CHIROPRO L and CHIROPRO Instructions for Use

Set CHIROPRO L REF 1700298-001

10 x

1 x REF 1600613-001

1 x REF 1600605-001

1 x REF 1600606-001

1 x REF 1303711-010

10 x

1 x REF 1600631-001

1 x REF 1303393-001

1 x REF 1500984-010

Set CHIROPRO REF 1700387-001

10 x

1 x REF 1600724-001

1 x REF 1600606-001

1 x REF 1303711-010

CA 20:1 L

CA 20:1

CA 20:1 L Micro-Series

REF 1600598-001

REF 1600632-001

1 x REF 1600752-001

10 x

1 x REF 1600631-001

1 x REF 1303393-001

1 x REF 1500984-010

Options

REF 1600605-001

REF 1600752-001

REF 1600692-001

10 x 10 x

10 x

REF 1600631-001

REF 1600606-001

REF 1303711-010

REF 1301560-010

REF 1500984-010

CHIROPRO L / CHIROPRO

Summary Starting display

CHIROPRO L Available values Torque in Ncm

Irrigation in ml/min

100 - 40’000 rpm

0.48 - 4.8 Ncm

30 ml/min 20%

with a CA 1 : 1

with a CA 1 : 1

60 ml/min 40%

Depends on the CA

Depends on the CA

120 ml/min 80%

MAIN MENU

Steps

Ratio

Speed in rpm

Implantology

Round bur 1

128:1

Endodontics

Round bur 2

64:1

Surgery

Drill 1

30:1

Drill 2

27:1

Drill 3

20:1

Drill 4

16:1

90 ml/min 60% 150 ml/min 100%

Tapping

10:1

Tap unscrewing

1:1

Implant screwing

1:2

Unscrewing

1:5

Implantology

Open pulp chamber

128:1

100 - 40’000 rpm

0.48 - 4.8 Ncm

30 ml/min 20%

Endodontics

endo file 1

64:1

with a CA 1 : 1

with a CA 1 : 1

60 ml/min 40%

Surgery

endo file 2

30:1

endo file 3

27:1

Depends on the CA

Depends on the CA

120 ml/min 80%

endo file 4

20:1

endo file 5

16:1

endo file 6

10:1

endo file 7

1:1

endo file 8

1:2

endo file 9

1:5

Implantology

Apical resection

128:1

100 - 40’000 rpm

0.48 - 4.8 Ncm

30 ml/min 20%

Endodontics

Tooth extraction

64:1

with a CA 1 : 1

with a CA 1 : 1

60 ml/min 40%

Surgery

Sinus lift

30:1

Free

27:1

Depends on the CA

Depends on the CA

120 ml/min 80%

90 ml/min 60% 150 ml/min 100%

90 ml/min 60%

20:1

150 ml/min 100%

16:1 10:1 1:1 1:2 1:5

Starting display

CHIROPRO Available values IMPLANT SYST.

Steps

Ratio

Speed in rpm

Torque in Ncm

Irrigation in ml/min

Implantology Straumann

Round bur 1

128:1

100 - 40’000 rpm

0.48 - 4.8 Ncm

30 ml/min 20%

Nobel Biocare

Round bur 2

64:1

with a CA 1 : 1

with a CA 1 : 1

60 ml/min 40%

Zimmer

Drill 1

30:1

Dentsply Friadent

Drill 2

27:1

Depends on the CA

Depends on the CA

120 ml/min 80%

Biomet 3i

Drill 3

20:1

Astra Tech

Drill 4

16:1

Thommen Medical

Tapping

10:1

Système

Tap unscrewing

1:1

Implant screwing

1:2

Unscrewing

1:5

90 ml/min 60% 150 ml/min 100%

Table of contents Contenu

1 Symbols Meaning of symbols

Page 34

3

Identification Intended use Environment Environmental protection and information for disposal of the instrument

35 35 35 35

Set supplied

36

4 Options

36

5 Technical description Technical data Electromagnetic compatibility

6 Installation 7 Description of keys and elements

37 38-39 40-41 42

8 Operation Description of functions Start-up Pre-settings (SETUP) Description of programs - Implantology - Endodontics* - Surgery*

9 List of errors / Troubleshooting

43 44 44-45 46

47

10 Default values Implantology Endodontics* Surgery*

48+129 48+130 48+130

11 Maintenance Overhaul Information Cleaning-disinfection Important

48 48 48 48

12 Generalities and guarantee General information Terms of guarantee

*only CHIROPRO L

48 48

33

ENG

2 Description

1 Meaning of symbols

0120

CE Marking with number of the notified body.

Protective earth (ground). Main switch ON - The instrument is switched on. OFF - The instrument is switched off. Fuse Ø 5 x 20 mm.

ENG

Alternating current. Device of type B.

CAUTION ! Dangerous voltage.

Element sensitive to electrostatic discharges.

CAUTION! Refer to the accompanying documents.

Danger of pinching. Do not put your fingers in rotating parts.

Variability in steps.

Symbol for “Water-cooling”.

Symbol for “peristaltic pump”.

Recyclable materials.

Recyclable electrical and electronic materials.

Sterilisable in autoclave up to the specified temperature.

Operating mode intermittent.

Manufacturer.

Light.

34

2 Description

Electronically controlled tabletop device allowing operation of an MX-LED CHIROPRO/MX CHIROPRO micromotor with variable speed control by a pedal. A peristaltic pump conveys the physiological liquid via a disposable irrigation line without being contaminated. The device's LCD display indicates the stage of implant fitting, the instrument's ratio, the bur speed, torque value and irrigation flow setting.

Intended use

Product intended for professional use only. Use in dentistry for implantology, dental surgery* and endodontic* work. Any use other than that for which this product is intended is unauthorised and may be dangerous. The medical device meets all the current legal requirements. The device is not authorised for use in an explosive atmosphere (anaesthetic gas).

Working

Temperature: Relative humidity: Atmospheric pressure:

Transport and storage

Environmental conditions for a period of max. 15 weeks Temperature: -25°C (-13°F) to +70°C (158°F) Relative humidity: 10% to 100%, including condensation Atmospheric pressure: 500 hPa to 1060 hPa

Environment

Environmental protection and information for disposal of the instrument

ENG

Identification

+10°C (50°F) to +25°C (77°F) 30% to 80%, including condensation 700 hPa to 1060 hPa

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

This device 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 device to its dealer or establish direct contact with an approved body for treatment and recovery of this type of equipment (European Directive 2002/96/EC).

*only CHIROPRO L

35

ENG

3 Set supplied Set CHIROPRO L REF 1700298-001

1x 1x 1x 1x 1x 1x 1x 1x 1x 1x 1x

CHIROPRO L control Micromotor MX-LED CHIROPRO Cable for MX-LED CHIROPRO micromotor Pack of 10 disposable sterile lines 10 attachment collars for fastening the sterile irrigation line to a cable Bracket for fluid bottle Pedal 3 buttons Cable system 3P, Switzerland, length 2.00 m Cable system 3P, Europe, length 2.50 m Cable system 3P, US/Asia, length 2.00 m Instructions

REF 1600613-001 REF 1600605-001 REF 1600606-001 REF 1500984-010 REF 1303711-010 REF 1303393-001 REF 1600631-001 REF 1300065-001 REF 1300066-001 REF 1300067-001 REF 2100219

Set CHIROPRO REF 1700387-001

1x 1x 1x 1x 1x 1x 1x 1x 1x 1x 1x

CHIROPRO control Micromotor MX CHIROPRO Cable for micromotor Pack of 10 disposable sterile lines 10 attachment collars for fastening the sterile irrigation line to a cable Bracket for fluid bottle Pedal 3 buttons Cable system 3P, Switzerland, length 2.00 m Cable system 3P, Europe, length 2.50 m Cable system 3P, US/Asia, length 2.00 m Instructions

REF 1600724-001 REF 1600752-001 REF 1600606-001 REF 1500984-010 REF 1303711-010 REF 1303393-001 REF 1600631-001 REF 1300065-001 REF 1300066-001 REF 1300067-001 REF 2100219

4 Options Contra-angle handpiece CA 20:1 L (light) Contra-angle handpiece CA 20:1 (without light) Contra-angle handpiece CA 20:1 L Micro-Series (light) Micromotor MX-LED CHIROPRO Micromotor MX CHIROPRO Cable for MX-LED CHIROPRO/MX CHIROPRO micromotor Pack of 10 disposable sterile lines 10 attachments collars for fastening the sterile irrigation line to a cable Pedal 3 buttons Cable system 3P, Switzerland, length 2.00 m Cable system 3P, Europe, length 2.50 m Cable system 3P, US / Asia, length 2.00 m 10x Fuse T4.0A L 250 VAC breaking capacity 40A

36

REF 1600598-001 REF 1600632-001 REF 1600692-001 REF 1600605-001 REF 1600752-001 REF 1600606-001 REF 1500984-010 REF 1303711-010 REF 1600631-001 REF 1300065-001 REF 1300066-001 REF 1300067-001 REF 1301560-010

5 Technical Description: Technical data Peristaltic pump Pump delivery: Hose for pump:

Voltage 100 – 240 VAC 50 / 60 Hz Fuses 2 fuses T4.0A L 250 VAC, breaking capacity 40A Power demand 300 VA Classification Class IIa in accordance with European Directive 93/42/EEC concerning medical devices. Electric insulation class I type BF, according to EN 60601-1 (apparatus protected against electric shocks). Degree of protection IP 40 (protection against insertion of objects larger than 1 mm). Dimensions L x W x H 309 x 220 x 123 mm. Height with bracket 506 mm Weight Housing 2.7 kg Cable 105 g

Pedal Bracket

830 g 115 g

Memory Implantology mode: Storage in memory of 8 implant fitting sequences of 10 steps each. Endodontics* mode: Storage in memory of an endodontics sequence of 10 steps. Surgery* mode: Storage in memory of 4 separate programs. Languages French, German, English, Italian, Spanish, Portuguese, Japanese and Russian.

From 30 to 150 ml/min. (5 levels). External Ø 5.60 mm, internal Ø 2.40 mm Wall thickness 1.60 mm.

Pedal REF 1600631-001 Dimensions (LxWxH) 250 x 205 x 54 mm with handle: 250 x 205 x 144 mm The pedal is waterproof (IP X8 in accordance with CEI 529). Cables Length of cables: Pedal cable 2.90 m Motor cable 2.00 m

ENG

Manufacturer Bien-Air Dental SA.

WARNING To prevent any risk of electric shock, this device should be connected only to a power supply network provided with protective earth. The apparatus is not adapted to the presence of an inflammable gas. Do not attempt to open the apparatus when it is connected to the electric mains. Beware of electric shocks. Parts applied Micromotor MX-LED CHIROPRO Micromotor MX CHIROPRO CA 20:1 L CA 20:1 CA 20:1 L Micro-Series CA 30:1 Irrigation lines

REF 1600605-001 REF 1600752-001 REF 1600598-001 REF 1600632-001 REF 1600692-001 REF 1600284-001 REF 1500984-010

Accuracy of displayed values Speed ± 5% Torque ± 5% Operating mode: Intermittent ON: 5 min. OFF: 40 min.

List of errors & Troubleshooting Page 47 Bracket Stainless steel Important see instructions Micromotor MX-LED CHIROPRO REF 2100161 Micromotor MX CHIROPRO REF 2100161 Cable for micromotor REF 2100163 Contra-angle CA 20:1, without light REF 2100209 Contra-angle CA 20:1 L, with light REF 2100209 Contra-angle CA 20:1 L Micro-Series, with light REF 2100209

*only CHIROPRO L

37

5 Technical Description: Electromagnetic compatibility

ENG

Precautions regarding Electromagnetic Compatibility (EMC)

Electro-medical equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in this document.

Frequency surgical equipment and similar equipment so that the HF cables are not routed on or near the device. If in doubt, please contact a qualified technician or Bien-Air Dental.

CHIROPRO L/CHIROPRO complies with the EMC requirements according to IEC 60601-1-2. Radio transmitting equipment, cellular phones, etc. shall not be used in close proximity of the device since they could influence the performance of the device. Particular precaution is required when using strong emission sources such as High

CHIROPRO L/CHIROPRO should not be used adjacent or stacked with other equipment. If adjacent or stacked use is necessary, CHIROPRO L/ CHIROPRO should be monitored to verify normal operation in the configuration in which it will be used.

WARNING!

The use of accessories, transducers and cables other than those specified, with the exception of transducers and cables sold by Bien-Air Dental as replacements parts for

internal components, may result in increased emissions or decreased immunity of CHIROPRO L/CHIROPRO.

Guidance and manufacturer’s declaration - electromagnetic emissions

CHIROPRO L/CHIROPRO is intended for use in the electromagnetic environment specified below. The customer or the user of CHIROPRO L/CHIROPRO should ensure that it is used in such an environment.

Emissions test

Compliance

Electromagnetic environment - guidance

RF emissions CISPR 11

Group 1

CHIROPRO L/CHIROPRO uses RF energy only for its internal function. 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

Not applicable

Voltage fluctuations/flicker emissions IEC 61000-3-3

CHIROPRO L/CHIROPRO is suitable for use in all Establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.

Compliant

Guidance and manufacturer’s declaration - electromagnetic immunity CHIROPRO L/CHIROPRO is intended for use in the electromagnetic environment specified below. The customer or the user of CHIROPRO L/CHIROPRO should ensure that it is used in such an environment. Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance Electrostatic ±6 kV contact ±6 kV contact Floors should be wood, concrete or ceramic tile. If floors discharge (ESD) are covered with synthetic material, the relative humidity ±8 kV air ±8 kV air should be at least 30%. IEC 61000-4-2 Electrical fast ±2 kV for power ±2 kV for power Mains power quality should be that of a typical commertransient/burst supply lines supply lines cial or hospital environment. IEC 61000-4-4 ±1 kV for lines no ±1 kV for lines no input/output input/output Surge ±0.5 kV line to line ±0.5 kV line to line IEC 61000-4-5 ±1 kV line to line ±1 kV line to line Mains power quality should be that of a typical commercial or hospital environment. ±0.5 kV line to earth ±0.5 kV line to earth ±1 kV line to earth ±1 kV line to earth ±2 kV line to earth ±2 kV line to earth Voltage dips, short <5% UT <5% UT interruptions and (>95% dip in UT) (>95% dip in UT) Mains power quality should be that of a typical commervoltage variations for 0.5 cycle for 0.5 cycle cial or hospital environment. If the user of CHIROPRO L/ on power supply CHIROPRO requires continued operation during power input lines 1 40% UT 40% UT mains interruptions, it is recommended that CHIROPRO L/ (60% dip in UT) (60% dip in UT) CHIROPRO be powered from an uninterruptible power for 5 cycles for 5 cycles supply or a battery. 70% UT 70% UT T T IEC 61000-4-11 (30% dip in U ) (30% dip in U ) for 25 cycles for 25 cycles

Power frequency (50/60 Hz) magnetic field IEC 61000-4-8

<5% UT (>95% dip in UT) for 5 sec

<5% UT (>95% dip in UT) for 5 sec

3 A/m

3 A/m

NOTE UT is the a.c. mains voltage prior to application of the test level.

38

Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

5 Technical Description: Electromagnetic compatibility Guidance and manufacturer’s declaration - electromagnetic immunity CHIROPRO L/CHIROPRO is intended for use in the electromagnetic environment specified below. The customer or the user of CHIROPRO L/CHIROPRO should ensure that it is used in such an environment. Immunity test

IEC 60601 test level

Compliance level

Electromagnetic environment - guidance Portable and mobile RF communications equipment should be used no closer to any part of CHIROPRO L/CHIROPRO, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance

3 Vrms 150 kHz to 80 MHz

3V 80 MHz to 800 MHz 800 MHz to 2.5 GHz

Radiated RF IEC 61000-4-3

3 V/m 80 MHz to 2,5 GHz

3 V/m

where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey,a should be less than the compliance level in each frequency range.b Interference may occur in the vicinity of equipment marked with the following symbol:

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. a

Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast 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 CHIROPRO L/CHIROPRO is used exceeds the applicable RF compliance level above, the CHIROPRO L/CHIROPRO should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the CHIROPRO L/CHIROPRO. b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

Recommended separation distances between portable and mobile RF communications equipment and the CHIROPRO L/CHIROPRO The CHIROPRO L/CHIROPRO is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the CHIROPRO L/CHIROPRO can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the CHIROPRO L/CHIROPRO as recommended below, according to the maximum output power of the communications equipment. Rated maximum output power of transmitter W

0.01 0.1 1 10 100

Separation distance according to frequency of transmitter m 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz

0.12 0.38 1.2 3.8 12

0.12 0.38 1.2 3.8 12

0.23 0.73 2.3 7.3 23

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE 1 NOTE 2

At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

39

ENG

Conducted RF IEC 61000-4-6

6 Installation

Fuse

= >

16 ON/OFF

Installation A. CHIROPRO L/CHIROPRO may be positioned on a table, on a trolley or another surface, but in no circumstances on the floor. Power plug 14 is the device for disconnection in case of problems, and it must be easily accessible at all times. B. The fuse box may be opened with a screwdriver. 100 - 240 Vac = fuse T-4.0 A L 250 VAC REF 1301560-010

Plug

C. The equipment is powered by your line voltage (100/115/230 Vac). Connect the power cable to the plug fig. 1.

fig. 1

ENG

D. Connect the pedal cable to the output provided on the rear panel, guiding the connector and plug by means of the index pin on the connector fig. 2.

Do not raise the pedal using the connection cable.

fig. 2

E. Connect the micromotor cable to the motor output, guiding the connector and plug by means of the index pin on the connector fig. 3.

7 fig. 3

F. Align and attach the bracket to the housing provided on the console’s rear and suspend the flask or bottle fig. 4.

fig. 4

G. Check the packaging integrity, as well as the expiry date of the irrigation line. Only lines supplied by Bien-Air Dental ensure trouble-free operation. These lines are sterile and for single use. Re-use may result in microbiological contamination of the patient.

fig. 5

40

6 Installation H. Remove the single-use sterile irrigation line from its pouch.

fig. 6

ENG

Fitting on the spray tube I. Connect the flexible hose of the irrigation line to the spray tube of the handpiece or contra-angle fig. 7.

fig. 7

Installation on the peristaltic pump J. Install the plastic cassette in the peristaltic pump. Check that the cassette is clipped correctly. Close the pump lid, fig. 8. If there is resistance to closing, open the lid again and check the correct positioning of the cassette.

Warning! Do not run the pump while the lid is open. Danger of pinching! fig. 8

REF 1303711-010

K. Perforate the cap of the physiological liquid flask with the pointed end of the irrigation line after removing the protective cap. L. Attach the irrigation line on the motor cable using the attachment collars REF 1303711-010 fig. 9.

fig. 9

Stopping procedure

The device can be safely stopped using the main switch 16 .

41

7 Description of keys and elements 0

DEVICE SCREEN

Name of program Instrument transmission ratio Torque setting

Only in SETUP mode Activation/deactivation of the stage

ROUND BUR

Reversal of motor rotation symbol

20:1 28.0 Ncm

Selection cursor

1’000

RPM

Irrigation stopped

ENG

Adjusting irrigation

1

COMMAND TO REVERSE THE ROTATION OF THE MICROMOTOR

2

“SETUP” MENU CALL-UP KEY

Motor overheating Speed adjustment

9

“PROGRAM” BUTTON ON PEDAL In implantology/endodontics* mode: - Short press: next stage - Long press: previous stage

:

BUTTON TO REVERSE THE ROTATION OF THE MICROMOTOR ON PEDAL

3

PARAMETERS BACKUP KEY

4

RETURN KEY

;

VARIABLE SPEED DRIVE ON PEDAL

u

COMMANDS DEVICE Down key cursor Up key Left key (–) adjusting Right key (+) Confirmation/selection key OK In implantology/endodontics* mode: next stage

<

PEDAL CONNECTOR

=

MAINS CONNECTOR (100/115/230 VAC)

>

FUSE HOLDER

6

PERISTALTIC PUMP LID

?

MAIN SWITCH ON THE DEVICE

7

MICROMOTOR CONNECTOR

@

LABEL

8

IRRIGATION ON/OFF CONTROL BUTTON ON PEDAL

A

BRACKET SUPPORT

B

MICROMOTOR

42

｝ ｝

*only CHIROPRO L

8 Operation Description of functions

1 2 CHIROPRO L

3

ENG

4

1 REV

The "reverse" function can be chosen directly in all the programs except endodontics*. Upon selection, a beep and the "reversal of motor rotation" icon indicate reverse rotation. For endodontics*, settings must be performed under SETUP (Auto-forward/Auto-reverse).

2 SETUP See next page. Stores the settings of a program: press the key until a beep is emitted, and the values that are flashing 3 SAVE will be stored in the memory directly.

4

ESC

Return function. With "ESC", you can leave the current screen. In “Implantology” and “Endodontics*” mode, can also be used to return to the previous stage. If the name of the program flashes when exiting, the changes will not be taken into consideration. The changes must always be confirmed with "SAVE", otherwise they will be lost.

ORANGE Program key: - Short press - Long press

next stage previous stage

BLUE Activation/Deactivation of the peristaltic pump.

GREY Activation/Deactivation of reversal of motor rotation.

Motor speed control pedal.

*only CHIROPRO L

43

8 Operation Start-up 1. System loading...

3. IMPLANT. SYSTEM

OK

ENG

Nobel Biocare

OK

LANGUAGE

Zimmer

English

Dentsply Friaden

Français

Biomet 3i

Deutsch

Astra Tech

Italiano

Thommen Medical

Espanol

System

Português

Select with Confirmation with OK

Russian

*6. MAIN MENU

Please check the pre-programmed values before inserting implant.

Straumann 2.

OK 4. <Name of selected system>

OK

Implantology Endodontics* Surgery* Select with Confirmation with OK

OK: continue ESC: back 5. INFORMATION

with OK: go directly to pre-setting with no possibility of deactivating the stages

OK

Key functions: move cursor UP

Japanese

move cursor DOWN

Select with Confirmation with OK

decrem./disable

or with SETUP, possibility of deactivating the stages with

increm./enable OK: continue

All the pre-programmed settings are indicative and MUST be validated by the user. This storing in memory takes place only at the first connection of the device and is subsequently maintained. These parameters can then be modified in SETUP. Pre-settings

SETUP

OK

OK

OK

Language

English

Language

Implant. system

Français

Implant. system

Endo* system

Deutsch

Endo* system

Ratio

Italiano

Ratio

Light

Español

Light

Footpedal

Português

Footpedal

Torque units

Russian

Torque units

Contrast

Japanese

Contrast Editor

Editor

Select the language wanted and confirm with OK.

System info

OK

Endo steps Endo parameters Select with then OK. If modifications with , the screen flashes. save with SAVE continue with OK. Without modification, continue with OK. ESC: back

System info Restore defaults

Restore defaults

OK

OK

OK

Language

Straumann

Implant. system

Nobel Biocare

Endo* system

Zimmer

Ratio

Dentsply Friadent

Light

Biomet 3i

Footpedal

Astra Tech

Torque units

Thommen Medical

Contrast Editor

System

System info Restore defaults

44

OK

Select the system wanted and confirm with OK. ESC: change

Language

128:1

Implant. system

64:1

Endo* system

30:1

Ratio

27:1

Light

20:1

Footpedal

16:1

Torque units

10:1

Contrast

1:1

Editor

1:2

System info

1:5

Restore defaults Select the ratio to be changed OK, then change of value with and with then save with SAVE. Continue with OK. ESC: back *only CHIROPRO L

8 Operation Pre-settings OK

OK

Language

Language

Implant. system

Implant. system Endo* system

Endo* system OK

Ratio

Light OFF

Light

Light

Light ON

Footpedal

ON or OFF with then OK. Display under light ON: Level: adjustment with Time delay: setting with , save with SAVE, continue with OK. ESC: back

Torque units Contrast Editor System info Restore defaults

OK

Footpedal

Implantology (Ncm)

Torque units

Endodontics* (mNm)

Contrast

Surgery* (Ncm) Adjustable with , save with SAVE, continue with OK. ESC: back

Editor System info Restore defaults OK

Language

OK

Language

Implant. system

Implant. system

Endo* system

Endo* system

Ratio

Ratio

Light

OK

Light

Footpedal

Implantology

Footpedal

Endodontics*

Torque units

Surgery*

Contrast

Torque units Contrast

System info

System Info: software version, serial number and electronics of the device.

Editor

ON/OFF or progressive with , save with SAVE, continue with OK. ESC: back

Editor

Contrast adjustment with , save with SAVE, continue with OK.

System info Restore defaults

Restore system: Can be used to reinitialise factory settings.

Restore defaults

OK OK

Language Implant. system Endo* system Ratio

Used to rename or customise the name of the system, tool or treatment. Select with then OK,choose the letters on the keypad by moving the cursor using then OK, save the new name with SAVE, ESC: back

Straumann Nobel Biocare Zimmer Dentsply Friadent Biomet 3i Astra Tech

Light

Thommen Medical

Footpedal

OK

Torque units Contrast Editor System info

OK

System names Tool names

Implantology (Ncm)

System OK

OK

Straumann

ROUND BUR 1

Nobel Biocare

ROUND BUR 2

Zimmer

DRILL 1

Apical resection

Dentsply Friadent

DRILL 2

Tooth extraction

Biomet 3i

DRILL 3

Sinus Lift

Astra Tech

DRILL 4

Free

Thommen Medical

TAPPING

Surgery* (Ncm) OK

Restore defaults

System

TAP UNSCREWING IMPLANT SCREWING UNSCREWING

*only CHIROPRO L

45

ENG

Ratio

8 Operation Description of functions

Name of program Instrument transmission ratio Torque setting

Only in SETUP mode Activation/deactivation of the stage

ROUND BUR

Reversal of motor rotation symbol

20:1 28.0 Ncm

1’000

Selection cursor

RPM

Irrigation stopped

ENG

Adjusting irrigation

MAIN MENU

Steps

Selection wanted and confirm with OK

Each of these stages can be activated or deactivated from the SETUP menu. See also info on the last page. OK: next step ESC: previous step

Implantology

ROUND BUR 1

Endodontics*

ROUND BUR 2

Surgery*

DRILL 1

Motor overheating Speed adjustment

Transmission ratio

Speed in rpm

Torque in Ncm

Irrigation in ml/min

Select with the cursor

Adjustable:

Adjustable:

Adjustable:

Adjustable:

then SAVE

then SAVE

then SAVE

then SAVE

DRILL 2 DRILL 3 DRILL 4 TAPPING TAP UNSCREWING

128:1

100 - 40’000 rpm

0.48 - 4.8 Ncm

30 ml/min 20%

IMPLANT SCREWING

64:1

with a CA 1:1

with a CA 1:1

60 ml/min 40%

UNSCREWING

30:1 Depends on the CA selected

120 ml/min 80%

27:1 Implantology

OPEN PULP CHAMBER

20:1

Endodontics*

ENDO FILE 1

16:1

Surgery*

ENDO FILE 2

10:1

ENDO FILE 3

1:1

ENDO FILE 4

1:2

ENDO FILE 5

1:5

90 ml/min 60% Depends on the CA selected

150 ml/min 100%

ENDO FILE 6 ENDO FILE 7 ENDO FILE 8 ENDO FILE 9 Implantology

Apical resection

Endodontics*

Tooth extraction

Surgery*

Sinus Lift Free Pre-programmed values, see pages 129-130

46

*only CHIROPRO L

9 List of errors & Troubleshooting Message

Release the pedal

Cause of error The pedal is pressed when starting the device. Safety The motor is blocked for more than 2 sec. The motor control card limits the power supplied to the motor to prevent motor overheating.

Safety

Action Release the pedal and press again.

Avoid extended use.

Equipment initialisation error The following error may occur at start-up of CHIROPRO L/CHIROPRO 1. Check on the integrity of the CHIROPRO L/CHIROPRO memory The memory is corrupt! The memory data check failed. Please contact Bien-Air Dental SA. ESC: restore

Press the ESC key to try to restore the memory. Contact Bien-Air Dental SA.

ENG

INIT ERROR 1

Device operating error The following errors may occur during operation of the device 1. Loss of pedal connection ERROR 1

The pedal is not connected! Please check the connection. ESC: exit

The pedal is not connected correctly.

Check pedal connection. Contact Bien-Air Dental SA.

Peristaltic pump motor overheating

Wait until the system cools. Contact Bien-Air Dental SA.

2. Peristaltic pump overheating ERROR 2

Irrigation pump overheating! Please wait for it to cool. ESC: exit

3. Peristaltic pump general error ERROR 3

Irrigation pump fault! Peristaltic pump electrical fault. Please contact Bien-Air Dental SA. ESC: exit

Contact Bien-Air Dental SA.

4. Loss of motor connection ERROR 4

The motor is not connected! Please check the connection. ESC: exit

Loss of motor phase fault. The motor is not connected correctly.

Check motor connection. Contact Bien-Air Dental SA.

Motor power fault. The motor cable may be defective.

Check motor cable. Contact Bien-Air Dental SA.

Overheating of motor control card (electrical control of motor).

Wait until the system cools. Contact Bien-Air Dental SA.

System electrical fault! Communication fault with motor Please contact Bien-Air Dental SA. control card: [EC100] ESC: exit Motor control card power supply undervoltage: [EC101]

Contact Bien-Air Dental SA.

5. Motor cable fault ERROR 5

Motor cable fault! Please change cable. ESC: exit

6. Motor control overheating ERROR 6

System overheating! Please wait for it to cool. ESC: exit

7. System electrical fault GEN ERROR [Error code]

Motor control card power supply overvoltage: [EC102] Other motor control card faults: [EC120] 47

10 Default values Implantology: Default values page 129 The table shows the default operating values for the 8 implantology systems pre-programmed in the system, namely: • Straumann • Nobel Biocare • Zimmer • Dentsply Friadent • Biomet 3i • Astra Tech • Thommen Medical • System, available to the user (default settings identical to the Straumann system).

Endodontics*: Default values page 130 The table shows the default operating values for the endodontics sequence. Surgery*: Default values page 130 The table shows the default operating values for 4 types of surgical operations proposed by the system, namely: • Root resection • Extraction of wisdom teeth • Sinus raising • Free program, left available to the user.

ENG

11 Maintenance Only use original Bien-Air Dental maintenance products and parts or those recommended by Bien-Air Dental. Using other products or parts may cause operational failure and/or void the guarantee. Overhaul Never disassemble the device. For any modification and repair, we recommend that you contact your regular supplier or BienAir Dental directly. Bien-Air Dental asks the user to have its dynamic instruments checked or inspected at least once a year. Information 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.

Cleaning-disinfection • Disinfect the surfaces of the console and pedal with a clean cloth soaked in a suitable product. • Do not exert any pressure on the screen. • Do not immerse in disinfectant solution • Not designed for an ultrasonic bath. • Use a new sterile irrigation line for each patient. Important For maintenance: - MX-LED CHIROPRO micromotor - MX CHIROPRO micromotor - Cable for micromotor - Contra-angle CA 20:1 L - Contra-angle CA 20:1 - Contra-angle CA 20:1 L Micro-Series

see instructions REF 2100161 REF 2100161 REF 2100163 REF 2100209 REF 2100209 REF 2100209

12 Generalities and guarantee General information The device must be used by a qualified person in compliance with the current legal provisions concerning industrial safety, health and accident prevention measures, and these working instructions. In accordance with such requirements, the operators: • must only use devices that are in perfect working order; in the event of irregular functioning, excessive vibration, abnormal heating or other signs that may indicate malfunction of the device, the work must be stopped immediately; in this case, contact a repair centre that is approved by Bien-Air Dental; • must ensure that the device is used only for the purpose for which it is intended, must protect themselves, their patients and third parties from any danger, and must avoid contamination through the use of the product. Terms of guarantee Bien-Air Dental grants the user a guarantee covering all functional defects, material or production faults. The device is covered by this guarantee for 12 months from the date of invoicing. In case of justified claim, Bien-Air Dental or its authorised

48

representative will fulfil the company’s obligations under this guarantee by repairing or replacing the product free of charge. Any other claims, of whatever nature, in particular in the form of a claim for damages and interest, are excluded. Bien-Air Dental shall not be held responsible for damage or injury and the consequences thereof, resulting from: •excessive wear and tear • improper use • non-observance of the instructions for installation, operation and maintenance •unusual chemical, electrical or electrolytic influences • poor connections, whether of the air, water or electricity supply. The guarantee does not cover flexible “fibre optic” type light conductors, or any parts made of synthetic materials. The guarantee shall become null and void if the damage and its consequences are due to improper manipulation of the product, or modifications to the product carried out by persons not authorised by Bien-Air Dental. Claims under the terms of the guarantee will be considered only on presentation, together with the product, of the invoice or the consignment note, on which the date of purchase, the product reference and the Serial No. should be clearly indicated. *only CHIROPRO L