Ultrasonic Endo Activation Device User Manual Changzhou Bomedent Medical Technology Co., Ltd.
Thank you very much for choosing the Ultrasonic Endo Activation Device of Bomedent To give full play to the function of this device, and operate and maintain it correctly and safely, please read this User Manual carefully before using it, and keep this User Manual properly for reference at any time Classification of device safety level: Classification of electric shock protection type: Class II Classification of electric shock protection level: Class B Classification of liquid entry preventio
Contents 1. Product Introduction............................................................................................................... 1 1.1 Brief Introduction............................................................................................................. 1 1.2 Model................................................................................................................................ 1 1.3 Scope of Application....................................................................
1. Product Introduction 1.1 Brief Introduction Ultrasonic Endo Activation Device (hereinafter referred to as “Actor I pro” or “device”) is an auxiliary device for dentists to perform root canal treatment. It is mainly used to effectively clean the root canal with the help of ultrasonic cavitation, so as to assist dentists to complete root canal treatment.
This device may not work properly due to the following environmental factors: 1) Portable or movable radio frequency transmitters are present nearby. 2) Electromagnetic interference may cause abnormal operation of this device. As with all electronic devices, this device has electromagnetic interference and should not be used on patients with cardiac pacemaker.
(1) This device may not cause harmful interference, and (2) This device must accept any interference received, including interference that may cause undesired operation. 2. Product Configuration 2.1 External Structure of Main Frame of Product 2.
Wireless foot switch (optional) 2.3 Accessories List Please see the packing list for the device configuration. 3.
Switch button ①: Power on: when the device is off, press and hold the switch button for 1 second, and the device will enter the standby state with the ring tone; Power off: in standby state, press and hold the switch button for 1 second, and the device will be turned off with the ring tone. Operation and stop: in standby state, press the switch button for 0.1 seconds, and the device will enter the working state and start vibrating. Press the switch button again to stop working.
The indicator light flashes in blue: it means that the device has been connected with the wireless foot switch, and they can communicate normally; The indicator light is off: the bluetooth is not turned on.
Please use the original working tip; The working tip has not been disinfected and sterilized before leaving the factory. Please use it after sterilization; After each treatment, the working tip should be cleaned, disinfected and sterilized. 4.3 Removal of Working Tip Align the wrench with the slot of the working tip, rotate the wrench counterclockwise to loosen the working tip, and continue to rotate the wrench until the working tip comes out.
Make sure there is enough flushing fluid in the root canal for cooling during the use of the device; Caution: Hold for 30 to 60 seconds at a time for a better cleaning effect. Switch between "high/low" power working states: in the working state of the device, press and hold the switch button for 1 second to switch between high and low power working states.
Please do not disassemble the working tip during the treatment, because it may scratch the operator or the patient. Caution: Please stop using this device when any abnormalities occur. This device is not suitable for all types of root canals. Please do not use this device for extremely deformed root canals. Please use disposable gloves and rubber dam during treatment; Be sure to remove the working tip after each treatment. 5.
Figure a Figure b Caution: When the battery power indicator light flashes in yellow, accompanied by the prompt tone, the battery power is low, and the device should be charged in time; The battery used in this product lacks of memory property and can be charged at any time; Please charge the device for at least 4 hours before the first charge; When the main frame is inserted into the charging base, but it does not enter the charging state, please stop charging it immediately and then contac
Actor I pro can be connected wirelessly with our wireless foot switch through bluetooth. After successful connection, the operation of Actor I pro can be controlled within 5 meters.
6. Troubleshooting Reference Fault Check items phenomenon The device does not work after starting up Fault analysis and handling method section The battery power is low. The time to press the switch button is too short The wrong power adapter is used The device is not charged properly The charging base is not powered on The main frame is not inserted into the charging base properly 1. The working tip is not tightened; The working tip fails to vibrate chapter or 2.
7． Cleaning, Disinfection and Sterilization Caution: No part of Actor I pro is sterilized before leaving the factory Warning: Please do not soak the main frame in the ultrasonic cleaning machine It is recommended to use a soft cloth soaked in alcohol to wipe and disinfect the surface of the main frame of Actor I pro; Please do not use liquid or spray cleaner directly on the main frame.
7.1 Cleaning and Sterilization of Working Tip, Wrench and Silicone Case 1) Cleaning Steps Parameters 1. Wash the working tip, wrench and silicone case with running water for 2 minutes to remove their Wash 2. Wipe 3. Scrub 4. Soak 5. Rinse 6. Dry surface contaminants. Wet the soft clean cloth in the cleaner, and then use it to wipe the surface of the working tip, wrench and silicone case thoroughly 5 times. Replace it with a new one after each wipe.
8. Storage, Maintenance and Transportation 1. Storage a. This product should be handled with care, kept away from earthquake source, and stored in a dry and ventilated place. b. This product should not be placed together with toxic, corrosive, flammable and explosive items. c. The relative humidity of the storage environment should be 10%~80%, the atmospheric pressure should be 500-1060hPa, and the temperature should be -10℃~ +50℃. 2. Maintenance a.
9. Technical Parameters Manufacturer Changzhou Bomedent Medical Technology Co., Ltd. Product name Ultrasonic Endo Activation Device Model Actor Ⅰ pro Dimensions Main frame: 169*26*28mm Charging base: 82*64*73 mm Weight 700g Power supply mode Lithium battery, DC 3.7V, 1600mAh Charging base Input: DC5V/1A Output: DC 5V, 0.5A max Power adapter Input: AC100-240V, 50/60Hz 0.
10. Symbol Description Warning: please read this manual Refer to the user manual before use Type B application device Class II device The product complies with the directive on WEEE. This device Serial number must be disposed of as municipal solid waste when abandoned Manufacturer Date of manufacture For indoor use Upward Damp-proof Fragile. Please handle it with care 11.
13. EMC Statement Special precautions regarding electromagnetic compatibility (EMC) should be taken for this Ultrasonic Endo Activation Device, and it must be installed and used in accordance with the EMC information specified in this manual. Portable and movable RF communication equipment may affect this device.
Guidance and manufacturer’s declaration – electromagnetic emissions The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that is used in such an environment. Immunity test Electrostatic discharge(ESD) EN 61000-4-2 IEC60601 test level Compliance Level Electromagnetic environment - guide Floors should be wood, concrete or ceramic ± 6kV contact ± 6kV contact tile.
Guidance and manufacturer’s declaration – electromagnetic emissions The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that is used in such an environment.
Recommended separation distances between portable and mobile RF communications equipment and the device The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF according to the maximum output power of the communications equipment.
After-sales service company: Changzhou Bomedent Medical Technology Co., Ltd. Tel: 0519-88991980 ChangZhou BoMedent Medical Technology Co.,Ltd. NO.
