Sirona C3 Plus Operating Instructions Manual

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Sirona Dental Systems GmbH Table of Contents

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Table of Contents

1General information .................................................................................................. 6

1.1 Dear Customer, ................................................................................................................................ 6

1.2 Contact data ..................................................................................................................................... 6

1.3 Notes on these Operating Instructions ............................................................................................. 7

1.4 Other valid documents...................................................................................................................... 8

1.5 Warranty and liability ........................................................................................................................ 8

1.6 Intended use ..................................................................................................................................... 9

2Safety instructions .................................................................................................... 10

2.1 Identification of the danger levels ..................................................................................................... 10

2.2 Information on the unit ...................................................................................................................... 10

2.3 On-site installation ............................................................................................................................ 11

2.4 Installing the treatment center .......................................................................................................... 11

2.5 Media quality..................................................................................................................................... 11

2.6 Connection to the public drinking water system ............................................................................... 12

2.7 Maintenance and repair .................................................................................................................... 12

2.8 Trouble-free operation ...................................................................................................................... 13

2.9 Vacuum system ................................................................................................................................ 13

2.10 Patient chair...................................................................................................................................... 13

2.11 Ventilation slots................................................................................................................................. 13

2.12 Intermittent operation........................................................................................................................ 14

2.13 Care, cleaning agents, and disinfectants.......................................................................................... 14

2.14 Modifications and extensions of the system ..................................................................................... 14

2.15 Electromagnetic compatibility ........................................................................................................... 15

2.16 Influencing of cardiac pacemakers ................................................................................................... 15

2.17 Dismantling / Installation................................................................................................................... 16

3Technical description ............................................................................................... 17

3.1 Standards / Approvals...................................................................................................................... 17

3.2 Technical data .................................................................................................................................. 19

4Controls and functional elements ........................................................................... 21

4.1 System overview of the C3+ ........................................................................................................................................ 21

4.2 Control panel on the dentist element ................................................................................................ 22

4.3 Control panel on the assistant element ............................................................................................ 26

5Putting the system into operation ........................................................................... 28

6Foot control ............................................................................................................... 30

6.1 Wireless foot switch C+ .................................................................................................................... 30

6.2 C+ foot switch.................................................................................................................................... 35

7Program selection ..................................................................................................... 37

7.1 Safety................................................................................................................................................ 37

7.2 MOVEMENT STOP! ......................................................................................................................... 38

7.3 Program selection............................................................................................................................. 39

Table of Contents Sirona Dental Systems GmbH

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8Positioning patients.................................................................................................. 40

8.1 Articulated headrest ......................................................................................................................... 40

8.2 Flat headrest .................................................................................................................................... 40

8.3 Motor-driven headrest...................................................................................................................... 41

8.4 MultiMotion headrest........................................................................................................................ 42

8.5 Chair movements adjustable by motor drive.................................................................................... 45

8.6 Programming patient positions ........................................................................................................ 46

9Dentist element and instrument functions ............................................................. 47

9.1 Dentist element ................................................................................................................................ 47

9.2 Positioning the dentist element ........................................................................................................ 48

9.3 General instrument functions ........................................................................................................... 49

9.4 Electric motor ................................................................................................................................... 51

9.5 Highspeed handpiece ...................................................................................................................... 52

9.6 SIROSONIC L scaler ....................................................................................................................... 53

9.7 SPRAYVIT L multifunctional syringe................................................................................................ 55

9.8 Saving the instrument programs ...................................................................................................... 56

9.9 Surgery with saline solution (NaCl).................................................................................................. 57

10 Operating light, tumbler filling, flushing of the cuspidor, purge.......................... 59

10.1 Operating light.................................................................................................................................. 59

10.2 Tumbler filling................................................................................................................................... 60

10.3 Flushing of the cuspidor................................................................................................................... 61

10.4 Purge / Auto Purge function (purging the water paths).................................................................... 61

11 Basic treatment center settings in the Mode dialog .............................................. 65

11.1 Mode key ......................................................................................................................................... 65

11.2 Mode: NACL PUMP OFF or ON for instrument holder .. ................................................................. 66

11.3 Mode: MAINTENANCE.................................................................................................................... 66

11.4 Mode: SERVICE ONLY START - STOP.......................................................................................... 66

11.5 Mode: FC CONTROL MODE ON/OFF - VARIABLE ....................................................................... 67

11.6 Mode: TIME - HOURS : MIN............................................................................................................ 67

11.7 Mode: DAY : MON : YEAR .............................................................................................................. 67

11.8 Mode: FOOT – CONTROL NORMAL - EXTENDED ....................................................................... 67

11.9 Mode: BOWL FLUSH. ON S YES - NO ........................................................................................... 68

11.10 Mode: CUP FILL ON S YES – NO................................................................................................... 68

11.11 Mode: WHITE BALANCE................................................................................................................. 68

11.12 Instrument settings via the Mode dialog:

REMOVE INSTRUMENT................................................................................................................. 70

11.13 Mode: # FUNCTION TOGGLE - MOMENTARY .............................................................................. 71

11.14 Mode: PURGE TIME... SEC ............................................................................................................ 71

11.15 Mode: PRESSURE PSI / BAR ......................................................................................................... 71

11.16 Mode: SPRACHE / LANGUAGE ENG / D / I / F / E......................................................................... 71

11.17 Mode: SIROLUX U - POS. ON – OFF ............................................................................................. 72

11.18 Mode: POLYLUX WITH CFS YES – NO ...................................................................................... 72

11.19 Mode: SUCTION WITH CFS YES – NO......................................................................................... 72

11.20 Mode: WHITE SCREEN YES – NO................................................................................................. 72

11.21 Mode: A/B VIDEO MODE ON – OFF.............................................................................................. 73

11.22 Mode: BLOW OUT SPRAY.............................................................................................................. 73

Sirona Dental Systems GmbH Table of Contents

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12 Assistant element...................................................................................................... 74

12.1 Positioning the assistant element ..................................................................................................... 74

12.2 Instrument tray for closed deposits................................................................................................... 74

12.3 Suction handpieces on the assistant element .................................................................................. 75

12.4 SPRAYVIT on the assistant element ................................................................................................ 76

12.5 Satelec Mini LED curing light............................................................................................................ 77

13 Water unit................................................................................................................... 82

13.1 Swiveling cuspidor (alternative equipment) ...................................................................................... 82

13.2 Adjusting the water amount for the cuspidor .................................................................................... 82

13.3 Amalgam rotor .................................................................................................................................. 83

13.4 Disinfection system (optional)........................................................................................................... 83

14 SIVISION 3 / SIROCAM 3 / SIROCAM C ................................................................... 84

14.1 SIVISION monitor ............................................................................................................................. 84

14.2 Camera versions............................................................................................................................... 85

14.3 SIROCAM 3 intraoral camera (extra equipment).............................................................................. 86

14.4 SIROCAM C intraoral camera (extra equipment) ............................................................................. 88

14.5 Operating modes of SIVISION 3....................................................................................................... 90

14.6 SIROCAM 3 / SIROCAM C integrated in the dentist element (video) .............................................. 92

14.7 SIROCAM 3 / SIROCAM C integrated in the dentist element (PC).................................................. 98

14.8 SIROCAM 3 / SIROCAM C integrated in the assistant element (video)........................................... 102

14.9 SIROCAM 3 / SIROCAM C integrated in the assistant element (PC) .............................................. 107

14.10 Switching between VIDEO mode and PC mode............................................................................... 110

14.11 SIVISION 3– second monitor function without SIROCAM3 / SIROCAM C...................................... 112

15 Extra equipment and accessories ........................................................................... 113

15.1 Media block on the patient chair....................................................................................................... 113

15.2 Hygienic motorized headrest protection ........................................................................................... 114

15.3 Seat cushion C ................................................................................................................................. 114

15.4 Folding armrest................................................................................................................................. 115

15.5 Hydrocolloid coolant supply .............................................................................................................. 115

15.6 X-ray image viewer on the lamp support tube .................................................................................. 116

15.7 Tray (extra equipment) ..................................................................................................................... 116

16 Maintenance............................................................................................................... 117

16.1 Care and cleaning instructions for the practice team........................................................................ 117

16.2 Inspection and maintenance............................................................................................................. 117

16.3 Safety checks ................................................................................................................................... 118

16.4 Maintenance Manual ........................................................................................................................ 118

17 Disposal ..................................................................................................................... 119

17.1 Returning electrical devices.............................................................................................................. 119

17.2 Battery disposal ................................................................................................................................ 120

1 General information Sirona Dental Systems GmbH

1.1 Dear Customer, C3+

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1 General information

1.1 Dear Customer,

We are delighted that you have chosen to equip your

practice with the Sirona C3+ treatment center.

Our aim is to recognize our customers' demands in good

time and to create innovative solutions. Together with

your trade partner, you have configured the unit to suit

your individual tastes. The new hub of your treatment

room is tailored to your personal needs.

With the C3+ you have chosen a treatment center that

epitomizes easy operation, innovative comfort,

high-quality design, and economic efficiency.

These Operating Instructions are designed to assist you

prior to initial use and whenever you require information

later on.

We hope the C3+ allows you to achieve optimum results

and satisfaction.

Your C3+ Team

1.2 Contact data

Customer Service Center In the event of technical queries, please use our online

contact form at www.sirona.com. In the navigation bar,

select "CONTACT" then "Customer Service Center" and

click on the "Contact form for technical questions" link.

Manufactu rer's address (wor ldwide)

Manufacturer's address Sirona Dental Systems GmbH

Fabrikstrasse 31

64625 Bensheim

Germany

Tel. : +49 (0) 6251/16-0

Fax: +49 (0) 6251/16-2591

E-mail: [email protected]

www.sirona.com

Sirona Dental Systems GmbH 1 General information

C3+1.3 Notes on these Operating Instructions

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1.3 Notes on these Operating Instructions

General information on the Operating

Instructions

Observe the Operating Instructions Please familiarize yourself with the unit by reading

through these Operating Instructions before putting it

into operation. It is essential that you comply with the

specified warning and safety information.

An abridged copy of the Operating Instructions is available

Tip: A quick guide containing brief operating instructions

has been provided to help you look up functions quickly.

Keep doc uments safe , Online portal, He lp

Keep documents safe Always keep the Operating Instructions handy in case

you or another user require(s) information at a later point

in time. Save the Operating Instructions on the PC or

print them out.

If you sell the unit, make sure that the Operating Instruc-

tions are included with it either as a hard copy or on an

electronic storage device so that the new owner can

familiarize himself with its functions and the specified

warning and safety information.

Online portal for technical documents We have set up an online portal for technical documen-

tation at http://www.sirona.com/manuals. From here,

you can download these Operating Instructions along

with other documents. Please complete the online form

if you would like a hard copy of a particular document.

We will then be happy to send you a printed copy free of

charge.

Help If you reach an impasse despite having thoroughly

studied the Operating Instructions, please contact your

dental depot.

Equipment options This document describes the full version of your system.

It may therefore cover components that are not included

in the system you purchased.

1 General information Sirona Dental Systems GmbH

1.4 Other valid documents C3+

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1.4 Other valid documents

Your treatment center can be equipped with additional

components that are described in separate sets of oper-

ating instructions. The instructions as well as any warn-

ing and safety information contained therein also must

be observed.

A separate manual of operating instructions exists for

each of the following Sirona products:

HUGO, CARL

• Treatment instruments and accessories

• LEDview operating light

• 15" and 22" flat-screen monitor

•SiroCam 3

• Dental treatment chairs

Care, cleaning, and disinfection of the treatment center

are described in the document entitled "Care and Clean-

ing by the Practice Team".

1.5 Warranty and liability

Warranty and liability

Warranty passport To safeguard your warranty claims, please complete the

attached "Installation Report / Warranty Passport"

together with the service engineer immediately after the

installation of your unit.

Maintenance Maintenance must be performed at scheduled intervals

to ensure the operational and functional reliability of your

product and to protect the safety and health of patients,

users and other persons. For further information, see

"Inspection and maintenance" on page 117.

The owner is responsible for making sure that all main-

tenance activities are performed.

As manufacturers of medical electrical equipment, we

can assume responsibility for the safety properties of the

unit only if maintenance and repairs on the unit are per-

formed either by us or by agencies which we have

expressly authorized and if components of the unit are

replaced by original spare parts in case of failure.

Exclusion of liability In the event that the system owner fails to fulfill its obli-

gation to perform maintenance activities or ignores error

messages, Sirona Dental Systems GmbH and its autho-

rized dealers cannot assume any liability for any dam-

age thus incurred.

Sirona Dental Systems GmbH 1 General information

C3+1.6 Intended use

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1.6 Intended use

This dental treatment center is designed to be used in

the field of human dentistry and must only be operated

by qualified dental personnel.

Contraindications for the use of the treatment center, if

any, are listed in the individual sections, e.g. Treatment

instruments.

This device is not intended for operation in areas subject

to explosion hazards.

This device is permanently installed. Operation is not

permitted in mobile vehicles.

Intended use also includes compliance with these Operat-

ing Instructions and the relevant maintenance instructions.

2 Safety instructions Sirona Dental Systems GmbH

2.1 Identification of the danger levels C3+

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2 Safety instructions

2.1 Identification of the danger levels

To prevent personal injury and material damage, please

observe the warning and safety information provided in

the present Operating Instructions. Such information is

highlighted as follows:

DANGER

An imminent danger that could result in serious bodily

injury or death.

WARNING

A possibly dangerous situation that could result in

serious bodily injury or death.

CAUTION

A possibly dangerous situation that could result in slight

bodily injury.

NOTICE

A possibly harmful situation which could lead to damage

of the product or an object in its environment.

IMPORTANT

Application instructions and other important information.

Tip: Information on making work easier.

2.2 Information on the unit

Accompanying documents

This symbol can be found next to the rating plate on the

unit.

Meaning: Observe the Operating Instructions when

operating the unit.

This symbol can be found on the rating plate on the unit.

Meaning: The accompanying documents are available

on the Sirona homepage.

Sirona Dental Systems GmbH 2 Safety instructions

C3+2.3 On-site installation

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2.3 On-site installation

The on-site installation must have been performed

according to our requirements. The details are described

in the document "Installation Requirements".

2.4 Installing the treatment center

Installation must be carried out by authorized techni-

cians in accordance with the installation instructions.

2.5 Media quality

The air and water supplies must meet the requirements

specified in the installation conditions.

To ensure compliance with the medical and national

legal requirements for water from treatment centers,

Sirona recommends equipping the treatment center with

a disinfection system. If you decide to operate the treat-

ment center without a disinfection system, you must

make alternative arrangements to ensure good water

quality.

As the owner of the treatment center, you are gener-

ally responsible for the water quality.

The colony count must fulfill the national regulations for

drinking water and must not exceed 500 CFU/ml under

any circumstances (CFU: colony forming unit).

In the event of an increased colony count, the indoor

installation must be checked and the cause of contami-

nation eliminated. Alternatively, a stand-alone water

supply can also be installed.

Before installation of the treatment center, an acceptable

microbiological water quality for the domestic water sup-

ply must be ensured and documented in the form of a

colony count. Sampling and the colony count must be

performed by a competent laboratory.

Check the treatment center water quality at regular inter-

vals; see "Microbiological inspection of the water" in the

document "Care and Cleaning by the Practice Team".

Please contact your specialized dealer or your relevant

dental association for the respective national require-

ments and measures. Where necessary, you must make

alternative arrangements to ensure good water quality if

you decide to operate the treatment center without a dis-

infection system.

Further information on the media quality requirements

are listed in the "Installation conditions" document.

Highly immunosuppressed patients should not come in

contact with water from the treatment center. The use of

sterile solutions is recommended.

2 Safety instructions Sirona Dental Systems GmbH

2.6 Connection to the public drinking water system C3+

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2.6 Connection to the public drinking water system

Connecti on to the public drinking wat er system

Free dis charge fo r option wit hout disinfection system

Treatment center with separation of the public

drinking water supply

Provided it is equipped with a disinfection system, the

treatment center fulfills the requirements of EN 1717

(free outlet with sections ≥20 mm) and the German Gas

and Water Association (DVGW). It is intrinsically safe in

accordance with worksheet W540 and therefore also ful-

fills the W270 requirements as well as the requirements

for plastics used in the transport of drinking water. It can

be connected directly to the public drinking water sys-

tem.

The treatment center therefore also bears the symbol for

the German Gas and Water Association (DVGW) along

with the rating plate.

Treatment center without separation to the

public drinking water supply

If compliance with EN 1717 is stipulated at a national

level, appropriate equipment must be installed beyond

the treatment center to protect the public drinking water

system.

This applies to device versions without a disinfection

system.

The treatment center then does not bear the symbol for

the German Gas and Water Association (DVGW).

Please always adhere to the national requirements with

regard to connecting treatment centers to the public

drinking water supply.

2.7 Maintenance and repair

Maintenance and repair

Authorized technical personnel and spare parts As manufacturers of dental medical units and in the

interest of the operational safety of your system, we

stress the importance of having maintenance and repair

of this unit performed only by ourselves or by agencies

expressly authorized by us. Furthermore, failed compo-

nents must always be replaced with original spare parts.

We suggest that you request a certificate showing the

nature and extent of the work performed from those who

carry out such work; it must contain any changes in rated

parameters or working ranges (if applicable), as well as

the date, the name of the company and a signature.

Maintenance intervals Despite the outstanding quality of your treatment center

and regular care by the practice team, in the interest of

operational safety, it is essential to have preventive

maintenance performed at scheduled intervals.

Sirona Dental Systems GmbH 2 Safety instructions

C3+2.8 Trouble-free operation

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In order to ensure the operational safety and reliability of

your treatment center and to avoid damage due to natu-

ral wear, you as the system owner must have your sys-

tem checked regularly by an authorized service engineer

from your dental depot. Furthermore, safety checks

must be performed. Please contact your dental depot to

obtain a maintenance offer. For further information, see

"Maintenance" on page 117.

2.8 Trouble-free operation

Trouble-free operation

Use of this unit is permissible only if it works properly

without malfunctions. If trouble-free operation cannot be

ensured, the unit must be taken out of service, checked

by authorized technicians for malfunctions and, if neces-

sary, repaired.

2.9 Vacuum system

The suction removal of aluminum and other metal oxides

from blasting devices via the amalgam separator and the

automatic separator installed in the treatment center is

prohibited! This would cause extreme wear and clogging

of the suction and water paths.

A separate vacuum system must be used in connection

with metal oxide blasting devices. Treatment centers

equipped with a central wet suction system are generally

suitable for suction removal of the above material. How-

ever, make sure to observe the instructions provided by

the manufacturer of your vacuum system.

No restrictions apply when using salt blasting devices in

connection with Sirona treatment centers. However, in

such cases, make sure that the system is subsequently

flushed with an adequate amount of water.

2.10 Patient chair

Patient chair

Please observe the patient chair's maximum load

capacity of 135 kg.

The weight distribution complies with ISO 6875. The

mechanical stability test is performed with a multiple

safety factor according to IEC 60601-1.

The maximum permissible weight of accessories

mounted on the patient chair is 5 kg.

The patient’s arms and legs must be resting on the

upholstery of the chair.

2.11 Ventilation slots

Ventilatio n slots

Under no circumstances may the ventilation slots on the

unit be covered, since otherwise the air circulation will be

obstructed. This can cause the unit to overheat.

wrong

right

2 Safety instructions Sirona Dental Systems GmbH

2.12 Intermittent operation C3+

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Do not spray liquids such as disinfectants into the venti-

lation slots. This may lead to malfunctions. Use only

wipe disinfection in the vicinity of the ventilation slots.

2.12 Intermittent operation

Intermittent operation

The motors of the treatment center and of the treatment

instruments are designed for intermittent operation cor-

responding to the dental mode of treatment.

Drive motors for patient chair and backrest: max. 6%

duty cycle (15 s "ON"/3 min, 55 s "OFF")

Other motors: Intermittent operation, max. 10% duty

cycle (max. 2 min "ON"/18 min "OFF")

2.13 Care, cleaning agents, and disinfectants

Unsuitable care and cleaning agents and disinfectants may

corrode the surface of the unit or impair its functioning.

Therefore, use only care and cleaning agents and disin-

fectants which have been approved by Sirona. For fur-

ther information, see the document "Care, cleaning

agents, and disinfectants", REF 59 70 905.

2.14 Modifications and extensions of the system

Modificat ions and extensio ns of the system

Modifications to this system which might affect the safety

of the system owner, patients or other persons are pro-

hibited by law.

For reasons of product safety, this product may be oper-

ated only with original Sirona accessories or third-party

accessories expressly approved by Sirona. The user is

responsible for any damage resulting from the use of

non-approved accessories.

If any devices not approved by Sirona are connected,

they must comply with the applicable standards, e.g.:

• IEC 60950-1 for information technology equipment

(e.g. PC) and

• IEC 60601-1 for medical electrical equipment.

The treatment center monitor must fulfill the require-

ments of the IEC 60950-1 standard.

The loudspeaker port of the monitor may only be con-

nected to a device that complies with IEC 60950-1

(e.g. a PC) or IEC 60601-1. Under no circumstances

may it be connected to a stereo system or similar.

Sirona Dental Systems GmbH 2 Safety instructions

C3+2.15 Electromagnetic compatibility

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If a system is created during the installation process, the

requirements of IEC 60601-1, 3rd edition, must be ful-

filled. The system author assumes responsibility for con-

formity of the system with 93/42/EEC Directive.

2.15 Electromagnetic compatibility

Medical electrical equipment is subject to special pre-

cautionary measures with regard to electromagnetic

compatibility (EMC). They must be installed and oper-

ated as specified in the document "Installation Require-

ments".

Portable and mobile RF communications equipment

may interfere with medical electrical equipment. There-

fore, the use of such devices (e.g. cellular phones) in

practice or hospital environments must be prohibited.

Operating an RF surgical device

Treatment with RF surgical devices creates strong elec-

tromagnetic fields, which may impact other electronic

devices. Do not place external RF surgical devices on

the shelf space of the treatment center and do not guide

the RF handpiece cable over this. Electromagnetic dis-

turbances can often be reduced, if the external RF sur-

gical device is operated with a neutral electrode.

Video system

Electromagnetic disturbances in the environment of the

treatment center may result in reduced image quality. In

such cases, it is advisable to repeat the exposure before

saving the image.

In case of line voltage drops, image data stored in the

video camera may be lost. Deposit the camera and

repeat the exposure.

Image artifacts may possibly occur as a result of

radio-frequency interference caused by the transmitters

of e.g. radio services or radio amateurs.

Wireless foot control

The wireless foot control may interfere with other

devices in the same frequency band (2.4 GHz) or

receive interfering signals from them. The safe condition

of the treatment center is guaranteed even if the wireless

transmission is compromised.

2.16 Influencing of cardiac pacemakers

The treatment center contains strong magnets. These

magnets can affect cardiac pacemakers implanted in

patients, users and technical personnel.

Therefore, please observe the safety information on

pages 40, 44, and 74.

2 Safety instructions Sirona Dental Systems GmbH

2.17 Dismantling / Installation C3+

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2.17 Dismantling / Installation

Dismantlin g / Installatio n

Follow th e installation instr uctions

When dismantling and reinstalling the unit, proceed

according to the installation instructions for new installa-

tion in order to guarantee its proper functioning and sta-

bility.

Sirona Dental Systems GmbH 3 Technical description

C3+3.1 Standards / Approvals

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3 Technical description

3.1 Standards / Approvals

The C3+ treatment center complies with the following

standards, among others:

• IEC 60601-1 (electrical, mechanical, and software

safety)

• IEC 60601-1-2 (electromagnetic compatibility)

• IEC 60601-1-6 (serviceability)

• ISO 6875 (patient chair)

• ISO 7494-1 (dental treatment units)

• ISO 7494-2 (dental treatment units, water and air

supply)

• ISO 9680 (operating light)

• ISO 11143 (amalgam separator), see also below

(provided amalgam separator option is available)

• EN 1717 (connection to the drinking water system),

see also below and the section "Connection to the

public drinking water system" on page 12

Original language: German

This product bears the CE mark in accordance with the

provisions of the Council Directive 93/42/EEC of

June 14, 1993 concerning medical devices (MDD).

The treatment center meets the requirements of the

Canadian Standard Association (CSA) in accordance

with CAN/CSA-C22.2 No. 60601-1.

The amalgam separator achieves a separation effi-

ciency of > 95 %. The requirements of the ISO 11143

standard are thereby fulfilled.

Type 1 separation process: Centrifugal system

The amalgam separator is approved by the German

Institute for Structural Engineering (DIBt) and by the

AFNOR (France).

Original language of the present document: German

The treatment center fulfills the requirements of the

directive on the restriction of hazardous substances,

2011/65/EU.

When equipped with a disinfection system, the treatment

center complies with the technical rules and require-

ments on safety and hygiene for connection to the public

drinking water supply.

0123

SIRONA

Dental Systems

GmbH

64625 Bensheim

Fabrikstrasse 31

Z-64.1-14

3 Technical description Sirona Dental Systems GmbH

3.1 Standards / Approvals C3+

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The unit is certified according to the requirements of the

German Technical and Scientific Association for Gas

and Water (DVGW). It is intrinsically safe in accordance

with worksheet W540. The unit thus fulfills the require-

ments of EN 1717, see also the chapter entitled "Con-

nection to the public drinking water system" on page 12.

This unit meets the requirements of BELGAQUA and

may therefore be connected to the public drinking water

supply in Belgium.

The wireless modules in the wireless foot switch and in

the treatment center meet the requirements of the

R&TTE Directive 1999/5/EC.

Standards:

• EN 60950-1

• EN 301489-1, EN 301489-17, EN 300328

The modules meet the requirements of the Federal

Communications Commission (Part 15 of the FCC

Rules).

FCC ID: SIFNANOLOCAVR0108

Industry Canada The modules meet the requirements of Industry Canada

(RSS210).

IC: 7654A-nanoLOCAVR

The current approvals of the wireless foot switch are

listed on the rating plate on the underside of the wireless

foot switch.

C3® is a registered trademark of Sirona Dental Systems

GmbH.

Sirona Dental Systems GmbH 3 Technical description

C3+3.2 Technical data

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3.2 Technical data

Dental treatment center

Model designation: C3+

Power connection: 100 V / 115 V / 230 VAC 50 / 60 Hz

Rated current: 11.5 A at 100 VAC

9.5 A at 115 VAC

4.5 A at 230 VAC.

In addition, max. 6 A for external devices

Overvoltage category: 2 acc. to IEC 60664-1

Main unit fuse: for 100/115 V AC: T 10 A H, 250 V AC , REF 10 77

460

for 230 V AC: T 6.3 A H, 250 V AC , REF 10 77 452

Protection class: Class I device

Device class in accordance

with Directive 93/42/EEC:

Class IIa equipment

Degree of protection against elec-

trical shock:

Type B applied parts

Except SIROCAM 3 / SIROCAM C. These are:

Type BF applied parts

Degree of protection against

ingress of water:

Ordinary equipment (without protection against

ingress of water)

The foot switch has an IP X1 degree of protection

against liquids (drip-proof).

Mode of operation Continuous operation with intermittent loading accord-

ing to the type of dental operation, see "Intermittent

operation" on page 14

This device is permanently installed. Operation is not

permitted in mobile vehicles.

Transport and storage conditions: Temperature: -40°C – +70°C

-40°F – +158°F

relative humidity: 10% – 95%

Air pressure: 500hPa – 1,060hPa

Operating conditions: Ambient temperature: 10°C – 40°C

50°F – 104°F

relative humidity: 30% – 85% (no condensa-

tion)

Air pressure: 700hPa – 1,060hPa

Installation location: ≤3,000 m above sea level

This treatment center is not suitable for operation in

areas subject to explosion hazards.

Pollution degree: 2 acc. to IEC 60664-1

Tests/Approvals: See "Standards / Approvals" on page 17

Year of manufacture: (on the rating plate of the patient chair)

-40

+70 1060

500

95

10

+10

+40 1060

700

85

30

3 Technical description Sirona Dental Systems GmbH

3.2 Technical data C3+

59 06 404 D 3390

20 D 3390.201.01.18.02

Foot switch wireless interface

IMPORTANT

Minimum PC requirements

See document "Installation instructions and system re-

quirements for PC configuration", (REF 59 11 321)

SIVISION 3.

Model designation: nanoLOC AVR

Frequency: 2,4 GHz – 2.4835 GHz (ISM band)

Transmitting power: < 2 mW (short-range device)

Modulation type: MDMA

Range: approx. 10 m

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