Care instructions ESTETICA E30
Always be on the safe side.
Manufacturer: Kaltenbach & Voigt GmbH Bismarckring 39 D-88400 Biberach www.kavo.com
Distributed by: KaVo Dental GmbH Bismarckring 39 D-88400 Biberach Phone +49 7351 56-0 Fax +49 7351 56-1488
Care instructions ESTETICA E30 Table of contents
Table of contents 1
2
3
User instructions ........................................................................................................................................ 2 1.1 User guide ....................................................................................................................................... 2 1.1.1 Abbreviations ...................................................................................................................... 2 1.1.2 Symbols .............................................................................................................................. 2 1.1.3 Target group ....................................................................................................................... 2 Reprocessing methods according to DIN EN ISO 17664 .......................................................................... 3 2.1 Instructions ...................................................................................................................................... 3 2.2 General instructions for the reprocessing of KaVo treatment centres ............................................. 4 2.2.1 Overview ESTETICA E30 reprocessing ............................................................................. 5 2.3 Reprocessing of the surfaces of treatment centre / upholstery ....................................................... 6 2.4 Preparation of the dentist element .................................................................................................. 8 2.4.1 Reprocessing of handle and holder pad/anti-slip mat ........................................................ 8 2.4.2 Reprocessing of the instrument holder of the TM table ...................................................... 8 2.4.3 Reprocessing of the instrument arm S table ...................................................................... 9 2.4.4 Preparation of the triple function handpiece KaVo One ................................................... 10 2.4.5 Preparation of triple function handpiece ........................................................................... 13 2.4.6 Preparation of the instrument hoses ................................................................................ 17 2.4.7 Servicing the turbine return air filter ................................................................................. 17 2.5 Reprocessing of the assistant element ......................................................................................... 18 2.5.1 Preparing the handpiece holder ....................................................................................... 18 2.5.2 Reprocessing of the suction hose connector ................................................................... 18 2.5.3 Reprocessing of sieve inserts and suction hoses ............................................................ 20 2.6 Reprocessing of the patient element ............................................................................................. 21 2.6.1 Reprocessing of the tumbler ............................................................................................ 21 2.6.2 Reprocessing of tumbler holder and tumbler filler ............................................................ 21 2.6.3 Reprocessing of the spittoon bowl ................................................................................... 22 2.7 Manual hygiene functions of the water-conducting system ........................................................... 23 2.7.1 Manual intensive germ reduction ..................................................................................... 23 2.8 Reprocessing of the suction system .............................................................................................. 25 2.8.1 Cleaning and disinfection of the suction system including suction hoses ........................ 25 Replenishing and checking the disinfectant ............................................................................................ 27 3.1 Replenishing KaVo OXYGENAL 6 when using the water bottle ................................................... 27 3.1.1 Filling the intensive germ reduction bottle ........................................................................ 29 3.2 Check the OXYGENAL 6 concentration ........................................................................................ 30
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Care instructions ESTETICA E30 1 User instructions | 1.1 User guide
1 User instructions 1.1 User guide Requirement Read these instructions prior to first use to avoid misuse and prevent damage. Note Comply with the Instructions for Use of the ESTETICA E30 treatment unit!
1.1.1 Abbreviations Abbre‐ viation IfU CI AI TI SC IEC RI EMC Scaler IR IrDA
Explanation Instructions for use Care instructions Assembly instructions Technician's instructions Safety checks International Electrotechnical Commission Repair instructions Electromagnetic compatibility Scaler (ZEG) Infrared Infrared Data Association
1.1.2 Symbols Refer to the chapter on Safety/Warning symbol Important information for users and service technicians Action request CE mark according to EC Directive 93/42 for medical devices Thermodisinfectable at up to 95 °C (203 °F)
Suitable for steam sterilisation at up to 135 °C (275 °F)
1.1.3 Target group This document is for dentists and dental office staff.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.1 Instructions
2 Reprocessing methods according to DIN EN ISO 17664 2.1 Instructions The reprocessing consists of the following basic steps: ▪ Cleaning and disinfection ( manually or automatically) ▪ Sterilisation Note Comply with national hygiene requirements, e.g. RKI guidelines.
CAUTION Risk of injury during cleaning of the treatment unit. Lack of instructions to the cleaning staff and lack of preparation of the treatment unit can lead to the cleaning personnel sustaining injuries. ▶ Only trained professionals and instructed cleaning personnel may be present in the treatment rooms. ▶ Position the chair for cleaning and turn the device off. CAUTION Product damage due to improper disinfection. Malfunctions. ▶ Use the disinfectant as prescribed by the manufacturer. ▶ No spray disinfection, perform wipe disinfection only. ▶ Do not immerse product or product parts in liquids. CAUTION Improper disinfection may lead to health hazards and material damage. Infection hazard to users and patients. Damage to the sterile product. ▶ No hot air sterilisation, no chemical cold sterilisation, do not sterilise with eth‐ ylene oxide. CAUTION Health hazard and property damage due to non-compliance with servicing schedule. Infection hazard to users and patients. Product damage. ▶ Comply with servicing schedule. Note The preparation methods for the instruments and motors are found in the sepa‐ rate instructions for use that accompany the instrument and motor packages.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.2 General instructions for the reprocessing of KaVo treatment centres
2.2 General instructions for the reprocessing of KaVo treatment centres Please comply with the general reprocessing instructions at all times. Detailed product-specific reprocessing instructions are provided subsequently. At the site of use
▶ Remove any surface contamination using a disposable cloth/paper towel.
Storage and transport
KaVo recommends reprocessing as soon as possible after use.
Preparations for cleaning
▶ Comply with product-specific reprocessing instructions.
Manual cleaning
Fixtures: ▪ Brush or cloth ▪ Tap water 30 °C ± 5 °C ▶ Rinse surface contamination off the product under running water.
Automatic cleaning
KaVo recommends thermodesinfection at up to 95 °C in accordance with ISO 15883-1 e.g. Miele G 7781 / G 7881 with the use of a alkaline cleaning agent with a maximum pH value of 10. ▶ For program settings as well as cleansers and disinfectants to be used, please refer to the Instructions for Use of the thermodisinfec‐ tor. ▶ Do not clean instruments and device components in the ultrasound bath.
Manual disinfection
▶ Perform wipe disinfection only, the use of spray disinfection and dis‐ infection baths is not feasible. ▶ Wipe all outer surfaces with a soft cloth and an approved disinfec‐ tant. Approved disinfectants: ▪ Mikrozid AF Liquid (made by Schülke & Mayr) ▪ FD 322 (Dürr) ▪ Incidin Liquid (Ecolab) ▪ CaviCide (Metrex) ▶ Use disinfectants according to the manufacturer's Instructions for Use. ▶ Please note the disinfectant safety data sheet.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.2 General instructions for the reprocessing of KaVo treatment centres Automatic disinfection
KaVo recommends thermodesinfection at up to 95 °C in accordance with ISO 15883-1 e.g. Miele G 7781 / G 7881 with the use of a alkaline cleaning agent with a maximum pH value of 10. ▶ For program settings as well as cleansers and disinfectants to be used, please refer to the Instructions for Use of the thermodisinfec‐ tor. ▶ Do not disinfect instruments and device components in the ultra‐ sound bath.
Manual drying
▶ Supply dry, clean and uncontaminated compressed air according to ISO 7494-2 only. ▶ Blow off the outside and inside with compressed air until water drops are no longer visible.
Automatic drying
Automatic drying usually is part of the cleaning/disinfection cycle of the thermodisinfector and should not be carried out above 95 °C.
Maintenance
▶ Discard damaged products.
Control and functional checks
▶ Perform a visual inspection checking for damage and wear and tear. ▶ Test products for function regularly.
Packaging
▶ Use standardised packaging material. Sealing should not be under tension. ▶ Use sterile goods packaging in order to ensure sterility.
Sterilisation
All sterilisable products are temperature-resistant up to max. 138 °C. KaVo recommends sterilisation in a steam steriliser (autoclave) accord‐ ing to EN 13060 / ISO 17665-1, e.g. STERIclave B 2200 / 2200 P (Ka‐ Vo) or Citomat K-Series (Getinge). ▶ Sterilise with a triple fractionated vacuum (B class steriliser); hold for 4 minutes; 134°C ± 1 °C; overpressure: 2.13 bar.
Storage
▶ Reprocessed products should be stored protected from dust with minimum exposure to germs in a dry, dark and cool place. ▶ Comply with the expiry date of the sterilised items.
2.2.1 Overview ESTETICA E30 reprocessing Reprocessing items/medical devices Surfaces Device
Cleaning manual
automatic
Disinfection manual automatic
X
X
Cushion
X
X
Light
X
X
Lights, handles
X
Dentist element Handle TM table / handle cup S table
X
X
X X
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Sterilisation automatic
See also: IfU KaVoLUX 540 LED / EDI / MAIA X X
Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.3 Reprocessing of the surfaces of treatment centre / upholstery Reprocessing items/medical devices Cannula triple-function handpiece
Cleaning manual X
automatic
Disinfection manual automatic X
Holder pad/anti-slip mat
X
Handpiece holder
X
X
Instrument arm S table
X
X
Assistant element Connection parts of the suction hose
X
Patient element Tumbler holder
X
X
Tumbler filler
X
X
Porcelain spittoon bowl
X
X
X
X
X
X
X
Sterilisation automatic X
X
X
X
X
2.3 Reprocessing of the surfaces of treatment centre / upholstery Position the chair for cleaning ▶ Adjust the backrest to vertical position and move the chair upward. See also: Instructions for useESTETICA E30
Turn device off ▶ Switch off the unit at the main switch.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.3 Reprocessing of the surfaces of treatment centre / upholstery
Cleaning and disinfecting the surfaces of treatment unit / upholstery CAUTION Non-colour-fast textiles. Non-colour-fast textiles can cause permanent discoloration. ▶ Remove discolourations with water immediately. Approved disinfectants: ▪ Mikrozid AF Liquid (made by Schülke & Mayr) ▪ FD 322 (Dürr) ▪ Incidin Liquid (Ecolab) ▪ CaviCide (Metrex)
▶ Clean the surfaces and upholstery with a soft cloth and water, and wipe-disin‐ fect them with an approved surface disinfectant. CAUTION Damage caused by spray disinfection. Disinfectant gets into cracks and loosens the paint. ▶ No spray disinfection. ▶ Only disinfect by wiping.
Cleaning and disinfection of the foot control CAUTION Damage caused by inappropriate use of water. Damage to the foot control. ▶ For cleaning, the foot control must not be immersed in water or placed under running water. ▶ Only wipe off. Do not spray.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.4 Preparation of the dentist element
2.4 Preparation of the dentist element 2.4.1 Reprocessing of handle and holder pad/anti-slip mat Note The handle of the TM table cannot be detached.
Cleaning and disinfection of the handle of the TM table / handle cup of the S table ▶ Clean the handle (TM table) / handle cup (S table) with a soft cloth and water, and wipe-disinfect it with an approved surface disinfectant.
Cleaning, disinfection, and sterilisation of holder pad/anti-slip mat ▶ Sterilise the holder pad and anti-slip mat by thermodisinfection.
2.4.2 Reprocessing of the instrument holder of the TM table Note The handpiece holder can be removed for better cleaning.
Cleaning and disinfection of the handpiece holder CAUTION Damage caused by thermodisinfection. ▶ Do not thermodisinfect the instrument holder.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.4 Preparation of the dentist element ▶ Pull the latches evenly outward and carefully remove the handpiece holder.
▶ Clean the handpiece holder under running water. ▶ Wipe-disinfect the instrument holder.
Sterilize the instrument holder CAUTION Damage caused by sterilisation. ▶ Do not sterilise the instrument holder.
2.4.3 Reprocessing of the instrument arm S table Note The instrument arm of the S table can be removed for better cleaning.
Cleaning and disinfection of the instrument arm S table CAUTION Damage caused by thermodisinfection. ▶ Do not sterilise the instrument arm S table by thermodisinfection.
▶ Take the handpieces off the hoses.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.4 Preparation of the dentist element ▶ Take the roller out of the instrument arm.
▶ Pull-off the instrument arm in an upward direction. ▶ Clean the instrument arm and roller under running water. ▶ Wipe the instrument arm S table with disinfectant.
Sterilisation of instrument arm S table CAUTION Damage caused by sterilisation. ▶ Do not sterilise the instrument arm S table
2.4.4 Preparation of the triple function handpiece KaVo One Note Wet the O-rings of the sleeves after sterilisation using silicone grease (Mat. no. 1.000.6403) or KaVo Rota Spray 2 (Mat. no. 0.411.7510). After replac‐ ing the cannula, the air channel must be blown out before the start of treatment to ensure that the air exiting during treatment is dry. Note For the cleaning/preparation of the cannula of the triple-function handpiece KaVo One, the cannula must be disassembled into the cannula tube and the taper sleeve.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.4 Preparation of the dentist element
Cleaning of triple-function handpiece KaVo One Automatic cleaning CAUTION Damage caused by improper cleaning/disinfection. ▶ Do not sterilise the single parts of the cannula in a hot-air steriliser. ▶ Do not place the single parts of the cannula in a disinfectant or ultrasonic bath. ▶ Single parts of the cannula should be subjected to thermodisinfection and sterilisation.
Manual cleaning Note Combine manual cleaning with disinfection.
Internal cleaning ▶ Leave the cannula and handpiece on the instrument, and activate the air and water for 60 seconds.
External cleaning Accessories required: ▪ Tap water 30°C ± 5°C ▪ Brush, e.g. medium-hard toothbrush ▶ Hold the valve body of the handpiece and screw off the cannula. ▶ Disassemble the cannula of the triple-function handpiece KaVo One into the cannula tube and the taper sleeve. ▶ Clean the cannula tube and taper sleeve by brushing them under flowing wa‐ ter (at least tap water quality). ▶ Immediately remove contamination from materials used in the dental practice (impression materials, caustic chemicals). ▶ Carefully wipe off contamination from the cannula tip with a soft Q-tip or soft cloth and alcohol. CAUTION Damage caused by using a nozzle needle that is too long. Damage to the internal hoses of the cannula. ▶ Use a short nozzle needle (Mat. no. 1.004.4986) to clean the media exit holes.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.4 Preparation of the dentist element
▶ Carefully remove contamination from the media exit ports using the short noz‐ zle cleaning needle.
Disinfection of triple-function handpiece KaVo One Manual disinfection See also: 2.2 General instructions for the reprocessing of KaVo treatment cen‐ tres, Page 4
External disinfection ▶ Wipe-disinfect the surfaces with a soft cloth.
Automatic disinfection CAUTION Damage caused by improper cleaning/disinfection. ▶ Do not sterilise the single parts of the cannula in a hot-air steriliser. ▶ Do not place the single parts of the cannula in a disinfectant or ultrasonic bath. ▶ Single parts of the cannula should be subjected to thermodisinfection and sterilisation.
Drying of triple-function handpiece KaVo One Manual drying ▶ Blow off the outside and inside with compressed air until water drops are no longer visible.
Automatic drying Not applicable.
Sterilisation of triple-function handpiece KaVo One Note The cannula can be subjected to sterilisation.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.4 Preparation of the dentist element ▶ Hold the valve body of the triple-function handpiece and screw off the cannula.
Sterilization in a steam sterilizer in compliance with DIN EN 13060 ▶ Remove the taper sleeve from the cannula tube weld in sterile goods packag‐ ing. ▶ Sterilise with a triple fractionated vacuum (B class steriliser); hold for 4 mi‐ nutes; 134°C ± 1 °C; overpressure: 2.13 bar.
CAUTION Damage caused by over-heating. Damage to the cannula. ▶ Immediately remove the parts from the steriliser after the sterilisation cycle is completed.
Storage ▶ Reprocessed products should be stored protected from dust with minimum ex‐ posure to germs in a dry, dark and cool place.
2.4.5 Preparation of triple function handpiece Note Wet the O-rings of the sleeves after sterilisation using silicone grease (Mat. no. 1.000.6403) or KaVo Rota Spray 2 (Mat. no. 0.411.7510). After replac‐ ing the cannula, the air channel must be blown out before the start of treatment to ensure that the air exiting during treatment is dry.
Cleaning of triple-function handpiece Automatic cleaning Not applicable.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.4 Preparation of the dentist element CAUTION Damage caused by improper cleaning/disinfection. ▶ Do not wash the gripping sleeve and the cannula in the thermodisinfector. ▶ Do not sterilise the gripping sleeve and the cannula in the hot-air steriliser. ▶ Do not place the gripping sleeve and the cannula in a disinfectant or ultra‐ sonic bath.
Manual cleaning Note Combine manual cleaning with disinfection.
Internal cleaning ▶ Leave the gripping sleeve and cannula on the instrument, and activate the air and water for 60 seconds.
External cleaning CAUTION Danger of injury if the valve body is hot (heating elements, high-pressure lamp). Risk of burn injury. ▶ Switch off the unit at the main switch. ▶ Let the handpiece cool after long use. Accessories required: ▪ Tap water 30°C ± 5°C ▪ Brush, e.g. medium-hard toothbrush ▶ Disassemble the gripping sleeve and cannula. ▶ Detach the key part from the gripping sleeve.
▶ Clean the key part, gripping sleeve and cannula by brushing them under run‐ ning water (at least tap water quality).
▶ Immediately remove contamination from materials used in the dental practice (impression materials, caustic chemicals).
▶ Carefully wipe off contamination from the cannula tip with a soft Q-tip or soft cloth and alcohol.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.4 Preparation of the dentist element CAUTION Damage caused by using a nozzle needle that is too long. Damage to the internal hoses of the cannula. ▶ Use a short nozzle needle (Mat. no. 1.004.4986) to clean the media exit holes.
▶ Carefully remove contamination from the media exit ports using the short noz‐ zle cleaning needle.
Disinfection of triple-function handpiece Manual disinfection External disinfection ▶ Wipe-disinfect the surfaces with a soft cloth.
Automatic disinfection Not applicable. CAUTION Damage caused by improper cleaning/disinfection. ▶ Do not wash the gripping sleeve and the cannula in the thermodisinfector. ▶ Do not sterilise the gripping sleeve and the cannula in the hot-air steriliser. ▶ Do not place the gripping sleeve and the cannula in a disinfectant or ultra‐ sonic bath.
Drying of triple-function handpiece Manual drying ▶ Blow off the outside and inside with compressed air until water drops are no longer visible.
Automatic drying Not applicable.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.4 Preparation of the dentist element
Care of triple function handpiece Requirement The multifunctional handpiece has been prepared. ▶ Apply KaVo silicone grease (Mat. no. 1.000.6403) or KaVo Rota Spray 2 (Mat. no. 0.411.7510) to the O-rings of the joint between the gripping sleeve and cannula. Use cotton buds for this purpose.
Sterilisation of triple-function handpiece Note The grip sleeve and cannula can be sterilised. ▶ Hold the handpiece at the taper sleeve and take off the cannula with a slight twisting motion.
▶ Pull the gripping sleeve off the valve body.
Sterilization in a steam sterilizer in compliance with DIN EN 13060 ▶ Weld the cannula and grip sleeve in sterile goods packaging. ▶ Sterilise with a triple fractionated vacuum (B class steriliser); hold for 4 mi‐ nutes; 134°C ± 1 °C; overpressure: 2.13 bar.
CAUTION Damage caused by over-heating. Damage to the gripping sleeve. ▶ Immediately remove the parts from the steriliser after the sterilisation cycle is completed.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.4 Preparation of the dentist element
Storage ▶ Reprocessed products should be stored protected from dust with minimum ex‐ posure to germs in a dry, dark and cool place.
2.4.6 Preparation of the instrument hoses Cleaning and disinfection of handpiece hoses ▶ Clean the hoses and couplings with a cloth and water. CAUTION Damage caused by spray disinfection. ▶ Do not subject instrument hoses to spray disinfection. ▶ Subject instrument hoses to wipe disinfection.
2.4.7 Servicing the turbine return air filter Cleaning the turbine return air filter Note The liquid collector must be checked weekly.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.5 Reprocessing of the assistant element ▶ If there is any liquid in the filter, drain the liquid and replace the O-rings of the multiflex couplings.
▶ If necessary, replace the turbine return air filter (Mat. no. 0.200.3098) and clean the filter holder. Note The turbine return air filter is in the same position in the dentist element variant with S table.
2.5 Reprocessing of the assistant element 2.5.1 Preparing the handpiece holder Note The handpiece holder can be removed. ▶ Wipe-disinfect the instrument holder.
2.5.2 Reprocessing of the suction hose connector ▶ Pull-off the connectors ① and ② from the suction hoses.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.5 Reprocessing of the assistant element ▶ Unscrew the connectors ③ and ④ from the suction hoses.
1
2
3
6
5 4
6
5
Cleaning and disinfection of the suction hose connector ▶ Clean the disassembled parts under running water. ▶ Thermodisinfect the disassembled connectors ① and ② for at least 10 mi‐ nutes at 93 °C (total cycle: approximately 20 minutes).
▶ Disinfect the connectors ③ and ④ by wipe disinfection. Note Connectors ③ and ④ cannot be subjected to thermodisinfection.
Sterilising the suction hose connector CAUTION Damage caused by sterilisation. ▶ Do not sterilise connectors ① and ②.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.5 Reprocessing of the assistant element Note Sterilise the suction cannulas according to the manufacturer's instructions. ▶ Sterilise connectors ③ and ④.
2.5.3 Reprocessing of sieve inserts and suction hoses Note Check the sieve inserts daily and after each surgery. The sieve inserts must be replaced at the latest when the suction performance decreases (Mat. no. 1.008.8638). Cleaning is not recommended for hygienic reasons. ▶ Pull the connector ⑤ off the suction hose. ▶ Clean the sieve ⑥ under running water. ▶ Remove the suction hoses from the holder. The suction motor starts automatically when the suction tubes are removed from the holder. ▶ Pull the sieve inserts out of the housing. ▶ Place a cloth under the sieve seat.
▶ If needed, insert a new sieve insert (Mat. no. 1.008.8638) into the seat. ▶ Wipe the suction tubes with disinfectant.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.6 Reprocessing of the patient element
2.6 Reprocessing of the patient element 2.6.1 Reprocessing of the tumbler ▶ Reprocess as specified by the manufacturer.
2.6.2 Reprocessing of tumbler holder and tumbler filler CAUTION Water in the device. Material damage from leaking water upon actuation of the "Tumbler filler" or "Bowl flush" keys. ▶ Make sure that the unit is turned off before removing the tumbler filler or the spittoon bowl. ▶ Always check the correct seating of tumbler filler and spittoon bowl before turning on the unit.
Cleaning and disinfection of the tumbler holder and tumbler filler
▶ Take off the tumbler holder (Mat. no. 1.008.9291). ▶ Clean the tumbler holder under running water. ▶ Subject the tumbler filler to wipe disinfection. CAUTION Damage caused by thermodisinfection. ▶ Do not subject the tumbler holder and tumbler filler to thermodisinfection.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.6 Reprocessing of the patient element
Sterilisation of tumbler holder and tumbler filler CAUTION Damage caused by sterilisation. ▶ Do not subject the tumbler holder and tumbler filler to sterilisation.
2.6.3 Reprocessing of the spittoon bowl CAUTION Water in the device. Material damage from leaking water upon actuation of the "Tumbler filler" or "Bowl flush" keys. ▶ Make sure that the unit is turned off before removing the tumbler filler or the spittoon bowl. ▶ Always check the correct seating of tumbler filler and spittoon bowl before turning on the unit.
Cleaning and disinfection of the spittoon bowl CAUTION Damage caused by inappropriate cleaning agents. ▶ Do not use acid-containing, sand-containing, and form-forming cleaning agents. ▶ Add a dose of DEKASEPTOL gel to the spittoon bowl and distribute the agent with a brush. ▶ For cleaning, allow the gel to act for approx. 5 minutes. ▶ For disinfection, allow the gel to act for approx. 15 minutes. ▶ After letting it work, press the "Spittoon bowl" button. ▶ Clean the spittoon bowl thoroughly using a brush. ▶ For thorough cleaning or thermodisinfection, rotate the spittoon bowl and lift it off.
The spittoon bowl made of porcelain can be subjected to thermodisinfection.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.7 Manual hygiene functions of the water-con‐ ducting system
2.7 Manual hygiene functions of the water-conducting system CAUTION Health damage due to germ formation. Infection hazard. ▶ Before start-up and after the device has not been used for a while (week‐ ends, holidays, vacations, etc.), rinse or purge with air the air and water lines. ▶ Actuate the tumbler filler several times. ▶ Carry out a manual intensive germ reduction. Note RKI recommends rinsing all water-conducting systems at the start of the work day for 2 minutes (with no handpieces attached) at all dispensing sites, such as, e.g., handpiece, turbine, motor dental scaler and tumbler filler. Note The "continuous germ reduction" hygiene function is available only with the water bottle kit. Treatment water that comes into contact with the patient (tumbler, dental instru‐ ments,..) can be germ reducted manually or intensively germ reducted manually. During normal operation of the treatment centre, the continuous germ reduction function (available with water bottle kit and added disinfectant KaVo OXYGENAL 6) ensures continuous germ reduction of the water-supplying systems. Manual rinsing and manual intensive germ reduction facilitate the rinsing and germ reduction of the water-supplying system. This counteracts the formation of micro-organisms in times of stagnation and ensures hygienic water supply for the patients.
2.7.1 Manual intensive germ reduction Note Observe the instructions for use for the instruments. Intensive germ reduction prevents the formation of microorganisms during exten‐ ded periods when the equipment is out of use. During intensive germ reduction, the afferent water ducts are manually filled with a higher concentration of KaVo OXYGENAL 6. Manual intensive germ reduction takes only 20 seconds for flushing and 20 seconds for rinsing of each handpiece. The time of exposure should be at least 30 minutes, and preferably over the weekend. An additional intensive germ reduction must be carried out during extended peri‐ ods on non-use (from 4 weeks).
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.7 Manual hygiene functions of the water-con‐ ducting system Intensive germ reduction must be carried out: ▪ At first start-up ▪ Before, during and after prolonged downtimes (more than 4 weeks) ▪ Over the weekend ▪ During vacations ▪ After treatment of patients at high risk
Order of manual intensive germ reduction ▶ Fill the intensive germ reduction bottle. See also: 3.1.1 Filling the intensive germ reduction bottle, Page 29 ▶ Press key while flushing.
▶ Flush each dental instrument for 20 seconds (without attachment handpieces or cannulas), including the triple-function handpiece. ▶ Fill tumble 3x. ▶ Then allow to act for at least 30 minutes, and preferably over the weekend. ▶ After the time of exposure, e.g. after the weekend, fill the tumbler 3x and rinse each dental instrument (without attachment handpieces or cannulas) for 20 seconds. Note The intensive germ reduction bottle must be newly filled prior to every intensive germ reduction process.
Intensive germ reduction during prolonged periods of non-use (> 4 weeks) During extended periods of non-use, e.g. semester breaks at university, intensive germ reduction must be carried out during the time of non-use. The disinfection fluid remains inside the system during the period of non-use.
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Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.8 Reprocessing of the suction system
2.8 Reprocessing of the suction system 2.8.1 Cleaning and disinfection of the suction system including suc‐ tion hoses Note Clean the suction hoses after each treatment and disinfect them with DEKASEP‐ TOL Gel daily.
Application of DEKASEPTOL Gel Note Regarding the air jet suction system (Venturi), only one aliquot may be drawn in‐ to each hose. ▶ Aspirate one tumbler of cold water with each suction hose. ▶ With the suction handpiece attached or by hand, press down the DEKASEPTOL dosing facility once each for the saliva ejector hose and the spray mist ejector. ▶ Aspirate the DEKASEPTOL Gel from the dosing facility. Note In suction processes with air jet suction systems (Venturi), the two following steps must not be carried out as they could lead to blockage of the thin hoses.
Without air jet suction system (Venturi) ▶ Aspirate another tumbler of cold water with each suction hose. ▶ Finally, aspirate another dose of DEKASEPTOL Gel and allow it to act.
With/without air jet suction system (Venturi) ▶ Place the suction hoses in the holder. DEKASEPTOL Gel basic set Mat. no. 1.000.7204
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DEKASEPTOL Gel refill canister Mat. no. 1.000.7205
Care instructions ESTETICA E30 2 Reprocessing methods according to DIN EN ISO 17664 | 2.8 Reprocessing of the suction system
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Care instructions ESTETICA E30 3 Replenishing and checking the disinfectant | 3.1 Replenishing KaVo OXYGENAL 6 when using the water bottle
3 Replenishing and checking the disinfectant 3.1 Replenishing KaVo OXYGENAL 6 when using the water bottle CAUTION Damage caused by defective water bottle. Malfunctions or failures from a leaky water bottle. ▶ Do not wash the water bottle in a dish washer, and do not rinse it with water hotter than 50 ℃. ▶ Do not use the water bottle if it is scratched, deformed or discoloured. ▶ Note the maximum useful life of the water bottle on the label. Water bottle complete: (Mat. no. 0.710.4151) Dosing attachment: (Mat. no. 1.002.0287)
Nameplate of water bottle and intensive germ reduction bottle
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Nameplate of water bottle / intensive germ reduction bottle
① Manufacturer ② Concentration ③ Use-by date ④ Material number
⑤ Month manufactured ⑥ Expiration date (year) ⑦ Storage temperature ⑧ Please comply with accompanying documents
Note The specified concentration of KaVo OXYGENAL 6 must not be exceeded.
Removing and cleaning the water bottle and intensive germ reduc‐ tion bottle ▶ Turn the device off.
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Care instructions ESTETICA E30 3 Replenishing and checking the disinfectant | 3.1 Replenishing KaVo OXYGENAL 6 when using the water bottle ▶ Remove the water bottle ① and intensive germ reduction bottle ② through a slow counterclockwise rotation.
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Note This allows the over-pressure to be released slowly from the water bottle. If the pressure supply to the equipment is not switched of, a permanent venting sound is audible. Note The water in the water bottle needs to be changed at least one daily. In order to ensure the efficiency of the measures, KaVo urgently recommends reprocessing the water with KaVo OXYGENAL 6. ▶ For cleaning, rinse the water bottle with water at less than 50 oC.
Filling the water bottle with the dosing facility ▶ Wipe up any spilled OXYGENAL immediately in order to prevent discoloura‐ tion of the surfaces. ▶ Remove the protective hose from the tube of the KaVo OXYGENAL 6 dosing facility. ▶ Guide the tube through the orifice of the coarse sieve of the KaVo OXYGENAL 6 bottle. ▶ Screw the KaVo OXYGENAL 6 dosing facility tightly to the KaVo OXYGENAL 6 bottle. ▶ Rotate the orifice in the lid to a filling level of 1.5 litres. Lid snaps-in in the filling position.
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Care instructions ESTETICA E30 3 Replenishing and checking the disinfectant | 3.1 Replenishing KaVo OXYGENAL 6 when using the water bottle
▶ Place the KaVo OXYGENAL 6 bottle on a level surface. ▶ Squeeze the KaVo OXYGENAL 6 bottle until the disinfection liquid rises above the red marker. In response to over-filling, the excess quantity above the tick mark is suc‐ tioned off automatically such that exact dosing is ensured.
3.1.1 Filling the intensive germ reduction bottle CAUTION Wrong disinfection solution or the dose is too high Injury hazard ▶ Use KaVo OXYGENAL 6 only. ▶ Do not exceed the maximum concentration of 0.25% KaVo OXYGENAL 6. ▶ Proceed like for filling the water bottle, but use a different dose of KaVo OXYGENAL 6.
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Care instructions ESTETICA E30 3 Replenishing and checking the disinfectant | 3.2 Check the OXYGENAL 6 concentration ▶ Fill the four-fold dose of KaVo OXYGENAL 6 (equivalent to 20 ml) in the inten‐ sive germ reduction bottle. Make sure that the spout of the KaVo OXYGENAL 6 dosing facility (nose) is situated right above the opening of the intensive germ reduction bottle.
▶ Then fill-up the intensive germ reduction bottle with tap water. Note Substances remaining in the dosing head are not contamination, but rather agents that are deposited there during extended periods of non-use after con‐ densation of the water. These deposits redissolve after several dosing process‐ es. ▶ Screw the intensive germ reduction bottle tightly to the treatment centre through a clockwise rotation. Apply compressed air to the intensive germ reduction bottle.
3.2 Check the OXYGENAL 6 concentration ▶ Fill the tumbler with water. ▶ Use Merckoquant peroxide test strips 100 to 1000 mg/l H2O2 (Mat. no. 0.229.5003) to determine the OXYGENAL 6 concentration in the wa‐ ter germ reduction system. The OXYGENAL 6 concentration should be in the range from 150 to 250 mg/l H2O2in normal operation.
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1.009.7934 · dw · 20130304- 02 · en