KaVo EXPERTsurg LUX 1.008.3500 Instructions For Use Manual

Instructions for use

EXPERTsurg LUX
REF 1.008.3500

Distributed by:
KaVo Dental Corporation
11729 Fruehauf Drive
Charlotte, NC 28273 USA
Phone: [phone]
Fax: [phone]

Manufacturer:
Kaltenbach & Voigt GmbH
Bismarckring 39
D-88400 Biberach
www.kavo.com

Table of contents

1 User instructions............................................................................................................................................. 6

1.1 User guide ............................................................................................................................................. 6

1.1.1 Symbols .................................................................................................................................... 6

1.2 Target group .......................................................................................................................................... 6

1.3 Service................................................................................................................................................... 6

1.3.1 Repair Service .......................................................................................................................... 6

1.4 Terms and conditions of warranty.......................................................................................................... 7

1.5 Transportation and storage.................................................................................................................... 7

1.5.1 Currently valid packaging regulations ....................................................................................... 7

1.5.2 Damage in transit...................................................................................................................... 7

1.5.3 Information on the packaging: Storage and transportation ....................................................... 8

2 Safety ............................................................................................................................................................. 10

2.1 Description of safety instructions ........................................................................................................... 10

2.1.1 Warning symbol ........................................................................................................................ 10

2.1.2 Structure ................................................................................................................................... 10

2.1.3 Description of hazard levels...................................................................................................... 10

2.2 Information about electromagnetic compatibility.................................................................................... 10

2.3 Disposal of electronic and electrical devices ......................................................................................... 11

2.4 Safety instructions ................................................................................................................................. 11

3 Product description......................................................................................................................................... 13

3.1 Intended use .......................................................................................................................................... 13

3.2 EXPERTsurg LUX ................................................................................................................................. 15

3.3 Controls ................................................................................................................................................. 17

3.4 Foot control ........................................................................................................................................... 18

3.5 Rating plates of EXPERTsurg LUX and foot control.............................................................................. 18

3.6 Technical Specifications of the EXPERTsurg LUX................................................................................ 19

3.7 Scope of delivery ................................................................................................................................... 20

4 First use.......................................................................................................................................................... 21

4.1 Unpacking.............................................................................................................................................. 21

4.2 Installing the bottle holder...................................................................................................................... 21

4.3 Plugging in the foot control .................................................................................................................... 21

4.4 Connecting the surgical motor ............................................................................................................... 22

4.5 Connecting the coolant container and hose set..................................................................................... 23

4.6 Electrical connection.............................................................................................................................. 27

5 Operation........................................................................................................................................................ 29

5.1 Switching the device on ......................................................................................................................... 29

5.2 Device settings ...................................................................................................................................... 29

5.2.1 Setting the language ................................................................................................................. 30

5.2.2 Setting the LUX brightness ....................................................................................................... 30

5.2.3 Setting the LUX afterglow time ................................................................................................. 31

5.2.4 Setting the operating mode of the foot control .......................................................................... 31

5.2.5 Setting the pump key operating mode of the foot control ......................................................... 32

5.2.6 Setting the clock time................................................................................................................ 32

5.2.7 Setting the date......................................................................................................................... 33

5.2.8 Setting the LCD brightness ....................................................................................................... 33

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5.2.9 Setting the volume .................................................................................................................... 34

5.2.10 Setting the key sound volume ................................................................................................... 34

5.2.11 Exporting settings ..................................................................................................................... 34

5.2.12 Importing settings...................................................................................................................... 35

5.2.13 Factory settings......................................................................................................................... 35

5.2.14 Version ...................................................................................................................................... 36

5.3 Surgical Motor INTRA LUX S600 LED .................................................................................................. 36

5.3.1 Attaching the straight or contra-angle handpiece ..................................................................... 36

5.3.2 Removing the straight or contra-angle handpiece .................................................................... 37

5.4 Setting and executing program steps .................................................................................................... 37

5.4.1 Factory settings......................................................................................................................... 39

5.4.2 Examples of program set sequences........................................................................................ 40

5.4.3 Selecting the program steps ..................................................................................................... 41

5.4.4 Selecting activities .................................................................................................................... 42

5.4.5 Limiting the program steps........................................................................................................ 42

5.5 Changing default values ........................................................................................................................ 43

5.5.1 Setting the maximum speed ..................................................................................................... 43

5.5.2 Setting the torque limit .............................................................................................................. 44

5.5.3 Setting the coolant flow............................................................................................................. 44

5.5.4 Changing the direction of motor rotation................................................................................... 45

5.5.5 Setting the transmission ratio.................................................................................................... 46

5.6 Rinsing function ..................................................................................................................................... 47

5.6.1 Manual rinsing function ............................................................................................................. 47

5.6.2 Program step Rinsing function.................................................................................................. 48

5.7 Activating the one-touch calibration....................................................................................................... 48

5.8 Foot control ........................................................................................................................................... 49

5.8.1 Changing the speed, coolant flow, and direction of motor rotation ........................................... 49

5.8.2 Selecting the program steps ..................................................................................................... 50

5.9 Changing the coolant container ............................................................................................................. 51

6 Decommissioning ........................................................................................................................................... 52

6.1 Disconnecting the electrical connection................................................................................................. 52

6.2 Disposal of the coolant hose.................................................................................................................. 52

6.3 Disconnecting the surgical motor........................................................................................................... 53

6.4 Disconnecting the foot control ............................................................................................................... 53

6.5 Dismantling the bottle holder ................................................................................................................. 53

7 Reprocessing steps in accordance with DIN EN ISO 17664.......................................................................... 55

7.1 Cleaning................................................................................................................................................. 55

7.1.1 Manual cleaning........................................................................................................................ 55

7.1.2 Machine cleaning ...................................................................................................................... 57

7.2 Disinfection ............................................................................................................................................ 57

7.2.1 Manual disinfection ................................................................................................................... 57

7.2.2 Automated disinfection.............................................................................................................. 57

7.2.3 Drying........................................................................................................................................ 58

7.2.4 Service, inspection and testing after preparation...................................................................... 58

7.3 Packaging .............................................................................................................................................. 58

7.4 Sterilisation ............................................................................................................................................ 59

7.4.1 Storage ..................................................................................................................................... 60

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8 Troubleshooting.............................................................................................................................................. 61

9 Run a software update ................................................................................................................................... 64

10 Safety checks ("STK") .................................................................................................................................... 65

11 Accessories .................................................................................................................................................... 66

12 Details on electromagnetic compatibility ........................................................................................................ 67

12.1 Guidelines and manufacturer's declaration - electromagnetic transmission.......................................... 67

12.2 Guidelines and manufacturer's declaration - electromagnetic resistance to jamming ........................... 67

12.3 Guidelines and manufacturer's declaration - electromagnetic resistance to jamming ........................... 68

12.4 Recommended safe distance between portable and mobile HF telecommunications equipment and

the EXPERTsurg LUX ........................................................................................................................... 70

Instructions for use EXPERTsurg LUX REF 1.008.3500

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Instructions for use EXPERTsurg LUX REF 1.008.3500

1 User instructions | 1.1 User guide

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1 User instructions

1.1 User guide

1.1.1 Symbols

Refer to the chapter on Safety/Warning symbol

Important information for users and service technicians

Thermodisinfectable

Sterilisable up to 135 oC

CE mark (European Community). A product bearing this mark meets the re­quirements of the pertinent EC directives, i.e. the standards applicable in
Europe.

1.2 Target group

This document is for dentists and dental office staff.

1.3 Service

Please direct all questions regarding the product, service and maintenance to the
KaVo Technical Service:
Toll-free: 1-888-ASK-KAVO (888-275-5286)
Email: [e-mail]
Please refer to the serial number of the product in all inquiries!

1.3.1 Repair Service

KaVo offers a fixed-price service check for the original factory maintenance. You can
use a loaner device for the time of the service check.

For repairs, please contact KaVo Repair Service.
For scheduling or if you have any questions, please contact:
KaVo Repair Service
KaVo Dental Corporation
11729 Fruehauf Drive
Charlotte, NC 28273 USA
Toll-free Direct Customer Service: 1-888-ASK-KAVO (888-275-5286)
Email: [e-mail]
www.kavousa.com

Instructions for use EXPERTsurg LUX REF 1.008.3500

1 User instructions | 1.4 Terms and conditions of warranty

1.4 Terms and conditions of warranty

KaVo provides the final customer with a warranty that the product cited in the han­dover certificate will function properly and guarantees zero defects in the material or
processing for a period of 12 months from data of purchase, subject to the following
conditions:
Upon justified complaints of flaws or a short delivery, KaVo will make good its war­ranty by replacing the product free of cost or repairing it according to the customer's
wishes. Other claims of any nature whatsoever, in particular with respect to compens­ation, are excluded. In the event of default and 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 due to natural wear,
improper cleaning or servicing, non-compliance with operating, servicing or connection
instructions, calcification or corrosion, contaminated air or water supplies or chemical
or electrical factors deemed abnormal or impermissible in accordance with factory
specifications.
The warranty does not usually cover bulbs, glassware, rubber parts and the colour­fastness of plastics.
Defects or their consequences that can be attributed to interventions on or changes
made to the product by the customer or a third party are excluded from the warranty.
Defects or their consequences that can be attributed to interventions on or changes
made to the product by the customer or a third party are excluded from the warranty.

1.5 Transportation and storage

1.5.1 Currently valid packaging regulations

Note

Only valid for the Federal Republic of Germany.

Dispose of and recycle the sales packaging appropriately in accordance with current
packaging regulations, employing waste management or recycling companies. Com­ply with the comprehensive return system. KaVo has had its sales packaging licensed
for this purpose. Please comply with the regional public waste-disposal system.

1.5.2 Damage in transit

In Germany

If the packaging is visibly damaged on delivery, please proceed as follows:

1. The recipient of the package must record the loss or damage on the delivery re­ceipt. The recipient and the representative of the shipping company must sign this
delivery receipt.

2. Leave the product and packaging in the condition in which you received it.

3. Do not use the product.

4. Report the damage to the shipping company.

5. Report the damage to KaVo.

6. Consult with KaVo first, before returning a damaged product.

7. Send the signed delivery receipt to KaVo.

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1 User instructions | 1.5 Transportation and storage

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If the product is damaged but there was no discernable damage to the packaging on
delivery, proceed as follows:

1. Report the damage to the shipping company immediately and no later than 7 days
after delivery.

2. Report the damage to KaVo.

3. Leave the product and packaging in the condition in which you received it.

4. Do not use a damaged product.

Note

Failure on the part of the recipient to comply with any of the above-mentioned oblig­ations will mean that the damage will be considered to have arisen following deliv­ery (in accordance with the General German Freight Forwarders´ Terms and Condi­tions, Art. 28).

Outside Germany

Note

KaVo shall not be held liable for damage arising from transportation.
The shipment must be checked on arrival.

If the packaging is visibly damaged on delivery, please proceed as follows:

1. The recipient of the package must record the loss or damage on the delivery re­ceipt. The recipient and the representative of the shipping company must sign this
delivery receipt.
Without this evidence, the recipient will not be able to assert a claim for damages
against the shipping company.

2. Leave the product and packaging in the condition in which you received it.

3. Do not use the product.

If the product is damaged but there was no discernable damage to the packaging on
delivery, proceed as follows:

1. Report any damage to the shipping company either immediately or no later than 7
days after delivery.

2. Leave the product and packaging in the condition in which you received it.

3. Do not use a damaged product.

Note

If the recipient fails to comply with any of the above-mentioned obligations, the
damage will be considered to have arisen following delivery
(in accordance with CMR law, Chapter 5, Art. 30).

1.5.3 Information on the packaging: Storage and transportation

Note

Please keep the packaging in case you need to return the product for servicing or
repair.

The symbols printed on the outside are for transportation and storage, and have the
following meaning:

Transport upright with the arrows pointing upwards!

Fragile - protect against impact!

Protect from moisture!

Instructions for use EXPERTsurg LUX REF 1.008.3500

1 User instructions | 1.5 Transportation and storage

Permissible stacking load

Temperature range

Humidity

Air pressure

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2 Safety | 2.1 Description of safety instructions

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2 Safety

2.1 Description of safety instructions

2.1.1 Warning symbol

Warning symbol

2.1.2 Structure

DANGER

The introduction describes the type and source of the hazard.
This section describes potential consequences of non-compliance.

▶ The optional step includes necessary measures for hazard prevention.

2.1.3 Description of hazard levels

Safety instructions distinguishing between three hazard levels are used in this docu­ment to prevent personal and property damage.

CAUTION

CAUTION
indicates a hazardous situation that can cause damage to property or mild to moder-

ate injuries.

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 in-

jury.

2.2 Information about electromagnetic compatibility

Note

Based on IEC 60601-1-2 (DIN EN 60601-1-2) concerning the electromagnetic com­patibility of electrical medical devices, we must draw your attention to the following
points:

• Medical electrical devices are subject to special precautions concerning the elec­tromagnetic compatibility and must be installed and operated in accordance with the
KaVo assembly instructions.

• High-frequency communications devices may interfere with electrical medical
devices.

See also:

2 12 Information about electromagnetic compatibility, Page 67

Instructions for use EXPERTsurg LUX REF 1.008.3500

2 Safety | 2.3 Disposal of electronic and electrical devices

Note

KaVo cannot guarantee the compliance of accessories, cables, and other compon­ents not supplied by KaVo with the EMC requirements of IEC 60601-1-2 (DIN EN
60601-1-2).

2.3 Disposal of electronic and electrical devices

Note

According to EC directive 2012/19 concerning used electrical and electronic
devices, this product is subject to the cited directive and must be disposed of ac­cordingly within Europe.

For more information, please visit www.kavo.com or contact your specialised dental
supplier.

For final disposal:

In Germany

To return an electrical device, you need to proceed as follows:

1. On the homepage www.enretec.de of enretec GmbH, you can download a form for
a disposal order under the menu item eom. Download the disposal order or com­plete it as an online order.

2. Enter the corresponding information to complete the order, and submit it as an on­line order or by fax [phone] to enretec GmbH.
The following contact options are also available for questions and for initiating a
disposal order:
Phone: [phone]
Email: [e-mail] and
Postal address: enretec GmbH, Geschäftsbereich eomRECYCLING®
Kanalstraße 17
D-16727 Velten

3. A unit that is not permanently installed will be picked up at the office.
A permanently installed unit will be picked up at the curb at your address on the
agreed date.
The owner or user of the device will have to bear the cost of disassembly, trans­portation and packaging.

International

For country-specific information on disposal, contact your dental supplier.

2.4 Safety instructions

WARNING

Application of un-authorised accessories or un-authorised modifications of the
product.

Accessories that have not been approved and/or inadmissible modifications of the
product could lead to hazards and/or personal injury or property damage.

▶ Only use accessories that have been approved for combination with the product

by the manufacturer or are equipped with standardised interfaces (e. g. MULTIflex
couplings, INTRAmatic).

▶ Do not make any modifications to the device unless these have been approved by

the manufacturer of the product.

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2 Safety | 2.4 Safety instructions

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CAUTION

Electrical sparks in the product.
Explosion and/or fire.

▶ Do not use product in areas subject to an explosion hazard.
▶ Do not operate the product in an oxygen-enriched atmosphere.

CAUTION

Damaged mains cable / missing protective conductor.
Electrical shock.

▶ Check the mains cable before use. The socket outlet must have a protective con-

tact and meet the respective national guidelines.

CAUTION

Damage by liquids.
Faults on electrical components.

▶ Protect openings of the product from any ingress of liquids.

CAUTION

Inadvertent penetration of liquids.
Electrical shock.

▶ Do not place the product in a tub-like container.
▶ Check the coolant containers and lines for absence of leakage. If any liquid is de-

tected on the device, do not touch the device and disconnect the device from the
mains supply without delay. Make sure that the surface of the device is com­pletely dry before plugging the main plug back in the socket.

CAUTION

Rotating parts while the pump is operating
Injuries

▶ Do not stick anything in the pump. Turn off the device when the pump is open.

CAUTION

Risks from electromagnetic fields.
Electromagnetic fields might interfere with the functions of implanted systems (such

as pacemakers).

▶ Ask patients if they have a cardiac pacemaker or other system implanted before

you start the treatment!

CAUTION

Impact of power failure.
Failure of the voltage supply or other errors can cause the surgical motor to come to a

standstill.

▶ Make sure that the power supply is working.

Instructions for use EXPERTsurg LUX REF 1.008.3500

3 Product description | 3.1 Intended use

3 Product description

The EXPERTsurg LUX is a surgical controller according to 21 CFR § 872.4200 (dental
handpiece and accessories). The device consists of a surgical control unit, a foot con­troller, a surgical motor (separate IFU) + motor cable, an instruments tray, a holder
and a tube set. As a functional principle the software-based surgical control unit con­trols the speed and torque of a dental micro motor. The unit is equipped with a pump
for the use with external irrigation tubing allowing irrigation of the working area. The
surgical control unit is operated through the buttons on the tabletop console or via foot
control. The device is intended to be used with the INTRA LUX S600 LED (separate
IFU) motor. Straight or contra-angle handpieces with a handpiece connection accord­ing to ISO 3964 can be equipped. The instrument tray allows the dentist to deposit the
handpieces in a safe position. The holder is intended to be used for general storage of
the bottle. The tube set is needed to deliver the external irrigation from the bottle to the
different handpieces. A power cord provides electric power to the unit. The EX­PERTsurg LUX will be delivered with software on the surgical control unit.

3.1 Intended use

Indications for use

This KaVo product is intended for surgery to expose and dissect oral tissue structures
or endodontic treatments (e.g. periodontal gap, gingiva, bone, jaw, extractions and im­plantations).

CAUTION

US Federal law restricts this device to sale by or on the order of a health care profes­sional / dentist.

For dental use only.

Proper Use

Note

The EXPERTsurg LUX is approved for use in surgical theatres.

The overarching guidelines and/or national laws, national regulations and the rules of
technology applicable to medical devices for start-up and use of the KaVo product for
the intended purpose must be applied and followed.

The user must ensure that the unit works properly and is in satisfactory condition be­fore each use.

The applicable national legal regulations must be observed during the use of the
device, in particular the following:

▪ Applicable regulations governing the connection and start-up of medical devices.

▪ Current occupational safety regulations.

▪ Current accident prevention regulations.

It is a responsibility of the user:

▪ to only use equipment that is operating correctly,

▪ to protect him or herself, the patient and third parties from hazards, and

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3 Product description | 3.1 Intended use

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▪ to prevent contamination from the product

To guarantee the consistent readiness for use and to preserve the value of the KaVo
product, the recommended maintenance services must be carried out in 2 year inter­vals.

The following persons are authorised to repair and service the KaVo product:

▪ Technicians of KaVo branch offices after appropriate product training.

▪ Specifically KaVo-trained technicians of KaVo franchised dealers.

Note

The permitted work is described in the Technician's Instructions available to the
trained service staff.

In Germany, operators, equipment managers and users are obliged to operate their
equipment in accordance with the MPG regulations.
The services encompass all the test tasks required in accordance with § 6 of the med­ical devices operator ordinance (Medizinprodukte-Betreiberverordnung, MPBetreibV).

After servicing, interventions, and repairs of the device, the device must be tested ac­cording to IEC 62353 (according to the state of the art) before re-use.

Note

The product must be cleaned and serviced according to instructions if it is not to be
used for an extended period of time.

Note

Any waste which is generated must be recycled or disposed of in strict compliance
with all applicable national regulations in a manner which is safe both for people
and the environment.

If you have any questions regarding proper disposal of the KaVo product, please
contact the KaVo branch.

Note

A recycling pass can be downloaded from www.kavo.com.

Instructions for use EXPERTsurg LUX REF 1.008.3500

3 Product description | 3.2 EXPERTsurg LUX

3.2 EXPERTsurg LUX

1

2

7

8

3

6

5

4

9

10

① Hand-held control panel ② Bottle holder
③ Hose pump ④ Hose fixation
⑤ Foot control ⑥ Surgical motor
⑦ Coolant hose ⑧ Handpiece tray
⑨ Motor cable ⑩ Symbol of type B applied part

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3 Product description | 3.2 EXPERTsurg LUX

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Rear

3

7

2

1

54

6

① Hose pump locking mechanism ② On-button
③ Mains plug ④ Please note the instructions for use
⑤ Follow the instructions for use ⑥ SD card slot
⑦ Foot control electrical outlet

Instructions for use EXPERTsurg LUX REF 1.008.3500

3 Product description | 3.3 Controls

3.3 Controls

3

2

6

7

8

1

4 5

1011 913 121415

① Program step ② Display of the activity
③ Maximal torque reached ④ Torque limit
⑤ Speed ⑥ Left arrow key
⑦ Plus key, increase value ⑧ Right arrow key
⑨ Minus key, decrease value ⑩ Back key
⑪ Transmission ratio ⑫ Direction of motor rotation
⑬ Coolant pump settings ⑭ Activation of one-touch calibration
⑮ Foot control status indicator / Service

check request

The back key has two functions. Pressing the back key briefly opens the selection of
program steps. Pressing the back key long opens the device settings.

Parameters can be selected using the arrow keys.

Use the plus key to increase the value.

Use the minus key to decrease the value.

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3 Product description | 3.4 Foot control

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3.4 Foot control

1

3

2

4

① Speed key (grey) ② Pump key (blue)
③ Programme key (grey) ④ Direction of motor rotation key (yellow)

3.5 Rating plates of EXPERTsurg LUX and foot control

The rating plates of EXPERTsurg LUX and foot control are affixed on the underside of
the housing and include the following symbols:

CE mark

VDE mark

CSA mark

Classification, type B

Please note the instructions for use

Please note the electronic instructions for use

Follow the instructions for use

Instructions for use EXPERTsurg LUX REF 1.008.3500

3 Product description | 3.6 Technical Specifications of the EXPERTsurg LUX

Operating mode: continuous operation with intermittent load

Alternating current (AC)

Supply voltage

Protection class II

Manufacturer

YYYY = Year manufactured
XXXXXXX = Serial number

Material number

Type: Device type

For disposal information, see Intended use

GOST R certification

HIBC Code

3.6 Technical Specifications of the EXPERTsurg LUX

Width 265mm

Depth 255mm

Height 100mm

Weight approx. 1.9 kg

Weight of foot control approx. 1.1 kg

Weight of motor approx. 125 g

Input voltage 100 - 240 V ~

Input frequency 50/60 Hz

Rated power max. 150 W

Speed 300 – 40,000 rpm

Max. torque on the motor 5.5 Ncm

Pump delivery rate 30 - 110 ml/min

Foot control: Class of protection IPX8

Foot control: cable length 2.5 m

Length of motor cable 6.5 ft (2 m)

Operating mode

Continuous operation with intermittent

load

30 sec. of operation/ 9 min. pause

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3 Product description | 3.7 Scope of delivery

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Note

The maximal motor load is 30 seconds operating time / 9 minutes pause (full load at
maximal speed).

Transportation and storage conditions

Ambient temperature -20 ℃ - +50 ℃

Relative humidity 5% - 95%

Air pressure 700 hPa - 1,060 hPa

Operating environment

WARNING

Inappropriate operating conditions.
Impairment of the electrical safety of the device.

▶ It is essential to comply with the operating conditions specified in the "Technical

Specifications" chapter.

Ambient temperature +10 ℃ - +35 ℃

Relative humidity 15% - 80%

Air pressure 700 hPa - 1,060 hPa

Max. elevation for operation up to 3,000 m

3.7 Scope of delivery

The scope of delivery of the EXPERTsurg LUX includes:

▪ EXPERTsurg LUX unit

▪ Foot control

▪ Surgical motor INTRA LUX S600 LED

▪ Motor cable S600

▪ Handpiece tray

▪ Hose set sterile S600 (5 units)

▪ Bottle holder

▪ Instructions for use for EXPERTsurg LUX

▪ Short instructions for the EXPERTsurg LUX

▪ Instructions for use INTRA LUX S600 LED

Instructions for use EXPERTsurg LUX REF 1.008.3500

4 First use | 4.1 Unpacking

4 First use

4.1 Unpacking

Note

You need to keep the cardboard box and all packaging materials to be able to
safely ship the unit in the future.

▶ Open the cardboard box.
▶ Remove the hose boxes.
▶ Take out the foot control and additional equipment.
▶ To take out the unit, pull it vertically upward and place it on a level surface.

4.2 Installing the bottle holder

▶ Slide the bottle holder ① in the guide on the underside of the unit.

ð The bottle holder ① snaps into place audibly and is then affixed.

4.3 Plugging in the foot control

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4 First use | 4.4 Connecting the surgical motor

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▶ Insert the plug of the foot control in the electrical outlet for the foot control. Make

sure that the marker arrows on the plug and the socket are aligned towards each
other.

▶ Slide the bracket into the designated recesses.

4.4 Connecting the surgical motor

Note

The delivered parts are not sterile (except for the coolant hose). Before the first
treatment of a patient, the surgical motor, motor cable, and the handpiece tray need
to be reprocessed.

See also:

2 Reprocessing steps in accordance with DIN EN ISO 17664