Miele G 679 Specifications

Instructions for useEXPERTtorque E679 - REF 1.006.9200EXPERTtorque Mini E675 - REF 1.006.6400, 1.006.0800

Description of hazard levelsThe safety instructions listed here, together with the three levels ofdanger will help avert property damage and injury.CA

DANGERDANGERindicates a maximal hazard due to a situation that can directly causedeath or fatal injury.2.2 Safety instructionsWARNINGHazards for the

WARNINGHazard from contraindication.If the soft tissue in the oral cavity is injured, the compressed air may en‐able septic substances to enter the ti

CAUTIONRisk of burn injury from hot handpiece head or hot handpiece lid.Burn injuries in the mouth may be caused if the handpiece overheats.▶ Never to

CAUTIONPremature wear and malfunctioning from improper storage during longperiods of nonuse.Reduced product life.▶ The medical device should be cleane

The following individuals are authorized to repair and service KaVo prod‐ucts:▪ Technicians at KaVo branches throughout the world▪ Technicians special

3 Product description▪ EXPERTtorque LUX E679 L Mat. no. 1.006.9200 Product description 14

▪ EXPERTtorque Mini LUX E675 L Mat. no. 1.006.6400▪ EXPERTtorque Mini LUX E675 LMW Mat. no. 1.006.0800 Product description 15

3.1 Purpose – Intended usePurpose:This medical device is▪ Only intended for dental treatment. Any other type of use or altera‐tion to the product is

Proper use:According to these regulations, this medical device may only be used forthe described application by a knowledgeable user. The following mu

Distributed by:KaVo Dental Corporation11729 Fruehauf DriveCharlotte, NC 28273 USATel. 847-550-6800Fax 847-550-6825Manufacturer:Kaltenbach & Voigt

3.2 Technical Specifications KaVo MULTIflex Midwest Stylus Cou‐pler XGTDrive pressure (psi) 30 - 61 39Drive pressurerecommended (psi)> 41 39Retu

KaVo MULTIflex Midwest StylusCoupler XGTAir consumption (Nl/min)39 - 51Idling speed (rpm) EX‐PERTtorque / EX‐PERTtorque Mini340,000 - 420,000 / 400,

3.3 Transportation and storage conditionsCAUTIONIt is hazardous to start up the medical device after it has been storedstrongly refrigerated.This ca

Air pressure: 700 hPa to 1060 hPa (10 psi to 15 psi)Protect from moistureProduct description 21

4 Start up and shut downWARNINGHazard from nonsterile products.Infection danger to the care provider and patient.▶ Before first use and after each u

CAUTIONDamage from soiled and moist cooling air.Contaminated and moist cooling air can cause malfunctions and lead topremature bearing wear.▶ Make sur

4.1 Checking the amount of waterCAUTIONOverheating of the tooth due to lack of cooling water.Insufficient spray water can cause the medical device t

3 Start up and shut down 25

4.2 Checking the pressuresCAUTIONCompressed air connection on devices.Contaminated and humid compressed air leads to premature wear andtear.▶ Supply

Drive pressure, drive pressure recommended, return air pressure,spray water pressure, and spray air pressure.See also: 3.2 Technical Specifications, P

Table of contents1 User instructions ...

5 OperationNoteAt the beginning of each workday, the water-conducting systems shouldbe rinsed for at least 2 min. without the instrument being attac

5.1 Attaching the medical deviceWARNINGDetachment of the medical device during treatment.A medical device that is not properly locked can detach fro

CAUTIONDamage from inaccurate coupling.Inaccurate coupling (especially during the afterglow period) can destroythe high-pressure lamp or the LED of th

5.2 Removing the medical device▶ Hold the coupling tight, and pull the medical device off while twistingslightly. Operation 31

5.3 Inserting the milling cutter or diamond grinderNoteOnly use carbide cutters or diamond grinders that comply with ISO1797-1 type 3, are made of s

WARNINGUse of unauthorised cutters or grinders.Injury to the patient or damage to the medical device.▶ Observe the instructions for use and use the cu

CAUTIONDanger of injury from cutters or grinders.Infections or cuts.▶ Wear gloves or fingerstalls.CAUTIONHazard from defective chucking system.The cut

▶ Forcefully press the push button with your thumb and simultaneouslyinsert the cutter or grinder all the way.▶ Check that the cutter or grinder is se

5.4 Removing the milling tool or diamond grinderWARNINGHazard from rotating cutter or grinder.Lacerations and damage to the chucking system.▶ Do not

▶ After the cutter or grinder has stopped rotating, press the press-but‐ton with your thumb and simultaneously pull out the drill bit or bur.Operation

5 Operation ...

6 Troubleshooting6.1 Cleaning the spray nozzleCAUTIONHazard from insufficient spray water.Overheating of the medical device and damage to the toot

▶ Use the nozzle needle (Mat. no. 0.410.0921) to free the water pas‐sage in the spray nozzles.6.2 Changing the water filter▶ Unscrew the sleeve ① in

▶ Unscrew the water filter ③ with the wrench (Mat. no. 1.002.0321)and take it out▶ Insert the new filter (Mat. no. 1.002.0271) and screw it in with th

7 Reprocessing methods according to ISO 176647.1 Preparations at the site of useWARNINGHazard from nonsterile products.There is a risk of infectio

7.2 CleaningCAUTIONMalfunctions from cleaning in the ultrasonic unit.Defects in the product.▶ Only clean manually or in a thermodisinfector.7.2.1

▶ Brush off under flowing tap water.7.2.2 Cleaning: Automated external cleaningKaVo recommends thermodisinfectors in accordance with ISO 15883-1,whi

▶ For program settings as well as cleansers and disinfectants to beused, please refer to the Instructions for Use of the thermodisinfec‐tor.▶ In order

7.2.4 Cleaning: Automated internal cleaningKaVo recommends thermodisinfectors in accordance with ISO 15883-1,which are operated with alkaline cleani

▶ In order to prevent negative effects on the medical device, makesure that the interior and the exterior of the medical device are dry,and then lubri

7.3.1 Disinfection: Manual external disinfectionKaVo recommends the following products based on material compatibili‐ty. The microbiological efficac

7.2.4 Cleaning: Automated internal cleaning ... 457.3 Disinfection .

▶ Spray the disinfectant on a cloth, then thoroughly wipe down themedical device and leave the disinfectant to soak in according to theinstructions fr

tion agent "neodisher® Z" and rinsing agent "neodisher® mielclear" andonly applies to the material compatibility with KaVo product

7.4 DryingManual Drying▶ Blow off the outside and inside with compressed air until water dropsare no longer visible.Automatic DryingThe drying proce

7.5 Care products and systems - ServicingWARNINGSharp cutters or grinders in the medical device.Risk of injury from sharp or pointed cutters or grin

NoteKaVo only guarantees that its products will function properly when thecare products used are those listed as accessories, as they were testedfor p

▶ Cover the product with the CLEANpac bag.▶ Place the product on the cannula and press the spray button for onesecond.Chuck careKaVo recommends cleani

▶ Carry out the servicing according to the instructions in the section,"Care with KaVo Spray".7.5.2 Care products and systems - Servicing:

▶ Servicing the product.Chuck careKaVo recommends cleaning and servicing the chuck system once aweek.See also: Instructions for use KaVo QUATTROcare 2

▶ Subsequently treat with the care products and care systems speci‐fied.7.5.3 Care products and systems - Servicing: Servicing with KaVoQUATTROcare

Servicing the clamping chuckKaVo recommends cleaning and servicing the chuck system once aweek.See also: Instructions for use KaVo QUATTROcare PLUSNot

8 Tools and consumables ...

▶ Press the handpiece together with the guide bush of the chuck to beserviced against the tip of the service coupling chuck.▶ Press the button showing

NoteClose the chuck service mode.Option 1: Place the dental handpieces in the QUATTROcare PLUS2124 A, close the front door and start theservice proced

7.6 PackagingNoteThe sterilisation bag must be large enough for the handpiece so that thebag is not stretched.The quality and use of the sterilisati

7.7 SterilisationSterilisation in a steam steriliser (autoclave) in accordance with ISO17665-1CAUTIONPremature wear and malfunctions from improper s

CAUTIONContact corrosion due to moisture.Damage to product.▶ Immediately remove the product from the steam steriliser after thesterilisation cycle!The

Select a suitable procedure (depending on the available autoclave) fromthe following sterilisation processes:▪ Autoclave with pre-vacuum:– at least 3

7.8 Storage▶ Reprocessed products should be stored protected from dust withminimum exposure to germs in a dry, dark and cool space.▶ Comply with the

8 Tools and consumablesAvailable from dental suppliers.Material summary Mat. No.Replacement turbine EXPERTtor‐que1.007.9313Replacement turbine EXPER

Material summary Mat. No.Instrument stand 2151 0.411.9501Insert for turbines 0.411.9902Nozzle pin 0.410.0921Cleanpac 10 units 0.411.9691KaVo MULTIflex

Only for the USAMaterial summary Mat. no.KaVo Spray America 2113 A 0.411.9660QUATTROcare plus Spray Ameri‐ca 2141 P1.005.4524Only for CanadaMaterial s

1 User instructionsDear UserCongratulations on purchasing this KaVo quality product. By following theinstructions below you will be able to work smo

9 Terms and conditions of warrantyThe following warranty conditions apply to this KaVo medical device:KaVo provides the end customer with a warranty

cordance with KaVo's instructions for use or other manufacturer's instruc‐tions. The warranty does not usually cover lamps, light conductors

1.007.9684 · kb · 20130122 - 05 - US · en

Action requestCan be sterilized with steam at 134 °C -1 °C / +4 °C (273 °F -1.6°F / +7.4 °F)ThermodisinfectableTarget groupThis document is intended f

2 Safety2.1 Description of safety instructionsWarning symbolStructureDANGERThe introduction describes the type and source of the hazard.This secti