iOptima Instructions for Use March 2022

Table of contents iOptima description ...4

iOptimaINT description ... 22

1

7

Symbols ... 5 1.1 1.2

2

Identification, Intended use and Notation .. 7 2.1 2.2 2.3

3 4

9

Description of symbols for iOptimaINT ... 23 Description of symbols for iOptimaINT accessories... 24

Identification, Intended use and Notation 25 8.1 8.2 8.3 8.4 8.5 8.6 8.7 8.8

Description ... 10

Identification... 25 Intended use... 25 Intended patient population... 26 Intended User... 26 Intended medical conditions ... 26 Patient contra-indications and Side-effects ... 27 In case of accidents... 27 Notation... 28

User and Patient safety: Warnings & Precautions for Use ... 29

10 Description ... 31

Install the iOptima app ... 17 Install the iOptima system ... 17

10.1 iOptimaINT system overview ... 31 10.2 iOptimaINT system table ... 31 10.3 Technical data ... 32 10.4 Performances ... 33 10.5 Environmental protection and information for disposal... 33 10.6 Limitation of liability ... 33 10.7 Electromagnetic compatibility (technical description) for iOptimaINT ... 34

Interface overview ... 19

11 Installation ... 37

Installation ... 17 5.1 5.2

6

8

Identification...7 Intended use...7 Notation...8

iOptima system overview ... 10 iOptima system table... 11 Set supplied... 11 Options ... 11 Technical data ... 12 Environmental protection and information for disposal... 13 Limitation of liability ... 13 Electromagnetic compatibility (technical description) for iOptima... 14

Symbols ... 23 7.1 7.2

User and Patient safety: Warnings & Precautions for Use ... 9 4.1 4.2 4.3 4.4 4.5 4.6 4.7 4.8

5

Description of symbols for iOptima unit ...5 Description of symbols for iOptima accessories...6

6.1 6.2 6.3

iOptima application... 19 Sound alerts ... 19 iPod touch® and iOptima connection / disconnection conditions ... 20

11.1 Install the iOptima app ... 37 11.2 Install the iOptimaINT system ... 37

12 Interface overview ... 38 12.1 iOptima application... 38 12.2 Sound alerts ... 38 12.3 iPod touch®/iPad mini® and iOptimaINT connection / disconnection conditions ... 39

1

iOptima/iOptimaINT operation ...40 13 Getting started ... 41 13.1 Back up data... 41 13.2 Use of the Touch screen... 41 13.3 Launch iOptima app ... 42 13.4 Quit iOptima app... 42 13.5 Welcome screen and disclaimer ... 43 13.6 Information ... 44 13.7 Settings ... 45 13.8 iOptima app update ... 45 13.9 Software update... 46

19 Maintenance ... 75 19.1 Servicing... 75 19.2 Cleaning ... 75 19.3 Important... 75 19.4 Replace 4VL seal... 76 19.5 iOptimaINT ... 76

20 Legal and general ... 77 20.1 General information ... 77 20.2 Trademarks... 77 20.3 Terms of guarantee ... 77

14 Operation - Restorative mode ... 47 14.1 Enter Restorative mode ... 47 14.2 Operative screen description... 47 14.3 Standard Use - Operating mode (Start) ... 49 14.4 Customize default operations ... 49 14.5 Create new operations (user-defined) ... 51

15 Operation - Endodontics mode ... 53 15.1 Enter Endodontics mode... 53 15.2 Operative screen description... 53 15.3 Standard Use - Operating mode (Start) ... 55 15.4 Customize settings ... 55 15.5 Add, sort or remove files ... 57 15.6 Restore (default) and delete (user-defined) systems... 58 15.7 Create new Brands and Systems... 59 15.8 CA ENDO / Reciproc option ... 60

16 Operation - Surgery mode ... 61 16.1 Enter Surgery mode... 61 16.2 Operative screen description... 61 16.3 Standard Use - Operating mode (Start) ... 63 16.4 Customize default operations ... 64 16.5 Create new operations (user-defined) ... 65

17 Operation - Piezo scaling mode ... 67 17.1 Enter Piezo scaling mode... 67 17.2 Operative screen description... 67 17.3 Standard Use - Operating mode (Start) ... 67 17.4 Customize default operations ... 68 17.5 Create new operations (user-defined) ... 70

18 List of errors & Troubleshooting ... 71 18.1 Alert messages (operating)... 71 18.2 Device operating error... 72 18.3 iOS compatibility errors (disclaimer screen),... 73

2

iOptima description

Rx Only

1 Symbols 1.1 Description of symbols for iOptima unit Symbol

5

Description

Symbol

Description

CE Marking with number of the notified body.

Non-ionizing electromagnetic radiation.

Manufacturer.

Alternating current.

REF

Catalogue number.

OFF (power).

SN

Serial number.

ON (power).

MD

Medical device.

Rx Only

Warning: In accordance with federal law (USA), this device is only available for sale upon recommendation by an accredited practitioner.

Sound alerts.

WARNING: hazard that could result in serious injury or damage to the device if the safety instructions are not correctly followed.

CAUTION: hazard that could result in light or moderate injury or damage to the device if the safety instructions are not correctly followed.

Separate collection of electric and electronic equipment.

Movement to the stop, in the direction indicated.

Refer to instruction manual/booklet (https://dental.bienair.com/en_ch/support/download-center).

4-hole connection and 4 electric (4VLM).

General symbol for recovery/recyclable.

Authorized EC Representative in the European Community.

MD

Data Matrix code for product information including UDI (Unique Device Identification).

ENG

1.2 Description of symbols for iOptima accessories Symbol

XXXX

Description

Symbol

Separate collection of electric and electronic equipment.

CE Marking with number of the notified body.

Manufacturer.

Description

SN

Serial number. Electrical safety. Applied part type B.

REF

Catalogue number.

MD

Medical device.

MD

Data Matrix code for product information including UDI (Unique Device Identification).

Authorized EC Representative in the European Community.

Rx Only

Warning: In accordance with federal law (USA), this device is only available for sale upon recommendation by an accredited practitioner.

135°C

Sterilization up to the specified temperature.

6

FIG. 1

2 Identification, Intended use and Notation 2.1 Identification

2.2 Intended use

iOptima Electronically controlled unit for dentistry allowing operation of a single MX2 micromotor with variable speed using the dental unit pedal. It is essential to connect a compatible iPod touch® using the lightning connector.

Product intended for professional use only. The iOptima systems are intended for use in restorative dentistry, endodontics, dental prophylaxis, and orthodontics by dentists and dental professionals in a dental office.

The unit provides power to the iPod touch® device as soon as it is connected. Under normal use (power supply = 32Vdc), the unit does not use any battery energy of the iPod touch®. The iOptima unit charges the iPod touch® battery when connected. The restorative, endodontics parameters are defined before operation using the iOptima application installed on the iPod touch®. The iOptima application indicates the operation steps, the ratio of the handpiece, tool speed, torque value, light intensity, footpedal mode and the micromotor rotation direction. iOptima application is compatible with Apple operating systems (iOS & iPadOS).

⚠ CAUTION In endodontic mode, the predefined torque and speed values are only intended as a guide. The file values used must be adapted according to the manufacturer instructions of the files.

7

FIG. 1 iOptima system connected to an iPod touch® that controls a MX2 motor. Any use other than that for which this product is intended is unauthorized and can be harmful. Note 1

ENG 2.3 Notation • A, B, C, etc. Text preceded by a letter indicates a procedure to be carried out step-by-step. •  Indicates a procedure result. • (1), (2), (3), etc. Text preceded by a number indicates text used in conjunction with an illustration. • OK, Save, Settings, etc. Text in bold italic font style indicates, on-screen elements such as buttons, menus, menu items, screen areas, values, fields when they are named and screen names. Tap Settings to open the Settings screen, change parameters and tap Done.

NOTES 1 The technical specifications, illustrations and dimensions contained in these instructions are given only as a guide. They may not be the subject of any claim. The manufacturer reserves the right to make technical improvements to its equipment, without amending these instructions. For all additional information, please contact Bien-Air Dental SA at the address indicated on the back cover.

8

3 User and Patient safety: Warnings & Precautions for Use To prevent any risk of explosion, the warning below must be observed:

⚠ WARNING According to IEC 60601-1:2005+A12012/AnnexG, electrified devices (motors, control units, couplers and attachments), can be safely used in a medical environment in which potentially explosive or flammable mixtures of anaesthetic substances are delivered to the patient only if: (1) The distance between the motor and the anaesthetic breathing circuit exceeds 25 cm. (2) The motor is not used simultaneously to the administration of the anaesthetic substances to the patient. To prevent any risk of electric shock, the warning below must be observed:

⚠ WARNING • The iOptima unit must be connected only to a power supply network provided with a protective earth. To prevent any risk of motor overheating, the cautions below must be observed:

⚠ CAUTION • Ensure that the micromotor hose is not bent. • The iPod touch® must never be disconnected from the iOptima dental unit during operation. To prevent any risk of injury (damage to bone, teeth, tissue) the caution below must be observed:

⚠ CAUTION • The parameters contained in the dental procedures are indicative only. Bien-Air Dental SA cannot be held liable for them.

9

• The iPod touch® must never be disconnected from the iOptima dental unit during operation. If the iPod touch® is disconnected during an operation, the micromotor stops immediately. To prevent any risk of injury and/or material damage the cautions below must be observed:

⚠ CAUTION • Never connect a handpiece on a running micromotor. • The power plug of the iOptima is the device used for disconnection in case of problems, it must be easily accessible at all times Note 1

NOTES 1 The predefined parameters may be subject to modification without notice.

ENG

4 Description 4.1 iOptima system overview The iOptima system consists of: • iOptima unit (3) with docking station for iPod touch® (4); • A MX2 micromotor (12) and MX2 hose (10, A); • A pneumatic 4-way connection input (6, B); • A power supply (2) and plug cord (C).

2

1

3

4

C

5

6

7

A

B

C

10

9

8

A

iOptima B

13 11

12

FIG. 1 (1) (2) (3) (4) (5) (6) (7)

Power supply cord Power Supply (C) iOptima unit iPod touch® [not provided in set] MX2 micromotor hose output (A) 4-way connector input, air and water inlet from your pneumatic unit (B) Power input connector (with lock) (C)

(8) Main power switch (9) MX2 micromotor hose* (A) (10) iOptima status light (green power on) (11) MX2 micromotor* (12) Handpiece* [not provided in set] (13) Dental unit with pedal (B) [not provided in set] *Applied parts (per IEC 60601-1)

10

4.2 iOptima system table Summary of the iOptima functions and technological features. Product

Device

Technology

Motor

Restorative

Endodontics

Oral surgery

Implantology

Prophylaxis

iOptima

iPod touch®

DMX2

MX2

X

X

-

-

X

4.3 Set supplied

iOptima set REF 1700547-001

4.3.1 iOptima system

Designation

REF number

iOptima unit (1x)

1600926-001

iOptima set REF 1700563-001

MX2 Micromotor hose (1x)

1600762-001

Designation

REF number

Power supply (1x)

1501938-001

iOptima unit (1x)

1600926-001

1300065-001

MX2 Micromotor (1x)

1600677-001

3P cable system, Switzerland, length 2.00 m (1x)

MX2 Micromotor hose (1x)

1600762-001

3P cable system, Europe, length 2.50 m (1x)

1300066-001

Power supply (1x)

1501938-001

3P cable system, US, length 2.00 m (1x)

1300067-001

3P cable system, Switzerland, length 2.00 m (1x)

1300065-001

3P cable system, Europe, length 2.50 m (1x)

1300066-001

3P cable system, US, length 2.00 m (1x)

1300067-001

Designation

REF number

iOptima bracket

1501988-001

Spraynet, cleaning spray 500 ml, box of 6 cans

1600036-006

4.4 Options

iOptima set REF 1700544-001

11

.

Designation

REF number

iOptima unit (1x)

1600926-001

MX2 Micromotor (1x)

1600677-001

MX2 Micromotor hose (1x)

1600762-001

Power supply (1x)

1501938-001

3P cable system, Switzerland, length 2.00 m (1x)

1300065-001

3P cable system, Europe, length 2.50 m (1x)

1300066-001

3P cable system, US, length 2.00 m (1x)

1300067-001

Dimensions L x W x H iOptima unit...125 x 145 x 75 mm iOptima unit (with iPod touch®)...125 x 145 x 160 mm MX2 hose ...L 1.7 m MX2 micromotor...Ø 21 x L 73.5 mm Power Supply ...130 x 75 x 45 mm Weight iOptima unit... 0.4 kg Power Supply ... 650 g MX2 micromotor... 94 g Electrical and pressure data Voltage...100-240 VAC Frequency ...47-63 Hz Nominal power ...90 W Max. input power...160 W Max. input pneumatic pressure ...5 bar / 72.5 psi Min. input pneumatic pressure ...3 bar / 43.5 psi Environmental conditions Environmental Operating conditions

Electric insulation class Class I per IEC 60601-1 (apparatus protected against electric shocks).

ENG

4.5 Technical data

Degree of protection IP 40 (protection against insertion of objects larger than 1 mm) Memory • Restorative Storage of 20 user-defined Operations • Endodontics Storage of 10 user-defined Brands Storage of 10 user-defined Systems Storage of 8 Files per System including adjustment of speed and torque values for each file List of errors & Troubleshooting See chapter “18 List of errors & Troubleshooting” on page 71. Important: Consult the Instructions for Use of the following devices: Product

Micromotor

IFU

Hose

IFU

iOptima

MX2 LED

2100199

MX2

2100223

Transport and storage (max. 15 weeks)

Temperature

+10°C (50°F) to +25°C (77°F)

-25°C (-13°F) to +70°C (158°F)

Relative humidity

30% to 80%

30% to 80%

Atmospheric pressure

700 hPa to 1060 hPa

500 hPa to 1060 hPa

Altitude

0 to 3'048 m (0 to 10'000 ft)

-

⚠ CAUTION Do not use iOptima outside the range of operating temperature. Classification Class IIa in accordance with European Directive 93/42/EEC concerning medical devices.

12

4.6 Environmental protection and information for disposal

The disposal and/or recycling of materials must be performed in accordance with the legislation in force.

This unit and its accessories must be recycled. Electrical and electronic equipment may contain dangerous substances which constitute health and environmental hazards. The user must return the unit to its dealer or establish direct contact with an approved body for treatment and recovery of this type of equipment (European Directive 2012/19/EU).

4.7 Limitation of liability Bien-Air Dental SA shall not be held liable for any non-compliant use of the iPod touch®. The conditions for and restrictions on use set by Apple must be respected (jailbreak, hardware modification, etc.). To ensure optimum operation of the iOptima application, iOS updates must be according to version used during validation of the application.

13

ENG

4.8 Electromagnetic compatibility (technical description) for iOptima 4.8.1 Electromagnetic compatibility warnings The intended EM environment (per IEC 60601-1-2 ed. 4.0) is Professional healthcare facility environment.

⚠ CAUTION The iOptima complies with the EMC requirements according to IEC 60601-1-2. Radio transmitting equipment, cellular phones, etc., should not be used in the immediate vicinity of the device, since this could affect its operation. The device is not suitable for being used close to high-frequency surgical equipment, magnetic resonance imaging (MRI) and other similar devices where the intensity of electromagnetic disturbances is high. In any case, ensure that no high frequency cables are routed above or near the device. If in doubt, contact a qualified technician or Bien-Air Dental SA. Special precautions should be taken when using strong emission sources such as high-frequency surgical equipment and other similar devices, to ensure that HF cables are not routed above or near the device. If in doubt, please contact a qualified technician or Bien-Air. 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 iOptima, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.

⚠ CAUTION The use of accessories, transducers and cables other than those specified, with the exception of transducers and cables sold by Bien-Air as spare parts for internal components, may result in increased emissions or decreased immunity.

⚠ CAUTION Since this device is intended to be used adjacent to or stacked with other equipment, the responsibility of verifying normal operation in the configuration in which it will be used falls onto the dental unit manufacturer.

4.8.2 Electromagnetic compatibility – emissions & immunity Guidance and manufacturer’s declaration - electromagnetic emissions iOptima is intended for use in the electromagnetic environment specified below. The customer or the user of iOptima should ensure that it is used in such an environment. Emissions test

Compliance

Electromagnetic environment - guidance

RF emissions CISPR 11

Group 1

The iOptima uses RF energy for its internal operation only. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

RF emissions CISPR 11

Class B

Harmonic emissions IEC 61000-3-2

Class A

Emissions due to voltage fluctuations IEC 61000-3-3

Conforming

The iOptima is suitable for use in any building, including residential buildings and those directly connected to the public low-voltage power supply network that supplies buildings used for residential purposes.

14

Guidance and manufacturer’s declaration – Electromagnetic immunity The iOptima is intended for use in the electromagnetic environment specified below. The customer or the user of the iOptima must ensure that it is actually used in such an environment. Immunity test

IEC 60601 test level

Compliance level

Electromagnetic environment - guidance

Electrostatic discharge (ESD) IEC 61000-4-2

±8 kV contact ±2 kV air ±4 kV air ±8 kV air ±15 kV air

±8 kV contact ±2 kV air ±4 kV air ±8 kV air ±15 kV air

Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.

Electrical fast transient burst IEC 61000-4-4

±2 kV for power supply lines ±1 kV for other lines

±2 kV for power supply lines ±1 kV for lines no input/output

Mains power quality should be that of a commercial or hospital environment.

Surge IEC 61000-4-5

±0.5 kV line to line ±1 kV line to line ±0.5 kV line to earth ±1 kV line to earth ±2 kV line to earth

±0.5 kV line to line ±1 kV line to line ±0.5 kV line to earth ±1 kV line to earth ±2 kV line to earth

Mains power quality should be that of a commercial or hospital environment.

0% UT for 0.5 cycle, at 0°, 45°, 90°, 135°, 180°, 225°, 270° and 315°

0% UT for 0.5 cycle, at 0°, 45°, 90°, 135°, 180°, 225°, 270° and 315°

0% UT for 1 cycle and 70% UT for 25/30 cycles at 0°

0% UT for 1 cycle and 70% UT for 25/30 cycles at 0°

Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11

15

Magnetic field due to mains frequency (50/60 Hz) IEC 61000-4-8

30 A/m

30 A/m

Conducted disturbances induced by RF fields IEC 61000-4-6

3 VRMS 0,15 MHz – 80 MHz 6 VRMS in ISM bands 0,15 MHz – 80 MHz 80% AM at 1 kHz

3 VRMS 0,15 MHz – 80 MHz 6 VRMS in ISM and amateur bands 0,15 MHz – 80 MHz 80% AM at 1 kHz

Radiated RF EM fields IEC 61000-4-3

3 V/m 80 MHz – 2,7 GHz 80 % AM at 1 kHz

3 V/m 80 MHz – 2,7 GHz 80 % AM at 1 kHz

Mains power quality should be that of a commercial or hospital environment. If the user of the iOptima INT requires continued operation during mains power interruptions, it is recommended that the iOptima be powered from an uninterruptible power supply or a battery. Magnetic fields generated by the mains frequency should be at levels characteristic of a typical location in a typical commercial or hospital environment. Field strengths from fixed RF transmitters, as determined by an electromagnetic site surveya should be less than the compliance level in each frequency range. Interference may occur in the vicinity of equipment marked with the following symbol:

Proximity fields from RF wireless communications equipment IEC 61000-4-3

IEC 60601 test level

Compliance level

Electromagnetic environment - guidance

Test freq. [MHz]

Max. power [W]

Immunity test level [V/m]

385

1.8

27

450

2

28

710, 745, 780

0.2

9

810, 870, 930

2

28

1720, 1845, 1970

2

28

2450

2

28

5240, 5500, 5785

0.2

9

ENG

Immunity test

Distance: 0.3 m

NOTE: UT is the AC mains voltage prior to application of the test level. Essential performance per IEC 60601-1: The essential performance is to maintain the visual luminous intensity of the LED and the motor speed. The maximum speed deviation is ±5%. a. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and mobile field radios, amateur radios, AM and FM radio broadcasts and TV broadcasts cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the iOptima is used exceeds the RF compliance level mentioned above, the iOptima should be observed to verify that it is operating normally. If abnormal operation is observed, additional measures may be necessary, such as reorienting or relocating the iOptima.

Note 1 - 2

NOTES 1

At 80 MHz and 800 MHz, the higher frequency range applies.

2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

16

1

FIG. 1

2

1

FIG. 2

2

3

FIG. 3

1

2

FIG. 4

5 Installation 5.1 Install the iOptima app A. Open the "App Store". B. Search the iOptima application. C. Install the iOptima application designed by Bien-Air Dental. Note 1

5.2 Install the iOptima system ⚠ CAUTION Before installing, please read carefully this product instruction. Note 2

FIG. 2 B. Connect the power cord (2) to the power supply (1) and plug to the mains. Note 3

⚠ CAUTION The power plug is the device used for disconnection in case of problems, it must be easily accessible at all times. FIG. 3 C. Connect the power supply cable (1) to the input connector (2) and turn right to lock.

⚠ CAUTION FIG. 1 A. Place the iOptima on a flat surface capable of bearing its weight.

⚠ CAUTION

⚠ CAUTION

Before connecting the MX2 cable ensure that all o-rings are correctly fitted and connectors are clean of dust.

It may be positioned on a table, on a trolley or any another surface but in no circumstances on the floor. It is not designed to be placed on wet surfaces or to come in contact with liquids.

17

Ensure that the power switch (3) is off «O».

FIG. 4 D. Connect the MX2 cable plug (2) to the output connector (1): • First sleeve up and carefully and firmly insert the cable plug, by guiding the connector and plug with the index pin on the connector; • Sleeve down and tighten (CW).

1 1

2

ENG

3

2

2

1

4 FIG. 5

FIG. 6

FIG. 5 E. Connect the MX2 cable (2) to the MX2 micromotor (1), by guiding the connector and plug with the index pin on the connector and tighten (CW).

⚠ CAUTION Never connect a handpiece on a running micromotor. FIG. 6 F. Connect the 4-way hose (1) to the 4-way connector of the iOptima unit (2): • First guide the sleeve and carefully and firmly insert the hose sleeve, by matching the connector and the coupling; • Tighten (CW). FIG. 7 G. Switch ON the water and power supply of the dental unit (refer to your dental unit instructions). H. Switch ON the iOptima (1) («I» = ON).

FIG. 7

NOTES 1 The iPod touch® must be correctly connected to a Wi-Fi network before the App Store is opened; refer to Apple's user guide for appropriate use of the iPod touch®. 2 In order to conform to the IEC 60601-1-2 standards, take into account the different routes of the wires through the system (bend, fold, section etc.) (see chapter “4.1 iOptima system overview” on page 10 and only use the power supply provided with the iOptima. In order to maintain warranty, this unit must be installed with the greatest care. Follow all the necessary instructions. Protect the unit from direct sunlight and dust. Keep the original packaging for storage and shipment. 3 The equipment is powered by your mains power supply (100240 VAC).

 The led (4) turns green (power ON).

I. Once it has been switched ON, connect the interface device «iPod touch®» (2) to the iOptima carefully sliding it along the lightning adapter (3).

 The iOptima is ready for use.

See chapter “6 Interface overview” on page 19.

18

FIG. 1 (iPod touch®)

6 Interface overview 6.1 iOptima application

6.2 Sound alerts

The iOptima application with iOptima allows to carry out restorative and endodontics dentistry operations.

⚠ CAUTION

Sound alert

Description

Always verify that the latest version of the software is used. It is recommended to connect the unit to the Internet periodically to detect if an app update is available.

One long beep

Entering in endodontics or restorative mode ENDO mode when selecting the first File

6.1.1 Compatibility The iOptima application is compatible with iPod touch® from 6th generation.

6.1.2 Notation In order to simplify the notation, in this manual: • iOptima application is referred to as «iOptima app»; • Restorative and Endodontics modes are referred to as «RESTO» and «ENDO».

19

Alternate short beeps

Message alert notifications Micromotor REVERSE running indicator

Alternate medium beeps Alternate long beeps

ENDO mode when the micromotor is running in reverse System failure notification

ENG 2

1

FIG. 2

6.3 iPod touch® and iOptima connection / disconnection conditions 6.3.1 Disconnection If the iPod touch® is disconnected, the iOptima system is in standby mode (micromotor stopped).

⚠ CAUTION

6.3.3 iOptima unit switched ON If the iOptima app is running and the iPod touch® plugged to the iOptima (switch ON): • The iPod touch® will charge up (even if the app is not running); • The sleep mode is deactivated; • The micromotor can be operated with the pedal (iOptima app in operative mode).

The iPod touch® must never be disconnected from the iOptima dental unit during operation. If the iPod touch® is disconnected during an operation, the micromotor stops immediately.

6.3.4 Replace 4VL seal

6.3.2 Connection

⚠ CAUTION

The micromotor can start only when the iPod touch® is connected and the application is in operative mode.

⚠ CAUTION If the footpedal is pressed before entering in operative mode, an alert message «Please release pedal…» will be displayed. The micromotor will not start to run until the footpedal is released and pressed again.

FIG. 2

Immediately replace any damaged or leaking O-rings and seals. Never use sharp tools! A. Switch off the water and the dental unit power supply. B. Switch OFF the iOptima unit «O». C. Unscrew and unplug the 4VL hose (1). D. Remove the damaged 4VL seal (2). E. Replace with a new 4VL seal (REF 1302403-010).

 Refit hose, switch ON units and water.

See chapter “5.1 Install the iOptima app” on page 17.

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