User Manual Newtron P5 - Support-acteon

User Manual Newtron P5 - Support-acteon

User Manual

Newtron P5

Contents

1 Documentation

1.1 Associated documentation

1.2 Electronic documentation

2 Required information

2.1 Indication for use

2.2 Operating principle

2.3 Date of inclusion of EC marking

2.4 Latest document update

2.5 Repairing or modifying the device

2.6 Accessory usage conditions

3 Removal from packaging, installation, connections

3.1 Unpacking your medical device

3.2 Positioning the medical device

3.3 Installing cords

3.4 Connecting the medical device to the water system

3.5 Connecting the medical device to the electrical network

3.6 Plugging the medical device to the electrical network

3.7 Installing the control pedal

3.8 Fix the medical device to a non-removable support

4 Description of the medical device

4.1 Control unit

4.2 Power configuration button

4.3 Adjusting ultrasound power

4.4 SLIM handpiece

4.5 Attach a tip or a file

4.6 Connecting and disconnecting accessories during use

4.7 Connecting the handpiece

4.8 Handpiece support

4.9 handpiece cord

4.10 Light indicator

4.11 Irrigation flow configuration button

4.12 Adjusting the irrigation

4.13 Initiating irrigation

4.14 Air inlets

4.15 Connection to water system

4.16 Control pedal

4.17 Activating ultrasounds using the pedal

4.18 Mains Connector

4.19 Switch

4.20 Fuse recess

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4.21 Cleaning the irrigation system

5 Cleaning, disinfecting and sterilizing

5.1 medical device cleaning and disinfection

5.2 Cleaning and disinfecting accessories

6 Monitoring and maintenance of the medical device

7 Maintenance

7.1 Replacing the water filter

7.2 Identifying incorrect operation

7.2.1 No operation

7.2.2 No spray

7.2.3 The power is not as expected

7.2.4 Ultrasounds not working

7.2.5 Water leakage

8 Technical specifications for the medical device

8.1 Identification

8.2 Control unit

8.3 Ultrasonic generator

8.4 Length of cords

8.5 Irrigation

8.6 Control pedal

8.7 Environmental characteristics

8.8 Environmental restrictions

8.9 Main performance characteristics

9 Regulations and standards

9.1 Official Texts

9.2 Medical class of the device

9.3 Standardised Symbols

9.4 Manufacturer identification

9.5 Branch addresses

9.6 Disposal and recycling

10 Index

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Foreword

The medical device SATELEC® that you are about to install and use in your practice is a medical device designed for professional use. It comprises the chosen tool with which you will provide treatment within the context of your work.

To ensure optimum safety for yourself and your patients, comfort in your daily practice and to benefit fully from the technology of your medical device, please read the documentation provided carefully.

If you have received this medical device by mistake, please contact the supplier to arrange for it to be collected.

Please refer to the instructions relating to the comprehensive range of dental ultrasonic generators SATELEC® for information about the following: l l l l l l l l documentation format; the documentation archiving period; warnings concerning user and patient populations; the treatment area; the medical device usage interactions, contraindications and prohibitions; electromagnetic compatibility; disposal and recycling of the medical device; manufacturer responsibility.

Please refer to the accessory cleaning, disinfection and sterilization protocols and the handpiece predisinfection, cleaning and sterilisation protocols for information about the following: l l l l preparation of parts for sterilization; detailed manual and automatic protocols; information concerning conditioning for sterilization; recommendations for the inspection of parts.

1 Documentation

This document contains the following information: l l l l l l l indications for use; description of the medical device; installation of the medical device; use of the medical device; preparation for cleaning and disinfection of the medical device; monitoring and general maintenance of the medical device; maintenance to be performed by the user.

1.1 Associated documentation

This document must be used in association with the following documents:

Document title

Cleaning, disinfection and sterilization protocols for Wrenches SATELEC

®

Cleaning, disinfection and sterilization protocols for Tips SATELEC

®

Cleaning, disinfection and sterilization protocols for Handpieces SATELEC

®

General instructions relating to the complete range ofSATELEC

® dental ultrasonic generators

Method for consulting electronic user instructions

Quick Clean Newtron

®

P5

Quick Start Newtron

®

P5

User Manual for Newtron

®

P5

User Manual for SLIM handpiece

References

J81001

J02001

J12911

J00011

J00000

J61001

J61000

J61101

J12921

1.2 Electronic documentation

The user instructions for your device are provided in electronic format and not in printed format. However, you can request a free printed copy of the user instructions within 7 days via our website, by telephone or in writing.

The electronic user instructions are available in PDF format (Portable Document Format) and you will need to have a PDF file read software installed to read the instructions.

The device user instructions can be consulted at the following address:

www.satelec.com/documents

It is important for you to have read and understood the content of the user instructions relating to the use of your device and its accessories prior to use.

We recommend that you visit the website regularly to consult and/or to download the latest version of your device's user instructions.

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2 Required information

2.1 Indication for use

This medical device is used in association with a dental utrasound handpiece to which an ultrasound instrument is attached. It is designed for the treatment of prophylaxis, periodontics, endodontics and preservation and restoration dentistry.

2.2 Operating principle

An electrical signal emitted by the medical device is supplied to the dental ultrasonic handpiece. This is connected to the medical device via a cord. The handpiece comprises a piezoelectric ceramic transducer, which transforms the electrical signal into ultrasonic vibrations. Mechanical vibrations are transmitted to a tip or a dental file attached to the end of the ultrasonic handpiece.

The Newtron® SLIM B.LED fitted with its Blue LED ring and used in conjunction with the F.L.A.G.™ disclosing liquid, shows up dental plaque during the scale removal or dental prophylaxis phase. Fitted with a white LED ring, the handpiece emits a white light providing the user with optimum visibility of the treatment area.

2.3 Date of inclusion of EC marking

2013

2.4 Latest document update

04/2013

2.5 Repairing or modifying the device

Contact the supplier of your device. Using the services of an unapproved repairer could render your device dangerous for you and your patients.

Do not repair or modify the SATELEC® without seeking the prior permission of .

If the device is modified or repaired, specific checks and tests must be carried out to ensure that the device is still safe to use.

In the event of doubt, contact an approved dealer or the SATELEC®customer service team :

www.acteongroup.com

[email protected]

SATELEC® at the request of technical personnel working for the network of dealers approved by

SATELEC®, provide all information required to repair the faulty parts on which they may perform repairs.

2.6 Accessory usage conditions

Accessories and SLIM handpiece must be cleaned, disinfected and sterilized prior to use.

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3 Removal from packaging, installation, connections

3.1 Unpacking your medical device

When you receive your medical device, check for any damage that may have occurred during transportation.

If you have received this medical device by mistake, please contact the supplier to arrange for it to be collected.

If you have any questions or requirements, contact your supplier.

The Newtron® P5 includes the following items: l a Newtron® P5 unit with non-detachable pedal cord, a non-detachable SLIM cord and a SLIM handpiece l l l l l l support; a Newtron® SLIM handpiece, depending on configuration , a Quick Start [J12900] and a Quick Clean

[J12930]; tips and wrenches depending on selected options; an attachment kit; a box containing FLAG disclosing liquid; a Quick Start Newtron® P5 [J61000]; a Quick Clean Newtron® P5 [J61000].

3.2 Positioning the medical device

Place the control unit in the position that is suitable for your activity.

Check that the cords do not hinder the movement or free circulation of anyone.

The medical device must be placed on a secure and flat surface or a surface with a maximum slope of 5 degrees.

Fix your medical device using the attachments provided to ensure that the device cannot be removed without the use of a tool.

Adjust the position of your medical device to correspond to your angle of vision and the characteristics of your workstation, e.g. lighting or distance between the user and the medical device.

Ensure that you can access your medical device quickly.

Do not install your medical device near or on another device.

3.3 Installing cords

Check that the cords do not hinder the movement or free circulation of anyone.

Never rotate the handpiece connector on its cord as this can damage your medical device.

Never wrap the handpiece cord around the medical device.

Make sure that it is not possible to wheel over or walk on the different cords.

The cord attached to its handpiece must be easily accessible. Make sure that the cord is slack during use.

Do not put the medical device cords in a cable cover or a cable tray.

3.4 Connecting the medical device to the water system

The information below only applies to medical device that need to be connected to the water system to operate.

Ask an approved dental installation technician to connect your medical device to the water system.

The water supply system pressure may vary throughout the day. The water supply system pressure must be adapted to the values recommended for your medical device. It is very important to make sure that the maximum

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pressure permitted for the medical device is never reached or exceeded. If in doubt, you are strongly advised to install or arrange for installation of a water pressure limiting system.

The water supply system must comply with the quality criteria compatible with the practice of dental treatments.

3.5 Connecting the medical device to the electrical network

Set the medical device to OFF position O and check that the mains voltage is compatible with that indicated on the medical device or its mains adapter. Next, connect the cord to the wall socket in compliance with the standards in force in the country of use.

A different voltage would cause damage to the medical device and could injure the patient and/or user. Any variation in the electrical network voltage or electromagnetic field that is non-compliant with the limits in force, could interfere with the medical device's operation.

medical devices equipped with a protective earth must be connected to a supply network equipped with a protective earth.

Do not plug the medical device into an extension lead and do not put the mains cord in a cable cover or cable tray.

3.6 Plugging the medical device to the electrical network

1. Set the medical device's mains switch to stop position O;

2. connect the mains cord to the control unit mains connector;

3. connect the mains cord to the electrical fixture wall socket. 

3.7 Installing the control pedal

The control pedal must be positioned near the feet of the operator and must be readily accessible.

3.8 Fix the medical device to a non-removable support

The medical device that you have just acquired is not designed for mobile use. To avoid accidently dropping the device, we recommend that you fix it in a precise place in your treatment room, using the screw and

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clamp [F61001] supplied in the packaging box, to ensure that it cannot be dismantled or moved without needing a tool.

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4 Description of the medical device

4.1 Control unit

The control unit incorporates technology Newtron® patented by SATELEC®.

The patented technology Newtron® controls the tips by Cruise Control®, an automatic system for setting the frequency and power in real time. This ensures that Satelec® tip vibration is gentle, regular and controlled.

4.2 Power configuration button

To ensure a quality treatment, you will need to use the tips at the power and irrigation flow settings recommended by SATELEC®.

The ultrasound power configuration button ensures: l

Configuration of the operating power: 1 to 20.

The configuration button has 4 colour sectors, each with 5 positions.

l l l l

Green: 1 to 6: very low to low power, used mainly for periodontics.

Yellow: 6 to 11: medium power, used mainly for endodontics.

Blue: 11 to 16: high power, used mainly for scale removal.

Orange: 16 to 20: very high power, used mainly for implant loosening.

The ultrasound power configuration button can be removed by the user to facilitate the cleaning and disinfection of the control unit. The button cannot be sterilised.

The removal of the button inhibits the activation of ultrasounds. The top surface of the control unit lights up white and the control pedal can be pressed to activate the purge function. The purge function can be stopped at any time by pressing the control pedal again.

4.3 Adjusting ultrasound power

Adjust the ultrasound power using the ultrasound power configuration button. The ultrasound power must be adjusted in accordance with the tip used and the required treatment. The operating power of the tips must be selected in compliance with the Satelec tips color coding system (CCS tips). Details of these indications are given in the adjustment table available at the address

www.satelec.com/documents

and on the treatment sheets.

4.4 SLIM handpiece

Only handpieces with SLIM connector SATELEC® can be connected to the medical device. There is a handpiece with SLIM connector without LED, and a handpiece with SLIM connector B.LED with white or blue LED. Refer to the handpiece user manual Newtron® [J12921] for more information.

4.5 Attach a tip or a file

A tip or a file vibrates correctly when it is perfectly tightened without being forced beyond its stop point. Tighten it moderately using the wrench provided to ensure optimum ultrasound operation. Over-tightening of the tip or file can result in breakage of the tip, file or handpiece.

To prevent self-locking of the tip or the file, the latter must be removed after each use.

4.6 Connecting and disconnecting accessories during use

Do not connect/disconnect the cord(s) or the handpiece when the medical device is switched on and your foot is on the pedal.

Do not tighten or loosen the tips when the handpiece is activated.

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4.7 Connecting the handpiece

Check for the absence of signs of humidity at the SLIM handpiece connections, and eliminate them if necessary

(wipe and blow using a multipurpose syringe).

Lubricate the irrigation system seal located behind the SLIM handpiece with dental instrument lubricant to extend its effectiveness and prevent leaks.

Connect the SLIM handpiece to the sleeve, by aligning the indexing points and by avoiding rotation movement.

Install the SLIM handpiece on the support.

4.8 Handpiece support

Le support permet de poser la pièce à main ou la douille du cordon.

The handpiece support can be fixed to the front face or the right side face of the medical device. To change the position of this support, unscrew the two screws located under the support, position the support over the two holes located on the right side face and insert and tighten the two fastening screws.

The two silicone supports can be removed by sliding them along the metal rod. They can be sterilised.

4.9 handpiece cord

The SLIM cord is only compatible with handpieces SATELEC® with SLIM connector.

The SLIM cord ensures irrigation circulation and electrical connection between the medical device and the SLIM handpiece.

4.10 Light indicator

The light indicator is designed to provide information about the status of the device.

When the light indicator is illuminated, the medical device is on and ready to use. The indicator's colour corresponds to the power level.

4.11 Irrigation flow configuration button

The irrigation flow configuration button stops the irrigation function at the stop at least and sets the irrigation flow: from "min" to "max".

The irrigation flow configuration button is not designed to be removed.

The purge function is activated by pressing the pedal for 4 minutes; it can be stopped by pressing the pedal again.

4.12 Adjusting the irrigation

Adjust the irrigation flow using the irrigation flow configuration button. This adjustment depends on the tip and the treatment.

As work habits, feedback and professional training differ from one professional to another, the user must make sure that the irrigation flow is perfectly adapted to the treatment to be carried out to avoid burning the treatment area.

4.13 Initiating irrigation

The medical device must be set to minimum power depending on the required irrigation flow rate. Press the pedal until a spray appears.

4.14 Air inlets

Air inlets ensure correct ventilation of the control unit. Leave them uncovered to allow air to circulate.

4.15 Connection to water system

The supply pipe connector is used to connect the medical device device to the domestic water distribution system. The connector is extended by a pipe to which a filter is attached. The filter needs to be cleaned and/or

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replaced regularly as specified in the chapitre Replacing the water filter page 21.

The water quality must meet the criteria required to perform dental treatments.

4.16 Control pedal

The ON/OFF type pedal is used by the practitioner to operate the medical device.

Pressing the pedal automatically activates the handpiece ultrasounds, and the irrigation function if it is not in 0 position.

The control pedal equipped with its cord cannot be disconnected. Its weight and antislip pad ensure good stability.

The light function remains active for approx. 9 seconds after the pedal is released.

4.17 Activating ultrasounds using the pedal

To activate the ultrasounds on your medical device, press the control pedal.

4.18 Mains Connector

The mains connector with its earthing pin is used to connect the device to the electrical network via a disconnectable mains cord.

4.19 Switch

The mains switch is used to switch on (position I) or to stop (position O) the medical device.

4.20 Fuse recess

The recess holds two mains fuses designed to protect the medical device in the event of overvoltage or an internal fault.

The following solutions are approved for use: l l l l l l

Hydrogen peroxide < 3%;

Chlorexidine < 3%;

EDTA Ethylenediaminetetraacetic acid < 15%;

Sodium Hypochlorite < 0.9%;

Sterile water, distilled water, deionised water, dimineralised water;

Saline solution at 0.9%.

The following solutions must not be used: l l

Hextril® Hexedrin;

Bleach.

4.21 Cleaning the irrigation system

After installation and before first use, at the end of the day and following a period of prolonged non-use of the medical device, it is important to clean the irrigation system.

Operate the device at minimum power, at maximum irrigation flow rate for two minutes.

When the irrigation system has been cleaned, perform the following operations:

1. disconnect the handpiece and refer to handpiece predisinfection, cleaning and sterilisation protocols

SATELEC® [J12910];

2. clean and disinfect the medical device as indicated in the chapitre medical device cleaning and disin-

fection page 17

3. follow the instructions for accessory cleaning, disinfection and sterilization protocols SATELEC®

[J81000] and [J02000].

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5 Cleaning, disinfecting and sterilizing

The instructions relating to accessory cleaning, disinfection and sterilization protocols provided by SATELEC®

have been approved for each medical device and accessory. The applicable guides are listed in chapitre Asso-

ciated documentation page 5

They can be downloaded at the following address:

www.satelec.com/documents

In all cases, the local regulations in force relating to the accessory cleaning, disinfection and sterilization protocols take precedence over the information provided by SATELEC®.

5.1 medical device cleaning and disinfection

The medical device must be in OFF or O stop position during cleaning and disinfecting procedures.

Refer to the instructions detailed in the chapitre Cleaning the irrigation system page 15

Avoid using cleaning and disinfection products that contain flammable agents.

Otherwise, ensure that the product has completely evaporated from or that there is not fuel left on the medical device and its accessories before switching it on.

Do not use abrasive product to clean the medical device.

Never apply sprays directly to the medical device to clean it. Always spray the product onto a wipe, then clean the medical device.

The medical device control unit, handpiece cord and control pedal must be cleaned and disinfected daily. The following cleaning and disinfection products can be used: l l l l l l l l l l

Unowipes wipes by Unodent;

Alcohol-free hard surface disinfectant wipes by Classic;

Spray alcohol-free hard surface disinfectant by Classic;

Hard surface disinfectant wipes by Classic;

Microzid wipes by Schülke;

Cyberclean by Cybertech;

SEPTOL wipes by Anios;

SEPTOL spray by Anios;

Dentasept spray 41 by Anios;

Anionyxspray WS by Anios.

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To prepare for cleaning, remove the various parts of Newtron® P5 as shown here.

5.2 Cleaning and disinfecting accessories

Refer to the accessory cleaning, disinfection and sterilization protocols listed in the chapitre Associated docu-

mentation page 5.

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6 Monitoring and maintenance of the medical device

Before and after each use, check that the device and its accessories are not faulty in any way. This is necessary to detect any isolation fault or damage. If necessary, replace damaged parts.

Monitor the cleanliness of the air inlets on the control unit to prevent any heating.

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7 Maintenance

The only preventive maintenance the medical device requires is: l l l l checking of accessories; everyday cleaning, disinfection and sterilisation procedures; cleaning; replacement of the water filter cartridge.

7.1 Replacing the water filter

The water filter must be cleaned regularly and must be replaced every 6 months.

Proceed as follows: l l l l l shut off the water supply; stop the medical device (position O); unplug the network plug; unscrew the two filter sections; using the two 10mm open-ended wrenches, remove the filter cartridge to be replaced [kit F10389] or l l l clean it with water spray; repeat the same process for the seal; perform the same operations in the reverse order for reassembly; check that the spray works correctly and that there is no leakage.

A damaged or blocked cartridge must be replaced.

7.2 Identifying incorrect operation

In the event of incorrect operation, refer to the tables below to quickly identify and repair the non-complex parts of the medical device.

If the incorrect operation is not described in the tables below, please contact your supplier or the After-Sales team at SATELEC®.

Do not use the medical device if it appears to be damaged or faulty. Isolate the medical device and make sure that it cannot be used.

7.2.1 No operation

Symptoms: the indicator light on the medical device is off and the medical device is not working.

Possible causes Solutions

No electrical current

Internal fuse not working

Contact your electrician

Return to After-Sales team SATELEC

®

Set the mains switch to position I Mains switch in position O

Faulty connection between the mains cord and the mains connector

Faulty connection between the mains cord and the electrical wall socket

Connect the mains cord to the mains connector.

Connect the mains cord to the electrical wall socket.

Mains fuses in the mains connector not working

Replace the mains fuses with fuses of the same type and rating

The medical device also has an internal fuse (ref. F1 on the printed circuit board) that cannot be accessed by the user.

7.2.2 No spray

Symptoms: There is no water spray at the tip.

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Possible causes

Dental cabinet water inlet in shut-off position

Flow configuration button on minimum

Faulty water pipe connection

Low water pressure

Blocked filter

Faulty solenoid valve

Tip or file blocked

Incorrect choice of tip

Inadequate amount of spray

Solutions

Open the water inlet

Adjust the flow configuration button

Check the water inlet

Check the water system pressure

Clean or change the filter

Return to After-Sales Department SATELEC

®

Unblock the tip or file

Check the tip

Adjust the spray

7.2.3 The power is not as expected

Symptoms: the tip does not vibrate at the expected frequency, the treatment is not progressing as normal and is taking longer or at a standstill.

Possible causes Solutions

Worn or distorted tip Replace the tip

Incorrect use: incorrect approach angle or inadequate pressure on the tooth

Refer to the configuration table available at

www.satelec.com/documents

Presence of liquid or humidity between the handpiece and cord

Thoroughly dry the electrical contacts

7.2.4 Ultrasounds not working

Symptoms: the tip does not vibrate, vibration cannot be heard.

Possible causes

Tip loose Tighten the tip using the wrench

Faulty connector contact

Handpiece cord wire(s) cut

Solutions

Clean the cord contacts

Return to After-Sales Department SATELEC

® to replace the cord

7.2.5 Water leakage

Symptoms: Water is leaking from one of the following places: l between the base of the SLIM handpiece and its cord.

Possible causes

Wear of 1.15mm x1mm SLIM handpiece seal

Solutions

Replace the seal using F12304 kit. Refer to the instructions in document

J12921

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8 Technical specifications for the medical device

8.1 Identification

Manufacturer

Nom du medical device

SATELEC®

N

EWTRON

® P5

8.2 Control unit

Width (in mm)

156

Height (in mm) 102

Depth (in mm)

Weight (in g)

186

1650 (with mains cord)

SLIM cord 1674 with pedal, SLIM cord and 300ml tank; 1712 with pedal,

Ingress protection rating: IPX0

8.3 Ultrasonic generator

Supply voltage 100 VAC - 240 VAC

Power consumption

Voltage supplied to handpiece

Output frequency

Power setting range

Operating mode

Type of leakage currents

Electrical rating

Internal fuse not accessible to the user

Fuse (mains connector)

60 VA

150 VAC

Minimum 28 kHz

1 to 20

Intermittent: 10 minutes ON / 5 minutes OFF

BF

1

Ref: FU1 / 1.5 AT - 125 V - SMD - Breaking capacity: 50 A

2 x 1 AT / 230 VAC fuses – 5mm x 20mm - Breaking capacity: 35 A

8.4 Length of cords

Scaler handpiece cord (in mm)

Control pedal cord (in mm)

>

2040

>

2000

8.5 Irrigation

Water pressure at inlet

Maximum water output flow at the end of the handpiece

8.6 Control pedal

Width (in mm)

Height (in mm)

Depth (in mm)

Weight (in g)

1 to 5 bars

80ml/min to 100ml/min at 5 input bars

70

30

95

150

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Ingress protection rating: IPX1

8.7 Environmental characteristics

Operating temperature +10°C to +30°C

Storage temperature

Operating humidity

Maximum storage humidity

Atmospheric pressure

Altitude

-20°C to +70°C

10 % à 100 %

70 %

Between 800 hPa and 1060 hPa

Less than or equal to 2000 metres

8.8 Environmental restrictions

Usage premises

Can be used at all medical premises. The medical device must not be used in an operating theatre, or outside.

Use in gas-filled atmosphere

Immersion

The medical device is not designed for use in a type AP or APG gas-filled atmosphere or in the presence of anaesthetic gases.

The SLIM handpiece must not be immersed.

8.9 Main performance characteristics

Ultrasonic vibrations of the tip or file fitted to the end of the conventional dental ultrasonic handpiece.

l l

Vibration frequency ≥ 28 kHz.

Tip amplitude ≤ 200 µm.

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9 Regulations and standards

9.1 Official Texts

This medical device complies with the essential requirements of European Directive 93/42/EEC. This equipment is designed and developed in compliance with Electrical Safety standard IEC60601-1 in force. It was designed and manufactured in accordance with an EN ISO 13485-certified quality assurance system.

9.2 Medical class of the device

This medical device is a class IIa device according to European Directive 93/42/EEC.

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9.3 Standardised Symbols

Symbols Meaning

Refer to the accompanying documentation

Consult the User Manual

Accompanying documentation in electronic format

I

YYYY

O

I

IPX1

LF type

Class 1

Alternating voltage

Sterilisation at 134°C in an autoclave

Sterilisation at 132°C in an autoclave

Washer disinfector for thermal disinfection

EC marking

Do not dispose of as household waste

Year of manufacture

Control pedal

Device OFF

Device ON

IP

: ingress protection ratings procured by a range

X

: no ingress of protection rating claim against the penetration of solids

1

: protects against the vertical falls of drops of water

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9.4 Manufacturer identification

SATELEC

A Company of ACTEON Group

17, avenue Gustave Eiffel

BP 30216

33708 MERIGNAC cedex

FRANCE

Tel. +33 (0) 556.34.06.07

Fax. +33 (0) 556.34.92.92

E.mail: [email protected]

www.acteongroup.com

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9.5 Branch addresses

FRANCE

SATELEC ACTEON GROUP

17 av. Gustave Eiffel

Zone industrielle du phare - B.P. 30216

33708 MERIGNAC cedex - France

Tel. +33 (0) 556 34 06 07

Fax. +33 (0) 556 34 92 92 e-mail: [email protected]

U.S.A.

ACTEON Inc.

124 Gaither Drive, Suite 140

Mount Laurel, NJ 08054 - USA

Tel. +1 856 222 9988

Fax. +1 856 222 4726 e-mail: [email protected]

GERMANY

ACTEON GERMANY GmbH

Industriestrasse 9 – 40822 METTMANN - GERMANY

Tel. +49 21 04 95 65 10

Fax. +49 21 04 95 65 11 e-mail: [email protected]

SPAIN

ACTEON MEDICO-DENTAL IBERICA, S.A.U.

Avda Principal n°11 H

Poligono Industrial Can Clapers

08181 SENTMENAT (BARCELONA) - SPAIN

Tel. +34 93 715 45 20

Fax. +34 93,715 32 29 e-mail: [email protected]

U.K.

ACTEON UK

Unit 1B - Steel Close – Eaton Socon, St Neots

CAMBS PE19 8TT - UK

Tel. +44 1480 477 307

Fax. +44 1480 477 381 e-mail: [email protected]

MIDDLE EAST

ACTEON MIDDLE EAST

Numan Center - 2nd Floor N° 205 - Gardens Street

PO Box 5746 - 11953 AMMAN - JORDAN

Tel. +962 6 553 4401

Fax. +962 6 553 7833 e-mail: [email protected]

CHINA

ACTEON CHINA

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Office 401 - 12 Xinyuanxili Zhong Street -

Chaoyang District - BEIJING 100027 - CHINA

Tel. +86 10 646 570 11/2/3

Fax. +86 10 646 580 15 e-mail: [email protected]

THAILAND

ACTEON (THAILAND) LTD

23/45 Sorachai Building 16th floor - Sukumvit 63

Road, Klongton Nua - Wattana, BANGKOK 10110

- THAILAND

Tel. +66 2 714 3295

Fax. +66 2 714 3296 e-mail: [email protected]

KOREA

ACTEON KOREA Corp.

8F Hanil B/D - 132-4 1Ga Bongrae-dong -

JOONG-GU – SEOUL - KOREA

Tel. +82 2 753 41 91

Fax. +82 2,753 41 93 e-mail: [email protected]

INDIA

ACTEON INDIA

B-94, GIDC Electronic Estate - Sector 25 –

GANDHINAGAR 382028 Gujarat - INDIA

Tel. +91 79 2328 7473

Fax. +91 79 2328 7480 e-mail: [email protected]

LATIN AMERICA

ACTEON LATIN AMERICA

Bogotà - COLOMBIA

Celular: +57 312 377 8209 e-mail : [email protected]

RUSSIA

ACTEON RUSSIA

Valdajski Proezd 16 – office 253

125445 Moscow - RUSSIA

Tel./Fax. +7 499 76 71 316 e-mail : [email protected]

AUSTRALIA/NEW ZEALAND

ACTEON AUSTRALIA/NEW ZEALAND

Suite 119, 30-40 Harcourt Parade

Rosebery NSW 2018

Australia

Tel. +612 9669 2292

Fax. +612 9662 2204 e-mail : [email protected]

TAIWAN

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ACTEON TAIWAN

14F-1, N°433, Jinping Rd.

Jhonghe Dist., New Taipei City 23563

TAIWAN (R.O.C)

Tel. + 886 926 704 505 e-mail : [email protected]

9.6 Disposal and recycling

As an item of Electrical and Electronic Equipment, the must be medical devicedisposed of via a specialist collection, removal, recycling or destruction channel. This applies in particular to the European market, in reference to Directive 2002/96/EC dated 27/01/2003.

When your medical device has reached the end of its service life, contact your nearest dental equipment dealer, or ACTEON GROUP head office or one of the company branches to find out how to proceed. The relevant

contact details are given in the chapitre Branch addresses page 28.

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- User Manual • Newtron® P5 • J61101 • V1 • (13) • 04/2013 • NBACEN040B

Index:

After installation

– indicator light

10 Index

A

After installation 15

air circulation 14

air inlets 19

Air inlets 14

Altitude 24

Amplitude 24

approved dealers 7

attachments 9

B

B.LED 13

Bleach 15

C

Chlorexidine 15 clean and disinfect the device 15 clean irrigation system 15

cleaned 7

color coding system 13

control pedal 10, 15

control unit 13

Cruise Control® 13

D

damage 19

deionised water 15

dental file 7

dental ultrasonic generators 5

dimineralised water 15

disinfected 7

disposal 30

distilled water 15

E

earthing pin 15

EDTA Ethylenediaminetetraacetic acid 15

Electrical Safety 25

electronic user instructions 5

end of the day 15

endodontics 7

European Directive 25

F

F61001 11

fall risk 10

fault 19

Filter 22

first inclusion of EC marking 7

first use 15

fuse 21

gas-filled atmosphere 24

G

H

Handpiece support 14

Handpieces 5

Hextril® Hexedrin 15

humidity 14

Hydrogen peroxide 15

I

incorrect operation 21

indexing points 14

indicator light 21

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Index: instructions relating to the comprehensive range of dental ultrasonic generators

– water filter instructions relating to the comprehensive range of

dental ultrasonic generators 3

irrigation flow 14

irrigation flow settings 13

K

kit F10389 21

kit F12304 22

L

LED 13

light function 15

light indicator 14

mains connector 10, 15 mains fuses 15 mains switch 15

Mains switch 21

Manufacturer 23

Medical class 25

M

N

non-use 15

P

pedal 15

periodontics 7

power settings 13

preservation and restoration dentistry 7

Pressure 24

printed copy 5

prophylaxis 7

purge function 13-14

Q

Quick Clean 5

Quick Start 5

recycling 30

removal of the button 13

repair 7 repairer 7

R

Saline solution 15

seal 22

silicone supports 14

SLIM cord 14, 23

Sodium Hypochlorite 15

spray 14, 21

Spray 17

Sterile water 15

sterilized 7

supply pipe 14

S

T

Temperature 24

tip 7, 22

Tip 22

Tips 5

treatment 13-14

ultrasonic vibrations 7 ultrasound instrument 7

ultrasound power 13

update 7

user instructions 5

User Manual 5

U

V

Vibration frequency 24

W

water filter 21

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- Newtron® P5 • J61101 • V1 • (13) • 04/2013 • NBACEN040B

water leak 22

water system 9

Wipes 17

Wrenches 5

Index: water leak

Wrenches

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Ref: J61101 • V1 • (13) • 04/2013 • NBACEN040B

A Company ofACTEON Group• 17 av.Gustave Eiffel • BP30216 • 33708 MERIGNAC cedex • France

Tel.+33 (0)556 34 06 07 • Fax.+33 (0)556 34 92 92

E-mail:[email protected] • www.acteongroup.com

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