KaVo INTRA 3610 N3 User manual

Instructions for use
INTRA surgical handpiece 3610 N3 - REF
0.524.5620

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

Contents
Contents 3
1 User instructions 6
1.1 Warranty terms and conditions 8
2 Safety 10
2.1 Description of safety instructions 10
2.2 Purpose – Proper use 12
2.3 Safety instructions 14
3 Product description 18
3.1 Technical data 18
3.2 Transportation and storage conditions 20
4 First use 22
4.1 Cooling medium supply 23
Contents 3

5 Operation 25
5.1 Attach the medical device 25
5.2 Remove the medical device 27
5.3 Insert the milling cutters or diamond grinders 28
5.4 Removing the milling tool or diamond grinder 32
5.5 Conversion for short handpiece cutters or grinders 33
6 Preparation methods according to ISO 17664 35
6.1 Preparations at the site of use 35
6.2 Disassemble the medical device 36
6.3 Assembling the medical device 37
6.4 Cleaning 37
6.4.1 Cleaning: Manual cleaning - external 37
6.4.2 Cleaning: Automated external cleaning 38
6.4.3 Cleaning: Manual cleaning of the inside 38
Contents 4

6.4.4 Cleaning: Automated internal cleaning 39
6.5 Disinfection 41
6.5.1 Disinfection: Manual disinfection - external 42
6.5.2 Disinfection: Manual disinfection - internal 43
6.5.3 Disinfection: Machine disinfection - external and internal 44
6.6 Drying 44
6.7 Care products and systems - Servicing 45
6.7.1 Care products and systems - Servicing: Care with KaVo Spray 47
6.7.2 Care products and systems - Servicing: Care with KaVo QUATTROcare 49
6.8 Packaging 52
6.9 Sterilization 53
6.10 Storage 55
7 Tools 56
Contents 5

1 User instructions
Dear user,
KaVo hopes that you enjoy your new high-quality product. Following the
instructions below will allow you to work smoothly, economically and safely.
© Copyright by KaVo Dental GmbH
Symbols
See the section Safety/Warning Symbols
Important information for users and technicians
User instructions 6

Disinfectable with heat
Sterilizable in steam up to 135°C (275°F)
CE mark (Communauté Européenne). A product with this mark
meets the requirements of the applicable EC directive.
Action request
Target group
This document is intended for dentists and their assistants. The section on
starting up is also intended for service technicians.
User instructions 7

1.1 Warranty terms and conditions
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 24 months from data of invoice, subject to the following conditions:
In case of justified complaints, KaVo will honour its warranty with a repair
or free replacement. 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 cannot be held liable for defects and their consequences that are or
may be due to natural wear, improper handling, cleaning or maintenance,
non-compliance with operating or connection instructions, calcination or
corrosion, contaminated air or water supplies or chemical or electrical fac‐
tors deemed abnormal or impermissible in accordance with KaVo's instruc‐
User instructions 8

tions for use or other manufacturer specifications. The warranty does not
usually cover lamps, light conductors made of glass and glass fibres, glass‐
ware, rubber parts and the colourfastness of plastic parts.
Defects or their consequences that can be attributed to interventions on or
changes made to the product by the customer or a third party not authorised
by KaVo are excluded from the warranty.
Service 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/delivery
note. The dealer, purchase date, unit number or type and serial number
must be clearly visible on this document.
User instructions 9

2 Safety
2.1 Description of safety instructions
Warning symbol
Structure
DANGER
The introduction describes the type and source of the danger.
This section describes the possible consequences of misuse.
▶The optional step contains necessary measures for avoiding haz‐
ards.
Safety 10

Description of hazardous steps
The safety instructions cited herein with the three levels of danger will help
avert property damage and injury.
CAUTION
CAUTION
indicates a hazardous situation that can lead to property damage or minor
to moderate injury.
WARNING
WARNING
indicates a hazardous situation that can lead to serious injury or death.
Safety 11

DANGER
DANGER
indicates a maximum hazardous situation that can directly cause serious
injury or death.
2.2 Purpose – Proper use
This medical device is
▪ only for dental treatment by a dental professional. The product may not
be changed or used for any other purpose since this may be hazard‐
ous. The medical device is intended for the following use: Surgery.
▪ A medical device according to relevant national statutory regulations.
Safety 12

According to these provisions, this medical device may only be used for the
described application by a knowledgeable user. The following must be ob‐
served:
▪ 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 properly operating equipment
▪ use the equipment for the proper purpose
▪ to protect himself, the patient and third parties from danger.
▪ to avoid contamination from the product
Safety 13

2.3 Safety instructions
CAUTION
Premature wear and malfunctioning from improper storage during long
periods of nonuse.
Shortened product life.
▶The instrument must be cleaned, serviced and stored dry if it has not
been used for a long period.
Safety 14

WARNING
Hazard to the care provider and patient
Damage, irregular noise during operation, excessive vibration, unusual
build-up of heat or if the cutter or grinder cannot be firmly held.
▶Stop work and seek service support.
CAUTION
Hazard from improperly putting away instruments.
Injury and infection caused by chucked cutters or grinders.
Damage to the chucking system when the instrument fails.
▶After treatment, place the cutter or grinder properly in the cradle with‐
out the tool.
Safety 15

Note
For safety reasons, we recommend that the tool holder system be checked
annually after the warranty period expires.
The following individuals are authorized to repair and service KaVo prod‐
ucts:
▪ Technicians at the KaVo branches throughout the world
▪ Technicians specially trained by KaVo
To ensure proper function, the medical device must be set up according to
the methods described in the KaVo instructions for use, and the care prod‐
ucts and methods 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 in‐
terval should take into account the frequency of use.
Safety 16

Service may only be provided by repair shops that have undergone training
by KaVo and that use original KaVo replacement parts.
Safety 17

3 Product description
INTRA surgical handpiece 3610 N3 (Mat. no. 0.524.5620)
3.1 Technical data
Drive speed max. 40,000 rpm-1
Identification 1 blue ring
Transmission 1:1
Maximum speed max. 40,000 rpm-1
Product description 18

The INTRA surgical handpiece 3610 N3 can be disassembled.
See also: 4 First use, Page 22
Handpiece cutters or grinders can be inserted.
After conversion, short handpiece cutters or grinders can be inserted.
The handpiece can be mounted on all INTRAmatic Lux motors, and motors
with a connection in accordance with ISO 3964 / DIN 13940.
Product description 19

3.2 Transportation and storage conditions
CAUTION
Starting up the medical device can be hazardous after it has been stored
in an excessively cold location.
The medical device can malfunction.
▶Prior to start-up, very cold products must be heated to a temperature
of 20 °C (68 °F) to 25 °C (77 °F).
Temperature: -20°C (-4°F) to 50°C (122°F)
Relative humidity: Non-condensing
Product description 20