KaVo INTRAcompact contra-angle 2061 CHC User manual

Instructions for use
INTRAcompact contra-angle 2061 CHC - REF 1.003.7714

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

Content
1 User instructions ....................................................................................................................................................................... 6
1.1 Terms and conditions of warranty ...................................................................................................................................... 9
2 Safety ................................................................................................................................................................................... 12
2.1 Description of safety instructions ..................................................................................................................................... 12
2.2 Purpose – Proper use .................................................................................................................................................... 16
2.3 Safety instructions ........................................................................................................................................................ 18
3 Product description .................................................................................................................................................................. 24
3.1 Technical Specifications ................................................................................................................................................ 25
Content 1

3.2 Transportation and storage conditions .............................................................................................................................. 27
4 First use ................................................................................................................................................................................ 29
5 Operation .............................................................................................................................................................................. 30
5.1 Attaching the medical device .......................................................................................................................................... 30
5.2 Removing the medical device ......................................................................................................................................... 33
5.3 Inserting the file ........................................................................................................................................................... 34
5.4 Removing the file ......................................................................................................................................................... 39
5.5 Application .................................................................................................................................................................. 41
Content 2

6 Reprocessing methods according to ISO 17664 ............................................................................................................................. 44
6.1 Preparations at the site of use ......................................................................................................................................... 44
6.2 Cleaning ..................................................................................................................................................................... 45
6.2.1 Cleaning: Manual external cleaning .................................................................................................................... 46
6.2.2 Cleaning: Automated external cleaning ............................................................................................................... 48
6.2.3 Cleaning: Manual internal cleaning ..................................................................................................................... 49
6.2.4 Cleaning: Automated internal cleaning ................................................................................................................ 51
6.3 Disinfection ................................................................................................................................................................. 52
6.3.1 Disinfection: Manual external disinfection ............................................................................................................ 53
Content 3

6.3.2 Disinfection: Manual internal disinfection ............................................................................................................. 55
6.3.3 Disinfection: Automated external and internal disinfection ....................................................................................... 56
6.4 Drying ........................................................................................................................................................................ 57
6.5 Care products and systems - Servicing ............................................................................................................................. 59
6.5.1 Care products and systems - Servicing: Servicing with KaVo Spray .......................................................................... 61
6.5.2 Care products and systems - Servicing: Servicing with KaVo SPRAYrotor .................................................................. 62
6.5.3 Care products and systems - Servicing: Servicing with KaVo QUATTROcare ............................................................. 63
6.6 Packaging ................................................................................................................................................................... 65
6.7 Sterilisation ................................................................................................................................................................. 66
Content 4

6.8 Storage ...................................................................................................................................................................... 69
7 Tools and consumables ............................................................................................................................................................ 71
Content 5

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
User instructions 6

Symbols
Refer to the Chapter on Safety/Warning symbol
Important information for users and service technicians
Action request
User instructions 7

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
User instructions 8

Target group
This document is intended for dentists and their assistants. The section on starting up is also
intended for service technicians.
1.1 Terms and conditions of warranty
The following warranty conditions apply to this KaVo medical device:
KaVo provides the end customer with a warranty of proper function and guarantees zero defects in
respect of material and processing for a period of 12 months from the date of the invoice, subject to
the following conditions:
User instructions 9

In case of justified complaints, KaVo will honour its warranty with a free replacement or repair. Other
claims of any nature whatsoever, in particular with respect to compensation, are excluded. In the
event of default, gross negligence or intent, this shall only apply in the absence of mandatory legal
regulations to the contrary.
KaVo shall not be liable for defects and their consequences that have arisen or may arise from
natural wear, improper handling, cleaning or maintenance, non-compliance with operating, mainte‐
nance or connection instructions, calcination or corrosion, contaminated air or water supplies or
chemical or electrical factors deemed abnormal or impermissible in accordance with KaVo's in‐
structions for use or other manufacturer's instructions. The warranty granted does not usually extend
to lamps, light conductors made of glass and glass fibres, glassware, rubber parts, and the colour‐
fastness of plastic parts.
User instructions 10

All liability is excluded if defects or their consequences originate from manipulations or changes to
the product made by the customer or a third party that is not authorised by KaVo.
Warranty claims will only be accepted if the product is submitted along with proof of purchase in the
form of a copy of the invoice or note of delivery. The dealer, purchase date, type, and serial number
must be clearly evident from this document.
User instructions 11

2 Safety
2.1 Description of safety instructions
Warning symbol
Safety 12

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 prevention.
Safety 13

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.
Safety 14

WARNING
WARNING
indicates a hazardous situation that can cause death or serious injury.
DANGER
DANGER
indicates a hazardous situation that can directly cause death or serious injury.
Safety 15

2.2 Purpose – Proper use
This medical device is
▪ intended for dental treatment only. Any other type of use or alteration to the product is imper‐
missible and can be hazardous. The medical device is intended for the following uses: , cavity
preparation, caries excavation.
▪ A medical device according to relevant national statutory regulations.
Safety 16

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.
Safety 17

2.3 Safety instructions
WARNING
Hazard to the care provider and patient.
In case of damage, irregular noise during operation, excessive vibration, atypical heating or when
the file cannot be firmly held.
▶Stop working and contact service support.
Safety 18