KaVo Dental 1.003.7710 Instructions For Use Manual
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KaVo Dental 1.003.7710 Instructions For Use Manual

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Instructions for use
INTRAcompact contra-angle 2080 CHC - REF
1.003.7710

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Summary of Contents for KaVo Dental 1.003.7710

  • Page 1 Instructions for use INTRAcompact contra-angle 2080 CHC - REF 1.003.7710...
  • Page 2 Distributed by: Manufacturer: KaVo Dental GmbH Kaltenbach & Voigt GmbH Bismarckring 39 Bismarckring 39 D-88400 Biberach D-88400 Biberach Tel. +49 7351 56-0 www.kavo.com Fax +49 7351 56-1488...

  • Page 3: Table Of Contents

    Table of contents Table of contents 1 User instructions ............................... 5 2 Safety ................................7 Description of safety instructions ......................7 2.1.1 Description of safety instructions: Warning symbol ..............7 2.1.2 Description of safety instructions: Structure ................7 2.1.3 Description of safety instructions: Description of danger levels ..........8 Safety instructions ..........................
  • Page 4 Table of contents 4 First use ................................19 Cooling medium supply ........................19 5 Operation ................................ 20 Attach the medical device ........................20 Remove the medical device ......................... 23 Insert the milling cutter or diamond grinder ..................23 Removing the milling tool or diamond grinder ..................27 6 Troubleshooting ..............................
  • Page 5 Table of contents Cleaning ............................... 34 7.2.1 Cleaning: Manual cleaning - external ..................34 7.2.2 Cleaning: Automated external cleaning ................... 35 7.2.3 Cleaning: Manual cleaning - internal ..................36 7.2.4 Cleaning: Automated internal cleaning ..................38 Disinfection ............................39 7.3.1 Disinfection: Manual disinfection - external ................
  • Page 6 Table of contents Packaging ............................. 50 Sterilisation ............................51 Storage ..............................53 8 Tools ................................55 9 Terms and conditions of warranty ........................56...

  • Page 7: User Instructions

    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 Safety/Warning symbol chapter Important information for users and service technicians...
  • Page 8 User instructions Action request CE mark (Communauté Européenne). 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.

  • Page 9: Safety

    Safety 2 Safety 2.1.1 Description of safety instructions: Warning symbol Warning symbol 2.1.2 Description of safety instructions: Structure DANGER The introduction describes the type and source of the hazard. This section describes the potential consequences of non-observance. ▶ The optional step includes necessary measures for hazard preven‐ tion.

  • Page 10: Description Of Safety Instructions: Description Of Danger Levels

    Safety 2.1.3 Description of safety instructions: Description of danger 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 11: Safety Instructions

    Safety DANGER DANGER indicates a hazardous situation that can directly cause death or serious injury. 2.2 Safety instructions 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. ▶...
  • 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 Risk of burn injury from hot handpiece head or hot handpiece lid.
  • Page 13 Safety CAUTION Risk due to incorrectly stored instrument. Injury and infection caused by chucked cutters or grinders. Damage to clamping system from dropping the instrument. ▶ After treatment, place the instrument properly in the cradle, without the cutter or grinder. The following individuals are authorized to repair and service KaVo prod‐...
  • Page 14 Safety 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 depends on the frequency of use and should be adjusted accordingly. Service may only be carried out by KaVo-trained repair shops using original KaVo replacement parts.

  • Page 15: Product Description

    Product description 3 Product description INTRAcompact contra-angle handpiece 2080 CHC (Mat. no. 1.003.7710)

  • Page 16: Purpose - Proper Use

    Product description 3.1 Purpose – Proper use Purpose: This medical device is ▪ Only intended for dental treatment. Any other type of use or alteration to the product is impermissible and can be hazardous. The medical device is intended for the following uses: Cavity preparation and caries excavation.
  • Page 17 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 ▪...

  • Page 18: Technical Specifications

    Product description 3.2 Technical Specifications Drive speed max. 40,000 rpm identification 1 blue ring Speed transmission 1 : 1 With press-button chuck. Contra-angle handpiece drill bits can be used. The contra-angle handpiece can be mounted on all INTRAmatic motors, and motors with a connection in accordance with ISO 3964 / DIN 13940.

  • Page 19: Transportation And Storage Conditions

    Product description 3.3 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 20 Product description Air pressure: 700 hPa to 1060 hPa (10 psi to 15 psi) Protect from moisture.

  • Page 21: First Use

    First use 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. 4.1 Cooling medium supply CAUTION Overheating of the tooth due to lack of cooling water. Thermal damage to the dental pulp.

  • Page 22: Operation

    Operation 5 Operation 5.1 Attach the medical device CAUTION Removing and attaching the handpiece while the drive motor is rotating. Damage to the catch. ▶ Never attach or remove the handpiece while the device is rotating!
  • Page 23 Operation 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 24 Operation ▶ Connect the medical device to the (LUX) motor coupling until it locks into place, and twist it until the catch audibly locks. ▶ Pull on it to make sure that the medical device is securely attached to the coupling.

  • Page 25: 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 Insert the milling cutter or diamond grinder Note Only use carbide cutters or diamond grinders that correspond to ISO 1797-1 type 3, are made of steel or hard metal and meet the following criteria: - Shaft diameter: 1.59 to 1.60 mm...
  • Page 26 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 27 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 28 Operation ▶ Forcefully press the push button with your thumb and simultaneously insert the cutter or grinder all the way. ▶ Check that the cutter or grinder is seated by pulling on it.

  • Page 29: 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 30 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.

  • Page 31: 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 32: 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 33 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. ▶...

  • Page 34: 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 35: 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 non-sterile products. There is a risk of infection from contaminated medical devices. ▶ Observe suitable personal protective measures. ▶...

  • Page 36: Cleaning

    Setup methods according to DIN EN ISO 17664 7.2 Cleaning CAUTION Malfunctions from cleaning in an 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 37: Cleaning: Automated External Cleaning

    Setup methods according to DIN EN ISO 17664 ▶ Brush off under flowing tap water. 7.2.2 Cleaning: Automated external cleaning KaVo recommends thermodisinfectors in accordance with EN ISO 15883 that are operated with alkaline cleaning agents at a pH of max. 10 (e.g. Miele G 7781 / G 7881 –...

  • Page 38: Cleaning: Manual Cleaning - Internal

    Setup methods according to DIN EN ISO 17664 ▶ 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). ▶ 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.
  • Page 39 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‐...

  • Page 40: Cleaning: Automated Internal Cleaning

    Setup methods according to DIN EN ISO 17664 7.2.4 Cleaning: Automated internal cleaning KaVo recommends thermodisinfectors in accordance with EN ISO 15883 that are operated with alkaline cleaning agents at a pH of max. 10 (e.g. Miele G 7781 / G 7881 – validation was performed with the ""VARIO-TD" programme, "neodisher mediclean"...

  • Page 41: Disinfection

    Setup methods according to DIN EN ISO 17664 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.

  • Page 42: 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. ▪ Microcide AF from Schülke&Mayr (liquid or cloths) ▪...

  • Page 43: Disinfection: Manual Disinfection - Internal

    Setup methods according to DIN EN ISO 17664 ▶ Spray the disinfectant on a cloth, then thoroughly wipe down the med‐ ical device and leave the disinfectant to soak in according to the in‐ structions from the disinfectant manufacturer. ▶ Follow the instructions for use of the disinfectant.

  • Page 44: Disinfection: Machine Disinfection - External And Internal

    Setup methods according to DIN EN ISO 17664 7.3.3 Disinfection: Machine disinfection - external and internal KaVo recommends thermodisinfectors in accordance with EN ISO 15883 that are operated with alkaline cleaning agents at a pH of max. 10 (e.g. Miele G 7781 / G 7881 – validation was performed with the ""VARIO-TD" programme, "neodisher mediclean"...

  • Page 45: Drying

    Setup methods according to DIN EN ISO 17664 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 cleaning program of the ther‐ modisinfector.

  • Page 46: 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 47: Care Products And Systems - Servicing: Care With Kavo Spray

    Setup methods according to DIN EN ISO 17664 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 proper use on our products. 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.
  • Page 48 Setup methods according to DIN EN ISO 17664 Servicing of the clamping chuck 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. ▶...

  • Page 49: 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. ▶ Place the product on the appropriate coupling of the KaVo SPRAYrotor and cover it with a CLEANpac bag.
  • Page 50 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. Chuck care KaVo recommends cleaning and servicing the chuck system once a week. See also: Instructions for use KaVo QUATTROcare...
  • Page 51 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...

  • Page 52: Packaging

    Setup methods according to DIN EN ISO 17664 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 ap‐ plicable standards and be suitable for the sterilisation procedure.

  • Page 53: Sterilisation

    Setup methods according to DIN EN ISO 17664 7.7 Sterilisation Sterilisation in a steam steriliser (autoclave) in accordance with EN 13060/ ISO 17665-1 (e.g. KaVo STERIclave B 2200 / 2200 P) CAUTION Premature wear and malfunctions from improper servicing and care. Reduced product life.
  • Page 54 Setup methods according to DIN EN ISO 17664 CAUTION Contact corrosion due to moisture. Damage to product. ▶ Immediately remove the product from the steam steriliser after the sterilisation cycle! The KaVo medical device has a maximum temperature resistance up to 138 ℃...

  • Page 55: 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 56 Setup methods according to DIN EN ISO 17664 ▶ Comply with the expiry date of the sterilised items.

  • Page 57: Tools

    Tools 8 Tools Obtainable from dental and medical 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 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...

  • Page 58: Terms And Conditions Of Warranty

    Terms and conditions of warranty 9 Terms and conditions of warranty 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 respect of material and processing for a period of 12 months from date of invoice, subject to the following conditions: In case of justified complaints, KaVo will honour its warranty with a free replacement or repair.
  • Page 59 Terms and conditions of warranty cordance with KaVo's instructions for use or other manufacturer's instruc‐ tions. No liability is assumed when defects or their consequences are derived from manipulations or changes to the product by the customer or a third party.

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