DKL L2-S600 User manual

Operating Instructions
Manufacturer:
DKL CHAIRS GmbH
An der Ziegelei 3
D-37124 Rosdorf
Germany
[phone]
[email protected]
www.dkl.de
L2-S600
Form no. GEN-L2600
Rev. 06 / 26.05.2023
Subject to change without
notice.
L2-C600

2
Contents
Annex
> Instructions for Use W&H Dentalwerk Bürmoos GmbH Electric motor EM-12L
> Instructions for Use W&H Dentalwerk Bürmoos GmbH Implantmed motor EM-19LC
> Instructions for Use W&H Dentalwerk Bürmoos GmbH Piezo Scaler PB 5
> Instructions for Use W&H Dentalwerk Bürmoos GmbH FOOT CONTROL S-NW
> Instructions for Use W&H Dentalwerk Bürmoos GmbH Peristaltic pump
> Operating Instructions DÜRR Dental Spittoon valve 3
> Operating Instructions DÜRR Dental CAS 1 Combi-Separator
> Operating Instructions DÜRR Dental CS 1 Combi-Sepamatic
> Use Manual Syringe Luzzani Minilight
> USER MANUAL FARO EVA
Symbols in the Operating Instructions 3
Symbols inside the Unit 4
Introduction 5
Electromagnetic Compatibility (EMC) 6
Safety Instructions - General 7
Safety Notes – Doctor’s Device, Assistant’s device and Cuspidor 8
Safety notes – Transmission Instruments 8
Technical Speci!cations 9
Media Requirements 10
Dimensions in Millimetres 12
Product Description 13
Foot Controller 16
Icons – Display 17
Icons – Navigation Touch Display 18
Icons – Setup 19
Moving the Treatment Chair 20
Putting the Treatment Unit into Operation 22
Creating a User 23
Managing Users 24
Main Menu Instruments 24
General Instrument Functions 25
Starting the Turbine 27
Starting the Turbine (Advanced Air) 27
Starting the Electric Motor 28
Starting the Piezo Scaler 30
Function Syringe Luzzani Minilight 31
Implantmed W&H EM-19LC 32
Operating Lamp LED.light EVA 38
Tray 41
Cuspidor 42
Suction 43
Suction System 44
Cleaning and Disinfection of the Suction Handpieces 45
Cleaning and Disinfection of the Suction System 47
Cleaning and Disinfection of the Surfaces 49
Cleaning and Disinfection of the Instrument Holders 52
Cleaning the Turbine Return Air Filter 52
Bottle Care System 53
Flushing Function with the Bottle Care System 54
Intensive Flushing with the Bottle Care System 55
Water Separation Unit (WSU) 56
Flushing Function with the Water Separation Unit (WSU) 58
Intensive Flushing with the Water Separation Unit (WSU) 59
Filling DK-DOX 150 into the Water Separation Unit 60
Setting Media Instruments 61
Maintenance and Inspection 62
Safety Inspections 62
Error Messages 63
Warrantee Declaration + Waste Disposal 65
EMC - Manufacturer‘s Declaration 66

3
Symbols in the Operating Instructions
WARNING"
(risk of injury)
General explanations,
without risk to
persons or objects
Thermodisinfectable Sterilisable up to the
speci!ed temperature Call customer service"
CAUTION"
(to prevent
damage occurring)
Symbols on the unit
Consult instructions for
use or consult electronic
instructions for use
ON / OFF Do not dispose of with
household waste
CE-marking with iden-
ti!cation number of the
noti!ed body
Type B application part
Manufacturing date Model (designation) Serial number
VElectrical voltage VA
AC
AHz
Electrical power con-
sumption
Current intensity Frequency of alter-
nating current
Electrical fuse
Alternating current
Foot controller
Manufacturer Medical device UDI - Product
Identi!cation

4
Symbols inside the Unit
Earth conductor connection -
Protective earth
Functional
earth
Symbols on the packaging
Transport upright; top
Permissible temperature range
Air humidity, limitation
Protect from moisture"
Do not stack"
Fragile
N
Connection point for
neutral conductor
Atmospheric pressure limitation

5
Introduction
For your safety and the safety of your patients
These operating instructions are intended to explain how to use your product. However,
we must also warn of possible dangerous situations. Your safety, the safety of your team
and, of course, the safety of your patients are very important to us.
Please observe the safety instructions!
Intended purpose
This treatment unit is used for the diagnosis and therapy of children and adults in the "eld of dentistry.
Improper use can damage the treatment unit and thus pose risks and
hazards to the patient, user and third parties.
Quali!cation of the user
The DKL treatment unit may only be used after medically, professionally and practically trained
personnel have been instructed. The development and design of the treatment unit were geared
towards the target group of dentists, dental hygienists, quali"ed dental employees (prophylaxis) and
dental assistants.
Production according to EU directive
The medical device complies with the provisions of regulation (EU) 2017/745.
0123
Responsibility of the manufacturer
The manufacturer can only be held responsible for the impact on the safety,
reliability and performance of the treatment unit if the following instructions
are observed:
> The dental unit must be used in accordance with these operating
instructions.
> If assembly, additions, new settings, changes or repair work is carried out
by DKL or trained technicians authorised by DKL or personnel of authorized
dealers trained by DKL.
> The electrical installation of the room must comply with the regulations of
the IEC 60364-7-710 standard („Erection of electrical installations in rooms
used for medical purposes“) or comply with the regulations applicable in
your country.
> The recommended annual maintenance is carried out and any repair work
in this context meets the requirements of EN 62353.
> „Repeat tests and pre-commissioning tests of medical electrical equipment
and systems – general regulations“are fully complied with.
> The national legal regulations are observed when using the device, in
particular the applicable health and safety regulations and accident
prevention measures.