KaVo INTRAcompact contra-angle 2967 LHC Instructions For Use Manual Download Page 1

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Instructions for use

INTRAcompact contra-angle 2967 LHC - REF 1.003.7704

Summary of Contents for INTRAcompact contra-angle 2967 LHC

Page 1: ...Instructions for use INTRAcompact contra angle 2967 LHC REF 1 003 7704...

Page 2: ...Distributed by KaVo Dental GmbH Bismarckring 39 D 88400 Biberach Tel 49 7351 56 0 Fax 49 7351 56 1488 Manufacturer Kaltenbach Voigt GmbH Bismarckring 39 D 88400 Biberach www kavo com...

Page 3: ...nstructions 6 1 1 Warranty terms and conditions 9 2 Safety 12 2 1 Description of safety instructions 12 2 2 Purpose Intended use 16 2 3 Safety instructions 18 3 Product Description 23 3 1 Technical Da...

Page 4: ...st Use 27 4 1 Cooling medium supply 28 5 Operation 29 5 1 Attaching the medical device 29 5 2 Removing the medical device 32 5 3 Insert the milling cutters or diamond grinders 33 5 4 Removing the cutt...

Page 5: ...ccording to ISO 17664 44 7 1 Preparations at the site of use 44 7 2 Cleaning 46 7 2 1 Cleaning Manual cleaning external 47 7 2 2 Cleaning Automated external cleaning 49 7 2 3 Cleaning Manual cleaning...

Page 6: ...ion Automated disinfection external and internal 57 7 4 Drying 58 7 5 Care products and systems Servicing 60 7 5 1 Care products and systems Servicing Care with KaVo Spray 62 7 5 2 Care products and s...

Page 7: ...7 6 Packaging 71 7 7 Sterilisation 73 7 8 Storage 76 8 Tools 78 Table of contents 5...

Page 8: ...ions 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 User...

Page 9: ...Symbols See the Safety Warning Symbols chapter Important information for users and technicians Disinfectable by heat User instructions 7...

Page 10: ...Steriliseable in steam up to 135 C 275 F CE mark European Community A product with this mark meets the requirements of the applicable EC directive Call to Action User instructions 8...

Page 11: ...s 1 1 Warranty terms and conditions The following warranty conditions apply to this KaVo medical device KaVo provides the end customer with a warranty of proper function and guarantees zero defects in...

Page 12: ...d their consequences that have arisen or may arise from to natural wear improper handling cleaning or maintenance non compliance with operating main tenance or connection instructions calcination or c...

Page 13: ...y be accepted if the product is submitted along with proof of purchase in the form of a copy of the invoice delivery note The dealer purchase date type and serial number must be clearly visible on thi...

Page 14: ...2 Safety 2 1 Description of safety instructions Warning symbol Safety 12...

Page 15: ...DANGER The introduction describes the type and source of the danger This section describes the potential consequences of non observance The optional step covers measures necessary for avoiding hazards...

Page 16: ...ty 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 mil...

Page 17: ...WARNING WARNING indicates a hazardous situation that can cause death or serious injury DANGER DANGER indicates a maximum hazardous situation that can directly cause serious injury or death Safety 15...

Page 18: ...ment Any other type of use or alteration to the product is im permissible and can be hazardous The medical device is intended for the following uses cavity preparation caries excavation endodontics A...

Page 19: ...le health and safety regulations the applicable accident prevention regulations these Instructions for use According to these regulations the user is required to only use equipment that is operating c...

Page 20: ...ING 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 a...

Page 21: ...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 referrin...

Page 22: ...alfunctioning 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...

Page 23: ...ters or grinders Damage to clamping system from dropping the instrument After treatment place the instrument properly in the cradle without the cutter or grinder Note For safety reasons we recommend t...

Page 24: ...d in the KaVo instructions for use and the care products and methods described therein must be used KaVo recommends specifying a service interval at the dental office for a licensed shop to clean serv...

Page 25: ...3 Product Description INTRAcompact contra angle 2967 LHC Mat no 1 003 7704 Product Description 23...

Page 26: ...3 1 Technical Data Drive speed max 40 000 rpm Identification 2 green rings Speed transmission 14 8 1 With press button chuck Usable with contra angle cutters or grinders Product Description 24...

Page 27: ...h ISO 3964 DIN 13940 3 2 Transportation and Storage Conditions CAUTION Starting up the medical device can be hazardous after it has been stored in an excessively cold location The medical device can m...

Page 28: ...Temperature 20 C to 70 C 4 F to 158 F Relative humidity 5 RH to 95 RH Air pressure 700 hPa to 1060 hPa 10 psi to 15 psi Protect from moisture Product Description 26...

Page 29: ...4 First Use WARNING Hazard from non sterile products Infection danger to the care provider and patient Before first use and after each use sterilise the medical device First Use 27...

Page 30: ...Cooling medium supply 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...

Page 31: ...al device during treatment A medical device that is not properly locked in place can become disconnected from the motor coupling and fall off Carefully pull on the medical device before each treatment...

Page 32: ...ION 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 Operatio...

Page 33: ...Connect the medical device to the LUX motor coupling until it locks into place and twist it until the catch audibly locks Operation 31...

Page 34: ...re that the medical device is securely attached to the coupling 5 2 Removing the medical device Unlock the medical device from the LUX motor coupling by twisting it slightly and then pulling it along...

Page 35: ...mond grinders 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 criteria shaft diameter 2 334 to 2 35 mm o...

Page 36: ...tters or grinders Injury to the patient or damage to the medical device Observe the instructions for use and use the cutter or grinder properly Only use cutters or grinders that do not deviate from th...

Page 37: ...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 35...

Page 38: ...CAUTION Danger of injury from cutters or grinders Infections or cuts Wear gloves or fingerstalls Operation 36...

Page 39: ...nder 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...

Page 40: ...Insert the cutter or grinder into the segment of the head drive by twisting the tool slightly and push to the stop Operation 38...

Page 41: ...Check that the tool is seated by pulling on it Operation 39...

Page 42: ...er 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 cont...

Page 43: ...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 41...

Page 44: ...spray nozzle CAUTION Hazard from insufficient spray water Insufficient spray water can cause the medical device to overheat and damage the tooth If the amount of spray water is insufficient unblock th...

Page 45: ...Use the nozzle needle Mat no 0 410 0921 to free the water passage in the spray nozzles Troubleshooting 43...

Page 46: ...of use WARNING Hazard from non sterile products There is a risk of infection from contaminated medical devices Observe suitable personal protective measures Remove any residual cement composite or blo...

Page 47: ...y when transporting it to be prepared Do not place it in a solution or the like Prepare the medical device directly after treatment Remove the cutter or grinder from the medical device Preparation met...

Page 48: ...7 2 Cleaning CAUTION Malfunctions from cleaning in an ultrasonic unit Defects in the product Only clean manually or in a thermodisinfector Preparation methods according to ISO 17664 46...

Page 49: ...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 Preparation methods according to ISO 17664 47...

Page 50: ...Brush off under flowing tap water Preparation methods according to ISO 17664 48...

Page 51: ...the program VARIO TD the detergent neodisher mediclean the neutraliser neodisher Z and rinse neodisher mielclear and only refers to the material compatibility with KaVo products The program settings...

Page 52: ...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 a...

Page 53: ...ng countries Germany Austria Switzerland Italy Spain Portugal France Luxembourg Belgium Netherlands United Kingdom Denmark Sweden Finland and Norway In other countries only automated interior cleaning...

Page 54: ...the program VARIO TD the detergent neodisher mediclean the neutraliser neodisher Z and rinse neodisher mielclear and only refers to the material compatibility with KaVo products The program settings...

Page 55: ...care products and systems provided by KaVo 7 3 Disinfection CAUTION Malfunctioning from using a disinfectant bath or disinfectant containing chlorine Defects in the product Only disinfect in a thermod...

Page 56: ...ual disinfection external KaVo recommends the following products based on material compatibility The microbiological ef ficacy must be ensured by the disinfectant manufacturer Preparation methods acco...

Page 57: ...x Tools required Cloths for wiping down the medical device Spray the disinfectant on a cloth then thoroughly wipe down the medical device and leave the disinfectant to soak in according to the instruc...

Page 58: ...infection internal For the effective re preparation the inside of the device must be cleaned automatically in a cleaning and disinfection unit in accordance with ISO 15883 1 The interior of this produ...

Page 59: ...formed with the program VARIO TD the detergent neodisher mediclean the neutraliser neodisher Z and rinse neodisher mielclear and only refers to the material compatibility with KaVo products The progra...

Page 60: ...ystems provided by KaVo 7 4 Drying Manual drying Blow off the outside and inside with compressed air until water drops are no longer visible Machine drying The drying procedure is normally part of the...

Page 61: ...Note Please observe the instructions for use of the thermodisinfector Preparation methods according to ISO 17664 59...

Page 62: ...oducts and systems Servicing CAUTION Sharp cutters or grinders in the medical device Injury hazard from sharp or pointed cutters or grinders Remove cutter or grinder Preparation methods according to I...

Page 63: ...educed product life Perform proper care regularly Note KaVo only guarantees that its products will function properly when the care products used are those listed as accessories as they were tested for...

Page 64: ...g the project after each time it 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...

Page 65: ...Chuck care KaVo recommends cleaning and servicing the chuck system once a week Preparation methods according to ISO 17664 63...

Page 66: ...Remove the cutter or grinder place the spray nipple tip in the opening and spray Preparation methods according to ISO 17664 64...

Page 67: ...Note Carry out servicing according to instructions in the section Care with KaVo Spray Preparation methods according to ISO 17664 65...

Page 68: ...o recommends servicing the project after each time it used i e after each automatic cleaning and before each sterilisation Place the product on the appropriate coupling of the KaVo SPRAYrotor and cove...

Page 69: ...Instructions for use KaVo SPRAYrotor 7 5 3 Care products and systems Servicing Care with KaVo QUATTROcare Cleaning and care unit with expansion pressure for effective cleaning and care Preparation met...

Page 70: ...KaVo recommends servicing the project after each time it used i e after each automatic cleaning and before each sterilisation Remove cutter or grinder Preparation methods according to ISO 17664 68...

Page 71: ...Service the product Chuck care KaVo recommends cleaning and servicing the chuck system once a week See also Instructions for use KaVo QUATTROcare Preparation methods according to ISO 17664 69...

Page 72: ...Remove the cutter or grinder place the spray nipple tip in the opening and spray Preparation methods according to ISO 17664 70...

Page 73: ...are 7 6 Packaging Note The sterilisation bag must be large enough for the instrument so that the bag is not stretched The quality and use of the sterilised product packaging must satisfy applicable st...

Page 74: ...Individually weld the medical device in the sterilised item packaging such as KaVo STERI clave bags Mat no 0 411 9912 Preparation methods according to ISO 17664 72...

Page 75: ...Autoclave 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 p...

Page 76: ...CAUTION Contact corrosion due to moisture Damage to product Immediately remove the product from the steam steriliser after the sterilisation cycle Preparation methods according to ISO 17664 74...

Page 77: ...res up to 138 280 4 F KaVo recommends e g STERIclave B 2200 2200P from KaVo Citomat K series from Getinge Depending on the device select a suitable process from the following sterilisation processes P...

Page 78: ...n minutes at 134 C 1 C 273 F 1 8 F Autoclave with gravitation process for at least 60 minutes at 121 C 1 C 250 F 1 8 F Follow the manufacturer s instructions for use 7 8 Storage Prepared products must...

Page 79: ...Note Observe the expiration date of the sterilised item Preparation methods according to ISO 17664 77...

Page 80: ...ols Obtainable from dental and medical suppliers Material summary Mat no Instrument stands 2151 0 411 9501 CLEANpac 10 units 0 411 9691 Cellulose pad 100 units 0 411 9862 Nozzle needle 0 410 0921 Tool...

Page 81: ...Material summary Mat no KaVo CLEANspray 1 007 0579 KaVo DRYspray 1 007 0580 KaVo Spray 2112 A 0 411 9640 ROTAspray 2142 A 0 411 7520 QUATTROcare plus Spray 2108 P 1 005 4525 Tools 79...

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