USER MANUAL - StomDevice.ru

USER MANUAL - StomDevice.ru
USER MANUAL
This manual is valid for:
LM-ProPower 100721741
LM-ProPower 100731751
LM-ProPower 100721741us
LM-ProPower 100731751us
LM-ProPower 100721741jp
LM-ProPower 100731751jp
Important!
Read this manual carefully
before using the product.
How to read this manual
Each chapter starts with a section with general instructions, which is
followed by sections with additional information. First read the general
section and then proceed to the section that applies to your product.
If there are any questions regarding the contents of this manual, please
contact LM-Instruments Oy.
Manufacturer, Marketing and Sales
LM-Instruments Oy
PL 88 (Norrbyn rantatie 8)
FI-21601 Parainen. Finland
Telephone: +358 2 4546 400
Fax: +358 2 4546 444
E-mail: [email protected]
Internet: www.lminstruments.com
Copyright
Copyright 2010 LM-Instruments Oy. All rights reserved. The contents
of this manual may be changed without notice. No part of this manual
may be reproduced in any form or by any means without permission in
writing from LM-Instruments Oy.
Printed in Sweden, May 2011.
2
0537
Contents
Safety ..................................................................................... 5
Consignes de securite (Canada) ......................................... 7
1 Unpacking ...................................................................... 9
1.1 General content of delivery ............................................. 9
1.2 Content of introkits ......................................................... 10
2 Equipment description ................................................. 11
2.1 General description ......................................................... 11
2.2 Control panel.................................................................... 12
2.3 Foot control ..................................................................... 13
2.4 Medicament bottle ........................................................... 14
2.5 Symbols on the equipment ............................................. 15
3 Installation ..................................................................... 16
3.1 General installation instructions ...................................... 16
3.2 Version for tap water ...................................................... 16
3.3 General installation instructions, continued .................... 17
4 Operating instructions ................................................. 18
4.1 General ........................................................................... 18
5 Cleaning and maintenance .......................................... 22
5.1 General cleaning procedure ............................................ 22
5.2 Recommended cleaning procedure ................................ 23
5.3 Maintenance ................................................................... 24
6 Troubleshooting UltraLED............................................ 25
7 Technical data ............................................................... 28
8 Warranty and Declaration of conformity ..................... 30
8.1 Warranty terms................................................................. 30
8.2 Declaration of conformity ................................................ 31
8.3 EMC - guidance ............................................................... 32
3
4
Safety
Safety
Intended use
This scaler is designed for dental purposes. It is designed for
removal of tartar or calculus on teeth and other dental work where
the ultrasonic vibration is beneficial. The unit should only be used
by licensed dental proffesionals trained in the proper use of scaling
devices. Do not use it for applications where it is not intended.
If you are unsure about your application, please contact your local
dealer or place of purchase.
General requirements
Service of the product is only to be performed by authorized service
personnel.
The product must be connected to electricity- and water supply
meeting the requirements specified in the Technical data section
page 28.
The product needs special precautions regarding EMC (Elektro
Magnetic Compability) and needs to be installed and put into
service according to the EMC information provided on page 33.
Portable and mobile RF (Radio Frequency) communications equipment can affect the product.
Contraindications
Do not use the scaler on patients with cardiac pacemakers. The scaler
may disturb the function of the pacemaker.
General precautions
• The product is not suitable for use in the presence of flammable gases.
• Only use the product in combination with LM-Instruments and Amdent scaler tips.
• If the handpiece tubing is damaged or worn-out, it must immedia
tely be replaced to avoid exposing the user or the patient to elec-
tric hazard.
• Use the original packaging when returning equipment for service.
Warnings
The product should not be used adjacent to or stacked with other
equipment.
If adjacent or stacked use is necessary, the product should be observed to verify normal operation in the configuration in which it will be
used.
5
Safety
Safety notices in this manual
WARNING
Caution
Warning indicates a potentially dangerous situation. Non-observance may lead to
death or injury.
Caution indicates a potentially harmful
situation. Non-observance may damage
the equipment.
Note indicates a situation where special
notice should be observed.
Note
66
Consigne de sécurité
Consigne de sécurité (Canada)
Utilisation prévue
Cet appareil à ultrasons est destiné à des applications dentaires.
Il est conçu pour éliminer le tartre ou les calculs des dents et pour
toute autre application dentaire où les vibrations ultrasonores sont
bénéfiques. Cet appareil doit être exclusivement manipulé par des
professionnels dentaires diplômés ayant suivi une formation relative
à l’utilisation correcte des dispositifs de détartrage. N’employez pas
cet appareil pour des applications pour lesquelles il n’est pas conçu.
Au cas où vous ne seriez pas sûr de son application, veuillez contacter
votre distributeur local ou le point de vente.
Conditions générales
Le service du produit doit être executé seulement par le
personnel de service autorisé avec les outils et le matériel appropriés.
Le produit doit être relié à l’approvisionnement de l’électricité et à
l’approvisionnement en eau répondant aux exigences définies dans la
section Caractéristiques techniques à la page 28.
Le produit exige des précautions spéciales concernant la CEM
(Compatibilité Electromagnétique) et doit être installé et mis en
service selon à la page 33. L’équipement de communication RF
(Radio Fréquence) portable et mobile peut affecter le produit.
Contres-indication
N’employez pas sur des patients avec les stimulateurs cardiaques.
Le produit peut déranger la fonction du stimulateur.
Précautions générales
•
•
•
•
Le produit n’est pas approprié pour l’usage en présence d’un
mélange anesthésique inflammable.
Utilisez seulement le produit en combinaison avec des inserts
de détartreur de LM-Instruments et Amdent.
Si la tuyauterie de pièce à main est endommagée ou usée, elle
doit immédiatement être substituée pour éviter d’exposer
l’utilisateur ou le patient au risque électrique.
Utilisez l’original empaquetage en renvoyant le matériel pour
le service.
Avertissement
Le produit ne doit pas être utilisé à proximité ou empilé avec d’autres
équipements. Si l’usage adjacent ou empilé est nécessaire, le produit
doit être surveillé pour une utilisation normale suivant la configuration
dans laquelle il sera utilisé.
7
Consigne de sécurité
Notifications de sûreté en ce manuel
WARNING
“Warning” indique une situation probablement dangereuse. La inobservance peut
mener à la mort ou des dommages.
“Caution” indique une situation probablement nocive. La inobservance peut endommager le matériel.
Caution
“Note” décrit si on observe la notification
spéciale.
Note
68
ance may lead to death or injury.
WARNING
1 Unpacking
Caution
Note
This chapter describes the
components of the delivery
and can be used as a check
list when unpacking. Contact your place of purchase
if anything is missing. For a
description of the features
of the equipment, read the
Equipment description section on page 11.
Caution indicates a potentially
harmful situation. Non-observance may damage the equipment.
Unpacking
Carefully unpack your LM-ProPower UltraLED unit and verify that
all accessories
and components
included according to the content
Note indicates
a situationare
where
lists below:
special notice should be observed.
1.1 General content of delivery
1. LM-ProPower UltraLED unit
2. Scaler handpiece connected to unit
3. Scaler introkit (see section 1.2 )
4. 500 ml medicament bottle or water hose 6 mm (1/4”)
5. Foot control
6. Foot control cable
7. Power cord
8.
LM-ProPower Fixer
6
7
1
4
3
6
5
2
8
9
Unpacking
1.2 Content of introkits
Content of UltraLED Scaler introkit
3 x Scaler tips
3 x ErgoGrips
3 x Torque Wrenches
3 x Tip Check Cards
10
Equipment description
2 Equipment description
2.1 General description
LM-ProPower UltraLED is an effective piezoelectric scaler in a
versatile and ergonomic appliance.
The device’s LED lights, advanced electronics, quality, and highdurability LM-DuraGradeMAX tips enhance the execution of
procedures which require great precision.
Ergonomically designed ErgoGrip handpieces with soft silicone handles give the user a comfortable, relaxed grip as well as an excellent
feel.
LM-ProPower is highly adaptable to any procedure or user approach.
It is not only an outstanding scaling and cleaning device, but it also
brings power and versatility to endodontics, implantology, restorative
treatments, minimally invasive treatments and apical surgery.
1
6
2
7
1. UltraLED Handpiece
(with an ErgoGrip and a tip
mounted)
4
2. Water flow control ring
3. Handpiece tubing
4. Control panel
3
5. Foot control
6. Medicament bottle
7. Depressurisation button
5
11
Equipment description
1. AC power input
2. Fuse holder
3. Water hose coupling (optional)
4. Foot control connection
5
5. Type plate
2
4
1
3
2.2 Control panel
14
1
1. Cleaning key
2. POWER ON key
3. POWER OFF key
13
6
4. Working mode 1 key = 0 to 40% power
5. Working mode 2 key = 0 to 70% power
12
5
6. Working mode 3 key = 0 to 100% power
7. StandBy indicator
9
11
4
10
8. POWER ON indicator
9. Dry mode indicator
10. Irrigation mode indicator
8
11. Working mode 1 indicator
12. Working mode 2 indicator
13. Working mode 3 indicator
14. Cleaning mode indicator
2
12
7
3
Equipment description
2.3 Foot control
11. Connection for foot control cable
12. OFF position
13. ON position
14. Diagnostic function, turn LED light
ON or OFF by a single-click on the
pedal
15. Irrigation position
16. Zero power position
17. Maximum power position
18. Power regulation
1
1
2
4
5
3
7
6
8
13
Equipment description
2.4 Medicament bottle (optional)
LM-ProPower has a medicament dispenser system, making the device independent of
a fixed water supply connection. The medicament bottle can be used for either medicament solutions or ordinary clean water.
The unit contains an electrically driven air compressor. When operating the unit the
compressed air forces the fluid from the bottle through the hose and to the handpiece
and the tip/nozzle.
1. Medicament bottle
2. Bottle connector
3. Depressurisation button
2
1
3
The LM-ProPower can be delivered either with the medicament dispenser system
or with fixed water supply connection without the bottle and bottle connector.
14
Equipment description
2.5 Symbols on the equipment
Working mode 1 = 0 to 40% power
Working mode 2 = 0 to 70% power
Working mode 3 = 0 to 100% power
Irrigation mode
Dry mode
Automatic cleaning function
Power ON
Power OFF
Example of type plate. The type plate is placed on the back side of the scaler
unit.
CLASSIFIED
9800163
Medical electrical equipment classified by ETL with respect to electric shock, fire,
mechanical, and other specified hazards in accordance with the Safety Standards
ANSI/AAMI ES 60601-1 and CAN/CSA C22.2 No 60601-1:08
Caution
Consult accompanying documents.
0537
Compliance label indicating compliance with the Medical Device Directive
93/42/EEC.
0537 is the ID-number of the Notified Body: VTT
Withstands autoclave temperature 135°C (275°F).
Type B applied part according to the degree of protection against electrical
shock.
Fuse
Input
Output
Please do not throw the equipment into the domestic refuse. Please use the return and collection systems available in your country for the disposal of this
product. The equipment can also be returned to the manufacturer for disposal.
15
Installation
3 Installation
WARNING
3.1 General installation instructions
Checklist
• Position the unit horizontally with the handpiece in the holder
and the hose hanging free.
• Position the unit where air is free to circulate on all sides and beneath it. Do not position the unit on a wall or next to a heat source.
• Avoid placing the unit in the immediate vicinity of sources of
electromagnetic radiation, for example an electrosurgery equipment.
• Connect the foot control cable to
the foot control and at the rear side
of the unit.
• Mount the scaler tubing in the
groove underneath the unit, as in
picture.
Caution
Caution
Do not place the unit on or
next to a heat source. Excessive heat may damage
the electronics.
Note
WARNING
Caution
Caution
Consult a qualified technician for connecting the scaler
to the water supply.
3.2 Version for tap water (optional)
Connecting to the water supply
1. Verify that the water supply can be turned off.
2. Verify that the water pressure conforms to the data in the Technical
data.
3. Verify that the water supply fulfills the medical demands of
hygiene.
4. Unscrew the nut from the nipple
and thread it on the hose.
5. Push the hose onto the coupling
nipple.
6. Tighten the nut firmly and insure
that the hose is securely attached
to the unit.
7. Connect the other end of the hose
to the water supply.
Note
6
16
WARNING
Warning indicates a potentially
dangerous situation. Non-observance may lead to death or injury.
Installation
3.3 General installation instructions,
Caution indicates a potentially
continued
harmful
situation. Non-observCaution
WARNING
The unit must be connected to an AC power outlet
provided with a protective
ground. USA and Canada:
The power cord and plug
must be classified as ”Hospital-Grade”.Note
• Verify
voltage
on the rear side match the voltage
ancethat
maythe
damage
therating
equipment.
of the AC power outlet.
• Verify that the AC power outlet is provided with a protective
ground.
Note indicates
a situation
where
• Connect
the power
cord to the
unit and the AC power outlet.
special
notice
should
be
obAll indicator lamps will illuminate for a short period during a
selfserved.
check of the unit.
• The unit is standby when the green indicator lamp is illuminated.
6
17
Safety notices in this ma
Operating instructions
4 Operating instructions
WARNING
Preparations (bottle version)
1. Fill the medicament bottle with water or medicament solution
according to the Medicaments that can be used, listed on page 29.
Caution
WARNING
2. Screw the bottle connector onto the bottle and push it onto the connector. See picture in section 2.4
A tip that is bent, altered,
worn more than 2 mm will
loose performance and must
be exchanged. Prolonged
use may cause tip breakage
and injury to the patient.
Note
3. Check that the power cord is connected and the unit is in stand-by
mode, the green indicator lamp is illuminated.
The operator should be
aware of that ultrasonic instruments with small diameters are subject to breakage
at any time. If not used correctly or with too much power or force the instrument
WILL break.
4.1 General
1. Gently slide the ErgoGrip on to the scaler handpiece.
Do not use nickel-titanium
files, since they easily break
at high frequenses.
2. Carefully place the tip in the torque wrench.
3. Use the torque wrench and screw the tip clockwise on to
the scaler handpiece. Tighten until resistance and the torque
wrench slides. The torque wrench prevents the tip from being
overtightened.
6
18
Warnin
dangero
ance m
Caution
harmfu
ance m
Note in
special
served.
WARNING
Operating instructions
4. Turn on the UltraLED scaler by ON key on the keyboard. The blue
indicator lamp illuminates and the scaler is activated.
Caution
Caution
Without cooling fluid, the
maximum operating time,
for the scaler handpiece, is
2 minutes followed by a
cooling-down period of 8
minutes. Operating without
cooling fluid Note
for more than
2 minutes may cause overheating of the scaler handpiece.
After above cycle has been
repeated 2 times, the scaler
handpiece has to cool down
for at least 60 minutes.
WARNING
5. The indicators next to the working modes are flashing to remind
that a working mode has to be selected. If several blue indicators are
flashing instead, check that the scaler hand piece is connected. If the
problem remains concern the trouble shooting section. Check the recommended working mode that is marked on the tip and
choose the working mode by pressing the corresponding working
mode key on the keyboard.
Safety notices in this manual
Caution
WARNING
Warningpress
indicates
potentially
6. A second
of thea“ON”
key activates the dry mode for scaling
dangerous
situation. Non-observwithout
water/medicament.
ance may lead to death or injury.
7. A third press of the “ON” key activates the irrigation mode.
The irrigation mode can also be activated in the scaling mode by
pressing down the foot control in the leftmost position.
Caution indicates a potentially
8. Byharmful
pressingsituation.
the “ON”Non-observkey repeatedly, it will toggle between normal
ance may
damage
the equipment.
scaling,
dry and
irrigation
mode.
Remember to choose the
9. Keep the handpiece over the cuspidor bowl and depress the foot
Safety
right workingnotices
mode if chang- in this manual
control in the leftmost position and adjust the water flow with the
ing scaler tip during the
treatment
New tips are not sterile upon
delivery. Sterilize
Note before use
according to the clinic’s
routines. WARNING
Keep the patient’s lips,
cheeks, and tongue out of
the way of the activated tip,
since contact may cause
burns because of friction
heat.
Caution
Note
6
ring
on the
handpiece
until the
water is dripping from handpiece as
Note
indicates
a situation
where
in special
picture notice
below. should
Recommended
be ob- flow: 20 ml/min.
Warning indicates a potentially
served.
dangerous situation. Non-observance may lead to death or injury.
Caution indicates a potentially
harmful situation. Non-observance may damage the equipment.
Notethe
indicates
a situation
where
10. Keep
patient’s
lips, cheeks
and tongue out of the way of the
special
notice
should
be
obtip and perform treatment according to “How to use the scaler”
served.on next page.
section
At low power settings there
will be no spray.
Increase the water flow if the
handpiece feels too warm.
19
Operating instructions
How
use the UltraLED scaler
How to
use theto
scaler
The side of the tip-end shall be applied to
The side of the tip-end shall be applied to the tooth so that the movement
the tooth so that the movement of the tip
oftothe
is parallel
to the
thescaler
tooth. The first 2 mm of the tip
is parallel
thetip
surface
of the tooth.
Thesurface
How
to useofthe
are
the
most
efficient!
Place
the
tip
on
the
before activating
first 2 mm of the tip are the most efficient!
The side of the tip-endtooth
shall besurface
applied to
control.
The before
power
is regulated
the foot
from 0 to
Place thethe
tipfoot
on the
tooth surface
the tooth
so that the with
movement
of thecontrol
tip
activating
the foot
switch.
is parallel
to the surface of the tooth. The
100%
within
each working
mode.
first 2 mmmore
of thethan
tip are
the most
efficient!
Normal scaling rarely requires
50%
power
level of each
Normal scaling rarely requires more than
50%
power
level.
Place
the
tip
on
the
tooth
surface
before
working mode. However, hard to remove calculus might require a higher
However, hard to remove calculus mightactivating
require a the
higher
footpower
switch.
setting. power setting.
Ensure that contact between
the tip and the tooth surface
is maintained during scaling.
Keep moving the tip slowly
back and forth and let the
instrument do the work.
Use short and long strokes
so that the whole surface of
Ensure
that contact
each tooth
is scaled.
Normal scaling rarely requires more than 50% power level.
However, hard to remove calculus might require a higher power
setting.
Ensure that contact between
the tip and the tooth surface
is maintained during scaling.
Keep moving the tip slowly
back and forth and let the
between
the tip and the tooth surface is maintained
instrument do the work.
during scaling. Keep moving
theand
tiplong
slowly
Use short
strokesback and forth and let the
do the
work.
andsurface
long of
strokes so that the whole
that short
the whole
The tip instrument
is normally aimed
towards
thesoUse
toothpocket.
surface of each tooth is each
scaled.
tooth is scaled.
The tip is normally
aimed
the toothpocket.
To keep
the tiptowards
working parallel
Theoftip
is normally
aimed towards the toothpocket.
to the surface
each
tooth, it is
important to follow the anatomy
of the tooth.
To keep the tip working parallel
to the surface of each tooth, it is
important to follow the anatomy
of the tooth.
With the correct power setting, appropriate pressure against
the tooth (approx. 20 grams but not exceeding 50) and the tip
operating parallel to the surface, treatment will be gentle, quiet
and efficient.
With the correct power setting, appropriate pressure against
To keep the tip workingthe
parallel
to the 20
surface
of each
tooth, it50)isand the tip
tooth (approx.
grams but
not exceeding
parallel
totooth.
the
If, during
the treatment,
a squeaking
sound
is heard
(loud
andsurface, treatment will be gentle, quiet
important
to follow
the operating
anatomy
of the
efficient.
dominating),
against
theand
tooth
might
be too low pressure against the tooth
Withthe
thepressure
correct
power
setting,
appropriate
or the tip not parallel to the surface of the tooth.
(approximately 20 grams but not exceeding 50) and the tip operating
If, during the treatment, a squeaking sound is heard (loud and
parallel to the surface, treatment
will be gentle, quiet and efficient.
dominating), the pressure against the tooth might be too low
If, during the treatment,ora the
squeaking
sound
is heard
and dominattip not parallel
to the
surface (loud
of the tooth.
ing), the pressure against the tooth might be too low or the tip not parallel
to the surface of the tooth.
20
Caution
Caution indicates a potentially
harmful situation. Non-observance may damage the equipment.
Operating instructions
After treatment
Note
Always set the water flow to
fully open before running the
cleaning cycle (dots in line,
see picture).
Note indicates a situation where
1. Run the automatic cleaning function, see instructions on page 22.
special notice should be observed.
2. After the cleaning cycle is finished, screw off the tip, counter
clockwise, with the torque wrench.
WARNING
3. Squeeze the ErgoGrip gently at the top and at the same
time slide it off the handpiece. Do not squeeze too hard at
the ErgoGrip as this can make the removal difficult.
Caution
Caution
Before cleaning and sterilizing; the handpiece water
control ring must be set to
fully open (dots in line, see
picture)
Note
4. Press the depressurization button (bottle version).
5. Pull the medicament bottle from the unit (bottle version).
6. Clean and sterilize the equipment/components according
to the Cleaning and maintenance section on page 22-23.
6
21
WARNING
Cleaning and maintenance
5 Cleaning and maintenance
Caution
5.1 General cleaning procedures
Automatic cleaning function
1. Make sure the water control is fully open. Place the scaler
handpiece over the bowl and start the cleaning cycle by pressing
the cleaning key “C”.
Note
Always set the water flow to
fully open before running the
cleaning cycle (dots in line,
see picture).
2. The cleaning cycle starts and stops automatically after 80 seconds.
Cleaning of the equipment/components
Wipe off with a soft cloth and use a surface disinfectant suitable
for hard plastics.
Cover and control panel
Wash at max 65°C (149°F)
Medicament bottle
Cap for medicament bottle
6
22
Warnin
danger
ance m
Cautio
harmfu
ance m
Note in
specia
served
WARNING
Caution
Caution indicates a potentially
harmful situation. Non-observance may damage the equipment.
Cleaning and maintenance
Autoclave in steam at max 135°C (275°F) or wash at max 95°C (203°F)
Scaler
tipsindicates a situation where
Note
Note
Autoclaving the handpiece
regularly may shorten the
life time of the scaler handpiece.
Therefore we recommend to
just autoclave the ErgoGrip
WARNING
and the scaler
tip after each
patient.
special notice should be observed.
Torque wrenches
LM-ErgoGrip LED
LM-ErgoGrip Focus LED
Safety notices in this manual
LM-ProPower scaler handpiece
Caution
Caution
Before cleaning and sterilizing; the handpiece
WARNINGwater
control ring must be set to
fully open (dots in line, see
picture)
Note
Caution
Note
Always set the water flow to
fully open before running the
cleaning cycle (dots in line,
see picture).
6
WARNING
Warning indicates a potentially
dangerous situation. Non-observance may lead to death or injury.
5.2 Recommended cleaning procedure
Beginning
the daya potentially
Cautionofindicates
harmful
situation.
Non-observRun the
automatic
cleaning
cycle with clean water. See instructions
ance
may
damage
the
equipment.
on page 22.
After each treatment
• Run the automatic cleaning cycle with clean water. See instructions
a situation where
on Note
page indicates
22.
special
notice
should
be ob• Wipe
off the
cover,
control
panel, handpiece and the hose with a
served.
soft cloth. Use a surface disinfectant suitable for hard plastics.
• Wash the ErgoGrip, the tip and possibly the scaler handpiece and
autoclave according to the clinic’s routines.
End of the day
• Run the automatic cleaning cycle with clean water. See instructions
on page 22.
• Remove and wash medicament bottle and bottle cap at a maximum
temperature of 65°C / 149°F (bottle version).
Caution
Caution
Do not sterilize any scaler
accessories using dry heat
or chemical autoclaves.
This may damage the
material.
Note
23
Cleaning and maintenance
Weekly (bottle version)
• Run the automatic cleaning cycle with an anti-microbial cleaning
agent solution in the bottle. See instructions on page 22.
We recommend to use a separate bottle for the cleaning agent
solution. Concerning exposure times of cleaning agent, follow
instructions given by manufacturer.
• Before patient treatment; to rinse the lines from cleaning agent
solution put clean water in the bottle and run the automatic
cleaning cycle until clean water comes out of the handpieces.
5.3 Maintenance
Power cord
Inspect the power cord, cables and the handpiece hose daily to insure
that the equipment is in good condition without mechanical damage.
O-rings (bottle connector)
Lubricate the O-rings regularly with a glycerine based, water soluble
lubricant. Vaseline may also be used, but it may shorten the durability
time of the O-rings.
Tips
When a tip is bent, altered, or worn more than 2 mm it will loose
performance and must be exchanged. Check the tip length weekly
by comparing the tip to a tip check card.
Exchanging fuses
1. Disconnect the power cord from the AC power outlet and the unit.
2. Open the fuse holder on the rear side of the unit.
WARNING
Safety notices in this ma
Caution
Caution
A petroleum based lubricant
on the o-rings may shorten
their durability time.
WARNING
Note
Caution
WARNING
A tip that is bent, altered,
scratched or worn more than
2 mm will loose performance and must be exchanged. Prolonged use may
cause tip breakage and injury to the patient.The
operaNote
tor should be aware of that
ultrasonic instruments with
small diameters are subject
to breakage at any time. If
not used correctly or with
too much power or force the
instrument WILL break.
3. Inspect the fuses for damages. Replace damaged fuses with new
ones. Verify the fuse specifications according to the Technical data
section on page 28.
4. Close the fuse holder.
24
Warni
dange
ance m
Cautio
harmf
ance m
Note i
specia
served
Troubleshooting
6 Troubleshooting UltraLED
Type of problem
Please see
A.Unit is not responding and no lights are lit on the control panel
Page 25
B.Lights are flashing on the control panel
Page 26
C.No tip vibration
Page 26
D.Weak tip vibration
Page 26
E.Insufficient or no water flow
Page 27
F.Tip does not fit smoothly onto the handpiece
Page 27
G.Difficulty to remove the ErgoGrip
Page 27
H.Handpiece is overheated
Page 27
I. Weak or no LED light
Page 27
A.Unit is not responding and no lights are lit on the control panel
1.
2.
3.
4.
Check that the power cord is connected properly and double check the voltage (120V/230V).
Check the fuse and replace if necessary. See Maintenance-section of the user guide.
Check that the wall outlet and the fuse panel of your clinic are OK.
If the problem still remains – contact your dealer for support and indicate Error Code E-X02.
25
Troubleshooting
B.Lights are flashing on the control panel
Four blue lights on the control panel
are flashing simultaneously.
Check that the foot control cable is connected at both ends and is not damaged.
The blue light next to the ON-key is
flashing alternately with three other
blue lights on the control panel.
Check that the scaler handpiece is properly
connected.
Three yellow lights are flashing in
sequence.
The Working Mode has not been selected.
Select the working mode by pressing one of
the keys next to the yellow lights.
The light next to the C-key is flashing.
The cleaning function has been activated.
Wait until the cleaning process has finished
and the light stops flashing.
C.No tip vibration
1. Check that the tip is firmly tightened. Preferably use a torque wrench and tighten clockwise
until the torque wrench slides. (The torque wrench prevents the tip from being overtightened.)
2. Check that the green light below the keys on the control panel is lit. If it is not lit, please see
Section A on page 25.
3. Check that the device has been turned on by pressing the ON-key and that the blue light next
to the ON-key is lit.
4. Check that the Working Mode has been selected by pressing one of the Working Mode keys
and that one of the yellow lights on the control panel is lit.
5. If you have an additional handpiece, try replacing the handpiece.
6. If you have an additional foot control cable, try replacing the foot control cable.
7. If you have an additional foot control, try replacing the foot control.
8. If the problem still remains – contact your dealer for support and indicate Error Code E S01.
D.Weak tip vibration
1. Check that the tip is firmly tightened. Preferably use a torque wrench and tighten clockwise
until the torque wrench slides. (The torque wrench prevents the tip from being overtightened.)
2. Check that the tip is not worn out. Use a tip check card to evaluate wearing or try an unused
tip. Use original LM-Instruments tips for reliable performance.
3. If you have an additional handpiece, try replacing the handpiece.
4. If the problem still remains – contact your dealer for support and indicate Error Code E-S02.
26
Troubleshooting
E.Insufficient or no water flow when foot switch is activated
1. If the unit are equipped with a water bottle: Check that the medicament/water bottle is
properly connected i.e. the cap is tightened and pushed in all the way onto the connector.
Check that the o-rings on cap and connector are in good condition. Replace o-rings if worn.
O-rings can be lubricated with a glycerine based lubricant (or vaseline).
2. If the unit are connected with tap water: Check that the tap water hose is properly connected
to the back of the device and that the tap water system is OK (tap/valve is open and possible
filter is OK).
3. Check that dry mode is not activated i.e. that the blue light next to the crossed-out water drop
is not lit. If it is lit, press the ON-key.
4. Adjust the water control ring on the handpiece to fully open (dots aligned).
5. Try with another tip.
6. Use the LM-ProPower Fixer to check that the water hose inside the handpiece has not stuck
in the autoclave. Insert the Fixer carefully into the handpiece from the hose connector side.
(To avoid the hose getting stuck, the water adjustment on the handpiece should be set to fully
open before sterilization in autoclave.)
7. If the problem still remains – contact your dealer for support and indicate Error Code E-S04.
F.Tip does not fit smoothly onto the handpiece
1. Clean handpiece threads with compressed air and try with a new tip.
2. If the problem still remains, the threads of the handpiece may be damaged and the handpiece
needs to be replaced. Contact your dealer and indicate Error Code E-S06.
G.Difficulty to remove the ErgoGrip from the handpiece
1. Grab the ErgoGrip gently near the lens and at the same time twist and slide it off the
handpiece.
2. If the problem still remains, replace the ErgoGrip.
H.Handpiece is overheated during use
1. Check that the fluid flow is sufficient (at least 20 ml/min).
2. If the problem still remains, replace the handpiece and contact your dealer.
I. Weak or no LED light.
1. Note that there are two versions of the ErgoGrip with different lenses and light pattern and
intensity: “ErgoGrip LED” and “ErgoGrip FocusLED”.
2. Check that lens in the ErgoGrip is clear and clean. Clean or replace if necessary.
3. If you have an additional handpiece, try replacing the handpiece.
4. If the problem still remains – contact your dealer for support and indicate Error Code E-S03.
27
Technical data
7 Technical data
Manufacturer
LM-Instruments Oy
PL 88 (Norrbyn rantatie 8)
FI-21601 Parainen, FINLAND
Model
LM-ProPower UltraLED
Classification
EN60601-1: Class 1, Type B
93/42 EU: Medical products, class IIa
L x W x H
270 x 140 x 165 mm (without bottle)
Weight
2900 g
Voltage
100 Vac, 50-60 Hz
115 Vac, 50-60 Hz
230 Vac, 50-60 Hz
Primary
fuse
T500 mAH, 250 V, Ø5x20 mm (100 Vac)
T400 mAH, 250 V, Ø5x20 mm (115 Vac)
T200 mAH, 250 V, Ø5x20 mm (230 Vac)
Power cord
Separate with protective earth plug
Power consumption
Max. 40 VA
Scaler power consumption
Max. 24 VA
Scaler power output
Max. 10 W (24 kHz - 28 kHz, automatic tuning)
Transport and storage
-40°C to 70°C (-40°F to 158°F)
Ambient temperature
Operation
10°C to 40°C (50°F to 104°F)
Transport and storage
10% to 100%
Relative humidity
Operation
10% to 95%
Water supply pressure
(version conn. to tap water)
1 - 10 bar (0,1–1,0 MPa, 14,5–145 PSI)
Water consumption
10 - 50 ml/min
Bottle volume
(bottle version)
500 ml
Installation and service of the product is only to be performed by aut­horized service
personnel by the manufacturer.
28
WARNING
Caution
WARNING
Immedately after using any
kind of medicament in the
medicament bottle, run the
automatic cleaning cycle
with clean water in the medicament bottle for both the
scaler and the
polisher unNote
til clean water comes out of
the handpieces.
Warning indicates a potentially
dangerous situation. Non-observance may lead to death or injury.
Technical data
Medicaments that can be used
Caution
• Clean
waterindicates a potentially
harmful situation.
Non-observ• Cetylpyridinium
chloride
ance
may
damage
the
equipment.
• Clorhexidine
• Essential oils
• Hydrogen peroxide, 3% USP
• Povidine iodine, 10% solution
Notesolution
indicates a situation where
• Saline
special
notice
should be ob• Sangurinara
extract
served.
• Sodium
hypochlorite 1% solution
6
29
Warranty and declaration
8 Warranty and Declaration of
conformity
..
8.1 Warranty Terms
The following warranty terms apply to the sale of LM-Instrument Oy’s products (hereinafter
“Products”) to a purchasing company or individual by LM-Instruments Oy (hereinafter
“Manufacturer”).
Manufacturer hereby warrants that the Products will be free from defects arising from faulty materials or workmanship for a period of twenty four (24) months from the date of purchase by a customer
from Manufacturer’s authorized dealer (hereinafter “Authorized Dealer”). The warranty period is
exceptionally three (3) months for products with a life inherently shorter than 24 months due to
normal wear and tear, for example tips of ultrasonic scalers, tips of endodontic files.
This warranty shall not apply to Products or parts thereof; which have been subject to abuse, misuse,
negligence or accident or are not connected to proper power supply; to which any modification,
alteration or attachment has been made without written consent of the Manufacturer; or which are
installed or operated violating instructions for installation, use and maintenance; which are normally
consumed in operation.
The sole and exclusive remedy under this warranty shall be limited to correct or circumvent
the errors or to repair or replacement of defective parts of Products by the Manufacturer, EXW
Manufacturer’s factory, providing that a written claim of the defect is sent to the Manufacturer within
the warranty period and the original part is returned to Manufacturer’s factory by the Authorized
Dealer, and Manufacturer’s inspection establishes the existence of such a defect.
The customer must contact the Authorized Dealer from whom the products were purchased to
request repair or replacement under this warranty and a written claim of the defects and send the
original Product the Authorized Dealer.
This warranty is void if service or repair is performed by persons not authorized by the manufacturer.
Any Products not manufactured by the Manufacturer, carries only such warranty, if any, as given by
any manufacturer thereof.
This warranty is the Manufacturer’s only warranty in respect of the Products and the Manufacturer
disclaims all other warranties, whether of merchantability, fitness for particular purpose or otherwise,
guarantees and liabilities, express or implied, arising by law or otherwise. In no event shall the
Manufacturer be liable for any general, consequential or incidental damages, loss of use or loss of
profits by reason of the manufacturer’s negligence or otherwise in connection with the sale, delivery,
installation, repair or use of the Products.
The Manufacturer shall have no liability whatsoever to the Authorized Dealer or customer or any
other person for or on account of any injury, loss or damage of any kind or nature, sustained by, or
any damages assessed or asserted against, or any other liability incurred by or imposed upon the
handling, use, operation, maintenance or repairs of Products by anyone other than the Manufacturer.
This exclusion of liability does not apply pursuant to the laws on product liability in case of personal
injury and property damage to privately used objects resulting from the Products.
30
...
WARNING
Warning indicates a potentially
dangerous situation. Non-observance may lead to death or injury.
Warranty and declaration
8.2 Declaration of conformity
Caution
WARNING
No modification of this
equipment is allowed.
Note
Caution indicates a potentially
The manufacturer hereby declares that the
harmful situation. Non-observLM-ProPower UltraLED unit
ance may damage the equipment.
Class I, type B according to EN60601-1 equipped with original accessories conforms to the essential requirements of the Medical Device
Directive 93/42/EEC with reference to the following harmonized
standards:
Note indicates a situation where
special notice
should be
obIEC 60601-1,
Third edition
2005
served. 2006
EN 60601-1:
Classification: Medical products, Class IIa:
0537
6
31
Warranty and declaration
8.3 EMC - Guidance and manufacturer’s declaration
Guidance and manufacturer's declaration - electromagnetic emissions
The LM-ProPower is intended for use in the electromagnetic environment specified below.
The customer or the user of the LM-ProPower should assure that it is used in such an environment.
Emission test
Compliance
Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1
The LM-ProPower uses RF energy only for its internal function.
Therefore, it's RF emissions are very low and are not likely to cause
any interference in nearby electronic equipment.
RF emissions
CISPR 11
Class B
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Not applicable
The LM-ProPower is suitable for use in all establishments, including
domestic establishments and those directly connected to the public
low-voltage power supply network that supplies buildings used for
domestic purposes.
Guidance and manufacturer's declaration - electromagnetic immunity
The LM-ProPower is intended for use in the electromagnetic environment specified below.
The customer or the user of the LM-ProPower should assure that it is used in such an environment.
IEC 60601
test level
Immunity test
Electrostatic
discharge (ESD)
Compliance level
±6 kV contact
±6 kV contact
±8 kV air
±8 kV air
±2 kV for power
supply lines
±2 kV for power
supply lines
±1 kV for input/output
lines
±1 kV differential
mode
±1 kV for input/output
lines
±1 kV differential
mode
±2 kV common mode
±2 kV common mode
Voltage dips, short
interruptions and
voltage varaiations
on power supply
input lines
<5 % U T
(>95 % dip in UT)
for 0,5 cycle
<5 % U T
(>95 % dip in UT)
for 0,5 cycle
40 % U T
(60 % dip in UT)
for 5 cycles
40 % U T
(60 % dip in UT)
for 5 cycles
IEC 61000-4-11
70 % U T
(30 % dip in UT)
for 25 cycles
70 % U T
(30 % dip in UT)
for 25 cycles
<5 % U T
(>95 % dip in UT)
for 5 sec
<5 % U T
(>95 % dip in UT)
for 5 sec
3 A/m
3 A/m
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
NOTE
32
U T is the a.c. mains voltage prior to application of the test level.
Electromagnetic environment guidance
Floors should be wood, concrete or
ceramic tile. If floors are covered with
synthetic material, the relative humidity
should be at least 30%.
Mains power quality should be that of a
typical commercial or hospital
environment.
Mains power quality should be that of a
typical commercial or hospital
environment.
Mains power quality should be that of a
typical commercial or hospital
environment. If the user of the
LM-ProPower requires continued
operation during power mains i
interruption, it is recommended that the
LM-ProPower be powered from an
uninterruptible power supply or battery.
Power frequency magnetic fields should
be at levels characteristic of a typical
location in a typical commercial or
hospital environment.
Warranty and declaration
Guidance and manufacturer's declaration - electromagnetic immunity
The LM-ProPower is intended for use in the electromagnetic environment specified below.
The customer or the user of the LM-ProPower should assure that it is used in such an environment.
Immunity test
IEC 60601 test level
Compliance
level
Electromagnetic environment - guidance
Portable and mobile RF communications equipment
should be used no closer to any part of the
LM-ProPower including cables, than the recommended
separation distance calculated from the equation
applicable to the frequency of the transmitter.
Recommended separation distance
Conducted RF
3 Vrms
IEC 61000-4-6
150 kHz to 80 MHz
Radiated RF
3 V/m
IEC 61000-4-3
80 MHz to 2,5 GHz
3V
d = 1,2√P
3 V/m
d = 1,2√P
80 MHz to 800 MHz
d = 2,3√P
800 MHz to 2,5 GHZ
were P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in metres (m).
Field strengths from fixed RF transmitters as determined by an electromagnetic site survey, a should be less
than the compliance level in each frequency range.b
Interference may occur in the vicinity of equipment
marked with the following symbol:
NOTE 1
At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.
a
b
Field strengths from fixed transmitters, such as base stations fro radio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess
the electromagnetic environment due to fixed RF transmitters. an electromagnetic site survey should be considered. If the
measured field strength in the location in which the LM-ProPower is used exceeds the applicable RF compliance level
above, the LM-ProPower should be observed to verify normal operation. If abnormal performance is observed additional
measures may be necessary, such as reorienting or relocating the LM-ProPower.
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
33
Warranty and declaration
Recommended separation distances between
portable and mobile RF communications equipment and the LM-ProPower
The LM-ProPower is intended for use in an electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the equipment can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the LM-ProPower as
recommended below, according to the maximum output power of the communications equipment.
Separation distance according to frequency of transmitter
m
Rated maximum output power of
transmitter
W
150 kHz to 80 MHz
80 MHz to 800 MHz
800
2,5MHz
GHz
150 MHz
kHz to 80
d = 1,2√P
d = 1,2√P
d = 2,3√P
0,01
0,12
0,12
0,23
0,1
0,38
0,38
0,73
1
1,2
1,2
2,3
10
3,8
3,8
7,3
100
12
12
23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres
(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output
power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
34
35
LM-Instruments Oy
9770090
9770035 Rev E
9770036
C8
PL 88 (Norrbyn rantatie 8)
FI-21601 Parainen, Finland
Tel: +358 2 4546 400
Fax: +358 2 4546 444
E-mail: [email protected]
Internet: www.lminstruments.com
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