Bien-Air Medical Technology
CHIROPRO series Instructions for Use Oct 2019
Instructions for Use
136 Pages
Preview
Page 1
CHIROPRO L / CHIROPRO FRA DEU ENG ESP ITA RUS JPN PRT
Instructions d’utilisation Bedienungsanleitung Instructions for use Instrucciones de uso Istruzioni per l’uso Инструкция по эксплуатации
Instruções de utilização
Version not for sale/use in the USA
REF 2100219-0007/2019.10
Set CHIROPRO L REF 1700298-001
10x
1x REF 1600613-001
1x REF 1600755-001
1x REF 1600606-001
1x REF 1303711-010
10x
1x REF 1600631-001
1x REF 1303393-001
1x REF 1500984-010
Set CHIROPRO REF 1700387-001
10x
1x REF 1600724-001
1x REF 1600825-001
1x REF 1600606-001
1x REF 1303711-010
10x
1x REF 1600631-001
1x REF 1303393-001
1x REF 1500984-010
Compatible items
CA 20:1 L
REF 1600755-001
REF 1600825-001
REF 1600598-001 REF 1600632-001
10x
REF 1600631-001
CA 20:1
10x
REF 1600606-001 REF 1303711-010 REF 1501621-010
CA 20:1 L Micro-Series
REF 1600692-001
10x
REF 1500984-010
CA 20:1 L KM
REF 1600785-001
10x
REF 1501635-010
CA 20:1 L KM Micro-Series
REF 1600786-001
10x
REF 1307312-010 REF 1303393-001
CHIROPRO L / CHIROPRO
Summary Starting display
Available values
CHIROPRO L
MAIN MENU
Steps
Ratio
Speed in rpm
Torque in Ncm
Irrigation in ml/min
Implantology
Round bur 1
128:1
100 - 40’000 rpm
0.48 - 4.8 Ncm
30 ml/min 20%
Endodontics
Round bur 2
64:1
with a CA 1 : 1
with a CA 1 : 1
60 ml/min 40%
Surgery
Drill 1
30:1
Drill 2
27:1
Depends on the CA
Depends on the CA
120 ml/min 80%
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
Identification Intended use Environment Environmental protection and information for disposal of the instrument
35 35 35 35
Set supplied
36
4 Compatible items
36
3
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 Servicing 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 CE Marking with number of the notified body. The instrument is switched on. The instrument is switched off. Fuse Ø 5 x 20 mm. Alternating current. Applied part type B.
ENG
Warning. CAUTION! Refer to the accompanying documents. Danger of pinching. Do not put your fingers in rotating parts. Thermo washer disinfectable. Variability in steps. Recyclable materials. Recyclable electrical and electronic materials. Sterilisable in autoclave up to the specified temperature. Manufacturer. Light. Expiration date. Disposable product.
STERILE EO
34
Sterilise with Ethylene Oxyde
2 Description
Identification
Electronically controlled tabletop device for dentistry allowing operation of an MX-i LED/MX-i 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
The system is to be used by dentists and surgeons in dental offices and hospitals. The system is designed to control a dental micromotor which can drive a dental hand-piece fitted with appropriate tools to cut hard and soft tissues in the mouth and to screw dental implants.
ENG
The system is intended for 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 intended EM environment (per IEC 60601-1-2 ed. 4.0) is Professional healthcare facility environment.
Environment
Environmental protection and information for disposal of the instrument
The device is not designed for use in an explosive atmosphere (anaesthetic gas). Working
Temperature: Relative humidity: Atmospheric pressure:
+10°C (50°F) to +25°C (77°F) 30% to 80%, including condensation 700 hPa to 1060 hPa
Transport and storage
Environmental conditions Temperature: Relative humidity: Atmospheric pressure:
-25°C (-13°F) to +70°C (158°F) 10% to 100%, including condensation 500 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-i LED Cable for MX-i LED 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 1600755-001 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-i Cable for micromotor MX-i 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 1600825-001 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 Compatible items Contra-angle handpiece CA 20:1 L (light) Contra-angle handpiece CA 20:1 L Micro-Series (light) Contra-angle handpiece CA 20:1 L KM (light) Contra-angle handpiece CA 20:1 L KM Micro-Series (light) MX-i LED micromotor MX-i micromotor Cable for MX-i LED micromotor Pedal 3 buttons Pack of 10 disposable sterile lines Kirschner/Meyer type detachable irrigation set for CA 20:1 L KM and CA 20:1 L KM Micro-Series, comprising 10 rings and 10 tubes Kirschner/Meyer pack of 10 disposable sterile lines 10 attachments collars for fastening the sterile irrigation line to a cable Bracket for fluid bottle Support 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 H 250 VAC
36
REF 1600598-001 REF 1600692-001 REF 1600785-001 REF 1600786-001 REF 1600755-001 REF 1600825-001 REF 1600606-001 REF 1600631-001 REF 1500984-010 REF 1501621-010 REF 1501635-010 REF 1303711-010 REF 1303393-001 REF 1301575-001 REF 1300065-001 REF 1300066-001 REF 1300067-001 REF 1307312-010
5 Technical Description: Technical data The use of the system with other handpieces, motors or cables has not been validated/certified Peristaltic pump Pump delivery: Hose for pump:
Fuses 2 fuses T4.0A H 250 VAC Power demand - 100 V /300 VA - 240 V /300 VA Classification Class IIa in accordance with European Directive 93/42/EEC concerning medical devices. Electric insulation class Class I, per IEC 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. List of errors & Troubleshooting Page 47 Bracket for physiological liquid flask Stainless steel
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).
ENG
Voltage 100 – 240 VAC 50 – 60 Hz
Cables Length of cables: Pedal cable 2.90 m Motor cable 2.00 m WARNING To prevent any risk of electric shock, this device must be connected only to a power supply network provided with protective earth. Modification of the device forbidden. The system is not adapted to be used in the presence of inflammable gases (e.g. anaesthetic gas). Do not attempt to open the apparatus when it is connected to the electric mains. Beware of electric shocks. Applied parts (per IEC 60601-1) MX-i LED micromotor MX-i Micromotor Cable for micromotor MX-i LED CA 20:1 L CA 20:1 CA 20:1 L Micro-Series CA 20:1 L KM CA 20:1 L KM Micro-Series Irrigation lines KM Irrigation lines KM detachable Irrigation set
REF 1600755-001 REF 1600825-001 REF 1600606-001 REF 1600598-001 REF 1600632-001 REF 1600692-001 REF 1600785-001 REF 1600786-001 REF 1500984-010 REF 1501635-010 REF 1501621-010
Operating mode: Intermittent ON: 5 min. OFF: 40 min.
Intended for use with: see instructions Micromotor MX-i LED REF 2100245 Micromotor MX-i REF 2100245 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 Contra-angle CA 20:1 L KM, light REF 2100209 Contra-angle CA 20:1 L KM Micro-Series, light REF 2100209
*only CHIROPRO L
37
5 Technical Description: Electromagnetic compatibility 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. 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 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 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. Dental professionals need to be aware of potential electromagnetic interference between electronic dental devices and active implantable medical devices, and should always inquire about any devices implanted in the patient.
ENG
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 specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result. 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
Class A
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.
Not applicable
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 ±8 kV contact ±8 kV contact Floors should be wood, concrete or ceramic tile. If floors Electrostatic ±2 kV air ±2 kV air are covered with synthetic material, the relative humidity discharge (ESD) ±4 kV air ±4 kV air should be at least 30%. IEC 61000-4-2 ±8 kV air ±8 kV air ±15 kV air ±15 kV air 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 N.A.
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 typical commercial or hospital environment.
Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11
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 250 cycles at 0°
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 250 cycles at 0°
Mains power quality should be that of a typical commercial or hospital environment. If the user of CHIROPRO L/ CHIROPRO requires continued operation during power mains interruptions, it is recommended that CHIROPRO L/ CHIROPRO be powered from an uninterruptible power supply or a battery.
Magnetic field due to mains frequency (50/60 Hz) IEC 61000-4-8
30 A/m
30 A/m
Magnetic fields generated by the mains frequency should be et levels characteristic of a typical location in a typical commercial or hospital environment.
38
5 Technical Description: Electromagnetic compatibility
Conducted disturbances induced by RF fields IEC 61000-4-6
Radiated RF EM fields IEC 61000-4-3 Proximity fields from RF wireless communications equipment IEC 61000-4-3
IEC 60601 test level 3 VRMS 0.15 MHz-80MHz 6 VRMS in ISM bands 0.15 MHz - 80MHz 80% AM at 1 kHz
Compliance level 3 VRMS 0.15 MHz-80MHz 6 VRMS in ISM bands 0.15 MHz - 80MHz 80% AM at 1 kHz
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
Test freq. [MHz]
Max. power [W]
Immunity test level [V/m]
385 450 710, 745, 780 810, 870, 930 1720, 1845, 1970 2450 5240, 5500, 5785
1.8 2 0.2 2 2 2 0.2
27 28 9 28 28 28 9
Electromagnetic environment - guidance 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. Interference may occur in the vicinity of equipment marked with the following symbol:
Distance: 0.3 m
ENG
Immunity test
NOTE UT is the a.c. mains voltage prior to application of the test level. Essential performance: The essential performance is the maintaining of the visual lighting intensity of the LED and the maintaining of motor speed. Maximum allowed speed deviation is ± 10%. 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.
39
6 Installation
Fuse
14
15
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 H 250 VAC REF 1307312-010
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 1
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
2
COMMAND TO REVERSE THE ROTATION OF THE MICROMOTOR
3
“SETUP” MENU CALL-UP KEY
4
PARAMETERS BACKUP KEY
5
6
Motor overheating Speed adjustment
10
“PROGRAM” BUTTON ON PEDAL In implantology/endodontics* mode: - Short press: next stage - Long press: previous stage
11
BUTTON TO REVERSE THE ROTATION OF THE MICROMOTOR ON PEDAL
RETURN KEY
12
VARIABLE SPEED DRIVE ON PEDAL
COMMANDS DEVICE Down key cursor Up key Left key (–) adjusting Right key (+) Confirmation/selection key OK In implantology/endodontics* mode: next stage
13
PEDAL CONNECTOR
14
MAINS CONNECTOR (100/115/230 VAC)
15
FUSE HOLDER
7
PERISTALTIC PUMP LID
16
MAIN SWITCH ON THE DEVICE
8
MICROMOTOR CONNECTOR
17
LABEL
9
IRRIGATION ON/OFF CONTROL BUTTON ON PEDAL
18
BRACKET SUPPORT
19
MICROMOTOR
42
*only CHIROPRO L
8 Operation Description of functions
1 2 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.
3
SAVE
Stores the settings of a program: press the key until a beep is emitted, and the values that are flashing 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
Please check the pre-programmed values before inserting implant.
Straumann
ENG
2. LANGUAGE
Nobel Biocare
OK
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
OK 4. <Name of selected system>
OK
Implantology Endodontics* Surgery* Select with Confirmation with OK
OK: continue ESC: back
with OK: go directly to pre-setting with no possibility of deactivating the stages
OK
5. INFORMATION 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
ENG
Ratio
OK
Language
OK
Language
Implant. system
Implant. system
Endo* system
Endo* system
Ratio
Ratio
Light
OK
Light
Implantology
Footpedal
Endodontics*
Torque units
Surgery*
Contrast
Footpedal 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
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
Ratio Light
Astra Tech
Footpedal
Thommen Medical OK
Torque units OK
Contrast Editor System info
System
System names Tool names
Implantology (Ncm)
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
Surgery* (Ncm) OK
Restore defaults
Sinus Lift
Astra Tech
DRILL 4
Free
Thommen Medical
TAPPING
System
TAP UNSCREWING IMPLANT SCREWING UNSCREWING
*only CHIROPRO L
45
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] Motor control card power supply ESC: exit undervoltage: [EC101] Motor control card power supply overvoltage: [EC102] Other motor control card faults: [EC120]
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]
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. Servicing 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: see instructions Micromotor MX-i LED REF 2100245 Micromotor MX-i REF 2100245 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 Contra-angle CA 20:1 L KM, light REF 2100209 Contra-angle CA 20:1 L KM Micro-Series, light REF 2100209
12 Generalities and guarantee General information The device must be used by a qualified professional in compliance with the current legal provisions concerning workplace 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.
In case of justified claim, Bien-Air Dental or its authorised 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.
Terms of guarantee Bien-Air Dental SA grants the user a guarantee covering all functional defects, material or production faults. The device is covered by this guarantee from the date of invoicing for: • 12 months for the hose; • 24 months for the iChiropro unit and CA 20:1 L Micro-Series; • 36 months for the MX-i micromotor.
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.
48
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.
*only CHIROPRO L