KaVo MASTERmatic LUX M10 L User manual

Instructions for use
MASTERmatic LUX M10 L - 1.009.3570

Distributed by:
KaVo Dental GmbH
Bismarckring 39
D-88400 Biberach
Phone [phone]
Fax [phone]
Manufacturer:
Kaltenbach & Voigt GmbH
Bismarckring 39
D-88400 Biberach
www.kavo.com

Table of contents
1User instructions....................................................................................................................................... 6
2Safety........................................................................................................................................................ 8
2.1 Description of safety instructions....................................................................................................... 8
2.2 Safety instructions........................................................................................................................... 11
3Product description................................................................................................................................. 18
3.1 Purpose – Intended use................................................................................................................... 19
3.2 Technical Specifications.................................................................................................................. 21
3.3 Transportation and storage conditions............................................................................................ 22
4Start up and shut down........................................................................................................................... 24
4.1 Check the amount of water.............................................................................................................. 25
5Operation................................................................................................................................................ 28
5.1 Attach the medical device................................................................................................................ 28
5.2 Remove the medical device............................................................................................................ 30
5.3 Insert the handpiece or contra-angle handpiece drill bit.................................................................. 31
5.4 Remove the handpiece or contra-angle handpiece drill bit............................................................. 35
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5.5 Conversion for contra-angle handpiece drill bit............................................................................... 36
6Troubleshooting...................................................................................................................................... 38
6.1 Check for malfunctions.................................................................................................................... 38
6.2 Troubleshooting............................................................................................................................... 41
6.2.1 Replacing the O-rings......................................................................................................... 41
6.2.2 Cleaning the spray nozzle.................................................................................................. 42
7Reprocessing steps in accordance with ISO 17664............................................................................... 44
7.1 Preparations at the site of use......................................................................................................... 44
7.2 Cleaning.......................................................................................................................................... 45
7.2.1 Manual cleaning - external.................................................................................................. 45
7.2.2 Automated external cleaning.............................................................................................. 46
7.2.3 Manual cleaning - internal................................................................................................... 47
7.2.4 Automated internal cleaning............................................................................................... 49
7.3 Disinfection...................................................................................................................................... 50
7.3.1 Manual disinfection - external............................................................................................. 53
7.3.2 Manual disinfection - internal.............................................................................................. 54
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7.3.3 Machine disinfection - external and internal....................................................................... 55
7.4 Drying.............................................................................................................................................. 56
7.5 Care products and systems - Servicing........................................................................................... 57
7.5.1 Care with KaVo Spray........................................................................................................ 59
7.5.2 Care with the KaVo SPRAYrotor........................................................................................ 61
7.5.3 Servicing with KaVo QUATTROcare 2104 / 2104A............................................................ 62
7.5.4 Servicing with KaVo QUATTROcare PLUS 2124 A........................................................... 65
7.5.5 Servicing with KaVo QUATTROcare CLEAN 2140 A......................................................... 68
7.6 Packaging........................................................................................................................................ 70
7.7 Sterilisation...................................................................................................................................... 71
7.8 Storage............................................................................................................................................ 73
8Tools and consumables.......................................................................................................................... 74
9Warranty terms and conditions............................................................................................................... 76
Contents 5 / 80

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.
© Copyright by KaVo Dental GmbH
Symbols
Refer to the chapter on Safety/Warning symbol
Important information for users and service technicians
1 User instructions 6 / 80

Can be steam-sterilised at 134 oC -1 oC / +4 oC (273 oF -1.6 oF /
+7.4 oF)
Thermodisinfectable
CE-Zeichen (Communauté Européenne). Ein Produkt mit diesem
Zeichen entspricht den Anforderungen der anwendbaren EG-
Richtlinie.
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 / 80

2 Safety
2.1 Description of safety instructions
Warning symbol
Structure
DANGER
The introduction describes the type and source of the haz‐
ard.
This section describes potential consequences of non-compliance.
▶ The optional step includes necessary measures for hazard prevention.
2 Safety 8 / 80

Description of hazard levels
The safety instructions listed here, together with the three levels of danger
will help avert property damage and injury.
CAUTION
CAUTION
indicates a hazardous situation that can cause damage to property or mild
to moderate injuries.
2 Safety 9 / 80

WARNING
WARNING
indicates a hazardous situation that can lead to serious or fatal injury.
DANGER
DANGER
indicates a maximal hazard due to a situation that can directly cause
death or fatal injury.
2 Safety 10 / 80

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 / 80

WARNING
Hazards for the care provider and the patient.
In the case of damage, irregular running noise, excessive vibration, un-
typical warming or when the cutter or grinder cannot be held.
▶ Do not use further and notify Service.
2 Safety 12 / 80

CAUTION
Risk due to incorrectly stored instrument.
Injury and infection caused by chucked cutters or grinders.
Damage to clamping system from dropping the instrument.
▶ After treatment, place the instrument properly in the cradle, without the
cutter or grinder.
2 Safety 13 / 80

CAUTION
Hazard from use as a light probe.
Do not use the device as a light probe since the rotating cutters or grind‐
ers can cause injury.
▶ Use an appropriate light probe for additional illumination of the oral
cavity or site of preparation.
2 Safety 14 / 80

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 / 80

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
For safety reasons, we recommend that the tool holder system be
checked annually after the warranty period expires.
2 Safety 16 / 80

The following individuals are authorized to repair and service KaVo prod‐
ucts:
▪ Technicians at KaVo branches throughout the world
▪ Technicians specially trained by KaVo
To ensure proper function, the medical device must be set up according to
the reprocessing methods described in the KaVo Instructions for Use, and
the care products and care systems described therein must be used. KaVo
recommends specifying a service interval at the dental office for a licensed
shop to clean, service and check the functioning of the medical device.
This service interval depends on the frequency of use and should be adjus‐
ted accordingly.
Service may only be carried out by KaVo-trained repair shops using origi‐
nal KaVo replacement parts.
2 Safety 17 / 80

3 Product description
MASTERmatic LUX M10 L (Mat. no. 1.009.3570)
3 Product description 18 / 80

3.1 Purpose – Intended use
Indications for use:
This medical device is
▪ intended for dental treatment only. All other types of use or modifica‐
tions of the product are not permitted and can be hazardous. The
medical device is intended for the following applications: Removal of
carious material, cavity and crown preparations, removal of fillings,
processing of tooth and restoration surfaces.
▪ A medical device according to relevant national statutory regulations.
Proper use:
According to these regulations, this medical device may only be used for
the described application by a knowledgeable user. You need to comply
with the following:
3 Product description 19 / 80

▪ the applicable health and safety regulations
▪ the applicable accident prevention regulations
▪ these Instructions for use
According to these regulations, the user is required to:
▪ only use equipment that is operating correctly,
▪ adhere to the specified intended use
▪ protect him or herself, the patient and third parties from danger, and
▪ avoid contamination from the product.
3 Product description 20 / 80