KaVo SMARTtorque LUX S619 L User manual

Instructions for use
SMARTtorque LUX S619 L - REF 1.008.1641
SMARTtorque Mini LUX S615 L - REF 1.008.1643
SMARTtorque S619 C - REF 1.008.1642

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
1 User instructions ............................................................................................................................................... 5
2 Safety ............................................................................................................................................................... 7
2.1 Description of safety instructions ............................................................................................................ 7
2.2 Safety instructions .................................................................................................................................. 9
3 Product description ......................................................................................................................................... 14
3.1 Purpose – Proper use .......................................................................................................................... 16
3.2 Technical Specifications ....................................................................................................................... 18
3.3 Transportation and storage conditions ................................................................................................. 20
4 Start up and shut down .................................................................................................................................. 22
4.1 Mount the MULTIflex (LUX) / MULTIflex LED coupling ........................................................................ 23
4.2 Checking the amount of water .............................................................................................................. 25
4.3 Checking the pressures ........................................................................................................................ 26
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4.4 Checking the O-rings ............................................................................................................................ 27
5 Operation ........................................................................................................................................................ 28
5.1 Attaching the medical device ................................................................................................................ 29
5.2 Removing the medical device .............................................................................................................. 31
5.3 Insert the milling cutter or diamond grinder .......................................................................................... 32
5.4 Removing the milling tool or diamond grinder. ..................................................................................... 36
6 Troubleshooting .............................................................................................................................................. 38
6.1 Exchanging the O-rings on the coupling on the supply hose ............................................................... 38
6.2 Cleaning the spray nozzle .................................................................................................................... 39
7 Reprocessing methods according to ISO 17664 ............................................................................................ 41
7.1 Preparations at the site of use .............................................................................................................. 41
7.2 Cleaning ............................................................................................................................................... 42
7.2.1 Cleaning: Manual external cleaning ........................................................................................ 42
7.2.2 Cleaning: Automated external cleaning ................................................................................... 43
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7.2.3 Cleaning: Manual internal cleaning ......................................................................................... 44
7.2.4 Cleaning: Automated internal cleaning .................................................................................... 46
7.3 Disinfection ........................................................................................................................................... 47
7.3.1 Disinfection: Manual external disinfection ............................................................................... 48
7.3.2 Disinfection: Manual disinfection - internal .............................................................................. 49
7.3.3 Disinfection: Machine disinfection - external and internal ....................................................... 50
7.4 Drying ................................................................................................................................................... 51
7.5 Care products and systems - Servicing ................................................................................................ 52
7.5.1 Care products and systems - Servicing: Servicing with KaVo Spray ...................................... 53
7.5.2 Care products and systems - Servicing: Care with KaVo SPRAYrotor ................................... 55
7.5.3 Care products and systems - Servicing: Servicing with KaVo QUATTROcare PLUS ............. 56
7.6 Packaging ............................................................................................................................................. 60
7.7 Sterilisation ........................................................................................................................................... 61
7.8 Storage ................................................................................................................................................. 64
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8 Tools ............................................................................................................................................................... 65
9 Warranty terms and conditions ....................................................................................................................... 67
Table of contents 4

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
User instructions 5

Action request
CE mark (European Community). A product bearing this mark
meets the requirements of the applicable EC directive.
Can be steam-sterilised at 134 °C -1 °C / +4 °C (273 °F -1.6 °F /
+7.4 °F)
Thermodisinfectable
Target group
This document is intended for dentists and their assistants. The section
on starting up is also intended for service technicians.
User instructions 6

2 Safety
2.1 Description of safety instructions
Warning symbol
Structure
DANGER
The introduction describes the type and source of the hazard.
This section describes the potential consequences of non-observance.
▶The optional step includes necessary measures for hazard preven‐
tion.
Safety 7

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.
WARNING
WARNING
indicates a hazardous situation that can cause death or serious injury.
Safety 8

DANGER
DANGER
indicates a hazardous situation that can directly cause death or serious
injury.
2.2 Safety instructions
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.
Safety 9

WARNING
Hazard from contraindication.
If the soft tissue in the oral cavity is injured, the compressed air may en‐
able septic substances to enter the tissue.
▶Treatment must be discontinued with instruments operated by com‐
pressed air when soft tissue is damaged in the oral cavity.
CAUTION
Burning hazard from hot instrument head and instruments cover.
If the instrument overheats, burns may arise in the oral area.
▶Never contact soft tissue with the instrument head.
Safety 10

CAUTION
Hazard from use as a light probe.
Do not use the device as a light probe since the rotating cutter grinder
can cause injury.
▶Use an appropriate light probe for additional illumination of the oral
cavity or site of preparation.
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.
Safety 11

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 location, according to instructions, before long periods of non‐
use.
Note
For safety reasons, we recommend that the tool holder system be
checked annually after the warranty period expires.
To ensure proper function, the medical device must be set up according
to the reprocessing methods described in the KaVo Instructions for Use,
Safety 12

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 adjusted accordingly.
Service may only be carried out by KaVo-trained repair shops using origi‐
nal KaVo replacement parts.
Safety 13

3 Product description
SMARTtorque LUX S619 L (Mat. no. 1.008.1641)
SMARTtorque Mini LUX S615 L (Mat. no. 1.008.1643)
Product description 14

SMARTtorque S619 C (Mat. no. 1.008.1642)
Product description 15

3.1 Purpose – Proper use
Purpose:
This medical device is
▪ Only intended for dental treatment. Any other type of use or altera‐
tion to the product is impermissible and can be hazardous. The med‐
ical device is intended for the following uses: Removal of carious ma‐
terial, cavities and crown preparations, removal of fillings, processing
of tooth and restoration surfaces.
▪ A medical device according to relevant national statutory regulations.
Product description 16

Proper use:
According to these regulations, this medical device may only be used for
the described application by a knowledgeable user. The following must
be observed:
▪ the applicable health and safety regulations
▪ the applicable accident prevention regulations
▪ these instructions for use
According to these regulations, it is the responsibility of the user to:
▪ only use equipment that is operating correctly,
▪ use the equipment for the proper purpose,
▪ protect him or herself, the patient and third parties from danger, and
▪ avoid contamination from the product.
Product description 17

3.2 Technical Specifications
SMARTtorque
LUX S619 L
SMARTtorque
Mini LUX
S615 L
SMARTtorque
S619 C
Minimal drive pressure 2.1 bar (30
psi)
2.1 bar (30
psi)
2.1 bar (30
psi)
Drive pressure 2.1 to 4.2 bar
(30 to 61 psi)
2.1 to 4.2 bar
(30 to 61 psi)
2.1 to 4.2 bar
(30 to 61 psi)
Air consumption 40 Nl/min 39 Nl/min 40 Nl/min
Idle speed 350,000 to
400,000 rpm
350,000 to
450,000 rpm
350,000 to
400,000 rpm
Power > 15 W > 12 W > 15 W
Head size Standard Mini Standard
Recommended oper‐
ating pressure
2 to 3 N 2 to 3 N 2 to 3 N
Product description 18