EDGEENDO EDGEAPEX Endodontic Motor Instruction Manual

EDGEENDO EDGEAPEX Endodontic Motor

Specifications

• Product Name: EDGEAPEX HP Endodontic Motor
• Usage: Cordless endodontic treatment motorized handpiece with root canal measurement capability
• Features: Cordless, portable, with combined length determination
• Rotation: 360 degrees rotation of contra angle
• Technology: Real-time feedback technology and dynamic torque control
• Accessories: Charging base, motor handpiece & contra angle, measuring wire, silicon cover (x2), spray nozzle, o-rings (x2), disposable sleeves (1 pack)

Product Usage Instructions

1. Charging the Device:

Ensure the device is fully charged before use by placing it on the charging base.

2. Assembling the Device:

Connect the motor handpiece and contra angle securely. Ensure all parts are properly fitted together.

3. Setting Up for Usage:

Confirm that the file is properly installed and locked in place within the contra angle before starting the motor handpiece.

4. Operating the Device:

Press the appropriate buttons to activate the motor for preparation and enlargement of root canals or for measuring canal length.

5. Maintenance:

After usage, clean the device with a disinfectant of neutral pH value or ethyl alcohol. Do not autoclave the motor handpiece.

FAQs

Q: Can I use a different power adapter with the device?

A: No, please always use the original power adapter provided with the device to prevent damage to the lithium battery and control circuit.

Q: Can I make modifications to the device?

A: No, any changes made to the device may violate safety regulations and cause harm to the patient. The manufacturer will not be liable for unauthorized modifications.

Please read this manual before operating

Product introduction

1.1 Product description
EDGEAPEX HP is mainly used in Endodontic treatment. It is a cordless endo motor with root canal measurement capability. It can be used as a endo motor for preparation and enlargement of root canals, or device for measuring canal length. It can be used to enlarge the canals while monitoring the position of the file tip inside the canal.
Features:
b
Cordless portable endo motor with combined length determination. c
360 degrees rotation of contra angle. d
Adopt real-time feedback technology and dynamic torque control,
1.2 Model and specification EDGEAPEX HP Endodontic Motor
1.3 Device parts and accessories The device is composed of charging base, motor handpiece & contra
angle. Additional accessories included in the box are: measuring wire,
silicon cover (x2), spray nozzle, o-rings (x2), disposable sleeves (1 pack).
1.4 Indications for Use EDGEAPEX HP Endodontic Motor is cordless endodontic treatment
motorized handpiece with root canal measurement capability. It can be used for preparation and enlargement of root canals, or measuring the canal length. And it can be used to enlarge the canals while monitoring the position of the file tip inside the canal.

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EDGEAPEX HP 2

1.5 Intended Use 1.5.1 The device can be used for preparation and enlargement of root canals, or device for measuring canal length. 1.5.2 The device must be operated only in hospitals and clinics by
1.5.3 CAUTION: Federal (US) law restricts this device to sale by or on the order of a licensed professional. 1.6 Contraindication
a) Doctors with a pacemaker are forbidden to use this device. b) This device may not be used on patients with cardiac pacemakers (or other electrical equipment) or those warned not to use small appliances (such as Electric razors, hair dryers, etc.). c) This device may not be used on hemophilia patients. d) Use with caution in patients with heart disease, pregnant women and young children. 1.7 Warnings 1.7.1 Please carefully read this Instruction Manual before first operation. 1.7.2 This device should be operated by professional and qualified
1.7.3 Do not directly or indirectly place this device near heat source. Operate and store this device in a suitable environment.
1.7.4 This device requires special precautions regarding electromagnetic compatibility (EMC) and must be in strict accordance with the EMC information for installation and use. Do not use this equipment especially in the vicinity of fluorescent lamps, radio transmitting devices, remote control devices, handheld and mobile highfrequency communication devices.
1.7.5 Please use the original contra angle. Otherwise the device will be unusable or cause adverse consequences.
1.7.6 Please do not make any changes to the device. Any changes may violate safety regulations, causing harm to the patient. The manufacturer will not be liable for any device changes made without the manufacturer’s consent.
1.7.7 Please use the original power adapter. Other power adapters will result in damage to the lithium battery and control circuit.
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1.7.8 The motor handpiece cannot be autoclaved. Use disinfectant of neutral pH value or ethyl alcohol to wipe its surface.
1.7.9 Do not press the push cover of contra angle before the contra angle stops rotating. Otherwise the contra angle will be broken.
1.7.10 Do not remove the contra angle before the motor handpiece stops rotating. Otherwise the contra angle and the gear inside motor handpiece will be broken.
1.7.11 Please confirm that the file is properly installed and locked in place before starting the motor handpiece.
1.7.12 Please set torque and speed as per the recommended
1.7.13 Error in replacing lithium batteries can lead to unacceptable risks, so use the original lithium battery and replace the lithium battery according to the correct steps in the instructions.
1.7.14 Please remove the battery if the motor handpiece is not likely to be used for some time.
1.7.15 Wireless charging will generate heat, and the surface temperature of charging base and motor handpiece will rise. It is recommended not to come in contact with the motor handpiece and charging base during wireless charging for more than 10 seconds.
1.8 Device safety classification 1.8.1 Type of operation mode: Continuous operating device 1.8.2 Type of protection against electric shock: Class II equipment with internal power supply 1.8.3 Degree of protection against electric shock: B type applied part 1.8.4 Degree of protection against harmful ingress of water: Ordinary equipment (IPX0) 1.8.5 Degree of safety application in the presence of a flammable anesthetic mixture with air, oxygen, or nitrous oxide: Equipment cannot be used in the presence of a flammable anesthetic mixture with air, oxygen, or nitrous oxide. 1.8.6 Applied part: contra angle, lip hook,file clip,touch probe. 1.8.7 The contact duration of applied part: 1 to 10 minutes. 1.8.8 The temperature of the surface of applied part may reach 46.6. 1.9 Primary technical specifications 1.9.1 Battery Lithium battery in motor handpiece: 3.7V /2000mAh
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1.9.2 Power adapter (Model: ADS-6AM-06N 05050/ UE08WCP-050100SPA)
Input: ~100V-240V 50Hz60Hz, 0.4A Max Output: 5V 1A 1.9.3 Torque range: 0.4Ncm-5.0Ncmc4mNm ~ 50mNm 1.9.4 Speed range: 100rpm~2500rpm 1.9.5 Wireless charging Frequency range: 112-205KHz Maximum RF output power of the product: 9.46dBuA/m@3m 1.10 Environment parameters 1.10.1 Environment temperature: +5 ~ +40 1.10.2 Relative humidity: 30% ~ 75% 1.10.3 Atmospheric pressure: 70kPa ~ 106kPa

Installation

2.1 Basic accessories of product

Motor handpiece

Contra angle

Charging base

Nozzle

Protective silicon cover 5

Power adapter

Measuring wire

File clip

Lip hook

Touch probe

Disposable insulation sleeves 2.2 Display Screens
2.2.1 Display Screens for 5 Operation Modes and Standby 2.2.1.1 EAL Mode This mode is for canal measurement. The motor handpiece does not run in this mode

2.2.1.2 CW Mode The motor handpiece rotates forward 360º, clockwise direction.

2.2.1.3 CCW Mode The motor handpiece rotates counterclockwise direction only. This mode is used to inject calcium hydroxide and other medicant. When this mode is being used, a double-beep sounds continuously.

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2.2.1.4 SGP Mode Safety Glide Path Mode F: Forward angle, R: Reverse angle
The rotation angle is adjustable, but the forward angle must be equal to the reverse angle.
2.2.1.5 ATR Mode ATR: Adaptive Torque Reverse function.
Normal continuous forward rotation, when the load of the file is greater than the set torque limit, the file will start to rotate forward & reverse alternately at the set angle.
2.2.2 Torque Display This appears when the motor is running. Meter shows the torque load
Set speed
Set torque Real time torque
2.2.3 Canal Measurement Display This appears when a file is inside the canal and the lip hook is in contact with the patient mouth. Bars in meter show the location of the be enlarged.
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The meter numbers 1.0, 2.0, 3.0 and digital numbers 00-16 do not represent the actual length from the apical foramen. It simply indicates the file progression towards the apex. The digital numbers -1 and -2
indicate that the file has reached the apex foramen. Subtract 0.5-1mm
used to estimate the canal’s working length. 2.3 Instructions for contra angle
2.3.1 The contra angle adopts precision gear transmission, and the transmission ratio is 6:1.
2.3.2 Before the first use and after treatments, please clean and disinfect contra angle with disinfectant of neutral PH value. After disinfection, lubricate it with specific cleaning oil. Finally, sterilize it under high temperature and high pressure (134, 2.0bar~2.3bar (0.20MPa~0.23MPa)).
2.3.3 The contra angle can only be used together with this device. Otherwise the contra angle will be damaged. 2.4 Installation and removal of contra angle.
2.4.1 Installation Align any locating pin of the contra-angle with the positioning slot on the motor handpiece and push the contra-angle horizontally. The three locating pins on the contra-angle are inserted into the three positioning holes on the motor handpiece. A “click” sound indicates that the installation is in place. The contra-angle can be rotated 360° freely.
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positioning slot locating pin
The contra-angle is free to rotate, adapting to the root canal of different positions, and it is convenient to watch the screen when operating.
2.4.2 Removal Pull out the contra angle horizontally when the motor handpiece has stopped running.
Warnings: the motor handpiece. has been properly installed.
head. Hold down the push button on the contra angle and insert the file. 9

and slips into place. Release the button to lock the file into the contra angle.
Warnings:
huck of contra angle.
Please use files with shanks that meet the ISO standard. (ISO standard: Ø2.334 ­ 2.350 mm)
Warnings: stopped.
Removing files without holding the push button will damage the chuck of contra angle.
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2.6 Canal measurement functional connection This is not required if the canal measurement function will not be
used. Connect the measuring wire to the motor handpiece. Line up the
measuring wire plug with the notch on the back of the motor and push it all the way in.
Connect the file clip plug into the socket (black) on the measuring wire. Connect the lip hook to the socket (white) on the measuring wire.
File clip
Black
White
Lip hook
Warnings: Connect the lip hook to the socket (white) on the measuring wire. Otherwise, the function of root canal preparation and root canal length measurement cannot be used together.
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2.7 Installation and removal of disposable isolation sleeves 2.7.1 Installation Before each use of the handpiece and after the handpiece is cleaned
and disinfected,put on a disposable isolation sleeve. Take the isolation sleeve out of the isolation sleeve box, then insert the isolation sleeve into the motor handpiece from the thin end of the handpiece, and install the isolation sleeve until there is no obvious wrinkle.
around the handpiece surface. After that, clean and disinfect the surface of the handpiece. Refer to Chapter 6.3 for cleaning and disinfection procedures.
2.7.2 Removing
sleeve from the thin end of the handpiece. Warning: Isolation sleeves are not reusable
3 Function and operation of product
a. Turn power on Press Main button to turn on motor handpiece.
motor handpiece. c. Customized program change Press Adjusting button “+”/”-” during standby sate. d. Parameter setting Press Setting button “P” to cycle through parameters, press Adjusting
button “+”/”-” to change them, then press Main button or wait 5 seconds
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e. Preset program selection Long press Setting button “P” to enter preset program during standby
button “P” to entry enter file number selection, press Adjusting button
f. Handpiece functions setting
and press Main button to enter handpiece functions setting, press Setting button “P” to cycle through settings, press Adjusting button “+”/”-” to

3.2 Screen display

Standby interface a. Customized program sequence number 0-9, in total 10 programs. b. Battery consumption c. Set speed d. Set torque e. Operation mode
Working interface a. Set speed b. Set torque c. Real time torque d. Torque display scale

Canal measurement mode interface b. EAL: Electronic apex locator

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Canal measurement state interface a. Canal length indicator bar b. Indication number Digital numbers 00-16 do not represent the actual length from the apical foramen. It simply indicates
apex. Number “00” indicates that
foramen. c. Apical foramen. Apical reference point setting interface
b. Apical foramen c. Digital “02” meter reading, very near physiological apical foramen.

CW
CCW SGP
ATR
Forward Angle Reverse Angle
EAL AP Apical Action

Clockwise rotation, forward ration
Counter clockwise rotation, reverse rotation
hydroxide and other solutions Safety Glide Path Mode Adaptive torque reverse ATR mode starts reciprocating motion when the set torque is reached; when torque reduces to normal value, the motor will rotate clockwise.
Electronic apex locator In this mode, the device will work like a standalone apex locator. Apical foramen.
point.

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Flash Bar Position apical action is triggered.

Auto Start

is inserted in the canal.

Auto Stop

is taken out of the canal.

Apical Slow Down approaches the apex. Activated in CW and CCW

operation mode when selected.

5 operation modes for canal shaping and

Operation Mode measurement.

Such as CW, CCW, SGP, ATR and EAL.

Speed

File rotation speed.

Torque (Torque Limit / Trigger Torque)

For CW and CCW modes, the torque value (Torque Limit) that triggers reverse rotation. For ATR mode, the torque value (Trigger Torque) that triggers ATR action.

Operation instruction

4.1.1 Starting and stopping of motor handpiece
and then the motor handpiece will enter Standby interface. The interface displays is as follows:

Standby interface b) Under Standby interface, press Main button, and then the motor handpiece will enter Working interface. The interface displays is as follows:

Working interface 15

c) Press the Main button again, and then the motor handpiece returns to Standby interface.
d) Hold down the Setting button “P”, then press Main button to turn
automatically shut down after 3 minutes without any button-pressing operation. The motor handpiece will also automatically shut down when put on charge. 4.2 Selecting customized program sequence number
The motor handpiece has 10 memory programs(M0-M9) and 5 preset programs, press Adjusting button “+”/”-” to change customized program sequence number during standby state.
M0-M9 is a memory program for canal shaping and measurement, every memory program has its own parameters such as Operation mode, speed and torque, all these parameters can be changed. 4.3 Parameter setting
Before starting of motor handpiece, please check the operation mode is correct.
make sure all the parameters are correct before starting of motor handpiece, otherwise there is
It has 5 operation modes for canal shaping and measurement: CW, CCW, SGP, ATR and
the explanations of these modes.) Press Setting button “P” once during standby state, press Adjusting button “+”/”-” to select correct Operation mode. CCW mode is used to inject calcium hydroxide and other medicant. When this mode is being used, a double-beep sounds continuously, used for indicating counter clockwise rotation happening. Repeatedly press Setting button “P” to check that all the next level parameters of this operation mode are correct, press Adjusting button “+”/”-” to make changes if not.
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The speed setting can be adjusted from 100 rpm to 2500 rpm. Press Adjusting button “+”/”-” to increase or decrease speed. Long press to fast increase or fast decrease speed. In ATR mode, speeds of 100~500rpm are available. In SGP mode, speeds of 100~500rpm are available. The torque setting can be adjusted from 0.4Ncm to 5.0Ncm. Press Adjusting button “+”/”-” to increase or decrease torque. Long press to fast increase or fast decrease torque. In ATR mode, Trigger Torques of 0.4Ncm~ 4.0Ncm are available. In SGP mode, torques of 2.0Ncm~5.0Ncm are available.
tip reaches the point inside the canal determined by the Flash Bar setting.
the reference point, the motor will response according to setting. It can be Reverse , Stop and OFF. P ress Adjusting button “+”/”-” to change.
as usual even if it reaches the reference point. Stop: automatic rotation stop when reference
will rotate again. Reverse: automatically reverses rotation when
pull upward a little bit, the rotation direction will change back again.
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inserted into the canal and the canal length indicator bar lights up more than 2 bars. P ress Adjusting button “+”/”-” to change.
into the canal. The Main button is used to start and stop the motor handpiece. ON: Motor starts automatically.
taken out of the canal and the canal length indicator bar lights up less than 2 bars before the
Press Adjusting button “+”/”-” to change.
of the canal. The Main button is used to start and stop the motor handpiece. ON: Motor stops automatically. This is the reference point where various apical actions are triggered. Press Adjusting button “+”/”-” to select
tip is located very near the physiological apical foramen.
to AP (Apex) on the meter.
tip approaches the reference point. P ress Adjusting button “+”/”-” to change. OFF: Disable Apical Slow Down function. ON: Rotation automatically slows down as the

Forward Angle .In the SGP mode, the Forward Angles of 20°~400° are available. In the ATR mode, the Forward Angle of 60°~400° are available.
Reverse Angle .In the SGP mode, the Reverse Angles of 20°~400° are available. In ATR mode, the reverse Angle cannot be greater than the forward Angle.
4.4 Preset program selection
system. Press Adjusting button “+”/”-” to switch to preset program(M0-M9, preset program 1-5 ), the interface will show as left. Long press Setting button “P” to enter preset program during standby state, the interface will show as left.
system.

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The parameters of the presets can also be If you want to change back to default setting, long press Setting button “P” to enter preset program during standby state, select a preset setting will be reloaded. The preset program can the motor handpiece and powering back on. Changing the preset program default setting is breakage. 4.5 Handpiece functions setting and press Main button to enter handpiece function settings, press Setting button “P” to cycle through settings, press Adjusting button “+”/”-” to
the Setting button “P” and press Main button to enter handpiece function settings, the software version number will appear on the display screen. After 3 seconds of displaying the version number on the screen, the “Auto Power OFF” can be changed, press Adjusting button “+”/”” to adjust, then press the “Main” button to
handpiece if no buttons are pressed. It can be set from 3 to 30 minutes in 1 minute increments.
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Press Setting button “P” again, the “Auto Standby Scr” can be changed, press Adjusting button “+”/”-” to adjust, then press to “Main”
This is the automatic return to standby display of motor handpiece when no buttons are pressed. It can be set from 3 to 30 seconds in 1 second increments. Press Setting button “P” again, the “Dominant Hand” can be changed, press Adjusting button “+”/”-” to adjust, then press to “Main” button to
set. Press Setting button “P”again, the “Calibration” can be changed, press Adjusting button “+”/”-” to select “ON”, then press “Main” button for calibration. Before calibrating, make sure the original contra angle is installed, and do not
it is calibrated without original contra angle or if there is any load on contra angle chuck, and
After replacement of contra angle, the contra angle should be calibrated before use. Press Setting button “P”again, the “Beeper Volume” can be changed ,press Adjusting button “+”/”-” to adjust, then press to “Main” button to
The”Beeper Volume”can be set from 0-3. Vol.0: Mute. Press Setting button “P” again, the “Restore Defaults” can be changed, press Adjusting button “+”/”-” to select “ON”, then press to “Main” button to restore defaults. 4.6 Protective function of automatic reverse During operation, if the load value exceeds the preset torque value,
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preset torque value again.

Load value is lower than preset torque value
Clockwise rotation

Load value is higher than preset torque value
Couterclockwise rotation

Load value is lower than preset torque value again
Clockwise rotation

Cautions: 1. Protective function of automatic reverse is ONLY suitable for CW mode. 2. This function is not available for CCW mode, ATR mode. 3. When the motor handpiece battery indicator indicates a low battery
to reach the torque value limit, therefore, the auto-reverse function will not work properly. Please charge it in time.
4. If the motor handpiece is under load all the time, the machine may stop automatically as a result of overheat protection. If it happens, turn
4.7 Motor operation Please set operation mode, torque and speed as per the recommended
Motor alone mode When using in motor alone mode, the torque bar will show on the screen. (more information about torque bar, please see chapter 3.2 Screen display )

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Motor combined with canal measurement function mode When using motor combined with canal measurement function, the measuring wire must be connected with motor handpiece by USB socket, and white socket connects with patient’s lip by lip hook, keep the black socket idle. The canal length indicator bar will show on the screen (more information about canal length indicator bar, please see chapter 3.2 Screen display) Set parameters of automatic functions as needed, such as Apical Action, Auto Start, etc(more information about automatic functions, please see chapter 4.3 Parameter setting). Connection testing It is strongly recommended to check the connection testing every time before use. Touch
contra angle and check that all the bars on the meter on the screen light up, and the motor should be reversed continuously, otherwise, the measuring wire or contra angle should be replaced.
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4.8 Canal measurement operation When using in standalone apex locator mode, we suggest putting the motor handpiece on the charging base to get better visual angle. Press Setting button “P” once during standby state, press Adjusting button “+”/”-” to select EAL Operation mode,
the explanations of Operation modes.) The measuring wire must be connected with motor handpiece by USB socket, white socket connects with patient’s lip by lip hook, and black socket connect The canal length indicator bar will show on the screen(more information about canal length indicator bar, please see chapter 3. 2 Screen display).
your thumb in the direction shown by the arrow. Clip the holder onto the metal the button.
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Connection testing It is strongly recommended to test the connection every time before use. Clip the holder onto lip hook and check that all the bars on the meter on the screen light up, otherwise, the measuring wire
Root canals not suitable for canal measurement Accurate measurement cannot be obtained for the root canal conditions shown below.
Root canal with a large apical foramen. Root canal that has an exceptionally large apical foramen due to a lesion or incomplete development cannot be accurately measured. The results may show shorter measurement than the actual length.
the opening.
of the root canal and contacts the gums, this will result in electrical leakage and an accurate measurement cannot be obtained. Wait for bleeding to stop completely. Clean the inside and opening of the canal throughly to get rid of all blood, and then make a measurement. Root canal with a chemical solution
An accurate measurement cannot be obtained if some chemical solution is
In this case, clean the canal and its opening. It is important to get rid of any solution
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Broken crown. If the crown is broken and a section of the gingival tissue intrudes into the cavity surrounding the canal opening, contact between the gingival tissue and
and an accurate measurement cannot be obtained. In this case, build up the tooth with a suitable material to insulate the gingival tissue. Fractured tooth. Leakage through a branch canal Fractured tooth will cause electrical leakage and an accurate measurement cannot be obtained. A branch canal will also cause electrical leakage.
percha. The gutta-percha must be completely removed to eliminate its insulating
the apical foramen and then put a little saline in the canal, but do not let it
Crown or metal prosthesis touching gingival tissue. Accurate measurement cannot be
prosthesis that is touching gingival tissue. In this case, widen the opening at
not touch the metal prosthesis before taking a measurement.
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Extremely dry canal. If the canal is extremely dry, the meter may not move until it is quite close to the apex. In this case, try moistening the canal with saline.
radiography. Sometimes the reading of apex locator and the X-ray image will not correspond. This does not mean that the apex locator is not working properly or that the X-ray exposure is a failure. An X-ray image might not show the apex correctly depending on the angle of the X-ray beam, and the location of the apex might seem to be other than it really is.
The actual apex for the canal is not the same as that for the anatomical apex. There are frequently cases where the apical foramen is located up towards the crown. In these cases, an X-ray might
apex even though it has actually reached the apical foramen.
4.9 Battery Charging The motor handpiece has built-in rechargeable lithium battery. When charging the battery, leave approximately 10cm around the
charging base for easy access to inlet and the power cord. Insert the power adapter plug into the charging base power socket
and confirm that they are correctly connected. Then insert the motor handpiece into the charging base (the motor handpiece needs to be correctly aligned with the charging base in the same direction for charging). When the blue indicator on the charging base flashes, it is charging. When the motor handpiece is fully charged, the blue indicator on the charging base is always on.
After charging, please unplug the power adapter. 4.10 Replacing Battery
Replace the battery if it seems to be running out of power sooner than it should. Please use the original lithium battery.
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b) Use tweezers etc. to open the rubber cover and then remove the screw.
c) Remove the battery cover. d) Remove the old battery and disconnect the connector. e) Connect the new battery and put it in the motor handpiece. f) Replace the cover and its screw. It is recommended to contact local distributors or manufacturer to replace the battery. 4.11 Oiling of contra angle Only the original oil injection nozzle can be used for oiling of contra angle. The contra angle needs to be lubricated after cleaning and disinfection, but before sterilization. 1. Firstly, screw the injecting nozzle into jet of oil bottle. (Around 1 to 3 circles) 2. Next, plug the nozzle into the end part of contra angle, and then
part. 3. Place the contra-angle upright for 30 minutes for leftover oil to
Warnings
Cautions
safely hold the contra angle while lubricating. b: Please use the appropriate nozzle suitable for handpiece
lubrication.
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Troubleshooting

Failure

Possible cause

Solutions

The motor handpiece Motor is on EAL mode, Change to CW, CCW,

does not rotate.

EAL mode is only for SGP or ATR mode.

canal measurement.

There is continuous The continuous beep Stop the motor

beep sounds after

sound is indicating that handpiece and change

starting the motor

the motor handpiece is the operating mode to

handpiece.

under CCW mode. CW Mode.

Contra angle

Calibration failure Clean the contra angle,

calibration failure

caused by strong

and recalibrate after oil

resistance of contra injection.

angle

The time of endurance Battery capacity

Please contact

becomes shorter after becomes smaller.

local distributor or

charging.

manufacturer.

No sound

Beeper Volume set to 0. Set Beeper Volume to

Vol.0: Mute.

1,2,3.

The continuously

Choose CCW Mode,

setting.

start the motor

the root canal.

Too high load torque of handpiece, and take the

Cleaning, Disinfection and Sterilization

6.1 Foreword

For hygiene and sanitary safety purposes, the contra-angle, the lip
be cleaned, disinfected and sterilized before each usage to prevent any
6.2 General recommendations 6.2.1 Use only a disinfecting solution which is approved for its
efficacy (VAH/DGHM-listing, CE marking, FDA and Health Canada approval) and in accordance with the DFU of the disinfecting solution manufacturer.
6.2.2 Do not place the contra-angle in a disinfectant solution or in an ultrasonic bath.
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Do not use chloride detergent materials. 6.2.3 Do not use bleach or chloride disinfectant materials. 6.2.4 For your own safety, please wear personal protective equipment (gloves, glasses, mask). 6.2.5 The user is responsible for the sterility of the product for the
dirty instruments where applicable after sterility. 6.2.6 The water quality has to be convenient to the local regulations
especially for the last rinsing step or when using a washer-disinfector. 6.2.7 To sterilize the endodontic files, refer to the manufacturer’s
instructions for use. 6.2.8 The contra-angle needs to be lubricated after cleaning and
disinfection, but before sterilization. 6.3 Cleaning and disinfection steps for the motor handpiece, the AC adapter and the base.
Before and after each use, all the objects that were in contact with infectious agents should be cleaned using towels impregnated with a disinfecting and detergent solution (a bactericidal, fungicidal and aldehyde free solution) approved by VAH/DGHM-listing, CE marking, FDA and Health Canada.
Warning: Do not sterilize the motor handpiece, the AC adapter
and the base. 6.3.1 Pre-Op processing Before each use, the handpiece, charger, and base must be cleaned
Warning: The handpiece, charger, and base cannot be
cleaned and disinfected with automatic equipment. Manual cleaning and disinfection is required.
6.3.1.1 Manual cleaning steps: 1. Take out the handpiece, charger, and base on the workbench. 2. Wet the soft cloth completely with distilled water or deionized water, and then wipe all the surfaces of the components such as the handpiece, charger, base, etc. until the surface of the component is not stained. 3. Wipe the surface of the component with a dry soft nap-free cloth. 4. Repeat the above steps at least 3 times. Note:
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a)Use distilled water or deionized water for cleaning at room temperature.
6.3.1.2 Manual disinfection steps: 1. Soak the dry soft cloth with 75% alcohol. 2. Wipe all surfaces of headpiece, charger, base and other components with a wet soft cloth for at least 3 minutes. 3. Wipe the surface of the component with a dry soft nap-free cloth. Note: a) The cleaning and disinfection must be performed within 10min before use. b) The disinfectant used must be used immediately, no foaming is allowed. c) In addition to 75% alcohol, you can use non-residue disinfectants such as Cavicide, but you must respect the concentration, temperature and time specified by the disinfectant manufacturer. d) After cleaning and disinfecting the handpiece, you must install a disposable isolation sleeve before use. 6.3.2 Post-Op processing After each use, clean and disinfect the handpiece, charger, and base
Tools: Nap-free soft cloth, tray 1. Remove the contra-angle from the handpiece, place it in a clean tray, and then remove the disposable isolation sleeve from the handpiece. 2. Soak the nap-free soft cloth with distilled water or deionized water, and then wipe all the surfaces of the components such as the handpiece, charger, base, etc. until the surface of the component is not stained. 3. Wet the dry soft cloth with 75% alcohol, and then wipe all surfaces of the handpiece, charger, base and other components for 3 minutes. 4. Put the handpiece, charger, base and other components back into the clean storage area. Note: a) The cleaning and disinfection must be performed within 10min before use. b) The disinfectant used must be used immediately, no foaming is allowed. c) In addition to 75% alcohol, you can use non-residue disinfectants such as Cavicide, but you must respect the concentration,temperature and time specified by the disinfectant manufacturer.
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6.4 The cleaning, disinfection and sterilization of contra-angle,lip
Unless otherwise stated, they will be hereinafter referred to as “products”.
Warnings: The use of strong detergent and disinfectant (alkaline pH>9 or acid pH <5) will reduce the life span of products. And in such cases, the manufacturer takes no responsibility. The products may not be exposed to temperature above 138. Processing limit The products have been designed for a large number of sterilization cycles. The materials used in manufacture were selected accordingly. However with every renewed preparation for use, thermal and chemical stresses will result in ageing of the products. The maximum number of sterilizations for products is 250 times. 6.4.1 Initial processing 6.4.1.1 Processing principles It is only possible to carry out effective sterilization after the
part of your responsibility for the sterility of products during use, only sufficiently validated equipment and product-specific procedures are used for cleaning/disinfection and sterilization, and that the validated parameters are adhered to during every cycle.
Please also observe the applicable legal requirements in your country as well as the hygiene regulations of the hospital or clinic, especially with regard to the additional requirements for the inactivation of prions.
6.4.1.2Post-operative treatment The post-operative treatment must be carried out immediately, no later than 30 minutes after the completion of the operation. The steps are as follows: 1. Remove the products from the base, and rinse away the dirt on the surface of handpiece with pure water (or distilled water/deionized water); 2. Dry the products with a clean, soft cloth and place it in a clean tray. Notes: a) The water used here must be pure water, distilled water or deionized water. 6.4.2 Preparation before cleaning Steps:
32

Tools: tray, soft brush, clean and dry soft cloth.
wire from the handpiece in sequence, and then put them into a clean tray; 3. Use a clean soft brush to carefully brush lip hook, file
clip,protective silicon cover,touch probe, head and back cover of the contra- angle until the dirt on surface is not visible. Then use soft cloth to dry the products and put them into a clean tray. The cleaning agent can be pure water, distilled water or deionized water.
Disassembling steps
b) When removing the protective silicon cover, pull it straight out slowly.
c) When inserting and removing the contra-angle, turn thehandpiece 6.4.3 Cleaning The cleaning should be performed no later than 24 hours after the operation. The cleaning can be divided into automated cleaning and manual cleaning. Automated cleaning is preferred if conditions permit. 6.4.3.1Automated cleaning · The cleaning device is proved to be valid by CE certification in accordance with EN ISO 15883. of the product.
33

· The cleaning procedure is suitable for the product, and the irrigating
It is recommended to use a washer-disinfector in accordance with
disinfection section in the next section “Disinfection”. Notes: a) The cleaning agent does not have to be pure water.It can be
distilled water, deionized water or multi-enzyme. But please ensure that the selected cleaning agent is compatible with the product.
b) In washing stage, the water temperature should not exceed 45 °C,
c) After cleaning, the chemical residue should be less than 10mg / L. 6.4.4 Disinfection Disinfection must be performed no later than 2 hours after the cleaning phase. Automated disinfection is preferred if conditions permit. 6.4.4.1Automated disinfection-Washer-disinfector
accordance with EN ISO 15883. ·Use high temperature disinfection function. The temperature does
not exceed 134 ° C, and the disinfection under the temperature cannot exceed 20 minutes.
·The disinfection cycle is in accordance with the disinfection cycle in EN ISO 15883.
Cleaning and disinfecting steps by using Washer-disinfector 1. Carefully place the product into the disinfection basket. Fixation of product is needed only when the product is able to move in the device. The products are not allowed to contact each other. 2. Use a suitable rinsing adaptor, and connect the internal water lines to the rinsing connection of the washer-disinfector. 3. Start the program.
disinfector, inspect (refer to section “Inspection and Maintenance”) and package (refer to chapter “Packaging”). Dry the product repeatedly if necessary (refer to section “Drying”).
Notes: a) Before use, you must carefully read the operating instructions provided by the equipment manufacturer to familiarize yourself with the disinfection process and precautions. b) With this equipment, cleaning, disinfection and drying will be
34

carried out together. c) Cleaning: (c1) The cleaning procedure should be suitable for the
product to be treated. The flushing period should be sufficient (5-10 minutes). Pre-wash for 3 minutes, wash for another 5 minutes, and rinse it for twice with each rinse lasting for 1 minute. (c2) In the washing stage, the water temperature should not exceed 45 °C, otherwise the
can be pure water, distilled water, deionized water or multi-enzyme solution, etc., and only freshly prepared solutions can be used. (c4) During the use of cleaner, the concentration and time provided by manufacturer shall be obeyed. The used cleaner is neodisher MediZym (Dr. Weigert).
d) Disinfection: For disinfection, the temperature is 93 ° C, the time is 5 min, and A0>3000 e) Only distilled or deionized water with a small amount of microorganisms (<10 cfu/ml) can be used for all rinsing steps. (For example, pure water that is in accordance with the European Pharmacopoeia or the United States Pharmacopoeia). f) After cleaning, the chemical residue should be less than 10mg / L.
h) Regularly repair and inspect the disinfector. 6.4.5 Drying If your cleaning and disinfection process does not have an automatic drying function, dry it after cleaning and disinfection. Methods:
product against the white paper (white cloth), and then dry the product with filtered dry compressed air (maximum pressure 3 bar). When no further liquid is sprayed onto the white paper (white cloth), the product drying is completed.
2. It can also be dried directly in a medical drying cabinet (or oven). The recommended drying temperature is 80~120 and the time should be 15~40 minutes.
Notes: a) The drying of product must be performed in a clean place. b) The drying temperature should not exceed 138 °C; c) The equipment used should be inspected and maintained regularly.
35

6.4.6 Inspection and maintenance 6.4.6.1 Inspection In this chapter, we only check the appearance of the product. 1. Check the product. If there is still visible stain on the product after cleaning/disinfection, the entire cleaning/disinfection process must be repeated. 2. Check the product. If it is obviously damaged, smashed, detached, corroded or bent, it must be scrapped and not allowed to continue to be used. 3. Check the product. If the accessories are found to be damaged, please replace them before use. And the new accessories for replacement must be cleaned, disinfected and dried. 4. If the service time (number of times) of the product reaches the
6.4.6.2 Maintenance Sterilizable Oil lubrication shall be applied to dried contra angle. The nozzle of cleaning lubricant is to be aligned with the air intake hole at the end of the contra angle to inject oil for 1-2 seconds.
6.4.7 Packaging Install the disinfected and dried product and quickly package it in a medical sterilization bag (FDA cleared wrap or pouch). Notes: a) The package used conforms to ISO 11607; b) It can withstand high temperature of 138 °C and has sufficient steam permeability; c) The packaging environment and related tools must be cleaned regularly to ensure cleanliness and prevent the introduction of contaminants;
6.4.8 Sterilization Use only the following steam sterilization procedures (fractional prevacuum procedure*) for sterilization, and other sterilization procedures are prohibited:
36

to EN 285 to comply with EN ISO 17665 or is cleared by FDA;

The validated sterilization cycle is one (1) fraction cycle, three (3)

consecutive half cycle and one (1) full cycle. The parameters are provid-

ed in the table below.

Mode Vacuum Temperature Cycle Exposure Time Drying Time

Fraction 30 seconds 20 minutes

Half 1

2 minutes

20 minutes

PreVac – 80 kPa (132-134) °C Half 2

2 minutes

20 minutes

Half 3

2 minutes

20 minutes

Full

4 minutes

20 minutes

. Notes:

are allowed to be sterilized; b) Before using the sterilizer for sterilization, read the Instruction
Manual provided by the equipment manufacturer and follow the instructions.
c) Do not use hot air sterilization and radiation sterilization as this may result in damage to the product;
d) Please use the recommended sterilization procedures for sterilization. It is not recommended to sterilize with other sterilization procedures such as ethylene oxide, formaldehyde and low temperature plasma sterilization. The manufacturer assumes no responsibility for the procedures that have not been recommended. If you use the sterilization procedures that have not been recommended, please adhere to related

• Fractional pre-vacuum procedure = steam sterilization with repetitive pre-vacuum.The procedure used here is to perform steam sterilization through three pre-vacuums.
  6.4.9 Storage 1.Store in a clean, dry, ventilated, non-corrosive atmosphere with a relative humidity of 10% to 93%, an atmospheric pressure of 70KPa to 106KPa, and a temperature of -20 °C to +55 °C; 2. After sterilization,the product should be packaged in a medical sterilization bag or a clean sealing container, and stored in a special storage cabinet. The storage time should not exceed 7 days. If it is exceeded, it should be reprocessed before use.
  37

Notes: a) The storage environment should be clean and must be disinfected regularly; b) Product storage must be batched and marked and recorded. 6.4.10 Transportation 1. Prevent excessive shock and vibration during transportation, and handle with care; 2. It should not be mixed with dangerous goods during transportation. 3. Avoid exposure to sun or rain or snow during transportation.

Storage, maintenance and transportation

7.1 Storage 7.1.1 This equipment should be stored in a room where the relative
humidity is 10% ~ 93%, atmospheric pressure is 70kPa to106kPa, and the temperature is -20°C ~ +55°C.
7.1.2 Avoid the storage in a too hot condition. High temperature will shorten the life of electronic components, damage battery, reshape or melt some plastic.
7.1.3 Avoid the storage in a too cold condition. Otherwise, when the temperature of the equipment increases to a normal level, there will be dew that will possibly damage PCB board. 7.2 Maintenance
7.2.1 This device does not include tools for repair, the repair should be carried out by authorized person or authorized after-service center.
7.2.2 Keep the equipment in a dry storage condition. 7.2.3 Do not throw, beat or shock the equipment. 7.2.4 Do not smear the equipment with pigments. 7.2.5 Calibration is recommended when using a new/other contra angle or after an extend period of operation, as the running properties can change with usage, cleaning and sterilization. 7.2.6 Replace the battery if it seems to be running out of power sooner than it should.
7.3 Transportation 7.3.1 Excessive impact and shake should be prevented in
transportation. Lay it carefully and lightly and don’t invert it. 7.3.2 Don’t put it together with dangerous goods during
transportation.
38

7.3.3 Keep out of direct sunlight and avoid getting wet in rain and snow during transportation.
8 Environmental protection
Please dispose according to the local laws.

After service

These products are designed for use in a dental office and this warranty is not applicable to other uses. The products are warranted against manufacturing defects in materials and workmanship for the following periods: Base, motor handpiece, power adapter: 2 years Contra-angle: one year Other spare parts: 6 months
Edge Endo will repair or replace products at its sole discretion. This warranty shall be limited to replacement or repair of the products or their parts and shall not extend to any other claims, including but not limited to loss of profit, cost of removal or replacement, incidental or consequential damages or other similar claims arising from use of this product. Damage to products resulting from acts of God, faulty installation, misuse, tampering, accident, abuse, negligence, alterations, unauthorized repairs or problems unrelated to materials and workmanship are not covered by this warranty.

10 Symbol instruction
Follow Instructions for Use

Serial number

Date of manufacture

Manufacturer

Type B applied part

Classequipment

Ordinary equipment

Recyclable

Used indoor only 39

Keep dry

Handle with care
Humidity limitation Atmospheric pressure for storage Made in China Distributor Unique device
Do not reuse

Appliance compliance WEEE directive Temperature limitation Sterilise at temperature
EU Importer Keep out of direct sunlight Medical Device
Warning

11 Statement
All rights of modifying the product are reserved to the manufacturer without further notice. The pictures are only for reference.
12 EMC-Declaration of conformity
The device has been tested and homologated in accordance with EN 60601-1-2 for EMC. This does not guarantee in any way that this device will not be effected by electromagnetic interference Avoid using the device in high electromagnetic environment.

40

Technical Description

Concerning Electromagnetic Emission
Table 1: Declaration – electromagnetic emissions
Guidance and manufacturer’s declaration – electromagnetic emissions
The model EDGEAPEX HP is intended for use in the electromagnetic environment specified below. The customer or the user of the model EDGEAPEX HP should assure that it is used in such an environment.

Emissions test
RF emissions CISPR 11
RF emissions CISPR11 Harmonic emissions lEC 61000-3-2
emissions lEC 61000-3-3

Compliance Group 1
Class B Class A Complies

Electromagnetic environment – guidance
The model EDGEAPEX HP energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.
The model EDGEAPEX HP is suitable for used in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.

Technical Description Concerning Electromagnetic Immunity
Table 2: Guidance & Declaration – electromagnetic immunity
Guidance & Declaration — electromagnetic immunity The model EDGEAPEX HP is intended for use in the electromagnetic environment specified below. The customer or the user of the model EDGEAPEX HP should assure that it is used in such an environment.

Immunity test

IEC 60601 test level

Electrostatic discharge ±8kV contact

(ESD)

±2, ±4, ±8, ±15kV

lEC 61000-4-2

air

Electrical fast transient/burst IEC 61000-4-4
Surge lEC 61000-4-5

±2kV for power supply lines ±1kV for Input/ output lines
±0.5, ±1kV line to line ±0.5, ±1, ±2kV line to earth

Compliance level

Electromagnetic environment guidance

±8kV contact ±2, ±4, ±8, ±15kV air

Floors should be wood, concrete
covered with synthetic material, the relative humidity should be at least 30 %.

±2kV for power supply Mains power quality should be

lines

that of a typical commercial or

hospital environment.

±0.5, ±1kV line to line Mains power quality should be

±0.5, ±1, ±2kV line to that of a typical commercial or

earth

hospital environment.

41

Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11

<5 % UT (>95% dip in UT.) for 0.5 cycle <5 % UT (>95% dip in UT.) for 1 cycle 70% UT (30% dip in UT) for 25 cycles <5% UT (>95 % dip in UT) for 250 cycles

<5 % UT (>95% dip in UT.) for 0.5 cycle <5 % UT (>95% dip in UT.) for 1 cycle 70% UT (30% dip in UT) for 25 cycles <5% UT (>95 % dip in UT) for 250 cycles

Mains power quality should be that of a typical commercial or hospital environment. If the user of the models EEDGEAPEX HP requires continued operation during power mains interruptions, it is recommended that the models EDGEAPEX HP be powered from an uninterruptible power supply or a battery.

Power frequency (50/60 Hz)
lEC 61000-4-8

30A/m

30A/m

should be at levels characteristic of a typical location in a typical commercial or hospital environment.

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

Table 3: Guidance & Declaration – electromagnetic immunity concerning

Conducted RF & Radiated RF

Guidance & Declaration – Electromagnetic immunity

The model EDGEAPEX HP is intended for use in the electromagnetic environment specified below.The customer or the user of the model EDGEAPEX HP should assure that it is used in such an environment.

Immunity test

IEC 60601 test Compliance

level

level

Electromagnetic environment – guidance

Portable and mobile RF communications equipment should be used no closer to any part of the models EDGEAPEX HP, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.Recommended separation distance

Conducted RF lEC 61000-4-6 Conducted RF lEC 61000-4-6 Radiated RF lEC 61000-4-3

3 Vrms 150 kHz to 80 MHz 6 Vrms ISM frequency band 3 V/m 80 MHz to 2.7 GHz

3V 6V 3V/m

d=1.2×P1/2 d=2×P1/2 d=1.2×P1/2 80 MHz to 800 MHz d=2.3×P1/2 800 MHz to 2.7 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).
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:

42

NOTE I At 80 MHz end 800 MHz. the higher frequency range applies.

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 model EDGEAPEX HP is used exceeds the applicable RF compliance level above, the model EDGEAPEX HP should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the model EDGEAPEX HP. b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3V/m.

Table 4: Recommended separation distances between portable and mobile

RF communications equipment and the model EDGEAPEX HP

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

Rated maximum output power
of transmitter W

Separation distance according to frequency of transmitter m

150kHz to 80MHz d=1.2×P1/2

80MHz to 800MHz d=1.2×P1/2

800MHz to 2,7GHz d=2.3×P1/2

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) accordable to the transmitter manufacturer. NOTE I At 80 MHz and 800 MHz. the separation distance for the higher frequency range applies.

43

Endodontic Motor Troubleshooting
This guide is suitable for the users who use Endodontic Motor for the first time, and those who get unstable readout because of improper operation.

Problems Possible Causes

Analysis

No readouts

File clip

File clip wire broken or poor contact

or unstable readouts

Measuring wire

Measuring wire broken or poor contact Poor contact between measuring wire and

socket

Root canal problem Endo is too small for a large root canal

The root canal is rinsed by pure water

Root canal is blocked by dentin chippings or

residual pulp

Root canal is blocked by gum

Root canal is too dry

Metal prosthesis

Metal prosthesis

Lip hook

Poor contact between lip hook and measuring

wire socket

The screen displays that endo reaches apical foramen before the endo
actually does

Endo Metal prosthesis
Dental crown problem

Endo hasn’t actually got into root canal Flush touches the metal prosthesis of dental
crown Endo touches metal prosthesis Blood oozes out to dental crown Dental crown is broken or gum hyperplasia

Pulp cavity problem

Root canal is cracked

There are residue, metal residue or debri in pulp

cavity

Perforation

Endodontic perforation

Cavity problem

Proximal caries

Handing method

File clip

shows that endo Root canal problem reaches

apical foramen,

but apex locator

shows it hasn’t

Poor contact in clip wire
The root canal is rinsed by pure water Root canal is too dry
There’s ledge in root canal(without X ray There are gums and dental debris

44

Solutions Replace the clip Replace the measuring wire Make sure of proper contact between socket and measuring wire

Use the endo with larger diameter Rinse root canal with saline solution Remove the dentin chippings or residual pulp

Remove the gum Moist the root canal with saline solution. Avoid endo touching metal prosthesis Reconnect the lip hook or replace lip hook

Keep pushing endo near to apical foramen, screen display will become normal

Reduce

avoid contacting metal prosthesis

Avoid endo touching metal prosthesis Completely stop bleeding and clean the blood Insulate the endo and dental crown with insulator or cut off the gum hyperplasia
Combine X-ray to get the length Remove residue, metal residue and debris

Repair perforation Clean necrotic tissue of the proximal caries, if it’s the same with adjacent dental
surface and periodontium, temporarily the adjacent surface Replace clip
Rinse root canal with saline solution Moist the root canal with saline solution With help of X ray avoid touching ledge with endo Remove the gutta- percha or debris and moist the root canal

45

Notes

Notes

46

47

EdgeApex HP statement regarding reciprocating function:
This EdgeApex HP features a new ATR mode that enables torque-based reciprocation. If the file torque is less than the set trigger torque value, the file will keep rotating in the cutting direction. When the file torque is more than the set trigger torque value, the file will automatically reciprocate in the non-cutting and cutting directions repeatedly at the set angles. Furthermore, ATR Mode can operate files for which the cutting direction is counterclockwise [EdgeOne Fire] as well as normal files for which the cutting direction is clockwise. (The cutting direction of the file is designated in the name of the ATR mode i.e. CW-ATR/CCW-ATR.)

The EdgeApex HP comes pre-programmed with 5 preset systems:

·

EdgeFile X7 Basic

·

EdgeFile X7 Advanced

·

EdgeTaper Basic S1 & SX & S2

·

EdgeTaper Basic F1-F5

·

EdgeTaper Platinum Basic S1 & SX & S2

A long press on “P” in any of the pre-programmed presets will open access to the full program of preset files

as listed in the chart below. Use “+”/”-” to highlight the desired file system and “P” to select and the Main on/

off button to confirm.

EdgeFile X7 Basic EdgeTaper Basic EdgeOne Fire A- SGP Mode (Forward 60, Reverse 150) Match Protaper Match K3 Match One Flare Match One Curve Match R-Endo

EdgeApex HP Preset Systems: EdgeFile X7 Advanced EdgeTaper Platinum Advanced EdgeOne Fire B- SGP Mode (Forward 70, Reverse 180) Match Pathfile Match TF Match One G Match 2Shape Match iRace

EdgeTaper Basic EdgeSequel Sapphire EdgeOne Fire C- CCW- ATR Mode (Forward 30, Reverse 150) Match Mtwo Match Revo-S Match Hero Gold Match Hero Shaper

Settings for other EdgeEndo systems: You can utilize the open program slots M0-M9 to customize and save as your favorites. The below chart details the recommended settings for customizing program slots M0-M9 for our given file systems.
Use the CW mode and adjust to the following ROTARY settings:

Torque Limit listed is specific to this handpiece:

EdgeFile X3, X5 and XR, EdgeEvolve

300-500 RPM, Torque Limit 2.9 N-cm

EdgeGlidePath

300-500 RPM, Torque Limit 2.0 N-cm

EdgeTaper Retreat

350 RPM, Torque Limit 3.0 N-cm

EdgeTaper Encore Platinum, EdgeV-Taper HT 300-400 RPM, Torque Limit 4.0 N-cm

EdgeMorphology

500 RPM, Torque Limit 1.5 N-cm

EdgeGates

800-1200 RPM

EdgeFind

300-500 RPM, Torque Limit 4.5 N-cm

Use the CCW-ATR mode and adjust to the following RECIPROCATING settings, each with Forward Angle 30°, Reverse Angle 150°, Trigger Torque listed is specific to this handpiece:

EdgeCoil EdgeCoil Glidepath EdgeOne Fire Glidepath

350 RPM, Trigger Torque .4 N-cm 300-500 RPM, Trigger Torque .4 N-cm 300-500 RPM, Trigger Torque .4 N-cm

01/2024 Rev. B

Made in China ZMN-SM-700 V1.0-20220526

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