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Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 1 User instructions Information on the packaging Catalogue number Serial number Legal Manufacturer Please note the electronic instructions for use Note: Please note accompanying documents EAC conformity mark (Eurasian Conformity) GOST R certification Transportation and storage conditions...
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Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 1 User instructions NOTICE In cases which – if not prevented – could lead to material damage. 7 / 28...
Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 2 Safety | 2.1 Infection hazard 2 Safety The instructions for use are a component of the product and must be read care- fully prior to use and be accessible at all times.
Repairs, servicing and safety checks may only be performed by trained service personnel. The following persons are authorised to do this: ▪ Service technicians of KaVo branches after the appropriate product training ▪ Service technicians of KaVo authorised dealers after the appropriate product...
Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 3 Product description | 3.2 Technical Specifications Proper use: According to these regulations, this product may only be used for the described application by a properly trained user.
Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 3 Product description | 3.3 Transportation and storage conditions 3.2.3 Contra-angle handpiece 2325 LN Identification 1 red ring Transmission ratio 1 : 4 Drive pressure 2.5 to 3.0 bar (29 to 44 psi) Air consumption...
Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 4 Start up and shut down | 4.1 Mount the MULTIflex (LUX) / MULTIflex LED coupling 4 Start up and shut down WARNING Hazard from contaminated products.
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Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 4 Start up and shut down | 4.2 Checking the amount of water 14 / 28...
Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 4 Start up and shut down | 4.3 Checking the pressures 4.3 Checking the pressures NOTICE Contaminated or moist compressed air at the compressed air connec- tion Premature wear ▶...
Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 5 Operation | 5.1 Attaching the medical device 5 Operation Note At the beginning of each workday, the water-conducting systems should be rinsed for at least 2 minutes (without transmission handpieces being at- tached) and if there is a risk of contamination from reflux or back suction, the system may also need to be rinsed for 20 to 30 seconds after each patient.
Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 5 Operation | 5.4 Removing INTRA LUX head from shanks 2307 LN or 2320 LN 5.4 Removing INTRA LUX head from shanks 2307 LN or 2320 LN ▶...
Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 5 Operation | 5.6 Removing the cutting tools or diamond grinder from the contra-angle 2325 LN ▶ Forcefully press the push button with your thumb and simultaneously insert the dental bur or diamond grinder all the way to the stop.
▶ Do not use Vaseline or other grease or oil. Note The O-rings on the coupling may only be lubricated with a cotton ball wetted with KaVo Spray. ▶ Press the O-ring between your fingers to form a loop. ▶ Push the O-ring to the front, and remove it.
Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 7 Reprocessing steps in accordance with ISO 17664 | 7.1 Preparations at the site of use 7 Reprocessing steps in accordance with ISO 17664 7.1 Preparations at the site of use WARNING Hazard from contaminated products.
Defects in the device. ▶ Disinfect manually only! KaVo recommends the following products based on compatibility of the materi- als. The microbiological efficacy must be ensured by the disinfectant manufac- turer and proven by an expert opinion. Approved disinfectants: ▪...
▶ Remove the tool from the medical device. ▶ Cover the medical device with the KaVo CLEANpac bag, and place it on the corresponding care adapter. ▶ Press the spray key for 1 to 2 seconds.
Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN - 0.535.6210 7 Reprocessing steps in accordance with ISO 17664 | 7.5 Packaging KaVo recommends servicing the chuck system once a week using the chuck servicing program integrated in the device. Note Handpieces must be taken off the service couplings before the chuck service can be started and performed.
Damage to product. ▶ Immediately remove the product from the steam steriliser after the steril- isation cycle. The KaVo medical device has a maximum temperature resistance up to 138 ℃ (280.4 °F). Sterilisation parameters: Select a suitable procedure (depending on the available autoclave) from the fol- lowing sterilisation processes: ▪...
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Cleanpac 10 units 0.411.9691 Nozzle pin 0.410.0931 Spray repair set 0.410.0610 2163 Material summary Mat. no. KaVo Spray USA and Canada 2113 A 0.411.9660 QUATTROcare plus Spray USA and 1.005.4524 Canada 2141 P Chuck servicing set 1.003.1253 25 / 28...
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12 months from the date of the invoice, subject to the following conditions: In case of justified complaints, KaVo will honour its warranty with a free re- placement or repair. Other claims of any kind whatsoever, in particular with re- spect to compensation, are excluded.
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