KaVo INTRA K-LUX 200 F Instructions For Use Manual
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KaVo INTRA K-LUX 200 F Instructions For Use Manual

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Instructions for use
INTRA K-LUX 200 – 1.000.6717
INTRA K-LUX 200 F – 1.002.1912

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Summary of Contents for KaVo INTRA K-LUX 200 F

  • Page 1 Instructions for use INTRA K-LUX 200 – 1.000.6717 INTRA K-LUX 200 F – 1.002.1912...
  • Page 2 Manufacturer: Distributed by: KaVo Dental GmbH KaVo Dental GmbH Bismarckring 39 Bismarckring 39 88400 Biberach 88400 Biberach Germany Germany Phone +49 7351 56-0 www.kavo.com Fax +49 7351 56-1488...

  • Page 3: Table Of Contents

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 Table of contents Table of contents 1 User instructions ....................... 2 Safety..........................2.1 Infection hazard ......................7 2.2 Explosion hazard ......................7 2.3 Electrical shock......................7 2.4 Improper use ........................

  • Page 4: User Instructions

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 1 User instructions 1 User instructions Dear user, Congratulations on purchasing this KaVo quality product. By following the notes below you will be able to work smoothly, economically and safely.
  • Page 5 Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 1 User instructions Serial number Manufacturer Note: Please note accompanying documents Follow the electronic instructions for use HIBC Code CE mark for medical devices EAC conformity mark (Eurasian Conformity)
  • Page 6 Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 1 User instructions CAUTION In cases which – if not prevented – can lead to material damage. 6 / 28...

  • Page 7: Safety

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 2 Safety | 2.1 Infection hazard 2 Safety NOTE All serious events occurring in relation to the product must be reported to the manufacturer and the competent authority of the member state, in which the user and/or patient resides.

  • Page 8: Electromagnetic Fields

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 2 Safety | 2.6 Electromagnetic fields 4 Check to make sure that the device is working properly and is in satisfactory condition before each use. 4 Have parts with sites of breakage or surface changes checked by the service personnel.

  • Page 9: Qualification Of Personnel

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 2 Safety | 2.8 Qualification of personnel 2.8 Qualification of personnel Application of the product by users without the appropriate medical training could injure patients, users or third parties.

  • Page 10: Disposal

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 2 Safety | 2.11 Disposal 2.11 Disposal This product is subject to the EC directive governing waste electrical and elec- tronic devices and must be submitted to special disposal in Europe.

  • Page 11: Description Of The Product

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 3 Description of the product | 3.1 Intended use 3 Description of the product INTRA K-LUX 200 (Mat. no. 1.000.6717) INTRA K-LUX 200 F (Mat. no. 1.002.1912) 3.1 Intended use...

  • Page 12: Technical Specifications

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 3 Description of the product | 3.2 Technical Specifications 3.2 Technical Specifications NOTE The motor is only approved in combination with the listed treatment units and small devices.

  • Page 13: Transportation And Storage Conditions

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 3 Description of the product | 3.3 Transportation and storage conditions Water requirements Water quality in accordance with DIN Tap water EN ISO 7494-2 7.2 - 7.8 Water filter, supplied by customer <...
  • Page 14 Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 3 Description of the product | 3.3 Transportation and storage conditions Temperature: -29 °C to +50 °C (-20 °F to +122 °F) Relative humidity: 5% RH to 85% RH absence of condensation...

  • Page 15: Startup And Shut Down

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 4 Startup and shut down 4 Startup and shut down WARNING Hazard from contaminated products. Infection hazard to the dentist and patient. 4 Prior to initial startup and after each use, reprocess the product and ac- cessories.

  • Page 16: Operation

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 5 Operation | 5.1 Connecting the motor to the supply hose 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 17: Removing An Instrument From The Motor

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 5 Operation | 5.4 Removing an instrument from the motor 4 Place the instrument on the motor, lightly press it against the motor while turning it in the direction of the arrow until the guide stud can be heard to lock into place.

  • Page 18: Checking For Malfunctions And Troubleshooting

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 6 Checking for malfunctions and troubleshooting | 6.1 Checking for malfunctions before initial start-up 6 Checking for malfunctions and troubleshooting 6.1 Checking for malfunctions before initial start-up CAUTION Danger from hot lamp.

  • Page 19: Replacing The Lamp

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 6 Checking for malfunctions and troubleshooting | 6.2 Troubleshooting 6.2.1 Replacing the lamp CAUTION Danger from hot lamp. Risk of burn injury. 4 Do not touch lamp after previous operation. Allow the lamp to cool down.
  • Page 20 Improper care of the O-rings. Malfunction or complete failure. 4 Do not use Vaseline or other grease or oil. 4 Spray a lint-free cloth with KaVo Spray and apply it to the O-rings on the coupling. NOTE If the connection to the instrument is not leak-proof, replace all O-rings.

  • Page 21: Reprocessing Steps In Accordance With Iso 17664-1 / Iso 17664-2

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.1 Preparations at the site of use 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 7.1 Preparations at the site of use...

  • Page 22: Manual Internal Cleaning

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.3 Automated reprocessing 4 Do not take sleeve ① off the motor. Manual external cleaning 4 Thoroughly wipe down the outer surfaces of the medical device with a CaviWipes cleaning and disinfection wipe to remove all visible deposits.

  • Page 23: Packaging

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.5 Packaging CAUTION Improper service and care. Risk of injury. 4 Service regularly with suitable agents.

  • Page 24: Sterilisation

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.6 Sterilisation 7.6 Sterilisation This product is not designed for sterilisation. NOTE Only the removable motor sleeve can be sterilised in an autoclave at up to 135°C.

  • Page 25: Consumables

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 8 Consumables 8 Consumables Available from specialised dental dealers. Material summary Mat. no. High-pressure lamp sterilisable 1.002.2928 KaVo MULTI LED lamp 1.007.5372 O-ring 8.3x0.68 0.200.6120 Airflow measuring tube 0.411.4441...

  • Page 26: Terms And Conditions Of Warranty

    Instructions for use INTRA K-LUX 200 – 1.000.6717, INTRA K-LUX 200 F – 1.002.1912 9 Terms and conditions of warranty 9 Terms and conditions of warranty This KaVo medical device is subject to the following warranty conditions: KaVo grants the end customer a warranty of proper function and guarantees...

This manual is also suitable for:

Intra k-lux 2001.000.67171.002.1912

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