Multi Function Ultrasonic Scaler

Varios 570

OPERATION MANUAL
Please read this Operation Manual carefully
before use, and file for future reference.

OM-E0500E 001
 Original Operation Manual ENGLISH
Classifications of equipment
• Type of protection against electric shock:
– Class II equipment
• Degree of protection against electric shock:
– Type BF applied part:
• Method of sterilization or disinfection recommended by the manufacture:
– See 12. Sterilization
• Degree of protection against ingress of water as detailed in the current edition of IEC 60529:
– Foot Control: IPX1 (Protected against vertically falling water drops)
• Degree of safety of application in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide:
– EQUIPMENT not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous
oxide.
• Mode of operation:
– Continuous operation

Intended to Use
This product is intended only for dental clinic /dental office use. This device generates ultrasonic waves intended for use in
dental applications such as scaling, root canal treatment, periodontal and cavity preparation.

1. Cautions for handling and operation

Read these cautions carefully and use only as intended or instructed.
Safety instructions are intended to avoid potential hazards that could result in personal injury or damage to the device.
Safety instructions are classified as follows in accordance with the seriousness of the risk.

Class Degree of Risk

A hazard that could result in bodily injury or damage to the device if the safety instructions are not
WARNING followed.
A hazard that could result in light or moderate bodily injury or damage to the device if the safety
CAUTION instructions are not followed.
NOTICE General information needed to operate the device safely.

WARNING
• TO PREVENT ELECTRIC SHOCK Do not unplug the AC Adaptor with wet hands.
• TO PREVENT ELECTRIC SHOCK Be sure to prevent water on the Control Unit.
• TO PREVENT ELECTRIC SHOCK Do not touch the handpiece backend electrical connections.
• TO PREVENT ELECTRIC SHOCK Use an electrical outlet that is grounded.
• If you feel any abnormality such as vibration, heat generation, abnormal noise, etc., prior or during the use of the unit, stop
using it immediately.
• This product is Medical Electrical equipment Electromagetic compatable (EMC).As described in the accompanying
documentation.
• Portable and mobile RF communications equipment can affect Electrical Medical equipment. Do not use RF equipment in
close proximity to the product.
• When installing the product, provide space of approximately 10cm around the Control Unit for easy access to the inlet and
the AC Adaptor.

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• USE ONLY NSK genuine Tips when using NSK Varios Ultrasonic Scaler (Varios 570 or Varios 570 Lux) problems such as
damage, failure and accident of Handpieces resulting from use of Non-NSK Tips are not included in the warranty. The
following are the possible failure that could happen when using the Non-NSK Tips;
· Vibration failure caused by using non conforming screws.
· Patients accidental ingestion of broken Tips.
· Damage of thread ridge of handpiece.
• You must use the Tip within the power range described on the Tip-Power Guide. If you use it out of the power range, the
Tip might break or damage an operative site.
• When operating the product always consider the safety of the patient.
• Use by medical professional, such as doctor or dental hygienist, is intended.
• Check the vibration outside the patient’s oral cavity before use. If any abnormalities are found, stop using immediately and
contact dealer.
• Do not drop or exsert an excessive shock to the Control Unit/Handpiece.
• To prevent possible tooth plane damage and handpiece overheating, Always use with sufficient water.
• Do not sterilize by ultraviolet light. Handpiece could discolor.
• Sterilize the Tip, Handpiece, Tip Holder, Tip Cover S and Tip Wrench by autoclaving. Wipe the Control Unit, AC Adaptor, Foot
Control and Handpiece Cord.
• If chemical, solvent or antiseptic solution is deposited on this product, immediately wipe it away. Discoloration or
deformation may occur if left.
• Do not disassemble or alter the handpiece/Control Unit.
• Keep away from patients with cardiac pacemakers.
• Keep away from explosive substances and flammable materials. Do not use for patients anesthetized under laughter gas.
(Nitrous Oxide)
• This product needs special precautions regarding EMC and needs to be installed and put into service according to the
EMC information.
• The use of ACCESSORIES, transducers and cables other than those specified, with the exception of transducers and
cables sold by the manufacturer of this product as replacement parts for internal components, may result in increased
EMISSIONS or decreased IMMUNITY of this product.
• This product should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is
necessary, this product should be observed to verify normal operation in the
!
 
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configuration in which it will be used.




• If any water drops remain on the handpiece after autoclaving, wipe them off.
Staining may result if left.
• There is the judgment that applies this product to a patient in the user side.
• Grounding reliability can only be achieved when the equipment is connected to  
"


an equipment receptacle marked "Hospital Only" or "Hospital Grade".  

"

CAUTION
• During operation, high frequency oscillations in the handpiece and handpiece cord may affect computer and LAN Noise
may be heard during operation near a radio receiver.
• Be sure to turn off the Power/Volume Knob after use. Remove the AC Adaptor and water inside of the Control Unit before
storage.
• Users are responsible for operational control, maintenance and inspection.
• Clean/sterilize the product immediately after using it. Then store it. Leaving it non-sterile might lead to failure.
• When you have not used the product for long time and use it again, check the operation before use.
• Eye damage may result if the LED is stared directly into, Do not look into or turn it to the eyes of the patient.
• When abnormalites are found with a Control Unit and /or an AC Adaptor, pull the AC adaptor from the AC Outlet
immediately.
• This product does not consider patient’s age (except infants), gender, weight or nationality.
• No special training is required for this device.
• Applied parts for patient and/or operator are/is Tip and Handpiece.
• Surface temperature of tip shall be more than 50 degree without using a tap water. To avoid this event, be sure to use a
tap water.

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 * Operation Principle
A sinusoidal electrical signal, at ultrasonic frequency (f>20kHz), is delivered by the generator. This signal is applied
to the ‘piezoelectric ceramic’ located inside the transducer. Piezoelectric ceramic converts this signal into mechanical

English
vibrations. These vibrations are at the same ultrasonic frequency as the electrical signal. The mechanical vibrations
are propagated towards the distal end of the transducer. The “TIP” insert, which is attached at the distal end of the
transducer, vibrates at ultrasonic frequencies and makes it possible to achieve the aimed purpose.

2. Component Names

DC Plug*3

1 Control Unit 1
2
2 Handpiece with Handpiece Cord Unshield 2M 1
(Varios2 or Varios2 Lux)
1
3 AC Adaptor Unshield cord 2M 1
4 Foot Control 1
5 Water Tube Set 1
6 Tip (G4,G6, G8) 1
7 Tip Wrench 1
8 Spanner Wrench (5x8) 2
9 O Ring 2
10 Tip Cover S (Option) -
11 Tip Holder (Option) -
1 By an area, AC Adaptor Shape change
2 Either one is contained with the set that you purchased
3 120 V Only

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 3. Name and Function of each part

Upside
Handpiece
Holder

Power/Volume
Knob

Water Volume
Knob

Power
Indicator

Handpiece
Output Cord
Indicator
Backside

Handpiece Holder

Water Tube Connector DC Connector Foot Control Connector

4. Prior to Operating System

4-1 Set the AC Adaptor
Insert each plug into appropriate connector. Plug Head
Set the AC Adaptor head like right Figure. Release button
Slide into the Plug Head to the AC Adaptor.
To release, push the button shown on the right figure, and
remove the Plug Head from the Adaptor.

CAUTION
If abnormalities are found with the Control Unit
and/or the AC adaptor, remove the AC adaptor from
the AC Outlet immediately.

Adaptor Body

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4-2 Connecting
Insert each plug into appropriate connector.

English
Connect Water Tube firmly into Water Tube
Connector.
Connect Foot Control firmly into Foot Control
Connector.
Connect AC Adaptor into DC Connector.
Fig.1

CAUTION
• Insert plugs firmly into the connector. Lose connection may be cause a malfunction.
• Ensure Power is OFF on the Control Unit during the AC Adaptor Connection. It may cause Fuse to blow.
• Do not connect the cord in wall outlet before connecting DC Connector.
• Do not pull the AC Adaptor forcibly.
• Do not disconnect the AC Adaptor while pressing on the Foot Control.
• Turn OFF the power to connect or disconnect the cords and plugs.

4-3 Disconnecting
4-3-1 Disconnect DC Plug and Foot Control Plug. PUSH
PULL
Simply pull out plugs from the Control Unit.
White Ring Water Tube
4-3-2 Disconnect Water Tube (Fig.2)
Pull out the Water Tube while pushing the
White Ring.
Fig.2

CAUTION
It requires the water removal before the Water tube disconnection.

5. Mounting and Removing the Handpiece

Align the Dots on the Handpiece and the Handpiece Cord. Push
handpiece into connector. Dots

To remove the handpiece, grip the Handpiece and Handpiece

Code then pull out it stright. (Fig. 3)

WARNING
To avoid Electrical Shock Do not touch the handpiece Handpiece Handpiece backend Handpiece Cord
backend electrical contacts.
Fig.3

CAUTION
Always confirm that the handpiece is correctly seated and locked into place.

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 6. Mounting and Removing Tip
Turn TIP lightly by hand, and install it.
Tip will insert from the bottom hole of Tip Wrench. Align the four corner of the Tip base area into the four corner of Tip
Wrench. And turn it clockwise until it clicks.
Do not touch the top part of TIP to avoid an injury. (SThere is the case that is longer than height of TIP WRENCH)
To remove the Tip, turn it counterclockwise with the Tip Wrench.
Tip Wrench
Loosen Tighten

Tighten

Loosen Fig.4

Caution for Tip Usage

• Check the Tip before use. (Flush, Damage, Bending or Rust)
• Do not exceed Maximum Power Level for Tip. Damage to tooth structure and Tip may result.
• Do not hit metal or prosthetic crown except for removing them. Tip could break and fall into mouth.
• Do not hit gingival, mucosa and/or skin directry etc. It could cause damage and/or burn injury.
• Do not sharpen and/or bend the Tip. Tip may damage and not generate enough vibration during scaling.
• During cutting, Tip will gradually wear away, as the Tip wears the stroke will get smaller and decrease cutting
efficiancy When level drops too far, change the Tip.(Tip Card check)
• DO ENSURE When securing tip to use the Tip Wrench as supplied, inefficient cutting will result.
• DO ENSURE before attaching Tip, Cleanliness of the tip screw, inefficient cutting will result.
• To avid personal injury DO ENSURE Tip is removed prior to disconnecting the handpiece or the handpiece cord.
• If you feel the Tip is not vibrating, remove it from an operative site, and press the Foot Control again. If this does
not improve the condition, Ensure the Tip is secure, turn the power off and restart it.
• When mounting the Tip, always use groves and Tip Wrench as supplied.
• Ensure that water Volumee must be “0”, when you use Tip which does not appear of water.
• Tip Wrench is consumable For reliable operation replace annually.

7. Operating Procedures
7-1 Power On
Connect the AC Adaptor to the wall outlet. Rotate the Power/Volumee Knob on the Control Unit. (Power indicator will light
on.)




Power
Indicator

Fig.5

6
7-2 Power Level Setting Power Level for each mode
DO ENSURE Power setting does not exceed the

English
recommended Power Level (Tip-Power Guide
included in the package.)
Set the power level with the Power/Volumee Knob
on the Front Panel. Make sure the power level is set
in the appropriate range for the attached Tip.
Fig.6

NOTICE
• Turn the Power/Volume Knob will increase or decrease the Power Level.
• If the Power Level is 0 (zero) and set the water Volumee, Tip will not oscillate but water comes out from the
handpiece.

7-3 Operate Varios 570 / 570 Lux

Tip vibration will begin when the Foot Control is depressed. Also,
Output indicator will be on.(For Varios2 Lux, Handpiece LED will
illuminate.)

7-3-1 Water Supply Volumee Adjustment

Turn the Water Volume Knob clockwise gradually to Increase
increase the supply Volumee. (Fig. 7)

During the Handpiece operation :

Possible: Power Level and Water Volumee adjustment.
Decrease
7-4 After the Treatment
Release the Foot Control and Power off the Control Unit. Close the
Unit Chair water valve. Fig.7

NOTICE
LED of the handpiece will remain ‘On’ for approx 5 seconds after Foot Control is released. (Varios2 Lux)

7-5 Protection Circuit

It may overheat inside when you use this Control Unit in more than Power 8 at G for long time. In this case, Protection
Circuit reduces the Power automatically. (Power 7)

If you need to increase more than Power 7, decrease the power less than 5 once and increase again.

NOTICE
During Protection Circuit function, the Control Unit can not increase the Power Level.

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8. Provided Scaler Tips
G4 The end of the Tip is thin and for supragingival fine scaling and interdental scaling. The
round cross-section allows tooth surfaces to be finished without causing damage.

Apply the top of the Tip on the tooth plane and move it sideways
finely in the same way as G8 Tip. (Fig. 8)

Fig.8

G6 Removal of supra and subgingival calculus. It provides easy access to interdental

spaces and narrow pockets.

Insert the top of the Tip into the periodontal pocket and move it
slowly. The top of the Tip is sharp so that it could remove tartar
on long coroner and retracted gingival. (Fig. 9)
Clean periodontal pocket at low power. (Set the level less than
“Power 5” at P mode.)

Fig.9

G8 Removal of supragingival and interdental calculus. This Tip can be used in all
quadrants and is very useful for the removal of hard calculus.

Apply the top of the Tip on the tooth plane and move it sideways
finely along the neck of tooth. (Fig. 10)

Fig.10

CAUTION
Tip is article of consumption. We recommend periodical replacement. About time of replacement, check the Tip
Card.

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How to use the Tip Card
1) Place the neck of the Tip in the cut out.

English
2) Check wear of the Tip.
3) See the green, yellow and red line to check wear of the Tip. *See below what each color means. At NSK we recommend
to replace a Tip when the Tip meets the yellow line (wear of 1mm) to guarantee safe and effective use.

Tip Card

Green: No wear - Tip is OK

Tip replacement is not necessary.
Neck

Yellow: Wear of 1mm - Tip is showing some wear

Tip replacement is recommended.
Handpiece

Red: Wear of 2mm - Tip is badly worn

Tip replacement is necessary.
Fig.11
The Tip Card can be used to check the following
tips : G1, G4, G6, G8, G9, P1/P1D, P10, and P20

CAUTION
1mm 2mm
Tips are consumables. The efficiency of dental scaling
decreases approximately 25% when the top of the Tip
wears 1 mm and approximately 50% when it wears 2 mm. 25%
In addition, the vibration condition changes owing to the Decrease
50%
wear, which may damage a patient’s tooth surface. Check Decrease
the Tip wear condition with the Tip Card periodically, and
replace the Tip with a new one in good time.
Efficiency Fig.12

9. How to Use Tip Cover S (Option)

Grip the Tip Cover S and insert it to the Tip.
To remove, grip the Tip Cover S and the handpiece & pull. Slit
(Fig. 13)
Tip
The Tip Cover S is not designed for use as a Tip changing
tool.

Tip Cover
CAUTION Tip-Handpiece Joint
Carefully insert the Tip Fig.13
into the Tip Cover S. Avoid
injuring the fingers.

Slit

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 10. Holder
10-1 Handpiece Holder
While the Handpiece is not in use, put the Handpiece on the Handpiece
Holder. (Fig.14)

Handpiece Holder

NOTICE
To prevent injury, always mount Scaler Tip Cover S.

Fig.14

CAUTION for Handpiece Holder

• Do not place in contact Tip with Handpiece Holder.
• Put straight the Handpiece. Do not incline it.
• Handpiece Holder may get dirt for water scale. In this case wipe it off with
alcohol immerses cloth.

Fig.15

10-2 Tip Holder (Option)

For a Tip removed from the handpiece, use the Tip Tip Holder
Tip
Holder. (Fig.16)

Fig.16

11. Care and Maintenance

11-1 Cleaning of Optic Fiber (Varios2 Lux) Optic Fiber End Face
Wipe the debris off the end of the Optic Fibers at the
handpiece with alcohol soaked cotton swab. (Fig.17)

CAUTION
Do not use any sharp pointed tools to clean the Optic
Fiber End Face. In case the light degridation, contact
dealer.
Fig.17

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11-2 Changing O-Ring O-Ring

Handpiece Cord

English
An O-Ring is located in the Handpiece Cord Connector. Use a pointed tool to remove,
and mount new O-Ring into the groove. (Fig. 18)
Optional O-Ring: Order Code 0310020080
11-3 Changing Water Filter Fig.18
Change the Water Filter as it may necessary.
1) Close the water valve of the dental unit.
2) Mount two Spanner Wrenches (5x8) and turn those as shown in Fig.19.
3) When the Water Filter case is separated, the Water Filter can be removed as shown in Fig. 20.
4) Replace with new (Order Code U387 042) and reassemble the filter in the reverse order.

O-Ring

Water Filter
Control Unit Side
Water Filter Case

Fig.19 Fig.20

12. Sterilization
• Autoclave sterilization is recommended.
• Autoclave sterilization required first time you use and after each patient as noted below. Take handpiece out of the
packing bag before sterilization.
• ONLY the Tip, Handpiece and Tip Wrench, Tip Holder and Tip Cover S (Option) can be autoclaved.
This handpiece can be cleaned and disinfected with a Thermo-Disinfector.

Autoclave Procedure
1) Remove the Tip after use. (Refer to 6. Mounting and Removing Tip)
2) Wipe dirt and debris from the products, and wipe clean with alcohol-immersed cotton swab or cloth. Do not use a wire brush.
3) Insert those into autoclave pouch. Seal the pouch.
4) Autoclavable up to max. 135˚C.
Ex.) Autoclave for 20 min. at 121˚C, or 15 min. at 132˚C.
5) Keep the products in an autoclave pouch to keep it clean until you use it.
Sterilization at 121°C for more than 15 minutes is recommended by ISO17664 and EN ISO17665-1.

CAUTION
• Do not sterilize by ultraviolet ray. The handpiece could discolor.
• If autoclaved with other instruments stained with chemical solution, it could strip the plating and make the surface
black.
• Do not autoclave any parts (the Control Unit, AC Adaptor, Foot Control, Handpiece Cord, O-Ring). Other than those
that can be subjected to autoclave sterilization. Perform alcohol disinfection to the Control Unit, AC Adaptor, Foot
Control, Handpiece Cord including after every patient.
• Do not wipe with, or clean or immerse in, high acid water or sterilizing solutions.

11
 13. Troubleshooting
When trouble is found, please check the followings prior to consulting your dealer.

Problem Probable Cause Cause Solution

Power Indicator
does not light, The AC Adaptor or the DC Plug is
Correctly insert the AC Adaptor or the Jack.
even if the Power/ disconnected.
Volume knob.
The Tip is not tightened firmly. Tighten the Tip until the Tip Wrench clicks.
Worn Tip. Replace the Tip.
No / Poor
vibration. The Tip does Power has not been correctly adjusted Adjust the power on the Power Guide or Tip case
not generate for the Tip. label. Do not exceed.
vibration, in spite
of depressing the The Foot Control is disconnected. Connect the Foot Control correctly.
Foot Control. Failure of vibrator in the handpiece. Contact dealer.
Failure of internal components of the
Contact dealer.
Foot Control.
The Tip is bent or Power has not been properly adjusted Adjust the power level on the Power Guide or Tip
—
broken. for the Tip. case label. Do not exceed.
The Tip is flying
— The Tip is not tightened firmly. Tighten the Tip until the Tip Wrench clicks.
away.
Power has not been properly adjusted Adjust the power level on the Power Guide or Tip
for the Tip. case label. Do not exceed.
Noise from the
— The Tip is not tightened firmly. Tighten the Tip until the Tip Wrench clicks.
handpiece.
Failure of vibration in the handpiece or
Contact dealer.
the Control Unit.
Power has not been properly adjusted Adjust the power level on the Power Guide or Tip
for the Tip. case label. Do not exceed.
The handpiece is
— The Tip is not tightened firmly. Tighten the Tip until the Tip Wrench clicks.
overheating.
Failure of vibration in the handpiece or
Contact dealer.
the Control Unit.
The water does
Check the water circuitry and supply to the Control
not reach to the —
Unit. Water pressure : 0.1-0.5MPa (1-5kgf/cm2)
Control Unit.
Turn the Water Volumee Knob and adjust to the
The Water Volumee Knob is closed.
No / Poor water. appropriate Volumee.
Check to see if
Disconnected Irrigation supply at low No problem. Turn the Water Volumee Knob and
water reaches the
Volumee range. (less than 10ml/min.) increase the Irrigation Volumee.
Control Unit.
Replace with new Water Filter (Refer to 11-3
The Water Filter is clogged.
Changing Water Filter (Option) ).
Water is leaking
from the joint
O-Ring at the handpiece cord is worn Replace with new O-Ring (Refer to 11-2 Changing
Water leakge between the
or damaged. O-Ring Handpiece Cord)
handpiece and
the cord.

12
 Problem Probable Cause Cause Solution
Water is leaking
The water circuitry in the Control Unit

English
Water leakage. from the Control Contact dealer.
is damaged.
Unit.
Handpiece
Tip oscillates, but
LED does not The handpiece is not connected into Firmly insert the handpiece into the Handpiece
Handpiece LED
illuminate. the Handpiece Cord correctly. Cord inmost.
turns on and off.
(Varios2 Lux)
Powerful output will weaken automatically while
continuous operation is over 10min at the setting
Loss of the power
Power output is of Maximum power at G mode. Releasing the foot
output without Protection Circuit is activated.
set 8 at G from the Foot Control. Decrease the Power less
operation.
than 5, once then increase the power again. (Refer
to 7-5 Protection Circuit)

14. Spare Parts

Model Products Order code Model Products Order code

Tip Wrench
Water Filter Set U387040 Z221076
(CR-10)

Water Supply
U387030 Tip Holder Z221080
Connector

Water Filter U387042 Tip Cover S Z217851

Spanner Wrench
Y1001301 O-Ring 0310020080
(5x8) x 2 pice

Autoclavable up to max135˚C.

15. Disposing product

Consult with dealer from whom you purchased it about waste disposal.

16 . Warranty
Manufacturer warrants its products to the original purchaser against defects in material and workmanship under normal
practices of installation, use and servicing. Such expendable items as O-Ring is not covered by this warranty.

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Symbols
TUV Rhineland of North America is a Nationally Recognized Testing Laboratory (NRTL) in the United States and is accredited by
the Standards Council of Canada to certify electro-medical products with Canadian National Standards.

Follow the waste of electric and electronic equipment (WEEE) Directive (2002/96/EC) to dispose of the product and
accessories.

Consult operation instructions. Manufacturer. Class II Equipment.

This conforms to CE European Directive of “Medical equipment directive 93/42/EEC.”

Type BF applied part. Authorised representative in the European community.

This product can be cleaned and disinfected with a Autoclavable up to Max.135°C. *for detail see Sterilization.
Thermo-Disinfector.

Protected against vertically falling water drops.

Marking on the outside of Equipment or Equipment parts that include RF transmitters or that apply RF electromagnetic energy
for diagnosis or treatment.

Guidance and manufacturer's declaration - electromagnetic emissions

The Varios 570 / Varios 570 Lux is intended for use in the electromagnetic environment specified below. The customer or the user of the Varios 570 / Varios 570 Lux
should assure that is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions The Varios 570 / Varios 570 Lux uses RF energy only for its internal function. Therefore, its RF emissions are
Group 1
CISPR11 very low and are not likely to cause any interference in nearby electronic equipment.
RF emmissions The Varios 570 / Varios 570 Lux is suitable for use in all establishments, including domestic establishments
class B
CISPR11 and those directly connected to the public low-voltage power supply network that supply network that
Harmonic emissions supplies buildings used for domestic purposes.
class A
IEC61000-3-2
Voltage fluctuations/flicker emissions
Complies
IEC61000-3-3

Guidance and manufacturer's declaration - electromagnetic immunity

The Varios 570 / Varios 570 Lux is intended for use in the electromagnetic environment specified below. The customer or the user of the Varios 570 / Varios 570 Lux
should assure that it is used in such an environment.
Immunity test IEC60601 test level Compliance level Electromagnetic environment - guidance
Electrostatic discharge (ESD) ±6kV contact ±6kV contact Floors should be wood, concrete or ceramic tile. If floors are
IEC61000-4-2 ±8kV air ±8kV air covered with synthetic material, the relative humidity should
be at least 30%.
Electrical fast transient/burst ±2kV for power supply lines ±2kV for power supply lines Mains power quality should be that of a typical commercial or
IEC61000-4-4 ±1kV for input/output ±1kV for input/output hospital environment.
Surge ±1kV line(s) to line(s) ±1kV line(s) to line(s) Mains power quality should be that of a typical commercial or
IEC61000-4-5 ±2kV line(s) to earth ±2kV line(s) to earth hospital environment.
Voltage dips, short <5% Ut (>95% dip in Ut) <5% Ut(>95% dip in Ut) Mains power quality should be that of a typical commercial
interruptions and voltage for 0.5 cycle for 0.5 cycle or hospital environment. If the user of the Varios 570 / Varios
variations on power supply 570 Lux requires continued operation during power mains
40% Ut (60% dip in Ut) 40% Ut (60% dip in Ut)
input lines interruptions, it is recommended that the Varios 570 / Varios
for 5 cycles for 5 cycles
IEC61000-4-11 570 Lux be powered from an uninterruptible power supply or
70% Ut (30% dip in Ut) 70% Ut (30% dip in Ut) a battery.
for 25 cycles for 25 cycles
<5% Ut (>95% dip in Ut) <5% Ut (>95% dip in Ut)
for 5 secs for 5 sec
Power frequency (50/60Hz) 3 A/m 3 A/m Power frequency magnetic fields should be at levels
magnetic field characteristic of a typical location in a typical commercial or
IEC61000-4-8 hospital environment.
NOTE: Ut is the a.c. mains voltage prior to application of the test level.
Guidance and manufacturer's declaration - electromagnetic immunity
The Varios 570 / Varios 570 Lux is intended for use in the electromagnetic environment specified below. The customer or the user of the Varios 570 / Varios 570 Lux
should assure that it is used in such an environment.
Immunity test IEC60601 test level Compliance level Electromagnetic environment - guidance
Portable and mobile RF communications equipment should be used
no closer to any part of the Varios 570 / Varios 570 Lux, including
cables, than the recommended separation distance calculated from
the equation applicable to the frequency of the transmitter.

Recommended separation distance

Conducted RF 3Vrms 3Vrms d = 1.2 P

IEC61000-4-6 150 kHz to 80MHz
d = 1.2 P 80MHz to 800MHz
Radiated RF 3V/m 3V/m d = 2.3 P 800MHz to 2.5GHz
IEC61000-4-3 80MHz 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 meters (m).
Field strengths from fixed RF transmitters as determined by an
electromagnetic site survey, should be less than the compliance level
in each frequency range.
Interference may occur in the vicinity of equipment
marked with the following symbol:

NOTE 1 At 80MHz and 800MHz, 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 mobiles 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 Varios 570 / Varios 570 Lux is used exceeds the
applicable RF compliance level above, the Varios 570 / Varios 570 Lux should be observed to verity normal operation. If abnormal performance is observed,
additional measures may be necessary, such as reorienting or relocating the Varios 570 / Varios 570 Lux.
b Over the frequency range 150kHz to 80MHz, field strengths should be less than 3 V/m.

Cables and accessories Maximum length Complies with

Handpiece cord 2m RF emissions, CISPR11, Class B/ Group 1
Foot Control 4m Harmonic emissions, IEC61000-3-2
Voltage fluctuations/ flicker emission, IEC61000-3-3
Electrostatic discharge (ESD) IEC61000-4-2
Electric fast transient / burst IEC61000-4-4
Surge IEC61000-4-5
Voltage dips, short interruptions and voltage variations on power supply input lines IEC61000-4-11
Power frequency(50/60Hz) magnetic field IEC61000-4-8
Conducted RF IEC61000-4-6
Radiated RF IEC61000-4-3

Recommended separation distances between portable and mobile RF communications equipment and the Varios 570 / Varios 570 Lux.
The Varios 570 / Varios 570 Lux is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of
the Varios 570 / Varios 570 Lux can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications
equipment (transmitters) and the Varios 570 / Varios 570 Lux as recommended below, according to the maximum output power of the communications equipment.
Separation distance according to frequency of transmitter
Rated maximum output power of transmitter m
W 150kHz to 80MHz 80MHz to 800MHz 800MHz to 2.5GHz
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 meters (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 800 MHz, the separation distance for 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.
Specification
Type NE253 Temperature 0 - 40 °C
Power Source AC 100 - 240 V 50-60Hz (The liquid must not freeze up)
Use Environment
Vibration Frequency 28 - 32 kHz Humidity 30 - 75 %
Atmospheric Pressure 700 - 1,060 hPa
Maximum Output 11 W
Rated power 25VA Temperature -10 - 60 °C
Store Environment Humidity 10 - 85 %
Lighting Varios 570 : No
Atmospheric Pressure 500 - 1,060 hPa
Varios 570 LUX : Yes
Dimensions W160 X D135 X H65 mm
(Without Cord)
Weight 0.43 kg (Without Attachment)

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