KaVo INTRA LUX KL702 Operating instructions

Brand: KaVo

Model: INTRA LUX KL702

Type: Operating instructions

KaVo INTRA LUX KL702 is a high-quality product for dental professionals. It can be used with a high-pressure lamp or the KaVo MULTILED lamp. The spray water regulation allows for precise adjustment of the water flow. Attachments can be easily connected and removed. The device has been designed to meet the highest standards of safety and reliability.

Instructions for use

INTRA LUX motor 702KL – 1.003.5622

- with high pressure lamp

- with KaVo MULTILED-lamp

Distributed by:

KaVo Dental GmbH

Bismarckring 39

D-88400 Biberach

Phone +49 7351 56-0

Fax +49 7351 56-1488

Manufacturer:

Kaltenbach & Voigt GmbH

Bismarckring 39

D-88400 Biberach

www.kavo.com

Contents

1User instructions....................................................................................................................................... 6

2Safety........................................................................................................................................................ 8

2.1 Description of safety instructions....................................................................................................... 8

2.1.1 Warning symbol.................................................................................................................... 8

2.1.2 Structure............................................................................................................................... 8

2.1.3 Description of danger levels................................................................................................. 9

2.2 Safety instructions........................................................................................................................... 11

3Product description................................................................................................................................. 19

3.1 Purpose – Proper use...................................................................................................................... 19

3.2 Technical Specifications.................................................................................................................. 22

3.2.1 Operation with high-pressure lamp..................................................................................... 27

3.2.2 Operation with KaVo MULTI LED lamp.............................................................................. 27

3.2.3 Transportation and storage conditions............................................................................... 28

3.2.4 Operating conditions........................................................................................................... 29

Contents 3 / 70

4First use.................................................................................................................................................. 30

4.1 Use of the enclosed KaVo MULTI LED lamp.................................................................................. 31

5Operation................................................................................................................................................ 32

5.1 Connection to the supply hose........................................................................................................ 32

5.2 Spray water regulation..................................................................................................................... 34

5.3 Connecting the attachments............................................................................................................ 35

5.3.1 Attaching............................................................................................................................. 38

5.3.2 Removal.............................................................................................................................. 38

6Troubleshooting...................................................................................................................................... 39

6.1 Check for malfunctions before initial startup.................................................................................... 39

6.2 Troubleshooting............................................................................................................................... 42

6.2.1 Replacing the high-pressure lamp...................................................................................... 42

6.2.2 Replacing the KaVo MULTI LED lamp............................................................................... 44

6.2.3 Exchanging the O-rings...................................................................................................... 47

7Preparation methods according to ISO 17664........................................................................................ 49

7.1 Preparation at the site of use........................................................................................................... 49

Contents 4 / 70

7.2 Cleaning.......................................................................................................................................... 50

7.2.1 Manual cleaning - external.................................................................................................. 50

7.2.2 Automated external cleaning.............................................................................................. 52

7.2.3 Manual cleaning - internal................................................................................................... 53

7.2.4 Automated internal cleaning............................................................................................... 55

7.3 Disinfection...................................................................................................................................... 55

7.3.1 Manual disinfection - external............................................................................................. 56

7.3.2 Manual disinfection - internal.............................................................................................. 57

7.3.3 Automated disinfection - external and internal.................................................................... 57

7.4 Drying ............................................................................................................................................. 58

7.5 Care products and systems - Servicing........................................................................................... 59

7.6 Packaging........................................................................................................................................ 61

7.7 Sterilisation...................................................................................................................................... 62

7.8 Storage............................................................................................................................................ 64

8Auxiliary equipment................................................................................................................................. 65

9Terms and conditions of warranty........................................................................................................... 66

Contents 5 / 70

1 User instructions

Dear User

Congratulations on purchasing this KaVo quality product. By following the

instructions below you will be able to work smoothly, economically and

safely.

Symbols

Refer to the chapter on Safety/Warning symbol

Important information for users and service technicians

1 User instructions 6 / 70

Can be steam sterilized at 134 oC -1 oC/+4 oC (273 oF -1,6 oF/+7,4

oF)

CE mark (European Community). A device bearing this mark

meets the requirements of the applicable EC guidelines.

Action request

Target group

This document is intended for dentists and their assistants. The section on

starting up is also intended for service technicians.

1 User instructions 7 / 70

2 Safety

2.1 Description of safety instructions

2.1.1 Warning symbol

Warning symbol

2.1.2 Structure

DANGER

The introduction describes the type and source of the haz‐

ard.

This section describes potential consequences of non-compliance.

2 Safety 8 / 70

▶ The optional step includes necessary measures for hazard prevention.

2.1.3 Description of danger levels

The safety instructions listed here, together with the three levels of danger

will help avert property damage and injury.

CAUTION

indicates a hazardous situation that can cause damage to property or mild

to moderate injuries.

2 Safety 9 / 70

WARNING

indicates a hazardous situation that can lead to serious or fatal injury.

DANGER

indicates a maximal hazard due to a situation that can directly cause

death or fatal injury.

2 Safety 10 / 70

2.2 Safety instructions

WARNING

Hazard from incorrectly reconditioned products.

An infection hazard exists from contaminated products.

▶ Take suitable personal protective measures.

2 Safety 11 / 70

WARNING

Hazard to the care provider and patient.

Irregular running noise, significant vibration, overheating, imbalance or in‐

sufficient grip.

▶ Stop working and contact service support.

WARNING

Risks from electromagnetic fields.

The functions of implanted systems (such as pacemakers) can be influ‐

enced by electromagnetic fields.

▶ Ask patients before treatment and counsel them about the risks.

2 Safety 12 / 70

WARNING

Electrical power

Electrical shock from incorrectly connecting a non-KaVo system to the

medical device.

▶ When installing and operating the medical device for treatments and

equipment from other manufacturers, observe the provisions of "Pro‐

tection from electrical shock," "Leakage current," and "Not grounding

the application part" in accordance with DIN EN IEC 60601-1.

▶ The medical device may only be combined with a treatment unit re‐

leased by KaVo.

2 Safety 13 / 70

WARNING

Hazard from direct exposure to radiation.

Blinding.

▶ Do not look directly into the high-pressure lamp or the KaVo MULTI

LED lamp.

2 Safety 14 / 70

CAUTION

Risks due to lack of control equipment.

Hazards can arise if control equipment is not available for changing the

speed and the direction of rotation.

▶ The dental treatment unit connected must have control equipment for

changing the speed and direction of rotation.

▶ A note is to be included in the documents accompanying the dental

treatment unit, referring to responsibilities arising from safety, reliability

and performance.

▶ The medical device may only be combined with a treatment centre re‐

leased by KaVo.

2 Safety 15 / 70

CAUTION

Damage from soiled and moist cooling air.

Contaminated and moist cooling air can cause malfunctions and lead to

premature bearing wear.

▶ Make sure that the supply of cooling air is dry, clean, and uncontami‐

nated in accordance with DIN EN ISO 7494-2.

CAUTION

Damage due to contaminated water.

Ensure that the water quality generally complies with DIN EN ISO 7494-2.

Permissible pH value 7.2 to 7.8.

2 Safety 16 / 70

CAUTION

Premature wear and malfunctioning from improper storage

during long periods of nonuse.

Reduced product life.

▶ The medical device should be cleaned, serviced and stored in a dry lo‐

cation, according to instructions, before long periods of nonuse.

Note

This medical device in conjunction with the dental treatment unit meets

the requirements of DIN EN IEC 60601-1.

2 Safety 17 / 70

The following individuals are authorized to repair and service KaVo prod‐

ucts:

▪ Technicians at KaVo branches throughout the world

▪ Technicians specially trained by KaVo

The present product is subject to the EC Directive on used electrical and

electronic devices and must be disposed within Europe at a special facili‐

ty. Further information can be obtained from KaVo or a dental distributor.

2 Safety 18 / 70

3 Product description

INTRA LUX Motor KL 702 (Mat. no. 1.003.5622)

3.1 Purpose – Proper use

Indications for use:

The sterilisable motor is:

3 Product description 19 / 70

▪ an electrical low-voltage motor for dental purposes according to DIN

EN ISO 14457 and DIN ISO 80601-2-60 and classified as a type B ap‐

plied part

▪ intended to drive / operate a dental handpiece / contra-angle hand‐

piece equipped with a handpiece connection according to ISO 3964

▪ not approved for use in areas at risk of explosion

▪ intended only for dental treatment by a dental professional; the prod‐

uct may not be modified or used for any other purpose since this may

be hazardous

▪ a medical device according to relevant national statutory regulations

3 Product description 20 / 70

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KaVo INTRA LUX KL702 Operating instructions

KaVo INTRA LUX KL702 Operating instructions

KaVo INTRA LUX KL702 Operating instructions

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