hPa (10 psi to 15 psi) Protect from moisture...
  • Page 26: Start Up And Shut Down

    4 Start up and shut down 26 / 74 4 Start up and shut down WARNING Hazard from non-sterile products. Infection hazard for care provider and patient. ▶ Before first use and after each use, prepare and sterilise the medical device and accessories accordingly.
  • Page 27: Check The Amount Of Water

    4 Start up and shut down 27 / 74 4.1 Check the amount of water CAUTION Overheating of the tooth due to insufficient amount of cool‐ ing water. Thermal damage to the dental pulp. ▶ Adjust the water amount for the spray cooling to a minimum of 50 ml/ min!
  • Page 28 4 Start up and shut down 28 / 74 CAUTION Hazard from insufficient spray water. Insufficient spray water can cause the medical device to overheat and damage the tooth. ▶ Check the spray water channels and clean the spray nozzles with the nozzle needle Mat.
  • Page 29 4 Start up and shut down 29 / 74...
  • Page 30: Operation

    5 Operation 30 / 74 5 Operation 5.1 Attach the medical device WARNING Release of the medical device during treatment. A medical device that is not properly locked in place can release from the motor coupling and fall off. ▶ Carefully pull on it before each treatment to ensure that the medical device is securely locked on the motor coupling.
  • Page 31 5 Operation 31 / 74 CAUTION Removing and attaching the handpiece while the drive mo‐ tor is rotating. Damage to the catch. ▶ Never attach or remove the reducing shank while the device is rotat‐ ing! ▶ Attach medical device to the (LUX) motor coupling and turn it until the latch audibly snaps into place.
  • Page 32: Remove The Medical Device

    5 Operation 32 / 74 ▶ Pull on the medical device to make sure that it is securely affixed to the coupling. 5.2 Remove the medical device ▶ Unlock the medical device from the motor coupling and then pull it off along its axis.
  • Page 33: Insert The Intra Lux

    5 Operation 33 / 74 5.3 Insert the INTRA LUX CAUTION Loosening of the medical device during treatment. If the head is not properly locked in place, it can fall out during treatment. ▶ Do not mount or remove the head while rotating. Before each treat‐ ment, check that the head is firmly seated and that the clamping ring is tight.
  • Page 34: Remove The Intra Lux

    5 Operation 34 / 74 ▶ Insert the head to the stop. Make sure that the catches are properly seated. ▶ Rotate the clamping ring in the opposite direction (-> close) and tight‐ en it. 5.4 Remove the INTRA LUX ▶...
  • Page 35: Troubleshooting

    6 Troubleshooting 35 / 74 6 Troubleshooting 6.1 Check for malfunctions CAUTION Missing or damaged O-rings. Malfunctions and premature failure. ▶ Make sure that all O-rings are on the coupling and undamaged.
  • Page 36 6 Troubleshooting 36 / 74 CAUTION Heating of the product. Burns or product damage from overheating. ▶ Do not use the product if it is irregularly heated. ▶ The medical device is too hot while idling: Check the amount of cooling air. ▶...
  • Page 37 6 Troubleshooting 37 / 74 ▶ When the speed drops or is uneven: Caring for the medical device. ▶ An O-ring is missing on the motor coupling: Replace O-ring.
  • Page 38: Troubleshooting

    Hazard from improper care of the O-rings. Malfunctions or complete failure of the medical device. ▶ Do not use Vaseline or other grease or oil. Note The O-ring on the coupling may only be lubricated with a cotton ball wet with KAVO spray.
  • Page 39: Cleaning The Spray Nozzle

    6 Troubleshooting 39 / 74 ▶ Press the O-ring between your fingers to form a loop. ▶ Shove the O-ring to the front, and remove it. ▶ Insert new O-rings into the grooves. 6.2.2 Cleaning the spray nozzle CAUTION Hazard from insufficient spray water. Overheating of the medical device and damage to the tooth.
  • Page 40 6 Troubleshooting 40 / 74 ▶ Use the nozzle needle (Mat. no. 0.410.0921) to free the water pas‐ sage in the spray nozzles.
  • Page 41: Changing The Water Filter

    6 Troubleshooting 41 / 74 6.2.3 Changing the water filter CAUTION Hazard from insufficient spray water. Insufficient spray water can cause the medical device to overheat and damage the tooth. ▶ Check the filter and exchange if necessary. ▶ Check the spray water channels and clean the spray nozzles with the nozzle needle Mat.
  • Page 44: Reprocessing Steps In Accordance With Iso 17664

    7 Reprocessing steps in accordance with ISO 17664 44 / 74 ▶ Remove all residual cement, composite or blood without delay. ▶ Reprocess the medical device as soon as possible after treatment. ▶ The medical device must be dry when transported for reconditioning. ▶...
  • Page 45: Manual Cleaning - External

    C ± 5 C (86 F ± 10 ▪ Brush, e.g. medium-hard toothbrush ▶ Brush off under flowing tap water. 7.2.2 Automated external cleaning KaVo recommends washer disinfectors in compliance with EN ISO 15883-1, which are operated using alkaline cleaning agents.
  • Page 46: Manual Cleaning - Internal

    Validated interior cleaning (residual protein removal) can only be accom‐ plished with KaVo CLEANspray and KaVo DRYspray. ▶ Cover the medical device with the KaVo CLEANpac bag, and place it on the corresponding care adapter. Press the spray button three times for 2 seconds each time.
  • Page 47 See also: 2 KaVo CLEANspray / KaVo DRYspray Instructions for Use Note KaVo CLEANspray and KaVo DRYspray for manual interior cleaning are only available in the following countries: Germany, Austria, Switzerland, Italy, Spain, Portugal, France, Luxem‐ bourg, Belgium, Netherlands, United Kingdom, Denmark, Sweden, Fin‐...
  • Page 48: Automated Internal Cleaning

    7 Reprocessing steps in accordance with ISO 17664 48 / 74 7.2.4 Automated internal cleaning KaVo recommends washer disinfectors in compliance with EN ISO 15883-1, which are operated using alkaline cleaning agents. ▶ For programme settings as well as cleansers and disinfectants to be used, please refer to the Instructions for Use of the washer disinfec‐...
  • Page 49: Disinfection

    7 Reprocessing steps in accordance with ISO 17664 49 / 74 7.3 Disinfection WARNING Hazard due to incomplete disinfection. Principally, KaVo recommends carrying out an final disinfection of the un‐ packaged item if complete disinfection cannot be guaranteed without this measure.
  • Page 50 7 Reprocessing steps in accordance with ISO 17664 50 / 74 CAUTION Malfunctioning from using a disinfectant bath or disinfectant containing chlorine. Defects in the product. ▶ Only disinfect in a thermodisinfector or manually.
  • Page 51 7 Reprocessing steps in accordance with ISO 17664 51 / 74 CAUTION Malfunctioning from using the disinfectant bath or chlorine- containing disinfectants. Defects in the device. ▶ Do not use an ultrasonic bath. CAUTION Never use alkaline or chlorine-containing disinfectants. The saline solution corrodes the metal parts.
  • Page 52: Manual Disinfection - External

    7 Reprocessing steps in accordance with ISO 17664 52 / 74 7.3.1 Manual disinfection - external KaVo recommends the following products based on material compatibility. The microbiological efficacy must be ensured by the disinfectant manufac‐ turer. ▪ Mikrozid AF made by Schülke & Mayr (liquid or cloths) ▪...
  • Page 53: Manual Disinfection - Internal

    The efficacy of manual internal disinfection must be demonstrated by the manufacturer of the disinfection agent. With KaVo products, use only disin‐ fection agents that have been released by KaVo with respect to the com‐ patibility of materials (e.g. WL-cid / made by ALPRO).
  • Page 54: Machine Disinfection - External And Internal

    7 Reprocessing steps in accordance with ISO 17664 54 / 74 7.3.3 Machine disinfection - external and internal KaVo recommends washer disinfectors in compliance with EN ISO 15883-1, which are operated using alkaline cleaning agents. ▶ For programme settings as well as cleansers and disinfectants to be used, please refer to the Instructions for Use of the washer disinfec‐...
  • Page 55: Drying

    7 Reprocessing steps in accordance with ISO 17664 55 / 74 7.4 Drying Manual Drying ▶ Blow off the outside and inside with compressed air until water drops are no longer visible. Automatic Drying The drying procedure is usually a part of the cleaning program of the ther‐ modisinfector.
  • Page 56: Care Products And Systems - Servicing

    Reduced product life. ▶ Perform proper care regularly! Note KaVo only guarantees that its products will function properly when the care products are used that are listed as accessories since they were tes‐ ted for proper use on our products.
  • Page 57: Care With Kavo Spray

    7.5.1 Care with KaVo Spray Note The shank can be serviced either alone or with a head attached to it. KaVo recommends servicing the product as part of the reprocessing after each use, i.e. after each cleaning, disinfection, and before each sterilisa‐ tion.
  • Page 58: Care With The Kavo Sprayrotor

    7.5.2 Care with the KaVo SPRAYrotor Note The shank can be serviced either alone or with a head attached to it. ▶ Place the product on the appropriate coupling of the KaVo SPRAYro‐ tor and cover it with a Cleanpac bag. ▶ Servicing the product.
  • Page 59: Servicing With Kavo Quattrocare 2104 / 2104A

    59 / 74 See also: 2 Instructions for use KaVo SPRAYrotor 7.5.3 Servicing with KaVo QUATTROcare 2104 / 2104A Note The shank can be serviced either alone or with a head attached to it. Cleaning and servicing unit with expansion pressure for effective cleaning...
  • Page 60 7 Reprocessing steps in accordance with ISO 17664 60 / 74 Note QUATTROcare 2104 / 2104 A is no longer included in the current delivery programme. Follow-up products: ▶ QUATTROcare PLUS 2124 A ▶ QUATTROcare CLEAN 2140 A Servicing and cleaning device with expansion pressure for the interior cleaning of inorganic residues and optimum care.
  • Page 61 7 Reprocessing steps in accordance with ISO 17664 61 / 74 KaVo recommends servicing the product as part of the reprocessing after each use, i.e. after each cleaning, disinfection, and before each sterilisa‐ tion. ▶ Remove the cutter or grinder.
  • Page 62: Servicing With Kavo Quattrocare Plus 2124 A

    7 Reprocessing steps in accordance with ISO 17664 62 / 74 7.5.4 Servicing with KaVo QUATTROcare PLUS 2124 A Note The shank can be serviced either alone or with a head attached to it. Servicing and cleaning device with expansion pressure for the interior cleaning of inorganic residues and optimum care.
  • Page 63: Servicing With Kavo Quattrocare 2140 A

    63 / 74 ▶ Servicing the product in the QUATTROcare PLUS. See also: 2 Instructions for Use KaVo QUATTROcare PLUS 2124 A 7.5.5 Servicing with KaVo QUATTROcare 2140 A Programme-controlled cleaning and servicing device for perfect servicing of handpieces and turbines.
  • Page 64: Packaging

    7 Reprocessing steps in accordance with ISO 17664 64 / 74 See also: 2 Instructions for use KaVo QUATTROcare CLEAN 2140 A 7.6 Packaging Note The sterilisation bag must be large enough for the handpiece so that the bag is not stretched.
  • Page 65: Sterilisation

    Sterilisation in a steam steriliser (autoclave) in accordance with EN 13060 / ISO 17665-1 CAUTION Premature wear and malfunctions from improper servicing and care. Reduced product life. ▶ Before each sterilisation cycle, service the medical device with KaVo care products.
  • Page 66 Damage to product. ▶ Immediately remove the product from the steam steriliser after the sterilisation cycle! The KaVo medical device has a maximum temperature resistance of up to 138 ℃ (280.4 °F). Select a suitable procedure (depending on the available autoclave) from the following sterilisation processes: ▪...
  • Page 67: Storage

    7 Reprocessing steps in accordance with ISO 17664 67 / 74 ▪ Autoclave using the gravity method: - at least 10 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4 °F) ▶ Use according to the manufacturer's Instructions for Use. 7.8 Storage ▶...
  • Page 68: Tools And Consumables

    8 Tools and consumables 68 / 74 8 Tools and consumables Available from dental suppliers. Material summary Mat. No. Instrument stand 2151 0.411.9501 Cleanpac 10 units 0.411.9691 Cellulose pad 100 units 0.411.9862 Nozzle pin 0.410.0921 Replacement filter 1.002.0271 Wrench 1.002.0321 O-ring 0.200.6120...
  • Page 69 8 Tools and consumables 69 / 74 Material summary Mat. no. KaVo CLEANspray 2110 P 1.007.0579 KaVo DRYspray 2117 P 1.007.0580 KaVo Spray 2112 A 0.411.9640 ROTAspray 2 2142 A 0.411.7520 QUATTROcare plus Spray 2140 P 1.005.4525...
  • Page 70: Warranty Terms And Conditions

    24 months from data of invoice, subject to the following conditions: In case of justified complaints, KaVo will honour its warranty with a free re‐ placement or repair. Other claims of any nature whatsoever, in particular with respect to compensation, are excluded.
  • Page 71 9 Warranty terms and conditions 71 / 74 ance with KaVo's instructions for use or other manufacturer's instructions. The warranty does not usually cover lamps, light conductors made of glass and glass fibres, glassware, rubber parts and the colourfastness of plastic parts.
  • Page 72 9 Warranty terms and conditions 72 / 74...

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