Chattanooga Intelect RPW 2 User manual

Operator and Installation Instructions
INTELECT RADIAL PRESSURE WAVE  RPW 
REF KIT V
REF KIT V
REF KIT V
Intelect®RPW 2
User Manual
EN

2CONTENTS EN
INTELECT®RPW 2 USER MANUAL
INTRODUCTION 
FOREWORD 5
INTENDED USER PROFILE 5
INTENDED ENVIRONMENT FOR USE 5
INTENDED USE 5
PRECAUTIONARY INSTRUCTIONS 5
HOME SCREEN DESCRIPTIONS 6
DESCRIPTION OF DEVICE MARKINGS 6
PAIN IN THE MUSCULOSKELETAL SYSTEM 8
INDICATIONS FOR USE 
CONTRAINDICATIONS 9
ADDITIONAL PRECAUTIONS 10
ADVERSE EFFECTS 10
PATIENT APPLIED PARTS 10
DEVICE DESCIPTION 
PRODUCT DESCRIPTION 11
COMPONENTS 12
IFU DOWNLOAD 13
SYSTEM START-UP 13
DEVICE CONNECTED TO THE MAINS 13
TO STOP TREATMENT 13
GENERAL WARNINGS AND 
PRECAUTIONS
CAUTION 14
WARNING 15
DANGER 16
SETUP INSTRUCTIONS 
UNPACKING THE DEVICE 17
DEVICE DESCRIPTION 19
FALCON HANDPIECE SET UP 20
POWERING UP THE DEVICE 21
SYSTEM 
OPERATING DATA AND RATINGS 22
FALCON HANDPIECE TECHNICAL SPECIFICATIONS 22
SOFTWARE 22
TRANSPORT AND STORAGE CONDITIONS 22
PATIENT PREPARATION 
TREATMENT TIPS 23
USER INTERFACE 
DEVICE USER INTERFACE 24
SCREEN DESCRIPTION 24
UNDERSTANDING YOUR BOTTOM BANNER 26

3CONTENTS EN
INTELECT®RPW 2 USER MANUAL
CHANNEL STATUS POSSIBILITES 27
BAR EXPLAINED 27
COMFORT MODE EXPLAINED 28
SETTINGS 29
HOME SCREEN 30
TREATMENT REVIEW SCREEN 31
GUIDELINES SCREEN 33
RADIAL PRESSURE WAVE OPERATION 33
SINGLE SHOT MODE 38
SPS (SUGGESTED PARAMETER SETUP) 40
TREATMENT DATA 43
CUSTOM PROTOCOLS 51
SHORTCUTS 56
UNASSIGN SHORTCUT 58
CLINICAL RESOURCES 59
MODALITY DESCRIPTIONS 62
PRINT SCREEN FUNCTION 62
TROUBLE SHOOTING CODES 63
ACCESSORIES 
REPLACEMENT ACCESSORIES 64
POWER CORDS 64
OPTIONAL ACCESSORIES 65
VACTOR HF HANDPIECE 
OPERATIONS, SETUP, CLEANING
AND MAINTENANCE
DEVICE DESCRIPTION 66
INSTALLATION INSTRUCTIONS 66
UNPACKING 66
SCOPE OF SUPPLY 66
CONNECTING THE HANDPIECE 67
OPERATION 68
START-UP 68
FUNCTIONAL CHECKS 68
STANDARD SETTINGS 68
TREATMENT 70
SAFETY INFORMATION 70
CARRYING OUT TREATMENT 70
CLEANING, MAINTENANCE, OVERHAUL 71
CHANGING THE SHOCK TRANSMITTERS 71
V25 AND V10
REPROCESSING THE HANDPIECE AND 71
SHOCK TRANSMITTERS
HANDPIECE 72
V25 AND V10 73
V40 73
TROUBLE-SHOOTING 74
ACCESSORIES AND SPARE PARTS 74

4CONTENTS EN
INTELECT®RPW 2 USER MANUAL
TECHNICAL SPECIFICATIONS 74
SYMBOLS AND LABELS 75
WARRANTY AND SERVICE 75
DEVICE MAINTENANCE 
WATER RESERVOIR 76
CLEANING THE INTELECT RPW 2 76
COPY OF MANUAL 76
INSTRUCTION FOR SOFTWARE UPGRADE 76
DEVICE MAINTENANCE 76
FALCON HANDPIECE CLEANING, 
MAINTENANCE; OVERHAUL
CLEANING 77
STANDARD SHOCK TRANSMITTERS 78
SPINE AND FASCIAE SHOCK TRANSMITTERS 79
CLEANING THE HANDPIECE 80
CLEANING THE SHOCK TRANSMITTERS 81
STANDARD SHOCK TRANSMITTERS 81
SPINE AND FASCIAE SHOCK TRANSMITTERS 82
CLUTCH FOR THE SPINE/FASCIAE SHOCK 82
TRANSMITTERS
OVERHAUL 83
OVERHAULING THE HANDPIECE 83
SERVICE & WARRANTY 
SERVICE LIFE 88
WARRANTY REPAIR/OUT OF WARRANTY REPAIR 88
WARRANTY 89
APPENDIX 
ELECTROMAGNETIC COMPATIBILITY (EMC) 90

5INTRODUCTION EN
INTELECT®RPW 2 USER MANUAL
This guide is intended for users of Intelect®RPW .
It contains general information on operation, precautionary
practices, and maintenance.
Before administering any treatment to a patient, the
users of this equipment should read, understand, and
follow the information contained in this guide for each
mode of treatment available, as well as the indications,
contraindications, warnings, and precautions. Consult
other resources for additional information regarding the
application of Radial Pressure Wave and Vibration therapies.
INTENDED USER PROFILE
The intended user of this device is a licensed medical
professional trained to properly use the device:
Physical Therapist, Occupational Therapist, Athletic Trainers,
Chiropractors, Osteopaths, Orthotists, Podiatrists, Sport’s
Medicine Therapists and Medical Doctors.
The device shall not be sold OTC to non professional users
The user should be able to:
• Read and understand the operator’s manual,
warnings, cautions and dangers.
• Sense auditory and visual signals.
• Read and understand cautions and contraindications
of the device
• The operator shall operate only one device at a time
and treat one patient at a time.
• The device is not intended to be operated by the
patient
FOREWORD
CAUTION
Text with a “CAUTION” indicator explains possible safety
infractions that have potential to cause minor or moderate
injury or damage to the equipment.
Text with a “WARNING” indicator explains possible safety
infractions that will potentially cause serious injury and
equipment damage.
Text with a “DANGER” indicator will explain possible safety
infractions that are imminently hazardous situations that
would result in death or serious injury.
The precautionary instructions found in this section and
throughout this manual are indicated by specific symbols.
Understand these symbols and their definitions before
operating this equipment. The definition of these symbols
are as follows:
PRECAUTIONARY INSTRUCTIONS
WARNING
DANGER
INTENDED ENVIRONMENT FOR USE
The device is intended to be operated in a clinical
environment, it can be moved from room to room.
The device is not intended to be regularly transported from
one facility to another. It is not intended for home use.
INTENDED USE
The Intelect RPW  device is intended to be used as a
therapeutic modality by clinicians needing to provide
patients with a powerful and proven method of treating
indications as pain, myofascial trigger points, disorders of
tendon insertions, activation of muscle and connective
tissue.
Individual results may vary. Neither DJO Global, Inc. nor any
of its subsidiaries dispense medical advice. The contents of
this document do not constitute medical, legal, or any other
type of professional advice. Information related to various
health, medical, and fitness conditions and their treatment
is not meant to be a substitute for the advice provided by a
physician or other medical professional.

6INTRODUCTION EN
INTELECT®RPW 2 USER MANUAL
HOME SCREEN ICON DESCRIPTIONS
Falcon Radial Pressure Waves
handpiece
Vibration Therapy handpiece V-Actor
Shortcut
SPS (Suggested Parameter Setup)
Custom Protocols
Treatment Data
Clinical Resources
Home
Settings
USB Drive
DESCRIPTION OF DEVICE MARKINGS
Refer to Instructional Manual and
Quick Start Guide Booklet
Warning, Caution, or Danger
Electrical type B equipment
Play
Pause
ON/OFF
Manufacturer
Date of manufacture
Catalogue number
Serial number
Fragile, handle with care
This end up
Keep dry
Temperature Range

7INTRODUCTION EN
INTELECT®RPW 2 USER MANUAL
Relative Humidity Range
Atmospheric Pressure Range
Testing agency
CE Mark of Conformity with
notified body number
Class  equipment
Radio frequency equipment
WEEE Directive conformity
Shelf life
Batch number
No condensation allowed
Read the instruction for use
AC Rated supply voltage
Markings are conform to ISO and ISO--"

8INTRODUCTION EN
INTELECT®RPW 2 USER MANUAL
PAIN IN THE MUSCULOSKELETAL SYSTEM
Before a treatment with Radial Pressure Wave, a correct
examination and diagnosis should be performed.
Please stay current with the latest developments and
medical publications on Radial Pressure Wave therapy for
details on contraindications and side eects not known at
the time of manufacturing.
RPW therapy is indicated for the following:
Myofascial Trigger Points (MTrP)
Localizing and Deactivating Trigger Points
Triggers are localized at the low energy level (approximately 
bar) by passing the transmitter over the muscle region being
treated (increased sensitivity to pain) and then deactivated
using a higher energy level (approximately  bar).
Activation of Muscle and Connective Tissue
Increasing Circulation
promotes blood flow through the
tissue and boosting metabolism.
Pulse vibration Massage
Soothing relief from muscle strain and stress.
Disorder of Tendon Insertions
Plantar Fasciitis, heel Pain, or heel Spur
Plantar Fasciitis is an inflammatory condition of the foot
caused by excessive wear to the plantar facia that supports
the arch
Tendinosis Calcarea/Supraspinatus-Tendon
Shoulder calcifications and chronic shoulder pain
Radial and Ulnar humeral Epicondylitis
Tennis elbow, inflammation of tendon attachments on
cubital or radial part of elbow joint (humeral)
Achillodynia
Pain due to inflammation of the Achilles tendon or the bursa
associated with it.
Retropatellar Pain Syndrome
Pain in the front of, behind, and around the kneecap.
Tibial Edge Syndrome
Pain located along or just behind the medial edge of the
tibia
Proximal Iliotibial band Friction Syndrome/Trochanteric
Insertion Tendonitis
Pain or aching on the outer side of the knee or hip

9INDICATIONS FOR USE EN
INTELECT®RPW 2 USER MANUAL
The Intelect®RPW  should NOT be used under the
following conditions:
• Brain or spinal column in the treatment area.
• On any body part during pregnancy.
• Direct application over cancerous tumors or lesions
due to its potential to increase blood flow to the area
of malignancy.
• Polyneuropathy area. A Diabetes patient often
experiences disturbed or reduced sensory and nervous
function in the polyneuropathic area.
• Cortisone therapy: Wait minimum  weeks after
local cortisone injection before treatment with radial
pressure waves.
• Haemophilia, Thrombosis, Deep vein thrombosis, or
other coagulation disorders.
• Anticoagulant pharmaceuticals.
• On any Neoplastic tissues or space occupying lesions.
• Reduced thermal sensitivity over the proposed area
of treatment, unless the physician in charge of the
patient is notified.
• Pulses must not be applied to target areas near large
vessels, the spinal column or head (apart from the
face).
CONTRAINDICATIONS

10 INDICATIONS FOR USE EN
INTELECT®RPW 2 USER MANUAL
ADDITIONAL PRECAUTIONS
When administering Radial Pressure Wave treatment, keep
in mind the following:
• Radial Pressure Wave treatment should be applied
with caution over bone where minimal (bony
prominence) or no (Stage IV wounds) soft tissue is
present.
• Hearing aids should be removed.
• The function of other patient connected equipment
may be adversely aected by the operation of the
pulsed radial pressure wave equipment. Maintain
maximum distance between devices in order to
reduce any tendency to interaction. Refer to the
EMC tables at the end of this manual for more
information.
• Any bleeding tendency is increased by heating
because of the increase in blood flow and vascularity
of the heated tissues. Care, therefore, should be used
in treating patients with therapeutic Radial Pressure
Wave treatment who have bleeding disorders.
• Frequent monitoring of intensity level and skin
response should occur during all treatments.
• Always apply the transmitter on the skin with small
circular movements.
• Never use Radial Pressure Wave therapy on the head.
• Do not treat direct in an area with a metal implant.
• Patients with active autoimmune diseases may not
respond positively with the treatment
ADVERSE EFFECTS
Side eects could occur after a treatment with Radial
Pressure Wave therapy. The majority will appear after -
days. Do not repeat a treatment until the previous side
eects have diminished. Common side eects include:
• Erythema, reddening
• Swelling
• Pain
• Hematoma
• Petechiae, red spots
• Skin lesions after previous cortisone therapy
• These side eects generally abate after  to  days
PATIENT APPLIED PARTS
Transmitters Material Applied part Type
A Steel . Type B
T Steel . Type B
C Ceramic Volcera Type B
DI  Titan grade  ELI Type B
F PTFE Type B
D-S Steel . Type B
D-S Steel . Type B
D-T Titan grade  ELI Type B
Ro Steel . Type B
R Steel . Type B
V POM-C LSG ( ACETRON) Type B
V POM-C LSG ( ACETRON) Type B
V POM-C LSG ( ACETRON) Type B
PERI ACTORS POM-C LSG ( ACETRON) Type B
SPINE ACTORS Polyvinylidenfluorid EpoFlon –
ECTFE (Halar) Type B
Ultrasonic gel Water de-ionized water Gel (PH) Type B

11 DEVICE DESCRIPTION EN
INTELECT®RPW 2 USER MANUAL
PRODUCT DESCRIPTION
The Intelect®RPW  is a compressed air-operated ballistic
shock wave generator. The shock waves in the device
are generated with a precision ballistic mechanism in the
handpiece. A projectile is accelerated by compressed air. The
motion and weight of the projectile produce kinetic energy.
When the projectile impacts against an immovable surface,
the shock transmitter, this kinetic energy is converted into
sound energy. This acoustic pulse is transmitted into the
tissue to be treated directly with the help of a gel.
These waves are physically classified as radial pressure
waves. The applied pressure pulse propagates radially within
the tissue and has a therapeutic eect on areas of the tissue
near the surface.
Note: This equipment is to be used only by a licensed medical
practitioner.

12 DEVICE DESCRIPTION EN
INTELECT®RPW 2 USER MANUAL
Gel Bottle
Gel for diagnostic and therapeutic medical procedures
should be water based with deionized water. No
formaldehyde, no fat. For external use only.
Pouch
COMPONENTS
Throughout these instructions the terms “left” and “right”
referring to the device sides are from the perspective of a
user standing in front of the device.
The components of the Intelect®RPW  are shown below.
Falcon Handpiece
Gel Holder
Cable Holders

13 DEVICE DESCRIPTION EN
INTELECT®RPW 2 USER MANUAL
IFU DOWNLOAD
. To download the IFU go to the Chattanooga website
www.chattanoogarehab.com
. Complete the registration to be informed of software and
IFU updates and register your device
. Select your INTELECT RPW  model
. Click download IFU to start the download
. A pdf viewer will be required to view IFU
SYSTEM START-UP
Complete the following steps for start-up of the Intelect®
RPW :
DEVICE CONNECTED TO THE MAINS
. Plug the power cord into the back of device. Plug the
other end of the cord into an electrical outlet.
Note: The Power Cord may be unplugged from the back of the device
in an emergency situation.
. Connect the Falcon handpiece on the right connector.
. Turn on the power switch located on the back of the
device.
TO STOP TREATMENT
Press Play/Pause button to pause treatment then press Stop
on touch screen. If device is on mains power press the On/O
button on the front panel then turn o the switch on the back
of the device.
Trigger the handpiece or press Start/Pause button to pause
treatment then press Stop on touch screen. If device is on
mains power turn of the switch on the back of the device.
Press and hold
for power o

14 GENERAL WARNINGS AND PRECAUTIONS EN
INTELECT®RPW 2 USER MANUAL
• This device should be operated at °C to +°C and % to % Relative Humidity (no condensation). The device should
be transported and stored at -°C to +°C and % to % Relative Humidity (no condensation).
• Atmospheric pressure requirements:  kPa to  kPa.
• The Falcon handpiece should be operated at °C to +°C and % to % Relative Humidity (no condensation).
The handpiece should be transported and stored at °C to +°C and % to % Relative Humidity (no condensation).
• The V-Actor HF handpiece should be operated at °C to +°C and % to % Relative Humidity (no condensation). The
handpiece should be transported and stored at °C to +°C and % to % Relative Humidity (no condensation).
• The time required for Intelect RPW  to warm from the minimum storage temperature between uses until Intelect RPW
 is ready for its intended use when the ambient temperature is °C is  hours.
• The time required for Intelect RPW  to cool from the maximum storage temperature between uses until Intelect RPW 
is ready for its Intended use when the ambient temperature is  °C is  hours
• Under single fault condition and extreme usage conditions, the maximum temperature of the hand piece can reach °C.
There is no particular health risk associated with this temperature besides your comfort.
• Use of parts or materials other than DJO’s can degrade minimum safety.
• Connect to this device only items and equipment that have been specified in this IFU as part of the Intelect RPW 
System or that have been specified as being compatible with the Intelect RPW  System.
• DO NOT disassemble, modify, or remodel the device or accessories. This may cause device damage, malfunction, electrical
shock, fire, or personal injury.
• Before using the therapy device, the operator must ascertain that it is in correct working order and operating condition.
The cables and connectors, in particular, must be checked for signs of damage. The device cannot be used if any part is
damaged as there is a risk of electrical shock.
• Before each use always oer the patient hearing protection.
• Apply a sucient amount of coupling gel to the patient’s skin in the treatment area and to the shock transmitter.
• The maximum energy level used during treatment must not cause the patient undue pain under any circumstances.
• DO NOT apply more than  shocks to the same spot during treatment.
• The surface of the transmitter can reach °C. Extended skin contact can cause minor burns. Interrupt therapy after a
maximum of  pulses to allow the transmitter to cool.
• Operating the device at pressures higher than  bar without an impact surface can result in damage to the handset.
• To avoid a trip hazard, keep all accessories and their cords separated during treatment by using the hook located on the
side of the device.
• Disconnect the instrument from the mains before starting any cleaning or overhaul work.
• Danger of injury due to pulse triggering when handpiece is open.
• Disconnect the handpiece from the control device before starting any cleaning or maintenance work.
• There are no user-serviceable parts inside the device. If a malfunction occurs, discontinue use immediately and contact
your local DJO oce via www.djoglobal.com for assistance and service information.
• Do not use while sleeping or operating heavy equipment.
CAUTION

15 GENERAL WARNINGS AND PRECAUTIONS EN
INTELECT®RPW 2 USER MANUAL
WARNING
• This equipment is not designed to prevent the ingress of water or liquids. Ingress of water or liquids could cause
malfunction of internal components of the system and therefore create a risk of injury to the patient.
• This device should be used only by a physician or licensed practitioner.
• Contaminated transmitters, and gel can lead to infection. Disinfect the handpiece after each treatment.
• DO NOT use the Intelect RPW  in water (Bath, Shower, etc.) that could cause electronic failure
• DO NOT operate the Intelect RPW  within the vicinity or environment of any microwave and RF shortwave diathermy
system.
• DO NOT operate this device in an environment where other devices are being used that intentionally radiate
electromagnetic energy in an unshielded manner.
• To avoid the risk of electric shock, this equipment must only be connected to a supply mains with protective earth.
• DO NOT apply more than  shocks to the same spot during treatment
• Avoid excessive pressure of the shock transmitter to the patient’s skin.
• DO NOT trigger pulses unless the pulse transmitter is in contact with the treatment zone.
• Portable RF communications equipment should be used no closer than  cm ( inches) to any part of the Intelect RPW
, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could
result.
• Use of accessories, handpieces and transmitters other than those specified or provided by the manufacturer of
this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this
equipment and result in improper operation.
• Device is designed to comply with electromagnetic safety standards. This equipment generates, uses, and can radiate
radio frequency energy and, if not installed and used in accordance with instructions for use, may cause harmful
interference to other devices in the vicinity. Harmful interference to other devices can be determined by turning this
equipment on and o. Try to correct the interference using one or more of the following:
» Reorient or relocate the receiving device
» Increase the separation between the equipment
» Connect the equipment to an outlet on a dierent circuit from that to which the other device(s)
are connected
» Consult your authorized DJO dealer for help.
• No modification of this equipment is allowed
• The Intelect®RPW  may be susceptible to Electro-Static Discharge (ESD) at greater than ± kV when first grasping
either the Falcon or V actor hand piece. In the event of such a discharge, the Intelect®RPW  may experience
communication loss. The Intelect®RPW  will terminate all active outputs, automatically place the device in a safe state.
• To prevent Electro-Static Discharge (ESD) at greater than ± kV:
»Grasp and hold the hand piece prior to starting treatment. If the applicator must be put down prior to completion
of treatment, stop the current treatment first and then place the applicator in the holder.
»Maintain humidity in the use environment to at least % relative humidity.
»Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material, DJO recommends
implementing additional controls to maintain relative humidity to at least %.
»Communicate these ESD-precautionary procedures to healthcare sta, contractors, visitors, and patients.
• DO NOT block the device's vents.
• Potential electromagnetic or other interference could occur to thsi or other equipment. Try to minimize this interference
by not using other equipment in conjunction with it.

16 GENERAL WARNINGS AND PRECAUTIONS EN
INTELECT®RPW 2 USER MANUAL
DANGER
• DO NOT connect the device to an electrical supply without first verifying that the power supply is the correct voltage.
Incorrect voltage may cause device damage, malfunction, electrical shock, fire, or personal injury. Your device was
constructed to operate only on the electrical voltage specified on the Voltage Rating and Serial Number Plate. Contact
your DJO dealer if the device is not properly rated.
• Device is not designed to be used in oxygen rich environment, Explosion hazard if the device is used in the presence of
flammable anesthetic mixture with air, oxygen, or nitrous oxide.
• If the device is not safe for operation, it must be repaired by a certified service technician and the operators must be
informed of the dangers posed by the device.

17 SETUP INSTRUCTIONS EN
INTELECT®RPW 2 USER MANUAL
UNPACKING THE DEVICE
The device is generally delivered with the packaging
material supplied by the manufacturer. As the device weighs
approximately  kg ( lbs), it must be unpacked by at least
 persons.
Proceed as follows:
• Position the transport packaging so that the arrows
are pointing upward.
• Remove the safety bands from the transport
packaging.
• Lift o the transport packaging upward.
• Remove the remaining foam material.
• Using at least  people, lift the device from the lower
packaging element.
• Inspect the device for any damages before
proceeding
Immediately upon unpacking the device, perform the
following steps:
. Verify the delivery documents to make sure that the
delivery is complete.
. Check the external components and accessories for
possible damage due to transport
. Verify that the packaging contains the following
• Intelect®RPW  device
• Intelect®RPW  Quick Start Guide
• USB Stick
• Pouch
• Gel Holder
• Cables Holder
• Power cord
• Conductor™Transmission Gel- ml (. oz) bottle
• Standard Accessory Kit that Includes the following:
» RPW Falcon Handpiece Applicator
» Projectile
» R  -  mm ESWT Transmitter
» D-S D-ACTOR® mm Transmitter
» Sealing Set
» Guide Tube
» Cleaning Brush
. Retain the original packaging. It may prove useful for any
equipment transport. Please refer to chapter to page ,
the Accessories Section for information. For information on
optional accessories.
. A pouch is provided with the device. This pouch can
be attached onto the side of the device handle, useful for
accessories storage.
a. Position the pouch on the side of the device, just below
the handle rail:
b. Get the attachment textile part above the rail
c. Attach the textile part to the Velcro band located on the
back of the pouch

18 SETUP INSTRUCTIONS EN
INTELECT®RPW 2 USER MANUAL
. The Gel Holder cup can be attached on the any side of the
device
. The cable holder is used to hang the handpieces cables
Throughout these instructions the terms “left” and“right”
referring to the machine sides are from the perspective of a
user standing in front of the device.
The components of the Intelect®RPW  are shown below.

19 DEVICE DESCRIPTION EN
INTELECT®RPW 2 USER MANUAL
DEVICE DESCRIPTION
Handle
Color Touch Screen
Play / pause button
Falcon Hand Piece Support
Transmitter Tray Holder*
USB Connector
Rotary adjustment
knob
V actor applicator
support
Switch
ON/OFF
Power Button
* Device delivered with  transmitters. Other transmitters displayed are optional.
* V-actor applicator is optional.

20 SETUP INSTRUCTIONS EN
INTELECT®RPW 2 USER MANUAL
FALCON HANDPIECE SET UP
. Unscrew the shaft from the handpiece and pull it out of
the handpiece handle. Use the supplied open-end spanner
for this purpose.
. Insert the new projectile into the fitted guiding tube
. Screw the shaft into the handpiece until finger-tight.
Using one hand, press the handpiece firmly onto the table
and tighten the shaft using the open-end spanner. It must
no longer be possible to unscrew the shaft by hand.
. Screw the transmitter screw cap with the required
transmitter firmly back onto the shaft. For two-part
transmitter caps: Make sure that the two cap parts are
screwed firmly in place and that the transmitter screw cap
is screwed firmly to the shaft.
. Connect the Falcon handpiece to the right connector on
the device