mectron Piezosurgery II Use And Maintenance Manual

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Manual of use and maintenance
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  • Page 1 English Manual of use and maintenance ����...
  • Page 2: Table Of Contents

    If there are any discrepancies between the descriptions contained 05.6 Instructions for use .......................18 in this manual and your equipment, please contact your dealer or the MECTRON After-Sale service 05.7 Permissible settings on the basis of the type of insert ...........19 for explanations.
  • Page 3: Intended Use

    Any such inserts should definitely not be used. It is necessary to instruct the patient to breathe through his nose during the treatment in order to avoid ingestion of the broken off fragment Mectron will not accept any liability for direct or incidental personal injury or damage to property in of the insert.
  • Page 4: Identification Data

    An exact description of the model including the serial number of the equipment will make it easier All equipment manufactured by MECTRON is thoroughly checked and tested, including all compo- for our After-Sale Service to respond quickly and efficiently to your queries.
  • Page 5: List Of Material Included In The Supply

    03.2 List of material included in the supply The material included in the supply may vary in case of promotional campaigns. � WARNING: Handpiece and cord can’t be detached. “Starter” configuration Casing of the device (Fig.3 - Ref.B). Piezosurgery handpiece complete with cord (Fig.3 - Ref.E). K5 torque wrench (Fig.3 - Ref.D).
  • Page 6: Installation

    - Open the door (Fig.4 - Ref.A) as far as it will go (Fig.4 - Ref.B). Mectron. The equipment will be installed in a suitable and handy place for it to be used, and is - Position the tube in the impeller (Fig.4 - Ref.C).
  • Page 7: Use

    05.0 Use 05.1 Controls This section illustrates the parts of the front panel (Fig.6) of the Piezosurgery unit, enabling the controls described in this manual to be located immediately. Description of the controls Ref. A - Graphic display. Function The display shows the following information: The type of power setting ROOT/BONE The output power level set in the ROOT mode.
  • Page 8: Description Of The Display And Functions

    Device in the BONE mode Fig. 8 - In the BONE mode, press the power-level key (Fig.6 - Ref.C) to set the following functions: QUALITY 1 QUALITY 2 QUALITY 3 SPECIAL To adjust the delivery rate of the pump press the + and – keys (Fig.6 - Rif.B). In the BONE mode, the speed can be set to between one and five.
  • Page 9: Safety Requirements During Use

    If this is not done, contact with the part to be treated or with other surfaces before start-up could - If the equipment is not working correctly, stop using it and call the Mectron Service cause tripping of the protection systems.
  • Page 10: Instructions For Use

    BONE 1* ÷ 2* ÷ 3* OT8L - OT8R BONE 1* ÷ 2* ÷ 3* insert to be used, consult Table 1 or the leaflet accompanying the Mectron insert you have IM3P BONE 1* ÷ 2* ÷ 3* ROOT PERIO purchased.
  • Page 11: Cleaning And Sterilisation

    After each treatment carry out the following operations: 06.0 Cleaning and sterilisation Remove the insert from the handpiece. Clean and disinfect the surfaces of the casing, the cords and their connectors using a low- 06.1 CLEAN function - Cleaning of the liquid circuit linting cloth moistened with a mild detergent solution (pH 6 to 9) and/or non-aggressive disinfectant having a neutral pH (pH 7).
  • Page 12: Cleaning And Autoclave Sterilisation Of The Inserts

    Soak the insert in the enzymatic detergent solution for 10 minutes at 40°C. Brush the surface of the insert gently with a soft nylon brush. Use a syringe to inject the enzymatic detergent into the cavity of the insert. Repeat this opera- tion three times in order to remove all the residues from the inner surface effectively.
  • Page 13: Autoclave Sterilising Of The Fitting Between The Cord And The Tube Of The Peristaltic Pump

    At the end of the life-cycle of this equipment, the purchaser is entitled to return the equipment to the dealer supplying new equipment. Instructions for disposal are available from Mectron; Failure to comply with the foregoing points may entail punishment in accordance with Directive 2002/96/EC.
  • Page 14: The Inserts

    � The footswitch will not work. Contact the nearest N.B.: Please read carefully the instructions for use. authorised MECTRON Service Centre. Type “B” applied part. A faint whistle can be heard The insert is not correctly...
  • Page 15 ERR appears on the ERR appears on the display. display). Lack of continuity of a lead in Contact the nearest the cord. authorised MECTRON The insert is worn, broken or Replace the insert. Service Centre. deformed (the message ERR Handpiece failure.
  • Page 16: Technical Data

    Alarms: The display on the front panel indicates error (see 13.0 Technical data point “Problem-solving”). Device in accordance with Directive 93/42/EEC: Class II a. Operating conditions: From +10°C to +40°C. Relative humidity from 30% to 75%. Class according to EN 60601-1: Type B Transport and storage conditions: From -10°C to +70°C.
  • Page 17 Guidance and manufacturer’s declaration - Electromagnetic immunity Guidance and manufacturer’s declaration - Electromagnetic immunity The PIEZOSURGERY // is intended for use in the electromagnetic environment specified below. The PIEZOSURGERY // is intended for use in the electromagnetic environment specified below. The customer or the user of the PIEZOSURGERY // should assure that it is used in such an environment.
  • Page 18: Guarantee

    In the event of failures due to accidents or improper use, or if the warranty has lapsed, repairs to MECTRON products will be charged on the basis of the actual cost of the materials and labour required for such repairs.
  • Page 19 Rivenditore - Reseller - Wiederverkäufer - Revendeur - Revendedor Mectron S.p.A. Via Loreto 15/A 16042 Carasco (Ge) Italy Tel. +39 0185 35361 Fax +39 0185 351374 www.mectron.com e-mail: mectron@mectron.com...

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