KaVo EXPERTmatic E15 C Instructions For Use Manual Download Page 10

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CAUTION

Risks due to lack of control equipment.

Hazards can arise if control equipment is not available for changing the

speed and the direction of rotation.

▶ The dental treatment unit connected must have control equipment

for changing the speed and direction of rotation.

▶ 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.

Safety

Summary of Contents for EXPERTmatic E15 C

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 KaVo Dental GmbH Bismarckring 39 D 88400 Biberach Phone 49 7351 56 0 Fax 49 7351 56 1488 Manufacturer Kaltenbach Voigt GmbH Bismarckring 39 D 88400 Biberach www kavo com ...

Page 3: ...description 13 3 1 Purpose Proper use 17 3 2 Technical Specifications E15 L E15 C 19 3 3 Technical Specifications E20 L E20 C 20 3 4 Transportation and storage conditions 21 4 First use 23 4 1 Check the amount of water 25 5 Operation 27 5 1 Attach the medical device 27 Table of contents 1 ...

Page 4: ...Troubleshooting 37 6 2 1 Troubleshooting Exchanging the O rings on the motor coupling 37 6 2 2 Troubleshooting Cleaning the spray nozzle 39 7 Setup methods according to DIN EN ISO 17664 41 7 1 Preparation at the site of use 41 7 2 Cleaning 42 7 2 1 Cleaning Manual cleaning external 42 7 2 2 Cleaning Automated external cleaning 43 7 2 3 Cleaning Manual cleaning internal 44 Table of contents 2 ...

Page 5: ...Machine disinfection external and internal 50 7 4 Drying 51 7 5 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 55 7 6 Packaging 58 7 7 Sterilisation 59 7 8 Storage 61 Table of contents 3 ...

Page 6: ...8 Tools and consumables 63 9 Terms and conditions of warranty 64 Table of contents 4 ...

Page 7: ... 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 Important information for users and service technicians User instructions 5 ...

Page 8: ...equirements 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 The section on starting up is also intended for service technicians User instructions 6 ...

Page 9: ...s 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 Safety 7 ...

Page 10: ...e dental treatment unit connected must have control equipment for changing the speed and direction of rotation 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 Safety 8 ...

Page 11: ...r 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 Never touch soft tissue with the handpiece head or handpiece lid Safety 9 ...

Page 12: ...dical 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 Do not use the medical device as a light probe Use an appropriate light probe for additional illumination of the oral cavity or site of preparation Safety 10 ...

Page 13: ...ined by KaVo 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 This service interval de...

Page 14: ...Service may only be carried out by KaVo trained repair shops using original KaVo replacement parts Safety 12 ...

Page 15: ...3 Product description EXPERTmatic LUX contra angle handpiece E15 L Mat no 1 007 5530 Product description 13 ...

Page 16: ...EXPERTmatic LUX contra angle handpiece E20 L Mat no 1 007 5540 Product description 14 ...

Page 17: ...EXPERTmatic contra angle handpiece E15 C Mat no 1 007 5531 Product description 15 ...

Page 18: ...EXPERTmatic contra angle handpiece E20 C Mat no 1 007 5541 Product description 16 ...

Page 19: ...ion 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 A medical device according to relevant national statutory regulations Product description 17 ...

Page 20: ...h and safety regulations the applicable accident prevention regulations these instructions for use According to these regulations it is the responsibility of the user to only use equipment that is operating correctly use the equipment for the proper purpose protect him or herself the patient and third parties from danger and avoid contamination from the product Product description 18 ...

Page 21: ...ication 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 Product description 19 ...

Page 22: ...ification 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 Product description 20 ...

Page 23: ...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 Temperature 20 C to 70 C 4 F to 158 F Relative humidity 5 RH to 95 RH absence of condensation Product description 21 ...

Page 24: ...Air pressure 700 hPa to 1060 hPa 10 psi to 15 psi Protect from moisture Product description 22 ...

Page 25: ...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 First use 23 ...

Page 26: ...d 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 First use 24 ...

Page 27: ...heck 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 cm3 min First use 25 ...

Page 28: ...ient 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 First use 26 ...

Page 29: ...al 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 Operation 27 ...

Page 30: ... 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 Do not connect or remove the medical device while pressing the footswitch Operation 28 ...

Page 31: ...ing 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 Operation 29 ...

Page 32: ...nd 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 teria shaft diameter 2 334 to 2 35 mm overall length max 22 mm Operation 30 ...

Page 33: ...structions for use and use the cutter or grinder prop erly Only use cutters or grinders that do not deviate from the specified data CAUTION Injury from using worn cutters or grinders Cutters or grinders could fall out during treatment and injure the patient Never use cutters or grinders with worn shafts Operation 31 ...

Page 34: ... 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 When checking inserting and removing use gloves or a fingerstall to prevent an injury or in fection Operation 32 ...

Page 35: ...s 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 Operation 33 ...

Page 36: ...der 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 Remove the cutter or grinder from the contra angle handpiece after treatment to avoid injury or infection while storing it Operation 34 ...

Page 37: ... After the cutter or grinder has stopped rotating press the press button with your thumb and simultaneously pull out the drill bit or bur Operation 35 ...

Page 38: ...ng 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 Troubleshooting 36 ...

Page 39: ...e When the speed drops or is uneven Caring for the medical device An O ring is missing on the motor coupling Replace O ring 6 2 1 Troubleshooting Exchanging the O rings on the motor coupling CAUTION Hazard from improper care of the O rings Malfunctions or complete failure of the product Do not use Vaseline or other grease or oil Troubleshooting 37 ...

Page 40: ...or 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 Insert new O rings into the grooves Troubleshooting 38 ...

Page 41: ...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 no 0 410 0921 Troubleshooting 39 ...

Page 42: ... Clean the water passage in the spray nozzles by using the nozzle needle Mat no 0 410 0921 Troubleshooting 40 ...

Page 43: ...ces Take suitable personal protective measures Remove all residual cement composite or blood without delay Recondition the medical device as soon as possible after treatment Remove the cutter or grinder from the medical device The medical device must be dry when transported for reconditioning Do not place it in a solution or similar Setup methods according to DIN EN ISO 17664 41 ...

Page 44: ... 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 Brush e g medium hard toothbrush Setup methods according to DIN EN ISO 17664 42 ...

Page 45: ...d 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 program neodisher mediclean cleaning agent neodisher Z neutralisation agent and neodisher mielclear rinsing agent and extends only to the compatibility of materials with respect to Ka Vo products Setup methods according to DIN EN ISO 17664 43 ...

Page 46: ...edical device are dry and then lubricate immediately with care agents from the KaVo care system 7 2 3 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 attachment...

Page 47: ...ual 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 land and Norway In other countries only automated interior cleaning with thermodisinfec tors in accordance with ISO 15883 1 Setup methods according to DIN EN ISO 17664 45 ...

Page 48: ... with the VARIO TD program neodisher mediclean cleaning agent neodisher Z neutralisation agent and neodisher mielclear rinsing agent and extends only to the compatibility of materials with respect to Ka Vo products For program settings as well as cleansers and disinfectants to be used please refer to the Instructions for Use of the thermodisinfector com plying with max pH value of 10 Setup methods...

Page 49: ...al 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 Defects in the product Only disinfect in a thermodisinfector or manually Setup methods according to DIN EN ISO 17664 47 ...

Page 50: ...n material compatibility The microbiological efficacy must be ensured by the disinfectant manufac turer Mikrozid AF Liquid made by Schülke Mayr FD 322 made by Dürr CaviCide made by Metrex Consumables required Cloths for wiping off the medical device Setup methods according to DIN EN ISO 17664 48 ...

Page 51: ...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 Immediately after internal disinfection lubricate the KaVo medical de vice immediately with care agents from the...

Page 52: ...7781 G 7881 validation was performed with the VARIO TD program neodisher mediclean cleaning agent neodisher Z neutralisation agent and neodisher mielclear rinsing agent and extends only to the compatibility of materials with respect to Ka Vo products For program settings as well as cleansers and disinfectants to be used please refer to the Instructions for Use of the thermodisinfector com plying w...

Page 53: ...with care agents from the KaVo care system 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 normally part of the cleaning program of the ther modisinfector Follow the instructions for use of the thermodisinfector Setup methods according to DIN EN ISO 17664 51 ...

Page 54: ... 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 Reduced product life Perform proper care regularly Setup methods according to DIN EN ISO 17664 52 ...

Page 55: ... 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 Remove cutter or grinder Cover the product with the CLEANpac bag Place the product on the cannula and press the spray button for one second Setup methods according to DIN EN ISO 17664 53 ...

Page 56: ...ervicing the chuck system once a week Remove the cutter or grinder place the spray nipple tip in the opening and spray Carry out the servicing according to the instructions in the section Care with KaVo Spray Setup methods according to DIN EN ISO 17664 54 ...

Page 57: ...h sterilisation Place the product on the appropriate coupling of the KaVo SPRAYrotor and cover it with a CLEANpac bag Service the product See also Instructions for use KaVo SPRAYrotor 7 5 3 Care products and systems Servicing Servicing with KaVo QUATTROcare Cleaning and care unit with expansion pressure for effective cleaning and care Setup methods according to DIN EN ISO 17664 55 ...

Page 58: ... 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 See also Instructions for use KaVo QUATTROcare Setup methods according to DIN EN ISO 17664 56 ...

Page 59: ...er 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 Setup methods according to DIN EN ISO 17664 57 ...

Page 60: ...tretched 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 Setup methods according to DIN EN ISO 17664 58 ...

Page 61: ... 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 Setup methods according to DIN EN ISO 17664 59 ...

Page 62: ...oisture 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 Setup methods according to DIN EN ISO 17664 60 ...

Page 63: ... F 7 4 F Autoclave using the gravitation method at least 10 minutes at 134 C 1 C 4 C 273 F 1 6 F 7 4 F or alternatively at least 60 minutes at 121 C 1 C 4 C 250 F 1 6 F 7 4 F Use according to the manufacturer s Instructions for Use 7 8 Storage Prepared products must be stored protected from germs as far as possi ble and dust in a dry dark cool room Setup methods according to DIN EN ISO 17664 61 ...

Page 64: ... Comply with the expiry date of the sterilised items Setup methods according to DIN EN ISO 17664 62 ...

Page 65: ...9501 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 Tools and consumables 63 ...

Page 66: ...y 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 KaVo shall not be liable for defects and their consequences that have arisen or may arise from natural wear improper handling cleaning ...

Page 67: ...stness of plastic parts All liability is excluded if defects or their consequences originate from ma nipulations or changes to the product made by the customer or a third party that is not authorised by KaVo Warranty claims will only be accepted if the product is submitted along with proof of purchase in the form of a copy of the invoice or note of delivery The dealer purchase date type and serial...

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