KaVo INTRAflex LUX 2 2313 LN Instructions For Use Manual
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KaVo INTRAflex LUX 2 2313 LN Instructions For Use Manual

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Instructions for use
INTRAflex LUX 2 2313 LN - 0.535.6220

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Summary of Contents for KaVo INTRAflex LUX 2 2313 LN

  • Page 1 Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220...
  • Page 2 Distributed by: Manufacturer: KaVo Dental Technologies, LLC Kaltenbach & Voigt GmbH 11727 Fruehauf Drive Bismarckring 39 Charlotte, NC 28273 USA D-88400 Biberach Phone: 847 550 6800 www.kavo.com Fax: 847 550 6825...

  • Page 3: Table Of Contents

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 Table of contents Table of contents 1 User instructions ........................ 4 2 Safety..........................6 2.1 Infection hazard ......................6 2.2 Technical condition......................6 2.3 Accessories and combination with other equipment ............7 2.4 Qualification of personnel....................

  • Page 4: User Instructions

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 1 User instructions 1 User instructions Dear User Congratulations on purchasing this KaVo quality product. By following the in- structions below you will be able to work smoothly, economically and safely.
  • Page 5 Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 1 User instructions 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 (Temperature range)

  • Page 6: Safety

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 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.

  • Page 7: Accessories And Combination With Other Equipment

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 2 Safety | 2.3 Accessories and combination with other equipment 2.3 Accessories and combination with other equipment Use of un-authorised accessories or un-authorised modifications of the device could lead to injury.

  • Page 8: Product Description

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 3 Product description | 3.1 Purpose – Intended use 3 Product description INTRAflex LUX handpiece 2313 LN (Mat. no. 0.535.6220) 3.1 Purpose – Intended use Indications for use: This medical device is ▪...

  • Page 9: Transportation And Storage Conditions

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 3 Product description | 3.3 Transportation and storage conditions Contra-angles drills can be used. Attachable to all MULTIflex (LUX) / MULTIflex LED couplings. 3.3 Transportation and storage conditions ▶ Do not store in a refrigerated environment.

  • Page 10: Start Up And Shut Down

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 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. Infection hazard for care provider and patient.
  • Page 11 Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 4 Start up and shut down | 4.2 Checking the amount of water 11 / 26...

  • Page 12: Checking The Pressures

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 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 ▶ Supply dry, clean and uncontaminated compressed air according to ISO 7494-2 only.

  • Page 13: Operation

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 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.

  • Page 14: Remove Handpiece Or Contra-Angle Drill From Handpiece 2313 Ln

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 5 Operation | 5.4 Remove handpiece or contra-angle drill from handpiece 2313 LN WARNING Use of impermissible cutters or grinders. Injury to the patient or damage to the medical device.
  • Page 15 Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 5 Operation | 5.5 Modification of the handpiece 2313 LN for contra-angle drills ▶ Use the enclosed hook to remove the bur stop. 15 / 26...

  • Page 16: Troubleshooting

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 6 Troubleshooting | 6.1 Replacing the O-rings on the coupling on the supply hose 6 Troubleshooting 6.1 Replacing the O-rings on the coupling on the supply hose NOTICE Improper care of the O-rings.

  • Page 17: Reprocessing Steps In Accordance With Iso 17664

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 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.

  • Page 18: Manual Disinfection - External

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 7 Reprocessing steps in accordance with ISO 17664 | 7.3 Automated reprocessing 7.2.3 Manual disinfection - external WARNING Incomplete disinfection. Infection hazard. ▶ Only use disinfection procedures that are verified to be bactericidal, fungi- cidal and virucidal.

  • Page 19: Servicing With Kavo Spray

    ▶ Remove the dental bur or diamond grinder, and, in the case of handpiece 2313 LN, close the chuck. ▶ 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.

  • Page 20: Packaging

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 7 Reprocessing steps in accordance with ISO 17664 | 7.5 Packaging Note Handpieces must be taken off the service couplings before the chuck service can be started and performed. ▶ Close the front door and press the chuck service button for at least three seconds until the spray canister control LED flashes three times consecut- ively.

  • Page 21: Storage

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 7 Reprocessing steps in accordance with ISO 17664 | 7.7 Storage 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-...

  • Page 22: Tools And Consumables

    Instructions for use INTRAflex LUX 2 2313 LN - 0.535.6220 8 Tools and consumables 8 Tools and consumables Available from dental suppliers. Material summary Mat.No. Instrument stand 2151 3.005.5204 Insert for INTRAflex 3.005.3089 Cellulose pad 100 units 0.411.9862 Cleanpac 10 units 0.411.9691...

  • Page 23: Terms And Conditions Of Warranty

    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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