Related Manuals for KaVo EXPERTmatic LUX E15 L
Summary of Contents for KaVo EXPERTmatic LUX E15 L
- Page 1 Instructions for use EXPERTmatic LUX E15 L - REF 1.007.5530 EXPERTmatic LUX E20 L - REF 1.007.5540 EXPERTmatic E15 C - REF 1.007.5531 EXPERTmatic E20 C - REF 1.007.5541...
- 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...
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Page 3: Table Of Contents
Table of contents Table of contents 1 User instructions ............................... 5 2 Safety ................................7 Safety instructions ..........................7 3 Product description ............................13 Purpose – Proper use ........................... 17 Technical Specifications E15 L / E15 C ....................19 Technical Specifications E20 L / E20 C ....................20 Transportation and storage conditions .................... - Page 4 Table of contents Remove the medical device ......................... 30 Inserting the milling tool or diamond grinder ..................30 Removing the milling tool or diamond grinder ..................34 6 Troubleshooting .............................. 36 Check for malfunctions ......................... 36 Troubleshooting ............................ 37 6.2.1 Troubleshooting: Exchanging the O-rings on the motor coupling ...........
- Page 5 Disinfection: Machine disinfection - external and internal ............50 Drying ..............................51 Care products and systems - Servicing ....................52 7.5.1 Care products and systems - Servicing: Care with KaVo Spray ..........53 7.5.2 Care products and systems - Servicing: Care with KaVo SPRAYrotor ........55 7.5.3 Care products and systems - Servicing: Servicing with KaVo QUATTROcare .......
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Page 6: Table Of Contents
Table of contents 8 Tools and consumables ..........................63 9 Terms and conditions of warranty ........................64... -
Page 7: User Instructions
User instructions 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 Refer to the Chapter on Safety/Warning symbol... - Page 8 User instructions Action request CE mark (European Community). A product bearing this mark meets the requirements of the applicable EC directive. Can be steam-sterilised at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4 °F) Thermodisinfectable Target group This document is intended for dentists and their assistants.
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Page 9: Safety
Safety 2 Safety 2.1 Safety instructions WARNING Hazard to the care provider and patient. In the case of damage, irregular running noise, excessive vibration, un- typical warming or when the cutter or grinder is not held firmly. ▶ Stop working and contact service support. - Page 10 ▶ A note is to be included in the documents accompanying the dental treatment unit, referring to responsibilities arising from safety, relia‐ bility and performance. ▶ The medical device may only be combined with a treatment centre released by KaVo.
- Page 11 Safety CAUTION Risk due to incorrectly stored handpiece. Injury and infection caused by chucked cutter or grinder. ▶ After treatment, place the handpiece properly in the cradle, without the cutter or grinder. CAUTION Risk of burn injury from hot handpiece head or hot handpiece lid. Burn injuries in the mouth may be caused if the instrument overheats.
- Page 12 Safety CAUTION Premature wear and malfunctioning from improper storage during long periods of nonuse. Reduced product life. ▶ The medical device should be cleaned, serviced and stored in a dry location, according to instructions, before long periods of nonuse. CAUTION Hazard from use as a light probe.
- Page 13 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 14 Safety Service may only be carried out by KaVo-trained repair shops using original KaVo replacement parts.
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Page 15: Product Description
Product description 3 Product description EXPERTmatic LUX contra-angle handpiece E15 L (Mat. no. 1.007.5530) - Page 16 Product description EXPERTmatic LUX contra-angle handpiece E20 L (Mat. no. 1.007.5540)
- Page 17 Product description EXPERTmatic contra-angle handpiece E15 C (Mat. no. 1.007.5531)
- Page 18 Product description EXPERTmatic contra-angle handpiece E20 C (Mat. no. 1.007.5541)
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Page 19: Purpose - Proper Use
Product description 3.1 Purpose – Proper use Purpose: This medical device is ▪ intended for dental treatment only. Any other type of use or alteration to the product is impermissible and can be hazardous. The medical device is intended for the following applications: preparation of cavities, caries excavation, endodontic applications, processing of tooth and restoration surfaces. - Page 20 Product description Proper use: According to these regulations, this medical device may only be used for the described application by a knowledgeable user. The following must be observed: ▪ the applicable health and safety regulations ▪ the applicable accident prevention regulations ▪...
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Page 21: Technical Specifications E15 L / E15 C
Product description Technical Specifications E15 L / E15 C Drive speed max. 40,000 rpm Identification 1 green ring Speed transmission 5.4 : 1 With press-button chuck. Usable with contra-angle cutters or grinders. The contra-angle handpiece can be mounted on all INTRAmatic (LUX) mo‐ tors, and motors with a connection in accordance with ISO 3964 / DIN 13940. -
Page 22: Technical Specifications E20 L / E20 C
Product description 3.3 Technical Specifications E20 L / E20 C Drive speed max. 40,000 rpm Identification 1 blue ring Speed transmission 1 : 1 With press-button chuck. Usable with contra-angle cutters or grinders. The contra-angle handpiece can be mounted on all INTRAmatic (LUX) mo‐ tors, and motors with a connection in accordance with ISO 3964 / DIN 13940. -
Page 23: Transportation And Storage Conditions
Product description 3.4 Transportation and storage conditions CAUTION It is hazardous to start up the medical device after it has been stored strongly refrigerated. This can cause the medical device to malfunction. ▶ Prior to start-up, very cold products must be heated to a temperature of 20°C to 25°C (68°F to 77°F). - Page 24 Product description Air pressure: 700 hPa to 1060 hPa (10 psi to 15 psi) Protect from moisture...
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Page 25: First Use
First use 4 First use WARNING Hazard from nonsterile products. Infection danger to the care provider and patient. ▶ Before first use and after each use, prepare and sterilise the medical device if needed. - Page 26 First use CAUTION Damage from soiled and moist cooling air. Contaminated and moist cooling air can cause malfunctions and lead to premature bearing wear. ▶ Make sure that the supply of cooling air is dry, clean and unconta‐ minated according to ISO 7494-2.
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Page 27: Check The Amount Of Water
First use 4.1 Check the amount of water CAUTION Overheating of the tooth due to lack of cooling water. Thermal damage to the dental pulp. ▶ Adjust the water amount for the spray cooling to a minimum of 50 /min... - Page 28 First use 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. no. 0.410.0921 if necessary.
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Page 29: Operation
Operation 5 Operation 5.1 Attach the medical device WARNING Detachment of the medical device during treatment. A medical device that is not properly locked in place can become discon‐ nected from the motor coupling and fall off. ▶ Carefully pull on the medical device before each treatment to ensure that it is securely locked onto the motor coupling. - Page 30 Operation CAUTION Removing and attaching the contra-angle handpiece while the drive motor is rotating. Damage to the drive. ▶ Never attach or remove the contra-angle handpiece while the drive motor is rotating! CAUTION Damage If the footswitch is pressed while you are connecting and removing the medical device, you can damage the medical device and motor coupling.
- Page 31 Operation ▶ Lightly spray O-rings on motor coupling with Mehrfunktionsspritze Spray. ▶ Attach the medical device to the motor coupling and turn it until the guide stud audibly snaps into place. ▶ Pull on the medical device to make sure that it is securely affixed to the coupling.
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Page 32: Remove The Medical Device
Operation 5.2 Remove the medical device ▶ Unlock the medical device from the motor coupling by twisting it slightly and then pulling it along its axis. 5.3 Inserting the milling tool or diamond grinder Note Only use carbide cutters or diamond burs that correspond to ISO 1797-1 type 1, are made of steel or tungsten carbide and meet the following cri‐... - Page 33 Operation WARNING Use of unauthorised cutters or grinders. Injury to the patient or damage to the medical device. ▶ Observe the instructions for use and use the cutter or grinder prop‐ erly. ▶ Only use cutters or grinders that do not deviate from the specified data.
- Page 34 Operation CAUTION Danger of injury from cutters or grinders. Infections or cuts. ▶ Wear gloves or fingerstalls. CAUTION Hazard from defective chucking system. The cutter or grinder could fall out and cause injury. ▶ Pull on the cutter or grinder to check that the chucking system is okay and the cutter or grinder is securely held.
- Page 35 Operation ▶ Press the push button firmly with your thumb and simultaneously insert the milling or grinding tool until it contacts the stop. ▶ Check that the cutter or grinder is securely attached by pulling on it.
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Page 36: Removing The Milling Tool Or Diamond Grinder
Operation 5.4 Removing the milling tool or diamond grinder WARNING Hazard from rotating cutter or grinder. Lacerations and damage to the chucking system. ▶ Do not touch rotating cutter or grinder.! ▶ Never press the press-button while the cutter or grinder is rotating! ▶... - Page 37 Operation ▶ After the cutter or grinder has stopped rotating, press the press-button with your thumb and simultaneously pull out the drill bit or bur.
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Page 38: Troubleshooting
Troubleshooting 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. CAUTION Heating of the product. Burns or product damage from overheating. ▶ Do not use the product if it is irregularly heated. -
Page 39: Troubleshooting
Troubleshooting ▶ The medical device is too hot while idling: Check the amount of cooling air. ▶ The medical device is too hot while working: Caring for the medical device. ▶ When the speed drops or is uneven: Caring for the medical device. ▶... - Page 40 Troubleshooting Note The O-rings on the motor coupling may only be lubricated with a cotton ball wetted with KaVo spray. ▶ Press the O-ring between your fingers to form a loop. ▶ Shove the O-ring to the front, and remove it.
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Page 41: Troubleshooting: Cleaning The Spray Nozzle
Troubleshooting 6.2.2 Troubleshooting: Cleaning the spray nozzle CAUTION Hazard from insufficient amount of spray water. Insufficient spray water can cause the medical device to overheat and damage the tooth. ▶ Check spray water channels and if necessary clean spray nozzles with the nozzle needle (Mat. - Page 42 Troubleshooting ▶ Clean the water passage in the spray nozzles by using the nozzle needle (Mat. no. 0.410.0921).
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Page 43: Setup Methods According To Din En Iso 17664
Setup methods according to DIN EN ISO 17664 7 Setup methods according to DIN EN ISO 17664 7.1 Preparation at the site of use WARNING Hazard from nonsterile products. There is a risk of infection from contaminated medical devices. ▶ Take suitable personal protective measures. ▶... -
Page 44: Cleaning
Setup methods according to DIN EN ISO 17664 7.2 Cleaning CAUTION Malfunctions from cleaning in the ultrasonic unit. Defects in the product. ▶ Only clean manually or in a thermodisinfector. 7.2.1 Cleaning: Manual cleaning - external Accessories required: ▪ Tap water 30 °C ± 5 °C (86 °F ± 10 °F) ▪... -
Page 45: Cleaning: Automated External Cleaning
Brush off under flowing tap water. 7.2.2 Cleaning: Automated external cleaning KaVo recommends thermodesinfectors in accordance with EN ISO 15883-1 that are operated with alkaline cleaning agents at a pH value of max. 10 (e. g. Miele G 7781 / G 7881 – validation was performed with the "VARIO-TD"... -
Page 46: Cleaning: Manual Cleaning - Internal
Can only be done with KaVo CLEANspray or 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. Remove the medical device from the spray... - Page 47 Setup methods according to DIN EN ISO 17664 ▶ Afterwards, rinse for 3-5 seconds with KaVo DRYspray. See also: 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‐...
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Page 48: Cleaning: Automated Internal Cleaning
Setup methods according to DIN EN ISO 17664 7.2.4 Cleaning: Automated internal cleaning KaVo recommends thermodesinfectors in accordance with EN ISO 15883-1 that are operated with alkaline cleaning agents at a pH value of max. 10 (e. g. Miele G 7781 / G 7881 – validation was performed with the "VARIO-TD"... -
Page 49: Disinfection
▶ In order to prevent negative effects on the medical device, make sure that the interior and the exterior of the medical device are dry, and then lubricate immediately with care agents from the KaVo care system. 7.3 Disinfection CAUTION Malfunctioning from using a disinfectant bath or disinfectant containing chlorine. -
Page 50: Disinfection: Manual Disinfection - External
Setup methods according to DIN EN ISO 17664 7.3.1 Disinfection: 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 Liquid made by Schülke & Mayr ▪... -
Page 51: Disinfection: Manual Disinfection - Internal
The efficacy of manual internal disinfection must be demonstrated by the manufacturer of the disinfection agent. With KaVo products, use only dis‐ infection agents that have been released by KaVo with respect to the com‐ patibility of materials (e.g. WL-cid / made by ALPRO). -
Page 52: Disinfection: Machine Disinfection - External And Internal
Follow the instructions for use of the disinfectant. 7.3.3 Disinfection: Machine disinfection - external and internal KaVo recommends thermodesinfectors in accordance with EN ISO 15883-1 that are operated with alkaline cleaning agents at a pH value of max. 10 (e. g. Miele G 7781 / G 7881 – validation was performed with the "VARIO-TD"... -
Page 53: Drying
In order to prevent negative effects on the medical device, make sure that the interior and the exterior of the medical device are dry, and then lubricate immediately with care agents from the KaVo care system. 7.4 Drying Manual Drying ▶... -
Page 54: Care Products And Systems - Servicing
Setup methods according to DIN EN ISO 17664 7.5 Care products and systems - Servicing WARNING Sharp cutters or grinders in the medical device. Risk of injury from sharp or pointed cutters or grinders. ▶ Remove cutter or grinder. CAUTION Premature wear and malfunctions from improper servicing and care. -
Page 55: Care Products And Systems - Servicing: Care With Kavo Spray
7.5.1 Care products and systems - Servicing: Care with KaVo Spray KaVo recommends servicing the product after each time it is used, i.e. after each automatic cleaning and before each sterilisation. ▶... - Page 56 Setup methods according to DIN EN ISO 17664 Care of chucking system KaVo recommends cleaning and servicing the chuck system once a week. ▶ Remove the cutter or grinder, place the spray nipple tip in the opening and spray. ▶...
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Page 57: Care Products And Systems - Servicing: Care With Kavo Sprayrotor
Setup methods according to DIN EN ISO 17664 7.5.2 Care products and systems - Servicing: Care with KaVo SPRAYrotor KaVo recommends servicing the product after each time it is used, i.e. after each automatic cleaning and before each sterilisation. ▶... - Page 58 Setup methods according to DIN EN ISO 17664 KaVo recommends servicing the product after each time it is used, i.e. after each automatic cleaning and before each sterilisation. ▶ Remove cutter or grinder. ▶ Service the product. Care of chucking system KaVo recommends cleaning and servicing the chuck system once a week.
- Page 59 Setup methods according to DIN EN ISO 17664 ▶ Remove the cutter or grinder, place the spray nipple tip in the opening and spray. ▶ Subsequently treat with the care products and care systems specified. See also: Care with KaVo QUATTROcare...
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Page 60: Packaging
The quality and use of the sterilisation packaging must satisfy applicable standards and be suitable for the sterilisation procedure! ▶ Individually weld the medical device in the sterilised item packaging (such as KaVo STERIclave bags Mat. no. 0.411.9912)! -
Page 61: Sterilisation
7.7 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 62 Setup methods according to DIN EN ISO 17664 CAUTION Contact corrosion due to moisture. Damage to product. ▶ Immediately remove the product from the steamsteriliserafter the sterilisation cycle! The KaVo medical device has a maximum temperature resistance up to 138 ℃ (280.4 °F).
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Page 63: Storage
Setup methods according to DIN EN ISO 17664 (Depending on the available autoclave,) select a suitable procedure from the following sterilisation processes: ▪ Autoclave with three times initial vacuum: – at least 3 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4 °F) ▪... - Page 64 Setup methods according to DIN EN ISO 17664 ▶ Comply with the expiry date of the sterilised items.
- Page 65 Cellulose pad 100 units 0.411.9862 Cleanpac 10 units 0.411.9691 Nozzle needle 0.410.0921 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 66 18 months from the date of the invoice, subject to the following condi‐ tions: In case of justified complaints, KaVo will honour its warranty with a free replacement or repair. Other claims of any nature whatsoever, in particular with respect to compensation, are excluded. In the event of default, gross negligence or intent, this shall only apply in the absence of mandatory legal regulations to the contrary.
- Page 67 Terms and conditions of warranty ical or electrical factors deemed abnormal or impermissible in accordance with KaVo's instructions for use or other manufacturer's instructions. The warranty granted does not usually extend to lamps, light conductors made of glass and glass fibres, glassware, rubber parts, and the colourfastness of plastic parts.