Voyager II L Operating Instructions Sept 2011

TABLE OF CONTENTS Page 1. OVERALL VIEW AND MAJOR COMPONENTS---------------------------- 1 2. DIMENSIONS AND SPECIFICATIONS 2-1. DIMENSIONS----------------------------------------------------------------- 2 2-2. SPECIFICATIONS------------------------------------------------------------ 2 3. OPERATING INSTRUCTIONS FOR UNIT 3-1. MASTER SWITCH----------------------------------------------------------- 3 3-2. DOCTOR TABLE SECTION------------------------------------------------ 3 3-3. CUSPIDOR SECTION------------------------------------------------------- 4 3-4. ASSISTANT INSTRUMENT HOLDER SECTION---------------------- 5 3-5. FOOT CONTROL SECTION------------------------------------------------ 5 3-6. SWING ARM SECTION----------------------------------------------------- 5 3-7. DOCTOR TABLE SAFETY LOCK DEVICE----------------------------- 5 4. OPERATING INSTRUCTIONS FOR CHAIR 4-1. MAIN SWITCH--------------------------------------------------------------- 6 4-2. CONTROLS-------------------------------------------------------------------- 6 4-3. SAFETY LOCK DEVICE---------------------------------------------------- 7 4-4. HEADREST OPERATIONS------------------------------------------------- 7 4-5. AUTO MODE POSITION ADJUSTMENT------------------------------- 7 5. RIGHT/LEFT HANDED DENTISTRY CONVERSION--------------------- 8 6. CARE AND MAINTENANCE 6-1. CARE AND MAINTENANCE FOR CHAIR----------------------------- 8 6-2. CARE AND MAINTENANCE FOR UNIT------------------------------- 9 7. ELECTROMAGNETIC COMPATIBILITY----------------------------------- 11 8. LIST OF COMPATIBLE HANDPIECES -------------------------------------- 14

Intended Use of the Product

This product is an active therapeutic device intended for the exclusive use for diagnoses, treatments and relative procedures of dentistry.

The product must be operated or handled by the qualified dentists or by dental staffs under

the supervision of the dentist.

Such dentists or dental staffs should instruct and/or assist the patients to approach to and leave from the product.

Patients should not be allowed to operate or handle the product unless he/she is so instructed. The product is supplied together with the handpieces like electric micromotor, air turbine

and/or motor, scaler and so on.

Environmental Requirements Ambient Temperature

Operating +5℃ - +40℃

Humidity 10 % - 80%

Storage -10℃ - +50℃

Atmospherical Pressure 600 hPa - 1060 hPa

Compatibility of Handpieces

Use the compatible handpieces as shown on the attached list for this unit. (List of compatible handpieces).

Important Notes

In case of the troubles, please contat Takara Belmont offices or your dealers.

Do not disassemble or attempt to repair.

Disassembly, repair or modifications shoud only be done by a qualified repair technician.

Attempts at disassembly, repair or modifications may lead to abnormal operation and accidents. In case of disposal of equipment

In case of disposal of equipment or of components dismounted from the unit, take full infection preventing measures, and carry out appropriate steps in accordance with the legal regulations at that time.

SYMBOLS Chair last position

Chair auto return

Chair preset1

Chair preset2

To raise the chair

To Recline the backrest

To lower the chair

To raise the backrest

Chair manual control

Non-ionizing radiation

Authorized representative in the European community

Manufacturer

Date of manufacture

Caution It means “caution, warnings, or possibility to danger”.

Separate collection for electrical and electronic equipment

Type B Applied Parts

㻨㻦

㻵㻨㻳

1. OVERALL VIEW AND MAJOR COMPONENTS

1

2

20

3

4

13

12 11 5

16

17 9

19

21

10

18

14 8

7

15

Chair base front left

6

Fig.1-1 Overall View and Major Parts MAJOR PARTS

13. Armrest

1. Light Pole 2. Cuspidor Bowl

14. Foot Switch

15. Power Switch

3. Cuspidor Unit 4. Assistant Holder

16. Pump Cover

5. Doctor Table

17. J-Box Cover

6. Doctor Arm 7. Doctor Arm Cover

18. Presuure Gauge

19. Stop Valve for Water

8. Foot Control 9. Headrest

20. Dental Light 048-VG 21. Handpieces

10. Backrest 11. Seat

(Micromotor, Air Turbine/Motor, Scaler and etc.) Manufacturers recommend to use the handpieces with CE markings

12. Seat Cover

-1-

2. DIMENSIONS AND SPECIFICATIONS 2-1. DIMENSIONS -mm-

°

0°

°

280

350

170

675

85°

430

575

13

80 R4

60

13

0° 570

305

°

215

°

72

370

730 470- 850

10°

70°

480

1740

75

58

650

1205

2015

565

1365

Fig.2-1 Dimensions

2-2. SPECIFICATIONS Chair Section Seat initial Height----------------------- 470mm Seat Lifting Stroke---------------------- 380mm Backrest Movement-------------------- 0˚ ~ 72˚ above Horizontal Auto Movements------------------------ 2 Preset, 1 Last Position Memory and 1 Auto Return Control Voltage-------------------------- DC12V Power Consumption-------------------- 230V, 50Hz, 3.7A Net Weight------------------------------- 140 kg Maximum Load------------------------- 135 kg Service Life------------------------------ 10 years Unit Section Doctor Side Handpiece---------------- 1 x High Speed Turbine Tubing 1 x Low Speed Air Motor Tubing 1 x 3-Way Syringe Assistant Side Handpiece-------------- Saliva Ejector (Central System Type) Vacuum (Central System Type) Bowl Flush------------------------------- Manual Control Cupfiller---------------------------------- Manual Control Dental Light----------------------------- 048-VG Type Net Weight------------------------------- 67 kg (With Dental Light) Service Life------------------------------ 10 years -2-

3. OPERATING INSTRUCTIONS FOR UNIT

Note : Before operation, confirm that air compressor is fully charged. The chair can be operated only when both the chair main switch and the master switch are ON. Refer to 4-1.

Master Switch

ON MA

IN

ON

OFF

OFF HP2

3-1. MASTER SWITCH (Fig.3-1 and Fig.3-2) Turn on the master switch located under the doctor table, the master switch indicator located on the front side of the cuspidor unit turns to green.

CAUTION Turn off the master switch after daily operation.

3-2. DOCTOR TABLE SECTION (1) Handpiece Spray Water Flow Control Knobs (Fig.3-1) The handpiece spray water flow control knobs located under the doctor table provide for individual adjustment. Each handpiece spray water flow control knob is lined up from the facing left hand side HP1, HP2... Turning a flow control knob counterclockwise increases flow volume and turning clockwise decreases. (2) 3-Way Syringe A. 3-Way Syringe Operation (Fig.3-3) Depressing either or both buttons, this syringe offers air, water and spray. Syringe tip can be rotated freely. To remove syringe tip : Keep depressing the lock ring and pull out the syringe tip. To set syringe tip : Keep depressing the lock ring, insert the syringe tip and release the lock ring.

HP1

Handpiece Spray Water Control Knobs

Fig. 3-1 Master Switch and Handpiece Spray Water Control Knobs

Master Switch Indicator

Cuspidor Unit

Fig. 3-2 Master Switch Indicator Syringe Tip

Lock Ring Water Button Air Button

Fig. 3-3 3-Way Syringe

B. 3-Way Syringe Flow Control Screws (Fig.3-5) Air and/or water flow of 3-way syringe can be Flow Control adjusted by the flow control screws located Screw (Water) bottom of the table. Decrease Increase Facing right hand side screw controls air and left hand side controls water. Hex Key Wrench Control Turning a flow control screw counterclockwise Flow Screw (Air) increases flow volume and turning clockwise decreases. Use the hex key wrench supplied. Fig. 3-4 3-Way Syringe Flow Control Screws ON

IN MA

OFF

HP2

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HP1

(3) Removing Table Top (Fig.3-5) Loosen 4-screws from the table bottom and remove the table top. The auto select valve and the handpiece pressure gauge are located in the table.

Table Top Cover

(4) Handpiece Drive Air Adjustment Screws (Fig.3-6 & Fig.3-7) Adjustment of drive air of each handpiece can be made by the screw on the auto select valve. It is important to set the drive air pressure in according with the handpiece manufacture's recommendation. Drive air pressure is indicated by the handpiece pressure gauge. Note : Refer to 3-5 for handpiece control Setting The Optimum Condition (Fig.3-7) Turn the appropriate dive air screw fully clockwise, then depress the drive air pedal of the foot control fully (maximum foot pressure) and turn the screw counterclockwise slowly. Stop turning the screw immediately when the handpiece pressure gauge shows the desired drive air pressure. (5) Handpiece Coolant Air Adjustment Screws (Fig.3-6 & Fig.3-7) Handpiece coolant air adjustment screws are provided for individual adjustment of handpiece coolant air. Turning a handpiece coolant air adjustment screw counterclockwise increases flow volume and turning clockwise decreases.

(6) Handpiece Refer to handpiece manufacturers operating instructions. 3-3. CUSPIDOR SECTION (1) Cupfiller (Fig.3-8) Keep pressing the cupfiller button until a cup is filled with water. (2) Bowl Flush (Fig.3-8) Turn the bowl flush control knob counterclockwise, water flushes into the cuspidor bowl. Further turning counterclockwise, increases the amount of flush water. -4-

ON MA

IN

OFF

HP2

HP1

Table Top Fixing Screws

Fig. 3-5 Removing Table Top Cover

Auto Select Valve View A

HP1

HP2

Handpiece Pressure Gauge

(HP3)

Fig. 3-6 Auto Select Valve and Pressure Gauge Drive Air Screw HP1 HP2

(HP3)

Coolant Air Screw View A

Fig. 3-7 Auto Select Valve Cupfiller Button

Decrease Increase Bowl Flush Control Knob

Fig. 3-8 Cupfiller and Bowl Flush

3-4. ASSISTANT INSTRUMENT HOLDER SECTION Pick up an instrument (Saliva Ejector or Vacuum Handpiece) from the assistant instrument holder, it starts working automatically. Returning the instrument to the assistant instrument holder stops it automatically.

Chip Blower Button Drive Air Pedal

ON OFF

3-5. FOOT CONTROL SECTION (Fig.3-9) (1) Drive Air Pedal Depressing the drive air pedal controls handpiece rotation speed and coolant air on/off.

Spray Water ON/OFF Switch

On Off

Chip Blower Button Coolant Water On/Off Switch

(2) Spray Water ON/OFF Switch Spray water ON/OFF switch allows water to be turned on or off. Refer to 3-2 (1) of this manual for adjusting water of each handpiece.

Drive Air Pedal

Fig. 3-9 Foot Control

(3) Chip Blower Button By depressing the chip blow button, chip blower comes out from handpiece without bur turning.

Upper Swing Arm Post Stopper Ring

(4) Safety Device by Foot Control When the drive air pedal is being depressed and handpiece is running, all the chair control switches are inactivated. This is to prevent the chair from unexpected movement by any switch being touched accidentally.

Lower Swing Arm

3-6. SWING ARM SECTION Table Height Adjustment (Fig.3-10) Hold and slightly lift up the doctor table, stopper ring will come up on upper swing arm post. Slide up or down the stopper ring to appropriate groove on upper swing arm post. Lower the doctor table to fix it at that height.

3-7. DOCTOR TABLE SAFETY LOCK DEVICE (Fig.3-11) If excess pressure (upward or downward) is applied to the doctor table by the movement of chair, safety device stops the chair movement to protect the table from being damaged.

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Fig. 3-10 Swing Arm

Upward

Doctor Table Downward

Fig. 3-11 Doctor Table Safety Lock Device

4. CHAIR OPERATING INSTRUCTIONS

4-1. MAIN SWITCH (Fig.3-1 & Fig.4-1) Turn on the master switch located at the left side of the pump cover, main switch illuminates in green. Note : Chair main switch will not activate unless master switch of unit is turned on. Refer to 3-1.

CAUTION

I (ON)

Operate the main switch only by hand. Turn off the main switch after daily operation.

Main Switch O (OFF)

Fig.4-1 Main Switch

4-2. CONTROLS (Fig.4-2)

CAUTION

Before operating the chair, confirm safety for the patient and the operator. All chair electrical movements can be controlled by the foot switch.

Foot Switch Disc

Preset-2

Preset-1

2

1

0

Auto Return

LP

Last Position Memory

(1) Manual Mode Control Fig.4-2 Foot Switch A. Seat Lifting Keep depressing ( ) side of the foot switch disc until the seat is lifted up to the desired

position. B. Seat Lowering Keep depressing (

) side of the foot switch disc until the seat is lowered to the desired

position. C. Backrest Reclining Keep depressing ( ) side of the foot switch disc until the backrest is reclined to the desired position. D. Backrest Raising Keep depressing ( position.

) side of the foot switch disc until the backrest is rased up to the desired

(2) Auto Mode Control E. Preset Control VOYAGER chair has two preset positions. (Preset-1 and Preset-2) Momentarily depress ( 1 ) button on the foot switch, the chair will move to the preset-1 position automatically. (Preset-2 is operated by ( 2 ) button.) F. Auto Return Momentarily depress ( 0 ) button on the foot switch, the chair will return to the initial position (The seat is fully lowered and the backrest is upright position.), G. Last Position Memory Momentarily depress (LP) button at treatment position, the backrest and seat will move to the mouth rinsing position automatically. Momentarily depress (LP) button again, the backrest and seat will return to the previous treatment position automatically. -6-

H. Emergency Stop During automatic procedure (Preset, Auto return and Last position memory), depressing any side of disc or button on the foot switch will cancel the automatic movement immediately. Note : Do not keep depressing auto mode button ( 1 )( 2 )( 0 )(LP) over 3 seconds. Memorized position in auto mode may be changed. 4-3. SAFETY LOCK DEVICE (Fig.4-3) All chair movements can be stopped automatically by the safety lock device when pressure is detected between the base and the lower link cover. In case that the safety lock device works, lift up the seat and remove a cause of pressure. Note : Seat lifting and backrest rasing can be operated by manual foot switch disc even when the safety lock device is working.

4-4. HEADREST (Fig.4-4) (1) Height Adjustment Press down or pull up the headrest to the desired height. (2) Angle Adjustment Push the headrest forward as required. Lift the headrest lever to rotate backward and release the lever at the desired angle.

Lower Link Cover Safety Lock Device Base

Fig.4-3 Safety Lock Device

Angle Adjustment

Headrest Lever Height Adjustment

Fig.4-4 Headrest 4-5. AUTO MODE POSITION ADJUSTMENT (1) Preset position Adjustment (Fig.4-5) Two preset positions can be memorized. A. Set the seat and the backrest to the desired preset position by manual control. B. Keep depressing ( 1 ) button until buzzer sounds (in about 3 seconds), then release it. C. The position is memorized in Preset-1. D. Preset-2 can be memorized by depressing ( 2 ) button as following A to C.

Foot Switch Disc

Preset-2

Preset-1

2

1

0

LP

Auto Return

Last Position Memory

Fig.4-5 Foot Switch

(2) Mouth Rinsing Position Adjustment (Fig.4-1) Mouth rinsing position in last position memory movement can be adjusted. A. Set the backrest and seat to the desired mouth rinsing position by manual control. B. Keep depressing (LP) button until buzzer sounds (in about 3 seconds) and release the button. C. This position is memorized as mouth rinsing position.

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5. RIGHT/LEFT HANDED DENTISTRY CONVERSION

1. Bring the chair to the initial position( at lowest height with backrest upright). 2. Swing the doctor table to cuspidor side fully. 3. Pull up two lock pins(A&B) on cuspidor mount arm, (Fig.5-1) and rotate the cuspidor unit to just behaind the chair. 4. Detach assistant handpiece holder from holder bar by lifting it up. Then rotate the assistant holder bar to the other side, and re-attach the handpiece holder on holder bar. 5. Rotate the cuspidor unit to the other side and set lock pins A& B on cuspidor mount arms to fix the unit. 6. Rotate dental light arm to the other side.

Pull

Knob A

Knob A

Knob B

Fig.5-1 Location of Knob

3

1

6

2

Knob B

5

4

Fig.5-2 Position for doctor table, cuspidor unit and dental light

6. CARE AND MAINTENANCE

CAUTION

Turn off the master switch and the main switch after daily operation or in long term interval.

6-1. CARE AND MAINTENANCE FOR CHAIR Other than cleaning, no scheduled maintenance of the chair is required.

CAUTION

Do not drench the chair for cleaning. Do not use polishing powder, solvents, strong disinfectant and hot water for cleaning. After cleaning, wipe with a dry soft cloth and keep dry. Upholstery can be cleaned with a neutral detergent. Paint parts, metal parts and plastic parts can be cleaned with DURR FD333 cleaner

( or equivalent). Do not drench the chair and unit. Wipe all surfaces dry after cleaning.

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6-2. CARE AND MAINTENANCE FOR UNIT (1) Cleaning Unit

CAUTION

Do not drench the unit for cleaning. Do not use polishing powder, solvents, strong disinfectant and hot water for cleaning After cleaning, wipe with a dry soft cloth and keep dry. All surfaces can be cleaned with DURR FD333 cleaner. Spray the cleaner (DURR FD333) on cloth and wipe the surfaces with the cloth. Do not drench the chair and unit. Wipe all surfaces dry after cleaning. Drain Cap

(2) Basket Strainer (Fig.6-1) Take out the drain cap and the basket strainer in centre of the cuspidor bowl and clean them.

Basket Strainer

Cuspidor Bowl

(3) Solid Collector (Fig.6-1) Pull out the solid collector with filter and clean it.

Solid Collector

Fig.6-1 Basket Strainer and Solid Collector (4) Handpiece Vacuum Tip 1. Vacuum Handpiece and Saliva Ejector (Fig.6-2) A. Pull and remove the top parts of each handpiece and clean strainer. Vacuum Cap B. After daily operation, run two cup of clean water through the handpieces to clean inside. Vacuum Handpiece Body

Saliva Ejector Tip

Saliva Ejector Handpiece Body

Sterilization Vacuum Tip/Saliva Ejector Tip/Vacuum Cap/ Slide Knob Slide Knob Vacuum Handpiece Body/Saliva Ejector Handpiece Body can be sterilized with autoclave. Vacuum Saliva Ejector Hose Vacuum handpiece body and saliva ejector body Hose must be assembled before autoclaving. Fig.6-2 Vacuum Handpiece and Saliva Ejector A. Wash off dirt of the handpiece with natural detergent. B. Rinse the handpiecwe with tap water. C. Insert the handpiece in a sterilization pouch and seal it. D. Autoclave for 20 min. at 121℃. Note: The slide knob can be autoclaved 100 times and is an expendable supply. CAUTION

• Skip dry cycle.

Note : After cleaning the handpieces, apply a white vaseline lightly on the rubber parts (O-Ring) and screws part for long life. Keep the handpieces in a clean place.

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2. Micro Motor / Air Motor / Turbine / Scaler Sterilize the handpiece according to manufacturer’s operating manual. 3. Belmont 77 Syringe (Fig.6-3 ) A. Remove the nozzle from syringe and clean it Sterilization A. Wash off dirt of the handpiece with natural detergent. B. Rinse the handpiecwe with tap water. C. Insert the handpiece in a sterilization pouch and seal it. D. Autoclave for 20 min. at 121℃.

Fig.6-3 Belmont 77 Syringe

CAUTION

• Skip dry cycle.

Keep the syringe in a clean place. 4. Tubing and Hose It is recommended that Durr FD333 be used to clean the exterior parts of tubing and hose

(5) Cleaning Oil Mist Separator (Fig.6-4) Handpiece oil mist separator is located rear side of the doctor table. Once a week open the oil mist separator and clean the oil mist filter.

(6) Flush Out System (Fig.6-5) (Option) Flush out switch is located under the doctor table. Take a handpiece from the handpiece holder. Turn on the flush out switch by pulling the lever toward outside. Water flushes from the handpiece to clean water line while the switch is on.

Oil Mist Filter Packing Cover

Fig.6-4 Cleaning Oil Mist Separator Flush Out Switch ON MA

IN

OFF

ON HP2

HP1

Fig.6-5 Flush Out Switch

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7.ELECTROMAGNETIC COMPATIBILITY(EMC) Medical electrical equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in this manual. Portable and mobile RF communications equipment can affect medical electrical equipment. The equipment or system should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the equipment or system should be observed to verify normal operation in the configuration in which it will be used.

Guidance and manufacture������������������������������������������ ’����������������������������������������� s declaration - electromagnetic emissions

The Voyager II L is intended for use in the electromagnetic environment specified below. The customer or the user of the Voyager II L should assure that it is used in such an environment. Emissions test Compliance Electromagnetic environment - guidance RF emissions The Voyager II L uses RF energy only for its internal CISPR 11 function. Therefore, its RF emissions are very low and are Group 1 not likely to cause any interference in nearby electronic equipment. RF emissions The Voyager II L is suitable for use in all establishments, Class B CISPR 11 including domestic establishments and those directly Harmonic emissions connected to the public low-voltage power supply network Class A IEC 61000-3-2 that supplies buildings used for domestic purposes. Voltage fluctuations/ Flicker emissions Complies IEC 61000-3-3

Guidance and manufacture����������������������������������������� ’���������������������������������������� s declaration - electromagnetic immunity

The Voyager II L is intended for use in the electromagnetic environment specified below. The customer or the user of the Voyager II L should assure that it is used in such an environment. IEC 60601 Electromagnetic environment Immunity test Compliance level test level guidance Electrostatic ±6 kV contact ±6 kV contact Floors should be wood, concrete or discharge (ESD) ±8 kV air ±8 kV air ceramic file. If floors are covered IEC 61000-4-2 with synthetic material, the relative humidity should be at least 30%. Electrical fast ±2 kV for power ±2 kV for power Mains power quality should be that transient/burst supply lines supply lines of a typical commercial or hospital IEC 61000-4-4 ±1 kV for input/output ±1 kV for input/output environment. lines lines Surge ±1 kV differential mode ±1 kV differential mode Mains power quality should be that IEC 61000-4-5 ±2 kV common mode ±2 kV common mode of a typical commercial or hospital environment. Voltage dips, short <5% UT <5% UT Mains power quality should be that interruptions and (>95% dip in UT) (>95% dip in UT) of a typical commercial or hospital voltage variations for 0.5 cycle for 0.5 cycle environment. If the user of the on power supply 40% UT 40% UT Voyager II L requires continued input lines (60% dip in UT) (60% dip in UT) operation during power mains IEC 61000-4-11 for 5 cycle for 5 cycle interruptions, it is recommended that 70% UT 70% UT the Voyager II L be powered from (30% dip in UT) (30% dip in UT) an uninterruptible power supply or a for 25cycle for 25cycle battery�. <5% UT <5% UT (>95% dip in UT) (>95% dip in UT) for 5 s for 5 s Power frequency 3 A/m 3 A/m Power frequency magnetic fields (50/60 Hz) should be at levels characteristic magnetic field of a typical location in a typical IEC 61000-4-8 commercial or hospital environment. NOTE UT is the a.c. mains voltage prior to applications of the test level.

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Guidance and manufacture��������������� ’�������������� s declaration ��–������������������������� ������������������������ electromagnetic immunity

The Voyager II L is intended for use in the electromagnetic environment specified below. The customer or the user of the Voyager II L should assure that it is used in such an environment. Compliance Immunity test IEC 60601 test level Electromagnetic environment - guidance level Portable and mobile RF communications equipment should be used no closer to any part of the ����������� Voyager II L���������������������������������������������������� , including cables, than the recommended separation distance calculated from the equation applications to the Frequency of the transmitter.

Conducted RF IEC 61000-4-6

3 Vrms 150 kHz to 80 MHz outside ISM bandsa

3 Vrms

Radiated RF IEC 61000-4-3

3V/m 80 MHz to 2.5 GHz

3 V/m

Recommended separation distance d = 1.2√P

d = 1.2√P 80 MHz to 800 MHz d = 2.3√P 800 MHz to 2.5 GHz 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 800MHz, the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by adsorption 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 Voyager II L is used exceeds the applicable RF compliance level above, the Voyager II L should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the Voyager II L. b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3V/m.

Essential performance (purpose of IMMUNITY testing) Unless operated by the switches for chair control, the chair section of the Voyager II L does not make any movements, except for sounding a buzzer and switching on/off the indicator.

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Recommended separation ����������������� distances�������� between Portable and mobile RF communications equipment and the Voyager II L

The Voyager II L is ����������������������������������������������������������������������������������������� intended��������������������������������������������������������������������������������� for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the Voyager II L can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Voyager II L as recommended below, according to the maximum output power of the communications equipment. Separation distance according to frequency of transmitter Rated maximum output power m of transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz W d = 1.2√P d = 1.2√P d = 2.3√P

0.01 0.12 0.12 0.23 0.1 0.38 0.38 0.73 1 1.2 1.2 2.3 10 3.8 3.8 7.3 100 12 12 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 At 80 MHz and 800MHz, the separation distance for the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by adsorption and reflection from structures, objects and people.

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8. LIST OF COMPATIBLE HANDPIECES DESCRIPTION Syringe

LUZZANI(3-way ) Minilight w/Light DCI (3-way)

Turbine

BIEN AIR BORA S36L / UNIFIX with LIGHT NSK Ti-Max X

Air motor

BIEN AIR Aquilon 830 / UNIFIX with LIGHT /PM1132 NSK EX-203 / EX-6

Micromotor Scaler

BIEN AIR MC3LK / PLMP021PCB. / PM1132 SATELEC SP4055 w/Light EMS Scaler NSK VARIOS VA 150 LUX(w/light)

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NOTE

Takara Belmont (UK) Ltd. Belmont House One St.Andrews Way,Bow, London E3 3PA U.K. Tel: (44)20 7515 0333 Fax:(44)20 7987 3596

TAKARA BELMONT CORPORATION

2-1-1, Higashishinsaibashi,Chuo-ku,Osaka, 542-0083, Japan TEL : 81-6-6213-5945 FAX : 81-6-6212-3680 BOOK NO. AEFT10E0 Printed in Japan 0911