B) Time setting: 10s, 20s, 30s. C) Working mode: Full. 1.3 Principle and usage 1.3.1 LED.Q adopts the principle of ray radiation to solidify the light-sensitive resin by shooting at it in a short time. 1.3.2 This product is used to restore teeth and solidify...
2. Structure and components LED.Q is composed mainly of main unit, optical fiber, light hood, high power LED and cable. (Picture 1) 3. Technical specifications 3.1 Dimensions: 248mm×26mm×26.5mm 3.2 Net weight: 127g 3.3 Configuration: Main unit *1 Optical fiber *1...
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Light hood *1 Instruction book *1 Product certificate *1 Warranty card *1 3.4 Power supply 3.4.1 According to the classification of power supply Connect to dental unit ~24V 3.4.2 Power input: ~24V 50Hz/60Hz 0.4A Max 3.5 Light source 3.5.1 3W high power blue LED light 3.5.2 Wave length: 420nm-480nm 3.5.3 Light intensity: 1000mW/cm ~1200mW/cm...
4.2 Take off the red cap from the optical fiber and insert the metal part into the front of the built-in LED.Q (Make sure to screw the fiber to the end by rotating it).
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5.2 After turning on the device, keep pressing the button in 1second, then the indicator light scroll shines. Now you can choose 10s, 20s, and 30sworking time. 5.3 While operating, put the light source alignment the position where needs to be solid, press the button in a short time, then with a “Di”...
6. Cleaning, Disinfection and Sterilization The cleaning, disinfection and sterilization of optical fiber is as follow. 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.
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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.
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6.3 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. 6.3.1 Automated cleaning •The cleaner is proved to be valid by CE certificationin accordance with ENISO 15883.
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6.4 Disinfection Disinfection must be performed no later than 2 hours after the cleaning phase. Automated disinfection is preferred if conditions permit. 6.4.1 Automated disinfection-Washer-disinfector ·The washer-disinfector is proved to be valid by CE certification in accordance with EN ISO 15883. ·Use high temperature disinfection function.
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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 carried out together. c) Cleaning: (c1) The cleaning procedure should be suitable for the product to be treated.
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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. g)The air used for drying must be filtered by HEPA.
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6.6 Inspection and maintenance In this chapter, we only check the appearance of the product. After inspection, if there is no problem, the optical fiber can only be used. 6.6.1 Check the product. If there is still visible stain on the product after cleaning/disinfection, the entire cleaning/ disinfection process must be repeated.
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introduction of contaminants; d) Avoid contact with parts of different metals when packaging. 6.8 Sterilization Use only the following steam sterilization procedures (fractional pre-vacuum procedure*) for sterilization, and other sterilization procedures are prohibited: 1. The steam sterilizer complies with EN13060 or is certified according to EN 285 to comply with EN ISO 17665;...
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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 effective standards and verify the suitability and effectiveness.
6.10 Transportation 1. Prevent excessive shock and vibration during transportation, and handle with care; 2. It should not be mixed with dangerous goodsduring transportation. 3. Avoid exposure to sun or rain or snow during transportation. The cleaning and disinfection of main unit are as follows. •...
8. Contraindication The heart disease patients, pregnant women and children should be cautious to use this equipment. 9. Maintenance 9.1 This product does include repair part, machine maintenance and repair shall be made by the designated professional or repaired at a repair shop. 9.2 Users can replace light hood and optical fiber on hand.
10.Trouble shooting Faulty Possible cause Solution 1, Wait for a few 1, Continuous use time minutes, it will be is too long, thermal back to normal. protection circuit 2,Check the working. indication connection of the 2, The device is not Non-act.
away from shaking point, installed or stored at shadowy, dry, cool and ventilated places. 11.2 Don't store it together with articles that are combustible, poisonous, caustic and explosive. 11.3 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 ℃...
14. Symbol instruction Class II equipment Type B applied part Ordinary equipment Used indoor only Date of manufacture Manufacturer Recovery Screw inside/ outside Keep dry Handle with care Temperature limitation for storage Humidity limitation for storage Atmospheric pressure for storage Appliance compliance WEEE directive Follow Instructions for Use...
15. Manufacturer’s right We reserve the rights to change the design of the equipment, the technique, fittings, the instruction manual and the content of the original packing list at any time without notice. If there are some differences between blueprint and real equipment, take the real equipment as the norm.
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