Operating Manual

Electric Motor E1

Version: first edition

Guangdong JINME Medical Technology Company Co.,Ltd

Copyright

©2016 All rights reserved. All copyrights are reserved by Guangdong

JINME Medical Technology Company Co.,Ltd.

The Company does not provide any guarantee to the manual. Including,
but not limited to, the implied warranties of merchant ability and fitness
for a particular purpose. The Company is not responsible for any errors
occurred in this manual or any derivative or other damages related to the
provision, execution or use of this manual. The information contained in
this document is subject to change without further notice. If you find
any problems in the document, please contact the Company. The
Company does not guarantee that there are no errors in this document.

Without the written permission of Guangdong JINME Medical

Technology Company Limited, no part of this document may be
photocopied, reproduced, altered or transferred in any form or by any
means such as electronic or paper, etc. by any person and any unit.

1
■Equipment Classification:
Classification of types of electric shock protection:

-- Category Ⅱ Equipment:

Classification by the degree of electric shock protection:

-- Type B applied part:

Classification according to the sterilization or disinfection methods

recommended by the manufacturer:
-- Please refer to Chapter 6 Sterilization

It shall be classified according to the degree of safety when used

under the cases of flammable anesthetizing gas mixed with air or
with oxygen or nitrogen oxide:

-- The equipment cannot be used under the cases with the

flammable anesthetizing gas mixed with air or with oxygen or
nitrogen oxide.

Classification by operation mode:

-- Continuous operation

Representation method of safety precautions and the

hazardous matters
■ Please read the following safety precautions carefully and have the
correct use method before using.
■ Please note the representing method of the hazardous matters, so as
not to cause damage to you and others due to the improper use. The
following items are classified according to the possible danger and/or

2
 the damage level, all of which are precautions related to the safe use.
You must read it carefully and observe accordingly.

Classification of The hazard or the severity of the damage may cause.

notice
WARNING It indicates a precaution that may result in personal
injury or damage to the articles.
Caution It indicates a precaution that may cause minor or severe
injury and damage to the articles.
Notice It indicates the precautions to be observed for the safety
sake.

WARNING

·Do not touch power cord with wet hand to prevent electric shock.
·Do not make the control unit adhere to liquids such as water, which may
cause the dangers such as electric shock and so on due to short circuit.
· Do not plug in and out the power outlet in a rough manner to prevent
electric shock.
· In case that there are abnormal conditions such as smoke, or smell
similar to the resin burning, please directly turn off the power switch,
pull out the power plug and entrust for repair immediately.
· Do not use in the room with explosion hazard or in the vicinity of
combustible substances.
·Use the power outlet with protective earthing to prevent electric shock.
· Full attention shall be paid as whether there are conditions such as
vibration, heat and noise and so on, and please stop immediately if you
feel abnormal conditions before use or in use.
· For the fuses within the adapter, please make sure to use the specified
2
 rated product.
Caution
·Priority shall be paid to the safety of patients; Hence, the safety must be
noted when using this product.
· This product is limited to the dental treatment by the personnel with the
dentist qualification. Do not use for oral surgery and implant treatment.
·Please make precise connection to each part, otherwise it may cause LED
light failure, water leakage or gas leakage.
·It is strictly forbidden to cause severe impact on this product, especially do
not let this product fall. Otherwise, it may cause malfunction.
· Please connect the handpiece tail pipe with ISO specification 9168,
Type B (Midwest 4 holes) or Type C (ISO standard 4 holes with light) to
this product.
· This product works normally in the places with the temperature of 0 ~
40 ℃ (32-104 ℉), humidity of 10 ~ 85%, pressure of 700 ~ 1060hPa, and
control components are not stained with water droplets. Use this product
in the place outside this may cause malfunction.
·Do not bend or twist the water supply pipeline or electrical conductor when
installing the control host or motor. Do not apply any abnormal force
during installation.
Caution
· Do not use the air contaminated with dust or moisture. If there is water
vapor or dust in the air, it may cause malfunction or overheat.
·Do not connect micro motors of this elextric motor E1 to products of other
models by other manufacturers, so as to avoid malfunction.

Control Host

· Unplug the power cord or the motor cord by holding the plug. If you
unplug by holding the wire, then the wire may break or cause
2
 malfunction.
·Do not replace the wire near the gas burner. Please do not repair the broken
motor line as it should be replaced with a new one.
· Full attention shall be paid as whether there are problems such as loose,
vibration, abnormal sound, heat (temperature), etc. Make sure to check it
by rotation outside the oral cavity of the patient. At this time, stop using
even if there is a slight abnormal condition, and please contact with the
our dealers.
·Do not spill water on the equipment; Otherwise it will cause the risk of a
fire or electric shock due to a short circuit.

Motor and handpiece (purchased separately)

·Do not use it for a long time under high load. Otherwise, it may cause heat.
·Disconnect the handpiece (purchased separately) after the motor has been
completely stopped.
·Do not connect/disconnect dental handpiece when it rotating..
·Make sure to adjust the rotation speed to the allowable speed range of the
dental handpiece (purchased separately) before use.
·Only 4-holes, 5-holes or 6-pin sleeves can be connected.
·Requirements for air supplied: dry, and do not contain water and grease.
Please equip a compressor with an air drying device. The air filter may be
installed as needed. Prior to installation, drain the pipeline with airflow.
· Do not perform high-temperature and high-pressure sterilization (or any
other high-temperature sterilization) on the control host, adapter, motor
cable, etc.
· The responsibility for operation and maintenance of equipment shall be
borne by the user.
·The responsibility for the correct operation and control, maintenance and

2
 inspection of the equipment shall be borne by the operator.

Notice
· If the computer or a LAN cables are placed in a position in the close
vicinity of the running motor or motor wire, sometimes it may cause
impact on it. In addition, if there are receivers such as radio, etc. near the
motor or the motor wire, sometimes it may cause noise.
·Turn off the power switch after use, and unplug the power plug when it is
not used for a long time, and clear the water from the control assembly,
handpiece pipe and the motor wire.
· The responsibility for operation, warranty inspection of the medical
equipment shall be borne by the user.
·Please store this product in the place without dust, sulfur and salt, and the
temperature of -10 ~ 60 ℃, humidity of 10 ~ 85% and the air pressure of
500 ~ 1060hPa.

Notes
Please read the following content carefully before use!
1. This device can only be used in the content involved in the manual,
and should not be used for other purposes. Please operate in strict
accordance with the operation manual. We will not be responsible for
any accidents caused by the operation due to failure in following the
manual.
2. Before using the primary power, make sure that the voltage is within
the operating range of the power adapter. The improper input voltage
will damage the device and cause harm to the operator and patients.
3. Please use original accessories, such as: motor. We will not be liable
for any problems and hazards arising from the use of the relevant
accessories not supplied from the Company.
4. As this product is an electronic product, do not insert any items into
2
the device, so as to avoid the hazard of electric shock.
5. When installing the control box, avoid the winding of connecting pipe
or the power cord.
6. Avoid liquids such as cleaning agents into the control box or adapter,
so as to prevent short circuits or other problems.
7. Cut off the power supply immediately if there is any abnormal
condition of the device. It is not allowed to perform the unauthorized
modification of equipment circuits or components. Any dis-assembly or
modification may cause the abnormal operation of drive or equipment.
8. Switch off the power after each use. For long-term placement,drain
the equipment and hose.
9. Avoid any strong electromagnetic interference to the equipment. Do
not place the device near the device with strong current, or place it near
a patient with a pacemaker.
10. The unstable voltage or magnetic field interference will affect the
normal operation of device.
11. This device is for the use by the professionals only.
12. For the first use, please first sterilize the dental handpiece and motor
of the electric motor.

2
1. List of Accessories
Control box (with motor) x1
Operation Manual x1

2. Scope of Application and Population

It is applicable to the general dental use, and the treatments such as
dental cavities repair, crown repair, crown finishing, filling and
polishing and so on when used with the ISO E-type straight handpiece
and contra angles and accessories with the constant speed, increased
speed or reduced speed.
This device is applicable for cutting, grinding and polishing of teeth. It
is only used by the trained dentists in the clinic or laboratory.

3. Specifications and Parameters

3.1 Requirements for power access:
Output voltage of power supply: 32VDC 4A (MAX)
Output power: 130W (MAX)
Output specifications of power supply: DC male head
5.5mm*2.1mm
Note: The power supply shall meet the medical standards 60601-1
certification, and the primary and secondary insulation shall meet
the 2mopp standard.
3.2 Motor
Motor model M1
Rectifying devices DC32V
Modes of operation Forward/reverse rotation
Speed range of standard mode 2000-40,000 rpm
Maximum torque of electric motor 3.5 N.cm
Consumption amount of cooling gas 6-8 NL/min (0.2MPa)
Sterilization temperature 134℃
Dimension Diameter Ф21.7× height 70.5mm
3.3 Control Host

4
 Model C1
Rectifying devices DC32V
Working air pressure 0.2MPa~0.6MPa
Dimension Length 135 × Width 135 × Height 67mm
3.4 Gas and water supply

Supply of spray water 65 ml/min and above (0.2 MPa)

Supply of spray gas 1.5 L/min and above (0.2 MPa)
Cooling water pressure 0.2MPa
4. Structure and Assembly
4.1. Names of Various Components

4 3

3
6

Fig. 1

5
 6 315074 Step-up board 1
5 203201 Tube assemblies 1
4 315026 Tube handle 1
3 203200 Motor 1
2 315062 Drive Board 1
1 203202 Controller 1
No. Code Name Qty.

Indication of Display of Indication of mode Adjustment of

store number rotating & drive ratio speed rotating speed
speed speed

Retriev Store light Reversal Selection of mode

e e
4.2. Connection of various parts

• When connecting to the control assembly, note that there shall

Caution
no air or water leakage in the handpiece tubes.
• When inserting the handpiece wire interface and the motor
wire interface, tighten the screws correctly to avoid any
abnormal rotation.
Caution
·Do not use the hose other than the one recommended by our Company
·Please confirm the drainage condition of the compressor again before use.
·Do not use the force above the required level to pull the motor wire.
·Do not use contaminated or humid air.

6
 4.2.1 Power supply Installation
As shown in Figure 2, connect the AC24v power cord to the booster
board's access port.

Output end
+ (red)

AC24V
Access to the
Output end
power cord
- (black)

Fig. 2
4.2.2 Installation of Pipelines
two-hole terminal socket (lamp control line)

Green: Motor cooling pipe

Yellow: Water pipe
Blue: atomizing pipe
Air pipe Inlet (air
pressure sensing)

Power switch
关

Three hole terminal

socket (motor line) Power sockets

Four hole terminal

socket (Controller line)

Fig. 3
7
As shown in Figure 3, control the shape of the four-hole handpiece tube
socket, firmly insert the handpiece lead plug from the chair, and tighten
the fixed handpiece connector plug nut. Firmly insert or connect the
sockets of each pipeline as shown in Figure 3.
4.2.3 Assemble and disassemble of motor/motor wires
As shown in Figure 4, insert the motor and motor wire interface
carefully and straightly until stop. Then firmly tighten the motor wire
nut. When disassembling, loosen the motor wire nut and pull it out
straightly.

Motor Motor wire interface

Motor wire nut Motor wire

Fig.4
4.2.4 Assemble and disassemble of motor/mobile phone
Insert the handpiece into the insertion part of the motor and turn during
the installation until you hear the sound of "clack", which suggests it is
coincided with the locating point. When disassembling, hold tight the
motor and the handpiece and pull it out straightly.
* handpiece needs to be purchased separately.

Handpiece (purchased separately)

Locating pin

Motor insertion part

8
 Caution
· Make sure to carefully use the mobile phone accessories (E-Type micro
motors) need to be greased. Place the handpiece vertically after greasing until
the excessive cleaning lubricating oil is drained. Wipe clean the phone before
connecting to the motor.
· Do not install or disassemble the handpiece while the motor is rotating.
· CAUTION: Do not connect the oiled handpiece to the motor when placing so
as to prevent the oil from spreading to the motor; thus causing a malfunction.
· Store the oiled handpiece separately, and then install it when using.
· Do not make water enter into the motor so as to avoid malfunction.

5. How to use
1) Align the plug of the power supply output
Symbol О I
(DC32V) to the interface jack of the controller
adapter and firmly insert in. Turn on the power
Status OFF ON
switch, and the controller's display series will
light.
Before turning on the power, make sure that the output voltage at
the output of the power supply is DC32V.
2) Press the selection button of reduction ratio [SET] and select the
reduction ratio of the handpiece to be used (Figure 5).

*When the rotation speed is set, the selected indicator for the
reduction ratio will be on. Please refer to the table below for details
on the display.

Handpiece Rotation speed Corresponding handpiece

transmission ratio display rotation speed /rpm
20：1 1~20 100~2,000
16：1 1~25 100~2,500
1：1 2~40 2,000~40,000
1：5 1~20 10,000 ~ 200,000

9
 Speed ratio indicator light

Press

Fig.5
3) Press the rotation speed adjustment button(SPEED/LUX【+】/【-】),
and the handpiece speed will be displayed on the screen in two digits.
Set by speed adjustment【+】 and【-】(Figure 6).
20: 1, which displays as 1 ~ 20. Corresponding to the speed from 100
RPM to 2,000 RPM, and each 100 RPM is one gear level.
16: 1, which displays as 1 ~ 25. Corresponding to the speed from 100
RPM to 2,500 RPM, and each 100 RPM is one gear level.
1: 1, which displays as 2 ~ 40. Corresponding to the speed from 2,000
RPM to 40,000 RPM, and each 1,000 RPM is one gear level.
1: 5, which displays as 1 ~ 20. Corresponding to the speed from
10,000 RPM to 200,000 RPM, and each 10,000 RPM is one gear
level.
When the speed setting value is the upper or lower limit of the speed in
the current gear ratio mode, the buzzer will give off the Bi-Bi sound to
indicate that the speed has reached the limit.

10
 Rotation speed display

Up

Down

Fig. 6

4) Forward and reverse 【REF】

Click It will change the direction of motor operation.

5) Program Archive [WR]

In the first time, click the program archive 【WR】 button, the storage
indicator will start flashing, and then press 【WR】 button to select the
number. Wait for two seconds to finish the automatic confirmation of the
change. All the current settings will be stored to facilitate the next call. A
total of four gear levels can be stored, which are M1, M2, M3 and M4 in
turn.

6) Program call
Click the program call [RD] button to select the user mode number. If
you select M2, then the M2 indicator light will be on, and the ventilation
will be operated in the mode stored based on M2.

7) Motor light adjustment

11
 On/Off: Single click the LED button to control the motor light.
Brightness adjustment: hold down the LED button and then press【+】
button and【 - 】 button simultaneously to modify the brightness of the
motor lights, and there are 5 levels of changes.
When the brightness setting value is the upper or lower limit, the buzzer
will give off the Bi-Bi sound to indicate that the brightness has reached
the limit.
Caution
When the supply air pressure is in the range of 0.05MPa ~

0.20MPa, in order to prevent the motor from overheating, the motor

rotation speed cannot reach the set value, and the actual output speed

is: set value*AD value/(air pressure AD value under 0.2MPa).

When the air pressure <0.05MPa, the motor does not rotate. When

0.6MPa ≥ air pressure ≥ 0.2MPa, the motor rotation speed will

operate according to the set value, and when the pressure ≥ 0.6MPa,

it exceeds the limit value, then the operation will be stopped to

protectthemotor.SeeFigure7 fordetails.

Figure 7
6. Sterilization
The sterilization treatment can only be conducted for the motor. The
company recommended that the autoclave shall be used for the
sterilization. At the initial use, or after the end of treatment of each
patient, perform autoclave as described below.

Parts can be treated with high temperature and high pressure sterilization:
motor and motor protection cover (anti-steam bolt).

■Autoclave method
1) Please switch off the power.
2) Remove the motor wire from the motor. (Refer to 4.2.3 Assemble

12
 and disassemble of motor/motor wires)
3) Remove the dirt on the motor surface with a brush (not made of
metal) and the like, and wipe with the cotton soaked with alcohol for
disinfection.
Anti-steam bolt
4) Screw the motor cap into the
motor wire connection part and
install the anti-steam bolt to the
Motor cap
motor insertion part (Figure 8).
Fig.8
5) Put into the autoclave bag and seal up.
6) Conduct the high pressure sterilization under the temperature of
up to 135 ℃.
e.g. 121 ℃ for 20 minutes or 132 ℃ for 15 minutes.
7) Always put into the bag for the high pressure sterilization before
use and keep it in a clean place.
* For EN13060 or ENIS017665-1, it is recommended that the
sterilization shall be conducted for more than 15 minutes under the
temperature of 121 ℃.

Caution

· Do not conduct the high pressure sterilization (or all the high temperature
sterilization) of the control component, adapter and motor wires.
· Do not lubricate for the motor.
· Do not use the oxidation potential water (strong acid water, ultra-acid
water) or sterilization solution for cleaning, dipping and wiping this
equipment; otherwise, it may cause the resin parts discolored or metal parts
corroded.
· The sterilization shall be conducted if there is dirt residual on the surface,
then it may be rusted.
13
 · When the O-ring at the motor head is disengaged, replace it with a new
O-ring (for motor protection) so as to avoid water flow into the motor and
cause failure.
*O-ring (for protection of motor): Product No. 315020
·To avoid loss, put the motor protection cover on a hook, etc. for storage and
do not store when it is connected to the motor, so as not to damage from
falling off.

7. Cleanliness and care

The deterioration of the O-ring will make it difficult to install the
mobile phone accurately, or cause water and air leakage. In this case,
please replace the O-ring.

1. Replace the O-ring

Remove the deteriorated O-ring at the
motor insertion position with the tools
such as needle, etc., and insert the new
O-ring into the O-ring slot.

O-Ring (Black): Product No. 315020

Caution
·There are a total of three O-rings.
·If the O-ring is deteriorated, it may cause the following problems:
Water leakage, no water flow
Air leakage, stuffiness
Vibration
Difficult to install the handpiece accurately

14
 8. Fault alarm

Fault code Fault description Treatment method

1. Turn on power switch again.
over-voltage/under- 2. Check if the input voltage meets the
E1 adapter requirements.
voltage 3. Check if there are any faults in the
adapter output.
Separate the handpiece from the object
E2 Motor overload
and power it on again
Temperature is too Switch off the power and power it on
E3
high again after 10 minutes
Default phase of Check the motor connection is good,
E4
motor and power it on again after connection.
Separate the handpiece e from the
E5 Locked-rotor object, and the motor automatically
restarts in 5 seconds.
Adjust the input air pressure to
E6 Over-pressure
0.2-0.6MPa

If you think there are any questions, please check again before sending
for repair; when any of the above conditions are not in conformity or no
improvement is shown after the inspection, please contact with the
retailer.

9. After-sale services
This product has undergone strict quality management and
previous-selling inspection, and in order to make you more reassured in
use, we especially attach the warranty certificate and warranty
registration card for you. If you do not have any questions after finishing

15
the settings, you are welcome to send us the warranty registration card
after filling in the necessary contents. If you do not send us the warranty
registration card, you will have to pay for the maintenance even it is in
the warranty period. In addition, please keep the warranty certificate
properly after filling in the contents.

10. Disposal of waste products

Please contact your dealer for advice on how to dispose the waste
products.

11. Warranty
The manufacturer shall be responsible for one-year warranty for the
quality of the product under the premise that it is used according to the
methods and procedures described in this operation manual from the
date of purchase.

Please note that we will not provide warranty if you fail to follow the
contents of this operation manual or use of disposable parts.

12. Sign indicators

TUV Rheinland North America is the National Recognized

Testing Laboratory (NRTL) in the United States, and the medical
electrical products of which is authorized by the Canadian Standards
Committee for the Canadian National Standard Verification.

Dispose of waste products and accessories in accordance with the

Waste Electrical and Electronic Equipment (WEEE) Directive

16
(2012/19/EU)
Class II instrument
Inquire operation manual
Manufacturer
Conform to CE European Directive of “Medical Device
Directive 93/42/EEC”
Type B Application Part
The maximum temperature of high temperature and high pressure
sterilization is up to135℃. *Please refer to sterilization for details
The external identification of device or device part indicate that RF
transmitter is included or the diagnosis or treatment can be
conducted with RF electromagnetic energy

13. EMC information (Electromagnetic compatibility information)

Caution：
 Dental electrical motor comply with YY0505-2012 standard
electromagnetic compatibility requirements.
 The user should according to the installation and use of information
provided by the EMC random file.
 Portable and mobile RF communication devices may affect the
performance of dental electrical motor, and avoid electromagnetic
interference, such as proximity to mobile phones, microwave ovens,
etc.;
 The instructions and manufacturers statements are attached to the
annex.

 Warning：
17
 The equipment or system should not be close to or overlapped with
other equipment. If it must be used in close proximity or
superposition, it should be observed and verified to operate
normally under its configuration.
 In addition to the equipment or system of spare parts manufacturers
as the internal components of the sale of the transducer and the
cable, using the specified accessories, transducer and cable
equipment or system may lead to increase or decrease the emission
immunity.
 The use of specified accessories, transducers or cables together
with equipment and systems may result in an increase in equipment
or system emissions or a decrease in immunity.
 The power cord length is 1.8 meters.
Enclosure：
Guidance and manufacturer's statement - Electromagnetic launch
Dental electrical motor E1 is expected for use in the electromagnetic
environment described below. Dental electrical motor E1 customers or users
shall ensure that their purchased products are used in this environment.
Launch test Conformity Electromagnetic Environment - Guide
RF emission Dental electrical motor E1 only uses RF
GB4824 energy in its internal functions. Therefore,
Group I the RF emission measure is extremely low,
and it is impossible to interfere with the
adjacent electronic equipment.
RF emission
Category B
GB4824 Dental electrical motor E1 is applicable for
Harmonic all installation environments, including civil
Type A
emission buildings installation environments, and

18
Gb17625.1 installation environments that are directly
Voltage connected to low voltage network power
fluctuation/flic supplies to power grids and civil buildings.
Comply
ker emission
GB17625.2

Guidance and manufacturer's statement -- electromagnetic immunity

Dental electrical motor E1 is expected for use in the electromagnetic
environment described below. Dental electrical motor E1 customers or users
shall ensure that their purchased products are used in this environment.
Immunity IEC60601 Test Electromagnetic
Compliance level
Testing Grade Environment- Guide
The floor boards shall
be made of wood,
（ESD）
±6 kV contact ±6 kV contact cement, or ceramic.
Electrostati
discharge discharge
c Discharge
If the floor board is
(ESD)
±8 kV air ±8 kV air laid with synthetic
GB/T
discharge discharge materials, then the
17626.2
relative humidity shall
be less than 30%.
Electric fast The quality of the grid
The power cord The power cord
transient power supply shall be
is ± 2kV is ± 2kV
/pulse train the typical commercial
GB/T electricity or hospital
17626.4 electricity.
Surging ±1kV line to line ±1kV line to line The quality of the grid
power supply shall be
GB/T
the typical commercial
17626.5 ±2kV to ground ±2kV to ground
electricity or hospital
19
 electricity.
The quality of the grid
0.5 cycle <5% Ut 0.5 cycle <5% Ut power supply shall be
voltage (voltage voltage (voltage the typical commercial
Voltage
drop > 95% Ut), drop > 95% Ut), electricity or hospital
waveform
5 cycles 40% Ut 5 cycles 40% Ut electricity. If dental
of voltage
voltage (voltage voltage (voltage electrical motor E1
drop and
drop at 60% Ut), drop at 60% Ut), users still need to
short
25 cycles 70% Ut 25 cycles 70% Ut continue operating the
interruption
voltage (voltage voltage (voltage equipment during grid
and input
drop at 30% Ut), drop at 30% Ut), power interruption, it
power line
<5% Ut voltage <5% Ut voltage is recommended to use
GB/T
(voltage drop > (voltage drop > uninterruptible power
17626.11
95% Ut), 5 95% Ut), 5 supply (UPS) or
seconds seconds battery to supply
power to E1.
It shall be at the same
Power
level as the power
frequency frequency magnetic
(50/60Hz) field at a typical
magnetic 3A/m 3A/m/50Hz location in a typical
field commercial or
GB/T hospital electricity
17626.8 utilization
environment
Note: Ut is the AC grid voltage before the test voltage.

Guidance and manufacturer's statement -- electromagnetic immunity

Dental electrical motor E1 is expected for use in the electromagnetic
environment described below. E1 customers or users shall ensure that their
purchased products are used in this environment.
20
Immunity EC60601 Compliance Electromagnetic Environment -
Testing Test Grade level Guide
Portable and mobile RF
communication devices should not
be used in any part of the
recommended isolation distance
from dental electrical motor,
including cables. The distance
should be calculated by the formula
corresponding to the transmitter
frequency.
Conducted Recommended isolation distance.
RF 3 Vrms d = 1 .2 P
GB/T 150 kHz 3 Vrms d = 1.2 P 80 MHz to 800 MHz
17625.6 to 80 MHz
d = 2.3 P 800 MHz to 2,5 GHz
Among them, P is based on
transmitter manufacturer to provide
the transmitter maximum output
Radiation 3 V/m rated power, to Watt (W) as the
RF 80 MHz to 3 V/m unit, D is the recommended
isolation distance, with m units.
b
GB/T 2,5 GHz
17626.3 The field strength of the fixed RF
transmitter is determined by the
electromagnetic field survey a, and
the B should be lower than the
coincidence level in each frequency
range.
Interference may be in the vicinity
of the following symbols marking
equipment.

21
Note 1 At the frequency points of 80MHz and 800MHz, it is applicable for
higher frequency range.
Note 2 These guidelines do not apply to all situations. The electromagnetic
transmission is affected by the device structure and the absorption/reflection
of objects and the body.
a Theoretically, it is unable to accurately predict the field strength generated
by fixed transmitters such as wireless (mobile phone/cordless) telephone base
stations and land mobile wireless, amateur wireless, AM and FM radio and
television broadcasts. In order to evaluate the electromagnetic environment
under the influence of the fixed RF transmitter, the electromagnetic
environment shall be considered to investigate on-site. If the field strength
measured at the use site of E1 exceeds the RF compliance level used above,
E1 shall comply with the principle of true normal operation. If abnormal
performance is found, other necessary measures shall be taken, such as
adjusting the E1 orientation, or installing the E1 to other fields.
b If it exceeds the frequency range of 150kHz-80MHz, the field strength shall
be less than 3V/m.

Portable and mobile RF communication equipment and recommended

spacing for dental electrical motor E1
Dental electrical motor E1 is expected for use in the RF interference
controlled electromagnetic environment. E1 customers or users shall make the
spacing between the portable and mobile RF communication equipment
(transmitter) and E1 shall be above the following recommended minimum
spacing, so as to avoid electromagnetic interference. The minimum
recommended spacing shall be calculated from the maximum output power of
the communication equipment.
Rated maximum The spacing calculated from the transmitter frequency /m

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 output power of 150kHz to 80MHz to 800MHz to
transmitter (W) 80MHz 800MHz 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
The transmitter rated maximum output power are not listed in the schedule,
the recommended isolation distance D, in meters (m) as a unit, can use the
corresponding transmitter frequency bar formula to determine, where P is the
maximum rated output power provided by the transmitter transmitter
manufacturers, by Watt (W) as a unit.
Note 1 At the frequency points of 80MHz and 800MHz, it is applicable for
higher frequency range.
Note 2 These guidelines do not apply to all situations. The electromagnetic
transmission is affected by the device structure and the absorption/reflection
of objects and the body.

14. Storage and transportation

· Place the device with care to avoid vibration. The installation and
storage environment shall be dry and cool.
· Avoid placing with the poisonous, corrosive, volatile and flammable
and explosive objects.
·Avoid vibration and shock during transport, and place with care.

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厂商：广东精美医疗科技有限公司
地址：佛山市南海区狮山镇罗村朗沙广东新光源产业基地核心区内
A 区 15 座
电话：+86-757-88777997/88777991
Manufacturer:Guangdong JINME Medical Technology Co.,Ltd
Add: A15,Guangdong New light Source Industrial Base,
Luocun ,Langsha, Shishan town, Nanhai District, Foshan, Guangdong,
China
Tel: +86-757-63825987

欧盟代表: 上海国际（欧洲）集团公司
地址：德国汉堡艾佛路 80 号
电话：+49-40-2513175 传真：+49-40-255726
EC representative :Shanghai International Holding Corp. GmbH
(Europe)
Add: Eiffestrasse 80, 20537 Hamburg，Germany
Tel: +49-40-2513175 Fax: +49-40-255726
Dimid No.:DE/0000040627
E-mail:shholding@hotmail.com
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