AIRFLOW Prophylaxis Master Instructions for Use Rev E Aug 2019

1. BEFORE USE CONGRATULATIONS!

You are now the owner of this new EMS device! Please read the instructions carefully before use 

TO AVOID the risk of electric shock, this equipment must only be connected to a mains supply with protective earth/grounding. This device uses a Class-I insulating system that requires protective earth. FOR USA AND CANADA: GROUNDING RELIABILITY CAN ONLY BE ACHIEVED WHEN EQUIPMENT IS CONNECTED TO AN EQUIVALENT RECEPTACLE MARKED “HOSPITAL ONLY” OR “HOSPITAL GRADE”. DO NOT modify this equipment and/or any of its accessories. No modification of any part of this medical device is allowed. DO NOT open the device. There are no serviceable parts inside. If any serious incident occurs that is directly or indirectly related to the device, report it immediately to the manufacturer and to the competent authority of your country and of where the patient is established (if different). Disconnect the mains plug from electrical outlet for the purposes of maintenance, in the case of malfunction or when the device is left unattended. Turn off the water inlet when not in use. The device is not equipped with Aquastop and the EG-110 water hose may disconnect or leak: risk of flooding. The Instructions for Use of the device, as well as the Treatment Recommendations(FB648) and Piezon Treatment Recommendations (FB-652), are provided in electronic format and are part of the product documentation. However, if you want these in hard copy, you can request one set free of charge on our website, by telephone or in writing, and receive it within 7 days. • The Instructions for Use of the device (FB-618), as well as the Treatment Recommendations (FB-648) and Piezon Treatment Recommendations (FB-652), are available for download in PDF format at www.ems-instruction.com using the Product/Key Code FT-229. A PDF reader is required and, in case of need, it can be downloaded from the same web site. • It is essential to first read and understand all the Instructions for Use of the device before operating it and using the related accessories. The Treatment Recommendations are an integral part of the device’s Instruction for Use and each one document is complementary to the other. Always keep this documentation close at hand. • We recommend that you visit our website regularly to consult and/or download the latest version of the documentation for your device at www.ems-instruction.com • Please contact EMS technical support or your local EMS representative for further information and support. ENGLISH

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1.1. Intended Use The device is a fixed table top unit combining:

- PIEZON®: ultrasound scaler - AIRFLOW®: air polishing technology

Intended for use in

PREVENTION, MAINTENANCE AND TREATMENT during dental prophylaxis to remove biofilm and calculus from natural teeth, restorations and implants 1.2. Application Fields Application on natural teeth including all smooth surfaces, pits, fissures and interproximal areas, dental restorations and dental implants. AIRFLOW ® applications include: • • • • • • • • •

Plaque removal for the placement of sealants Surface preparation prior to the bonding/cementation of inlays, onlays, crowns and veneers Surface preparation prior to placing composite restorations Effective plaque and stain removal for orthodontic patients Cleaning prior to the bonding of orthodontic brackets Cleaning the implant fixture prior to loading Stain removal for shade determination Plaque removal prior to a fluoride treatment Plaque and stain removal prior to a whitening procedure

PERIOFLOW® applications include: • • •

Maintenance of periodontal deep pockets up to 9 mm following initial treatment Removal of periodontal biofilm Cleaning of implants

PIEZON® applications include: • • • • • • • • • • • • •

Removal of supragingival calculus Removal of subgingival calculus Periodontal treatment Preparation of approximal cavities Luting tooth-shaded inlays and onlays with highly thixotropic, dual-curing cements Endodontics: preparation, cleaning and irrigation of root canals Endodontics: retrograde preparation of root canals Endodontics: condensing gutta-percha Endodontics: removal of crowns and bridges Restorative: Preparation of cavities Restorative: Cementation of restorations Restorative: Condensing of amalgams Restorative: Removal of crowns, bridges, inlays and posts

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1.3. Intended Users Only qualified dentists, dental hygienists and dental professionals must use this device by fully complying with their respective country’s regulations, accident prevention measures, and strictly follow these instructions for use. The device must be prepared and maintained only by persons who have been instructed in infection control, personal protection and patient safety.

Improper use (e.g. due to lack of hygiene or routine maintenance), non-compliance with our instructions, or the use of accessories and spare parts that are not approved by EMS invalidates all claims under warranty and any other claims.

No specific training other than initial professional training is required to use this medical device. The practitioner is responsible for performing the clinical treatments and for any dangers that may arise due to a lack of skill and/or training. For optimal patient comfort, safety and efficiency, we suggest that you regularly follow our: SWISS DENTAL ACADEMY Training Program Do you know the Guided Biofilm therapy? If not:

GET TRAINED NOW

Please contact your local EMS representative for further information. Professional product installation and product introduction by EMS certified person is highly recommended for optimal setup and reliability.

1.4. Patient Population PIEZON® devices are intended for use on patients requiring dental treatment, including scaling (e.g. subgingival and supragingival calculus, stains), endo (e.g. root canal treatment), restorative (e.g. cavities, amalgams), periodontics and dental prophylaxis, regardless of age or gender. AIRFLOW® devices are intended for use on patients requiring dental treatment, including cleaning and polishing of teeth (natural or implant) by the projection of water, air and dental powders onto the tooth surface, regardless of age or gender. This medical device is not intended for use on newborn (neonate) and infant (< 2 years old) patient populations.

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1.5. Contraindications Suggestion for alternatives:

Treatments contraindications: ®

and

®

are contraindicated with

®

is contraindicated with

®

is contraindicated with

®

is contraindicated with

Patients with severe or unstable upper respiratory tract infections, chronic bronchitis/asthma 1. Pregnant and breastfeeding patients Patients with severe inflammation and/or osteonecrosis. Patients with a cardiac pacemaker, defibrillators and any implantable electronic device.

PIEZON® AIRFLOW® and PIEZON® PS AIRFLOW® PLUS and PIEZON® PS AIRFLOW® PLUS

The decision to use AIRFLOW® and/or PERIOFLOW® on contagious patients or on patients with risk of infection, has to be taken by the dentist/medical doctor on an individual basis following practitioner protection level, patient risk assessement and specific country regulations. On patients under Bisphosphonate therapy, the decision to use AIRFLOW® and/or PERIOFLOW® has to be taken by the dentist/medical doctor depending on the oral health of the patient. Suggestion for alternatives:

AIRFLOW ® powders contraindications:

CLASSIC powder

is contraindicated with

Low-salt diet patients.

Flavored CLASSIC powder

is contraindicated with

Patients allergic to flavor aroma.

PLUS powder

is contraindicated with

PERIO & SOFT powder

is contraindicated with

Patients allergic to Chlorhexidine. Patients allergic to Glycine (Glycocoll).

AIRFLOW® PLUS AIRFLOW® PLUS/PERIO and CLASSIC NEUTRAL AIRFLOW® PERIO AIRFLOW® PLUS

1.6. Compatibility This device is compatible with the following accessories: ®

Powders

Handpiece ® Handpiece ® Handpieces ® Scaling and Periodontal instruments ®

®

Endodontics instruments

®

Conservative measures instruments Cavity preparation instruments

®

1

PLUS powders: DV-082, DV-086 series CLASSIC powders: DV-048 series PERIO and SOFT powders: DV-070, DV-071 series EL-308 EL-354 EN-060, EN-061 PS, A, B, C, P, PSR, PSL, PL1, PL2, PL3, PL4, PL5, HPL3, DPL3, PI RT1, RT2, D, H, ESI, Files ISO 15, 20, 25, 30, 35, Endochuck 180°, 120° and 90°, RT3, RE2, BERUTTI E, F, G, SP SM, PF, SD, VE, SB, SBD, SBM

Related to possible powder inhalation during AIRFLOW® treatment.

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Applied Parts The following items are Medical Device Applied Parts: • AIRFLOW® (EL-308) Handpiece • PERIOFLOW® (EL-354) Handpiece • PIEZON® (EN-060 and EN-061) Handpieces Applied Parts, under certain operating conditions, may exceed 41°C of temperature and reach a maximum temperature of 51°C.

1.7. General Precautions

PS Instrument

USE EMS ACCESSORIES ONLY! The use of any other accessories could lead to patient injury, malfunction or damage to the device

DO NOT use this device in the presence of flammable anesthetics or oxidizing gases (such as nitrous oxide (N2O) and oxygen) or in close proximity to volatile solvents (such as ether or alcohol), as explosion may occur. DO NOT store the powder near acids or heat sources. TAKE the following precautions to prevent any adverse events to the patient and/or to the user in case of electromagnetic disturbances: • Always refer to the information listed in the chapter “ • Electromagnetic Compatibility”. • In case of a wireless pedal malfunction, presumably caused by electromagnetic disturbances, use the wired pedal instead. • In case of a device malfunction, presumably caused by electromagnetic disturbances, first verify the cabling, and then move any portable RF communications equipment and mobile devices placed nearby as far away as possible to rule out interference. • Stop using the device if the electromagnetic disturbances persist and contact EMS technical support for assistance.

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2. INSTALLATION 2.1. Equipment included in the box Check contents for any damage that may have occurred during transportation. AIRFLOW Prophylaxis Master ® Unit

Quick Guide

AIRFLOW ® PLUS Prophylaxis Powder

Powder Chambers

with Master Screw, water & air filters installed FT-229/A

12x DV-082

AIRFLOW ® CLASSIC Prophylaxis Powder 2x DV-048

Power cord

providing links to eIFU download and product registration

Plug type depends on country

Air hose EH-142

PLUS : EL-607 CLASSIC: EL-606

Water hose

NIGHT CLEANER

CLIP+CLEAN

EG-110

2x AB-613 (Package EL-655)

DV-154AU (800 ml)

One of the following pedals: AIRFLOW Handpiece cord

Boost wireless pedal

EM-145

EK-404A with 2x AA 1.5V type lithium batteries

PIEZON® Handpiece cord

Foot switch (Wired pedal)

®

PIEZON® bottle EG-111

NIGHT CLEANER

bottle

EG-120

EM-146

EK-410

BIOFILM DISCLOSER DV-158

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FS-447

FS-462

FS-443

1 2

EL-308: AIRFLOW® Handpiece AB-470A/A: Easy Clean

1 2

EN-060 : PIEZON® Handpiece 3x DS-016A : Instrument PS

1

3

EL-651: Cord gaskets

3

4x AB-340: Light guide

2

4 5

El-600: Water filter EL-599: Air filter

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3 4 5

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EL-354: PERIOFLOW® Handpiece AB-358/B Nozzle extractor (under) 10x AB-327A/A: PERIOFLOW® nozzle 6x DT-064: Instrument PI DT-018: Flat wrench (on top) DS-010: Endochuck 120°

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2.2. Step-by-step installation Find an appropriate area to place the device. Place the medical device (control unit) within the dental cabinet in a suitable position for your activity and leave enough free space to allow easy handling and proper aeration. Keep a minimum of 10 cm clearance around the unit. Do not stack it with other equipment. The medical device must be placed on a secure and flat surface (with a maximum slope of 5 degrees).

Check for proper water and air supply lines. Verify that your dental cabinet has a filtered tap water source and a compressed air source using air and water hoses EG-110 and EH-142, respectively. In case your cabinet water and air lines are not provided with the required hoses EG-110 and EH-142, a proper installation by qualified personnel is required. Call EMS Service for support. In order to prevent retro contamination, connect the cable to EN-1717 or DVGW 2 compliant fluid sources.

Check for a proper and safe power grid. This device uses a Class-I insulating system that requires protective earth. Plug the unit only into an FI protected mains supply (FI = Residual current protection). For USA and Canada: connect only to a hospital-grade outlet. Check that the rated voltage of the device is suited for the local line voltage to prevent damaging the unit, risk of fire and electric shock. The mains plug of the unit must be accessible at all times. DO NOT INSTALL the device in case your dental cabinet does NOT have protective earth. If you have any concerns about this, call EMS Service for on-site support by qualified personnel.

Be aware The use of cables and accessories other than those supplied by EMS may negatively affect EMC performance. Use only parts supplied by EMS. The device uses a low power radio, 8 dBm EIRP max, Bluetooth® 2.4 GHz, to communicate with the wireless pedal. Interference may occur in the vicinity of this equipment. The Bluetooth® radio is automatically disabled (powered off) when a wired pedal is connected. Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the device, including cables. Otherwise, degradation of the performance of this equipment could result. 2

German Technical and Scientific Association for Gas and Water

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Connect air and water hoses Turn the device over and place it upside down. 1

Pressure: 4.5 to 7 bar

Connect the air hose EH-142 to the cabinet/dental unit. Dry air. Max. humidity: 1.032 g/m3 Push the hose connector into the air jack firmly (it may be hard).

Filtration: max. 1 μm

Connect the water hose EG-110 to the cabinet/dental unit. 2

To prevent retro contamination, connect the cable to an EN-1717 or DVGW compliant fluids source. DO NOT install the PIEZON® or NIGHT CLEANER bottle before connecting the air and water lines.

Drinking water Pressure: 2 to 5 bar Salinity: max. 0.2% Temperature: 10°C to 30°C

Install accessories Continue to keep the device upside down and disconnected from the power grid!

1 5

6

5

6

2

3

4

3

4

5

4

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3

1

2

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EH-142 Air hose – filter pre-installed PUSH VERY HARD EG-110 Water hose – filter pre-installed Power cord into socket (Fuse holder in the socket) EK-410 Wired pedal ONLY IF APLICABLE EM-145 AIRFLOW® handpiece cord + lock actuator PUSH HARD EM-146 PIEZON® handpiece cord + lock actuator PUSH HARD

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Check the cord connections

PUSH

1. HARD 2.

PUSH The handpiece cord is not fully connected.

PUSH HARD to lock in. The system is well connected & locked.

To disconnect the handpiece cord system, unlock the connection and pull at the same time.

Fix the device You will find a “Master Screw” provided on the bottom center of the device. Unscrew the Master Screw first and use it to secure the device firmly to a table or onto the AL-125 device support in your cabinet (the AL-125 part is available through our after-sales support and dealers).

Table

Master Screw usage

Master Screw placement

Fix your device with the provided “Master Screw” in order to ensure that the unit cannot be removed without the use of a tool. Check the position of the medical device so that it corresponds to your line of sight and the characteristics of your personal workstation (the lighting and the distance between the user and the device). The device must remain quickly and easily accessible at all times. Check that the water and air lines and the power cord do not hinder physical movement.

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Power your device You can now connect the power cord to the mains grid. Protective earth is required! Be sure your power grid has an efficient protective earth.

Voltage: 100-240 Vac Frequency: 50 to 60 Hz. Operating current: 4 A max.

Installation of the wireless pedal Insert two (2) AA 1.5V lithium batteries into the wireless pedal. Close the cover and operate your device. Risk of fire: use only batteries that have current limiter/short-circuit and over-temperature protection (compliant to IEC 60086-4:2014 Safety of lithium batteries). The optional wireless pedal supplied with your device is already paired and ready to use (Note: A pedal can only command one single device at a time. Pairing is maintained even if the batteries are removed). When you receive your new machine, all you need to do is insert the two (2) AA lithium batteries into the wireless pedal and your device is ready to work. In case you replace your pedal, you will need to pair it with your device. For instructions, please read the specific Maintenance & Troubleshooting chapter. The Bluetooth® radio is automatically disabled (powered off) when a wired pedal connected. The wireless pedal uses a low power, 8 dBm EIRP max, Bluetooth® 2.4 GHz radio, to communicate with the control unit. Interference may occur in the vicinity of this equipment. Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the device, including cables. Otherwise, degradation of the performance of this equipment could result.

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2.3. Powder Chambers Clinical risk: Only use PLUS or PERIO Powder with the PLUS Powder chamber. Clinical risk: Only use PLUS Powder chamber (red) for subgingival treatments. PLUS

CLASSIC

The PLUS Powder chamber is designed for the PLUS Powder. It can be used for supra and subgingival treatments. Pressure is automatically reduced for compatibility with subgingival treatments, including Perioflow treatments (Supra applications also possible). Compatible EMS Powders: PLUS and PERIO (refer to paragraph “Compatibility” for details).

The CLASSIC Powder chamber is designed for the CLASSIC Powder and can only be used for supragingival treatments. Sodium Bicarbonate: Use only this powder and chamber for supragingival applications. Compatible EMS Powders: CLASSIC and SOFT (refer to paragraph “Compatibility” for details).

Check bottle and powder chamber integrity: There should be no crack on the body. The powder chamber is pressurized during use. Replace faulty parts immediately. Make sure that the powder chambers are dry. Use only PLUS or PERIO Powders for restorations, crowns, bridgework, implants and orthodontics. Do not sterilize the powder chambers and their caps/parts by steaming or dry thermal reprocessing. Use only ambient temperature active disinfectant and cleaning agents.

By hand only: remove the powder chamber cap to refill powder up to the indicated MAX level, then insert the cap back fully onto the bottle. Pour the powder in freely. The central tube can be fully filled without problem.

Before pressurizing, position the powder chamber into the device. Magnetic attraction will position it correctly. Do not insert upside-down.

Do not fill the chamber higher than the indicated MAX level. The powder level will go down slightly a few minutes after the filling (powder compaction).

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2.4. Water supply and PIEZON® bottle Without Bottle:

PIEZON® & AIRFLO W® use external water supply.

AIRFLOW® uses external water supply. PIEZON® uses bottle liquid supply.

2

1

The CLIP+CLEAN shall be previously cleaned and disinfected before use. Non-disinfected CLIP+CLEAN may contaminate the device.

With Bottle connected:

Place the CLIP+CLEAN into the device’s bottle receptacle for dust protection.

Connect the PIEZON® bottle Only use the PIEZON® bottle EG-111 (transparent) for disinfectant solutions.

The PIEZON® bottle is compatible with the following solutions: Avoid unwanted chemical reactions or ingestion of residues of solution. Always rinse the liquid circuit with drinking water before using a different solution or undergo a regular treatment requiring water only. For treatment application use the percentage of solution as per discretion and per local country regulations and recommendations. Solution Sodium Hypochlorite Chlorexidine Carbanilides Povidone iodine Quaternary ammonium compound Cetylpyridin chloride Citric acid Physiological water (NaCl %) Ethanol Isopropanol

Concentration Up to 5% Up to 1% Up to 0.05% Up to 12% Up to 0.7% Up to 1% Up to 5% Up to 0.9% Up to 5% Up to 5%

Do not sterilize the PIEZON® bottle and its nozzle cap by steaming or dry thermal reprocessing. Use only ambient temperature active disinfectant and cleaning agents.

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2.5. AIRFLOW® and PERIOFLOW® Handpieces AIRFLOW® and PERIOFLOW® Handpieces are reusable, but they shall have been previously reprocessed: cleaned, disinfected and sterilized. Not reprocessed Handpieces and accessories may cause bacterial or viral infections.

Connect the AIRFLOW® or PERIOFLOW® Handpiece.

Follow the “Reprocessing of EMS parts” instructions and the present-day regulations on reprocessing enforced in your country. In case the AIRFLOW® Handpiece gets clogged, refer to the “Maintenance & Troubleshooting” section for instruction.

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2.6. PIEZON® Handpiece and Instruments PIEZON® Instruments and Handpieces are reusable, but they shall be reprocessed before use: cleaned, disinfected and sterilized. Not reprocessed handpieces and accessories may cause bacterial or viral infections. Follow the “Reprocessing of EMS parts” instructions and the present-day regulations on reprocessing enforced in your country. Check tip length and tip thread through the cover right folder of your Quick Guide. If tip extremity is in the red area, it can have excessive and uncontrolled vibration. Replace the tip.

Accessories are available from EMS and authorized dealers.

1

2

3

Mount the tip / insert using the EMS CombiTorque® tool

Connect the PIEZON® Handpiece

Nose cap and light guide

Once the instrument is screwed all the way in, give an extra quarter of a turn to obtain the required torque and remove the CombiTorque®.

Blow-dry the connections to remove any presence of liquid and to ensure a proper electrical contact.

Always use the handpiece with the light guide and the nose cap installed and correctly tightened. For replacing the light guide, refer to the “PIEZON® light guide check & replace” section.

Use only the CombiTorque® to tighten the EMS Instrument on the handpiece to the correct torque to avoid tip unscrewing or breaking.

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3. DEVICE USE 3.1. Interfaces 2

1

BOOST Press hard NORMAL Press gently

4

3

7 6

1

2

ON/OFF-mode Standby

Powder chamber pressurization / depressurization

5

ON: the device goes into operating mode. OFF: the device reverts back to standby. (After 1 hour of inactivity, the unit switches to off-mode standby) Powder chamber is pressurized or depressurized. A white light illuminating the powder chamber will turn on when pressurized. During chamber depressurization, the AIRFLOW® cord will automatically purge and the white light will turn off at the end of the process. Entering Standby mode: The powder chamber depressurizes automatically. Powder chamber depressurization may take up to 10 seconds to complete. During this time, it is recommended that you leave the AIRFLOW® Handpiece in its holder with the nozzle facing down to avoid spraying the purged air and residual powder upwards.

Power setting

3

Place your finger in the groove below the numbers to adjust AIRFLOW® air pressure and PIEZON® power: • 0 (water only, blue indicator) • 10 (Maximum) Memorization of the preselected settings. 4

PIEZON® water

Sets the PIEZON® water flow rate.

5

AIRFLOW ® water

Sets the AIRFLOW® water flow rate.

6

Pedal (normal)

Press the edge of the pedal for normal operation. The pedal is deactivated when both handpiece cords are placed in their holders.

Pedal BOOST

Pressing hard on the center of the wireless pedal activates power boost. For easy boost activation: leave the foot on the pedal and put the heel up.

7

(Only on the wireless pedal)

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PIEZON® power setting

The unit is equipped with NO PAIN® technology which provides an adaptive response in function according to the load applied to the instrument. The following table shows the maximum output power as per user power setting:

PIEZON® Power

Power Setting

0

1

2

3

4

5

6

7

8

9

10

Max Output Power [W] 0

0.4

1.2

2.1

3.0

3.9

4.8

5.6

6.4

7.2

8.0

Risk of tip breakage: with ENDO files, do not exceed 2.5W (power setting “3” max.)

AIRFLOW® pressure setting

Both the PLUS and CLASSIC powder chambers have an integrated dynamic pressure regulator that automatically set the optimal pressure range for the selected powder chamber and related powder type as detailed in chapter “Powder Chambers”. The following table shows the static and approximate dynamic pressures 3 as per selected powder chamber and user power setting:

AIRFLOW® Pressure

Pressure Setting

0

1

2

3

4

5

6

7

8

9

10

Static [Bar]

/

2.5

2.7

3.0

3.2

3.5

3.7

4.0

4.2

4.5

4.7

CLASSIC dynamic [Bar]

/

1.9

2.1

2.3

2.6

2.8

3.0

3.2

3.5

3.7

3.9

PLUS dynamic [Bar]

/

1.5

1.7

1.9

2.0

2.2

2.4

2.6

2.7

2.9

3.1

3 Dynamic pressures depend on handpiece and powder type too. The listed pressures are for information purpose and referring to the commonly used EL-308 AIRFLOW® Handpiece with DV-082 and DV-048 powders.

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PIEZON® and AIRFLOW® BOOST

BOOST effect Pressing hard on the center of the wireless pedal activates the BOOST mode and results in an increase of power, as the following table shows:

AIRFLOW® Boost

PIEZON® Boost

Power Setting

0

1

2

3

4

5

6

7

8

9

10

Corresponding Boost Level

0

6

7

8

8

8

9

10

10

10

10

Power Setting

0

1

2

3

4

5

6

7

8

9

10

Corresponding Boost Level

0

6

7

8

9

10

10

10

10

10

10

Risk of tip breakage: use BOOST only with a tip suited for high power usage. DO NOT use BOOST with ENDO files.

Wireless pedal battery saving Each time the wireless pedal is released, it enters into a low power mode. Even if unused for long, it is not required to remove the batteries. To avoid an involuntary depletion of the wireless pedal batteries, in case the pedal remains pressed without interruption for 10 minutes, it will automatically enter into switch-off mode. To resume from the switch-off mode, it is required to first release the wireless pedal and then power cycle the device (switch off for 30s and then power on again).

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Water temperature and acoustic feedback settings AIRFLOW® and PIEZON® liquids’ temperature is 40°C by default. To adjust the water temperature or the acoustic feedback, follow the procedure below: 1. Turn the device ON. 2. Securely place both handpieces (AIRFLOW® and PIEZON®) back into their holders. 3. Press  +  simultaneously to access the menu. (See image below – place fingers in the groove below the numbers)

4. Colors will appear on the numbers: • 0 to 4 for setting water temperature (5 is not used) • 6 to 10 for setting acoustic feedback (5 is not used) Water temperature 4

Acoustic feedback

0

1

2

3

4

6

7

8

9

10

No Heating

25°

30°

35°

40°

No sound

Low volume

Medium volume

High volume

Maximum volume

5. Change the settings according to your wish. 6. Press the ON/OFF button to save the setting and exit. Note: • •

Changes are applied to both AIRFLOW® and PIEZON® liquid temperatures. After a few seconds of keyboard inactivity, the device automatically exits the mode.

The target temperature is determined into the device’s body. On AIRFLOW® side, water temperature decreases along the cord. Air spray also decreases the temperature. Final temperature of AIRFLOW® spray is lukewarm, lower than 40°C. On PIEZON® side, PIEZON® Handpiece warms up the waterline which compensates natural cooling along the cord. Please adjust the temperature setting for maximizing patient comfort. 4

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