3M Elipar DeepCure-L User manual

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LED Curing Light
Светодиодное устройство для фотополимеризации
стоматологических материалов
Светодиодна лампа за полимеризация
LED svjetiljka za polimerizaciju
Gyors polimerizációt biztosító LED-lámpa
Diodowa lampa do polimeryzacji
Lampă de fotopolimerizare cu LED
LED Polymerizačná lampa
Polimerizacijska LED luč
Polymerační LED lampa
LED Işık Cihazı
LED-valguslamp
Gaismas diodes lampa
Diodinis švitintuvas
Стоматологічна лампа для світлової полімеризації
LED полимеризациона лампа
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Operating Instructions
Инструкция по эксплуатации
Инструкции за експлоатация
Upute za upotrebu
Használati utasítás
Instrukcja użycia
Instrucţiuni de utilizare
Návod na použitie
Navodila za uporabo
Návod k použití
Kullanma Talimatları
Kasutusjuhend
Lietošanas pamācība
Naudojimo instrukcija
Інструкції з експлуатації
Упутство за употребу
Elipar™
DeepCure-L

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Elipar™DeepCure-L
LED Curing Light
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Safety Instructions
PLEASE NOTE!
Prior to installation and start-up of the device, please
read these instructions carefully!
As with all technical devices, the proper function and
safe operation of this device depend on the user’s
compliance with the standard safety procedures as well
as the specific safety recommendations presented in
these Operating Instructions.
1. Use of the device is restricted to professional person-
nel in
accordance with the instructions below. The
manufacturer assumes no liability for any damage
arising from any other or improper use of this device.
2. The charger must be accessible at all times. Do not
use the charger for any use other than the charging of
the Elipar™DeepCure-L handpiece. Disconnect the
handpiece from the mains by unplugging the charger
from the USB socket before use.
Treating patients using the handpiece while it is still
connected to the charger is disabled for safety
reasons. Light-curing is possible only after the char-
ger has been disconnected.
3. Use only the 3M charger which is provided with the
device. The use of any other charger can result in
damage to the battery.
4. CAUTION. Do not stare at source. May be harmful to
the eyes. Restrict exposure to the area of the oral
cavity in which clinical treatment is intended. Protect
patient and user from reflection and intensive scattered
light by taking the appropriate precautions, e.g., glare
shields, goggles, or coverings.
5. CAUTION! As it is the case for all high-intensity light-
curing devices, the high light intensity is accompanied
by heat generation on the exposed surface. This heat
can result in irreversible damage if there is longer
exposure in the proximity of the pulp or soft tissue. The
exposure times given in the manufacturer’s instructions
must be observed exactly to avoid any such damage.
Uninterrupted exposure times of the same tooth
surface in excess of 20 seconds and direct contact
with oral mucosa or skin must be strictly avoided.
Scientists working in this field are in agreement that the
irritation caused by heat generated during light curing
can be minimized by taking two simple precautions:
• Polymerization with external cooling from an air flow
• Polymerization at intermittent intervals (e.g.,
2 exposures lasting 10 seconds each instead of
1 exposure lasting 20 seconds).
6. Elipar DeepCure-L may be operated only with
the supplied light guide or original 3M replacement
and accessory light guide.
Table of Contents Page
Safety Instructions 1
Product Description 3
Indications 3
Technical Data 4
Charger 4
Handpiece 4
Charger and Handpiece 4
Transport and Storage Conditions 4
Installation of the Unit 4
Factory Settings 4
Initial Steps 4
Charger 4
Light Guide/Handpiece 5
Battery Charging 5
Battery Power Level Display on Handpiece 6
Operation 6
Selection of Exposure Time 6
Activating and Deactivating the Light 7
Inserting and Removing the Light Guide
from/into the Handpiece 7
Positioning the Light Guide 7
Testing of Light Intensity 7
Recommended Cure Techniques with 3M
Adhesives 8
Sleep Mode 8
Audible Signals
- Handpiece 8
Troubleshooting 9
Maintenance and Care 10
Care of the Handpiece 10
Reprocessing the Light Guide 10
Cleaning and Disinfecting Charger,
Handpiece and Glare Shield 12
Storage of the Handpiece during
Extended Periods of Non-Use 12
Return of Old Electric and
Electronic Equipment for Disposal 12
Customer Information 12
Warranty 13
Limitation of Liability 13
Symbol Glossary 13

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blems in the
operation of this or other devices, mo-
ve the device to
a different location.The EMC ma-
nufacturer’s declara
tion is listed in the appendix.
16. CAUTION! Portable high-frequency communica-
tion devices including their accessories should
keep a minimum distance of 30 cm to Elipar Deep-
Cure-L. Otherwise, the performance characteris-
tics of the device may be reduced.
17. Prior to each use of the device ensure that the
emitted light intensity is sufficient to safely guaran-
tee
polymerization. Check the light guide and the
light guide mounting port to make sure they are
clean. If necessary, the light guide mounting port
and the light guide can be cleaned as described in
the section “Maintenance and Care” (see also the
section “Testing of Light Intensity”).
Please report a serious incident occurring in relation to
the device to 3M and the local competent authority
(EU) or local regulatory authority.
The light guide must be seen as an applied part.
The use of other light guides may result in a reduc-
tion or increase in the light intensity. The product’s
warranty does not cover any damage resulting from
the use of third-party light guides.
7. Use only genuine 3M parts when replacing
defective components as directed in these
Operating Instructions. The product’s warranty
does not cover any damage resulting from the
use of third-party replacement parts.
8. Should you have any reason to suspect the safety
of the device to be compromised, the device must
be taken out of operation and labeled accordingly
to prevent third parties from inadvertently using
a possibly defective device. Safety may be
compromised, e.g., if the device malfunctions or is
noticeably damaged.
9. Keep solvents, flammable liquids, and sources of
intense heat away from the device as they may
damage the plastic housing of the device, the seals,
or the operating buttons.
10. Do not allow any cleaning agents to enter the devi-
ce
during cleaning as they could cause an electri-
cal short or a dangerous malfunction.
11. Only service centers authorized by 3M Deutsch-
land GmbH may open the device housing and
repair the device.
12. CAUTION: this device must not be modified wi-
thout the manufacturer’s permission.
13. Individuals with a history of cataract surgery may
be particularly sensitive to the exposure to light and
should be discouraged from Elipar DeepCure-L
treatment unless adequate safety measures, such
as the use of protective goggles to remove blue
light, are undertaken.
14. Individuals with a history of retinal disease should
seek advice from their ophthalmologist prior to
operating the device. In operating the Elipar
DeepCure-L device, this group of individuals must
take extreme care and comply with any and all
safety precautions (including the use of suitable
light-filtering safety goggles).
15. This device has been developed and tested in ac-
cordance with the relevant EMC regulations and
standards. It is in conformity with legal require-
ments. Since various factors such as power sup-
ply, wiring, and the ambient conditions at the place
of operation can affect the EMC properties of the
device, the possibility that, under unfavorable con-
ditions, there will be EMC disruptions cannot be
completely excluded. If you should notice pro-

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The handpiece must be connected to the charger at
the latest when the battery power level display glows
red steadily so that the battery is charged (cf.“Battery
Power Level Display on Handpiece”).
The device is shipped with a light guide with 10 mm
diameter. It is not permissible to use the light guides of
other devices.
The handpiece is equipped with a sleep mode to mini-
mize the device’s energy consumption. The handpiece
switches to sleep mode if it is not used for a period of
about 5 minutes or the incorrect charging voltage is de-
tected.
The charger uses a maximum of 0.2 W when ready for
operation.
+These Instructions for Use should be kept for the
duration of product use. The product may only be
used when the product labeling is clearly readable.
For details on all additionally mentioned products
please refer to the corresponding Instructions for
Use.
Intended Purpose
Intended purpose: curing light for light curing dental
materials.
Intended users: educated dental professionals who
have theoretical and practical knowledge on usage of
dental products.
Patient target group: all patients requiring dental treat-
ment, unless the patient’s condition limits the use.
Clinical benefit: initiates the curing reaction of light
curing dental materials.
Indications
• Polymerization of light-curing dental materials with
photo initiator for the wavelength range 430
- 480 nm.
- Most light-curing dental materials respond to this
light wavelength range. In case of doubt, please
contact the respective manufacturer.
Contraindications
Do not use Elipar DeepCure-L in patients with a history
of photobiological reactions (including individuals with
urticaria solaris or erythropoietic protoporphyria) or who
are currently on photosensitizing medication (including
8-methoxypsoralen or dimethylchlorotetracycline).
Potential Undesirable Side Effects and Complica-
tions
Heat generation can result in pulp or tissue damage.
Unprotected light exposure can result in eye damage.
Refer to chapter safety instructions for correct handling.
Light guide
Handpiece
Glare shield
Product Description
Elipar DeepCure-L is a high-performance LED light
source for the polymerization of light-curing dental
materials. The device has two components: a wireless
handpiece with a built-in battery which can be replaced
by 3M customer care and a charger. The device
is a medical electrical device in accordance with
IEC 60601-1and is available as a tabletop device.
Wall-mounting is not possible.
In comparison with conventional light-curing devices,
Elipar DeepCure-L features excellent beam collimation
and a uniform beam profile, directing more of the light
energy to the restoration being polymerized and
producing a deep, uniform, and complete curing of the
restoration.
The light source is a high-performance light diode
(LED). The beam emerging from the device covers
the light wavelength range of 430 to 480 nm relevant,
for instance, for camphor quinone products and is
suitable for use with the majority of light-curing dental
materials, including materials for fillings, liners, core
build-ups, fissure sealings, temporary restorations,
and cements for indirect restorations.
See the manufacturer’s information for the exposure
time required for the specific dental material.
Settable exposure times:
• 5,10, 15, 20 sec
• Continuous mode (120 sec)
• Tack-cure mode (1 sec)
Place the handpiece on a flat surface when not in use.
The handpiece can be connected to the charger
between applications so that the battery is charged.

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Technical Data
Charger Model CPS008050100
Operating voltage: 100 - 240 V 50/60 Hz
Nominal consumption: 0.2 A max
Dimensions without
country-specific adapter: Length: 65 mm
Width: 40 mm
Depth: 31 mm
Weight: 75 g
Classification: Protection class II,
Manufacturer: Click Technology Co., Ltd.
Model: CPS008050100
Charger Model GTM96060-0606-1.0
Operating voltage: 100 - 240 V 50/60 Hz
Nominal consumption: 0.6 A max
Dimensions without
country-specific adapter: Length: 74 mm
Width: 44 mm
Depth: 37 mm
Weight: 107 g
Classification: Protection class II,
Manufacturer: GlobTek, Inc.
Model: GTM96060-0606-1.0
Handpiece
Power supply: Lithium-ion battery,
nominal voltage 3.7 V,
capacity 2300 mAh
Utilizable wavelength
range: 430
- 480 nm
Wavelength peak: 444 - 452 nm
Light intensity (between
400 and 515 nm): 1470 mW/cm2
- 10% / +20%
(independent of battery
power level)
Light emission area: 60 - 65 mm2(optically active)
Intermittent operation: The device has been desi-
gned solely for short-term
operation.
Typical operating time at
room temperature (23°C):
7 min, at 40 °C ambient tem-
perature: 1min on, 15 min
off (cooling-off period)
Total exposure time
with new, fully
charged battery: Typically 120 min
Dimensions: Diameter: 28 mm
Length: 270 mm
Weight: 180 g (incl. light guide)
Charger and Handpiece
Time to charge
empty battery: Approx. 2 h
Operating temperature: 10° C up to 40°C /
59°F up to 104°F
Relative humidity: 30% up to 75%
Atmospheric pressure: 700 hPa up to1060 hPa
Transport and Storage Conditions:
Ambient temperature range: - 20°C up to +40° C /
- 4°F up to +104°F
Relative humidity: 30% up to 75%
Atmospheric pressure: 700 hPa up to 1060 hPa
Subject to technical modification without prior notice.
Installation of the Unit
Factory Settings
The factory settings of the device are as follows:
• 10 sec exposure time
Initial Steps
Charger
ESelect the plug adapter specific to the country and
place it on the charger.
+40°C
+104°F
–20°C
–4°F
max.
75%
30%
hPa
1060
700

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Charger Model CPS008050100
Charger
Charger Model GTM96060-0606-1.0
ERemove the plug adapter by pushing the slider
switch in the direction of the arrow.
Light Guide / Handpiece
EPlace the glare shield on the front of the device.
EAutoclave the light guide prior to first use.
EThen attach the light guide to the handpiece until it
noticeably locks into place (see Section “Removing
and Inserting the Light Guide from/into the Hand-
piece”).
EIf the device malfunctions, insert the charger plug
into the charging socket of the handpiece. The
device will reset itself and can then be used again.
Battery Charging
E
The device contains a powerful lithium-ion recharge-
able battery. This type of battery does not have any
memory effect and can therefore be recharged at
any time by inserting the charger plug into the
charging socket of the handpiece (see the section
“Battery Power Level Display on Handpiece”).
EBefore using the handpiece for the first time,
connect it to the charger for a period of about
2 hours so that the new battery is completely
charged for the first time. Make sure the colors line
up correctly.
Plug adapter
1333

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The green status light on the handpiece blinks while
the battery is charging. The green status light glows
steadily when the device is fully charged. As a safety
precaution, light-curing is not possible while the
device is charging.
Status LED Operating status
Handpiece Charger
without charger connected
Steady green Handpiece Charging has
light ready for been completed
operation
Flashes green –– Battery is being
charged
Steady red light Low battery Problem during
charge charging
Flashes red Battery fully Problem in
discharged, charging, battery
exposure is defective
cycle will be or cannot be
completed or, charged
if in continuous
mode, stopped
Battery Power Level Display on Handpiece
LED showing
exposure times
{
START button
TIME button
Operation
Selection of Exposure Time
0 1 2 3 4 5 6 7 8 9 10
Distance (mm)
Light intensity (%)
100
90
80
70
60
50
Exposure time options: 5,10, 15, 20 sec, continuous
mode (120 sec), tack-cure mode (1sec).
ESee the instructions for use for the specific dental
material when selecting the exposure time.
EThe indicated exposure times assume that the light
guide is held at the exact position over the material
being polymerized.
EIf the distance between the light guide and the
restoration is increased, the exposure time must be
adjusted accordingly because the light intensity
weakens (see graph).
Status LED
133333333
Select the exposure time by pressing the TIME button.
- The selected exposure time is indicated by the
4 green LEDs.
- Each time the button is briefly pressed, the
setting advances to the next (higher) value. All
4 green LEDs will be turned on for a setting of
20 sec. Pressing the button again will turn off all
of the LEDs and enable the continuous mode.
- The display advances through the available
settings, if the button is kept depressed.
- While exposure is ongoing, the button for selec-
tion of the exposure time is inactive.

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Activating and Deactivating the Light
E
Briefly press the START button; the light will turn on.
- The LEDs first indicate the set exposure time;
all 4 LEDs light up for 20 sec. Every 5 sec, as
the time runs down, the LEDs will turn off one at
a time; at 15 sec remaining time, 3 LEDs will still
be on, at 10 sec remaining time 2 LEDs, etc.
- The LEDs do not come on at all in continuous
mode; an audible signal is emitted every
10 seconds.
EIf desired, the light can be turned off by pressing
the START button again before the exposure time
is over.
EHolding down the START button activates the
tack-cure mode: the devxice emits a single short
light pulse which enables the defined curing of
Protemp™Crown temporary restorations or a light-
curing cement excess (e.g., RelyX™Unicem) to
enable easy removal.
Inserting and Removing the Light Guide from/into
the Handpiece
EAttach the light guide to the handpiece by inserting
it with a slight rotation until it clicks firmly into place
and there are no gaps between the neck of the light
guide and the handpiece (see picture).
- Damaged light guides substantially reduce
the light intensity and must be replaced
immediately, sharp edges may cause serious
injury!
Testing of Light Intensity
Depending on the layer thickness of the filling material
being cured, it is possible to check the function of the
curing light using curing disks for composites:
EPlace the curing disk on a mixing pad.
E
Fill your preferred composite into a bore of the curing
disk at least twice as deep as the recommended
layer thickness of your composite.
ECure the composite in the curing disk for the time
recommended by the composite manufacturer.
EScrape off soft material from the bottom of the
cured material with a plastic spatula.
EThe solid thickness of the cured material in the
curing disk divided by two is the layer thickness
which can be properly cured.
E
If you have doubts about the correct function of your
curing light, clean the light guide and the protection
glass in the light guide mounting hole and ensure
proper fit of the light guide in the handpiece and
repeat the intensity test.
EIf you have still doubts about the correct function of
your curing light, contact 3M service.
The curing disk must only be used to test the func-
tion of the curing light! For clinical depth of cure,
please refer to the Instructions for Use of
the filling material.
Commonly available devices for measuring light intensity
can also be used; their measurement values should
not be regarded as absolute values. When such devices
are used, we recommend recording the intensity of the
curing light before its first use and measuring it again at
regular intervals so that any decrease in light intensity
ERemove the light guide by turning slightly and
pulling it out of the handpiece.
Positioning the Light Guide
ERotate the light guide into the desired position for
polymerization.
E
To make full use of the light intensity provided, place
the light guide as close to the filling as possible.
Avoid directly contacting the filling material!
- Keep the light guide clean at all times to obtain
full light intensity.

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can be detected. The light
intensity testing unit in
an Elipar DeepCure-S base station has a device for
measuring intensity on a percentage basis.
Recommended Cure Techniques with 3M Adhe-
sives
• Rotate the light guide into the desired position for
polymerization.
• A barrier sleeve may be used. Note that sleeve can
impact power and irradiance of a curing light. It is
critical to ensure the sleeve is powder free and the
seam is not over the tip of the light guide and that
the sleeve fits well. Intermediate level disinfection
(manual disinfection with ready-to-use disinfectant
wipes) is indicated when a sleeve is used, otherwise
the light guide should undergo high level disinfection
(manual disinfection using disinfectant bath, see
“Reprocessing the Light Guide”).
The following sleeves have been tested:
Sleep Mode
The handpiece begins charging automatically when
connected to the charger (green status light blinks) if
the battery requires charging. If the charging voltage
is not correct (e.g., there is dirt on the contacts in the
charger socket or the charger), the handpiece goes
into sleep mode. If the handpiece is not connected to
the charger and is not used for a period of about
5 minutes, it also goes into sleep mode. In this opera-
tion mode, all of the displays and signals of the hand-
piece are turned off so that power consumption is
reduced to a minimum.To terminate the sleep mode
press the START button.
- The sleep mode termination signal (two short
audible signals) is emitted indicating that the
handpiece is ready for operation; the handpiece
displays the latest selected exposure mode and
time settings.
Audible Signals - Handpiece
An audible signal is emitted
• every time a button is pressed,
• every time the light is turned ON,
• 1time after 5 sec exposure time, 2 times after 10 sec,
3 times after 15 sec.
Exception: in continuous mode; an audible signal is
emitted every 10 seconds.
Two audible signals are emitted
• every time the sleep mode is terminated by pressing
the START button,
• every time the light is turned OFF.
A 2 sec-error signal is emitted, if
• the handpiece over-heats,
• the battery lacks sufficient charge.
The audible signals from the handpiece can be turned
off (except for the 2-sec error signal). Follow these
instructions to turn them off. Plug the charger into a
functioning power outlet, then press and hold down the
TIME and START buttons at the same time with one
hand. With the other hand, connect the charging cable
from the power supply to the charging socket of the
handpiece. An audible signal confirms that there has
been a change from “Audible signals activated” to
“Audible signals deactivated”. Release the two buttons
and disconnect the handpiece from the charger. Repeat
the above procedure to activate the audible signals.
Sleeve Impacts
Power or
Irradiance
Cure Sleeve®Tip Covers (short) – Kerr No
Complete Curing Light Sleeves-Demi
– Kerr No
TIDIShield™ Custom Fit Curing Light
Sleeves – TIDI Products No
SmartLite®Max Lens Cover Sleeve –
Dentsply No
Curelastic™ Cure-Light Sleeve
(Steri-Shield) Yes

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Troubleshooting
Error Cause
ESolution
The status display on
the handpiece glows
red steadily.
The status display of
the handpiece flashes
red.
The ongoing exposure
is interrupted (light off
signal is emitted)
followed by a 2 sec-
error signal; the hand-
piece switches to
“sleep” mode and
resists further activa-
tion.
The status light on the
handpiece blinks red
whenever the hand-
piece is connected to
the charger.
The handpiece has
not been used for a
long time and now it
cannot be turned on.
The handpiece does
not respond to the
pressing of either
button.
While the handpiece
is connected to the
charger, pressing
the START button
will not start the light
emission.
The remaining battery
charge is adequate only for
typical 5 10-sec exposure
cycles.
EConnect the handpiece
to the charger and
recharge the battery.
The battery lacks sufficient
charge.
EConnect the handpiece
to the charger and
recharge the battery.
Charging problem. The
battery is defective or at the
end of its useful life.
EContact 3M
Service.
There is not enough charge
in the battery to turn on the
handpiece.
EConnect the handpiece
to the charger and
recharge the battery.
Software crash possible.
EPlug the included
charger into an outlet
and connect it to the
handpiece. This causes
the light-curing device
to reset itself.
The handpiece is connected
to the charger. Light-curing
is prevented as a safety
precaution.
EDisconnect the charger
from the handpiece and
restart the light emission.
Error Cause
ESolution
The light emission
does not start when
the START button
is pressed; an error
signal sounds for
2 sec.
During light emission
in continuous mode,
an error signal sounds
for 2 sec, the emission
is stopped, and the
handpiece changes
to sleep mode.
The light intensity is
too low
The dental material
does not cure
completely.
The light guide cannot
be attached to the
handpiece.
The information about inter-
mittent operation under the
header “Technical data
-
handpiece” has not been
observed.
The handpiece has become
overheated in the course
of use. The handpiece can
be used again once it has
cooled down.
EAllow the handpiece to
cool for 3 minutes, then
start the next exposure
by pressing the START
button.
The information about inter-
mittent operation under the
header “Technical data
-
handpiece” has not been
observed.
The handpiece has become
overheated in the course
of use. The handpiece can
be used again once it has
cooled down.
EAllow the handpiece to
cool for 3 minutes, then
start the next exposure
by pressing the START
button.
EClean the light guide and
the protecting glass in the
light guide mounting hole
(please refer to “Cleaning
the Light Guide”).
EClean the light guide and
the protecting glass in the
light guide mounting hole
(please refer to “Cleaning
the Light Guide”).
ECheck to see that the
correct light guide has
been attached.
EThe light guide is not
designed for use with the
Elipar DeepCure-L.

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Maintenance and Care
The Elipar DeepCure-L device is maintenance-free.
No periodic maintenance is required. See the informa-
tion contained in this chapter to secure problem-free
operation.
Care of the Handpiece
EUse only the charger included with the product.
The use of other chargers may damage the battery
cells or result in inadequate charge.
Do not immerse the handpiece in water or incinerate!
Please also observe the chapter on “Safety”.
Reprocessing the Light Guide
The light guide is not sterile when delivered and must
be reprocessed before being used for the first time
and after each patient use.
Follow manufacturer’s instructions for preparation,
temperatures, contact time and rinsing off the clean-
ing1and disinfecting solution2exactly.
An enzymatic detergent should be used as the clean-
ing solution.
Material Resistance
Make sure that the cleaning and disinfectant agents
you have chosen do not contain any of the following
materials:
- Organic, mineral, and oxidizing acids (minimum
acceptable pH value 5.5)
- The pH value of the cleaning and disinfecting
solution should be between pH 7 and 11
- Oxidation agents (e.g., hydrogen peroxide)
- Halogens (chlorine, iodine, bromide)
- Aromatic/halogenized hydrocarbons
Observe the manufacturer’s information about the
cleaning and disinfecting agents.
The light guide must not be exposed to temperatures
higher than 135 °C (275 °F).
The light guide has been tested for up to 500 steriliza-
tion cycles.
Limitations on Reprocessing
This medical device is safe to use if it is reprocessed
according to these instructions and no visible damage
is seen.
Inspect the device carefully before each use and dis-
card if there is any damage.
Point of use / Pre-Treatment
The contaminated light guide must be placed in an
approved, sealed container during transport from the
point of use to the reprocessing area.
The pre-treatment must be carried out before either
automatic or manual cleaning and disinfecting. Imme-
diately after using (within a maximum of 2 hours),
remove gross contaminations from the light guide.
For this, rinse the light guide thoroughly under running
water (drinking water quality as a minimum) for at least
10 seconds.
Use a soft brush or a soft cloth to manually remove
any remaining contamination. Remove polymerized
composite with alcohol; a plastic spatula may help in
removing the material. Do not use any sharp or point-
ed tools to protect the surface of the light guide from
scratching.
Cleaning and Thermal Disinfecting (Automated
Washer-Disinfectors / CDD (Cleaning and Disinfec-
tion Device))
EAfter the light guide has been pre-treated, place it in
the wire or sieve basket of the washer-disinfector.
Make sure that the devices do not touch one anoth-
er in the washer-disinfector.
ERemove the light guide from the washer-disinfector
unit at the end of the drying cycle and store it under
low germ count conditions.
EExamine the light guide for visible impurities. If any
impurities are visible, repeat the cycle in the wash-
er-disinfector.
Automated washer-disinfectors that meet the
following requirements are suitable for use:
• The device generally has a certified effectiveness in
accordance with ISO 15883. The washer-disinfector
is regularly serviced and tested.
• If available, use a tested cycle for thermal disinfec-
tion (A0 value > 600 or, for older devices, at least 5
min at 90 °C/194 °F).
• The water used for rinsing is minimum drinking wa-
ter quality. Use low-germ and low-endotoxin water
for final rinsing.
• The air used for drying should be filtered (oil-free,
with low microbiological and particulate contamina-
tion).
Note: The evidence of suitability for automatic cleaning
and disinfection took place using the Miele G7336 CD
washer-disinfector (Gütersloh) and the cleaning agent
Thermosept RKN-zym (Schülke & Mayr). The program
D-V-THERMO0905, without drying time was used un-
der worst case conditions.
Cleaning
steps Parameters
Pre-rinse Temperature: 10 ° ± 2 °C
Time: 1 min

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11
ENGLISH

en
ECleaning takes place in the immersion bath with a
soft brush for at least 5 minutes.
EThen remove the light guide from the solution, thor-
oughly rinse with low-germ-count water (drinking
water quality as a minimum), and dry with a lint-free
cloth.
Manual Disinfection (High Level Disinfection)
EA disinfecting agent containing o-Phthalaldehyde
(e.g., Cidex OPA by Johnson & Johnson) is recom-
mended. It is compatible with the light-curing de-
vice.
ETo disinfect, place the cleaned light guide for the
specified application time (≥ 12 min) into the solu-
tion, making sure that it is completely covered.
EThe instruments in the disinfection bath must not
touch each other during this process.
EThen remove the light guide from the solution, thor-
oughly rinse with low-germ-count water (drinking
water quality as a minimum) for at least 3 minutes,
and dry with a lint-free cloth.
EThen check the light guide (see “Check”).
1Cleaning agent Thermosept RKN-zym (Schülke &
Mayr) for the washer-disinfector and Cidezyme®/
Enzol®and CaviWipes™ were used for manual
cleaning.
2Cidex OPA, ready-for-use solution, was used for vali-
dation of the high level disinfection and CaviWipes™
for validation of intermediate level disinfection.
Packaging for Sterilization
Package the light guide in single wrapped sterilization
pouches (one-way packaging or double packaging).
Sterilization
Effective cleaning and disinfection are absolutely es-
sential requirements for effective sterilization.
A fractionated vacuum procedure (at least 3 vacuum
stages) or a gravity procedure (with adequate product
drying) must be used for the sterilization. The use of
the less effective gravity procedure is permissible sole-
ly if the fractionated vacuum procedure is unavailable.
The user is solely responsible for selection of the pa-
rameters required for the gravity procedure; the user
must therefore calculate or validate these parameters
in accordance with the loading configuration. The dry-
ing time actually required is also directly dependent on
parameters that are in the sole responsibility of the us-
er (loading configuration and density, sterilizer condi-
tion, etc.) and must consequently be determined by
the user.
• Steam sterilizer in conformity with DIN EN
13060/DIN EN 285 or ANSI AAMI ST79 (for USA:
FDA clearance)
Cleaning and disinfection of the light guide by wip-
ing is only permitted in combination with a corre-
sponding protective sleeve
Manual Cleaning
EClean the light guide after every application for 30
seconds with ready-to-use disinfectant wipes (e.g.,
CaviWipes™ based on the active substances alco-
hols and quaternary compounds (QAV)) or equiva-
lent cleaning agents.
EFollow the cleaning agent manufacturer’s directions
for use.
EClean with the wipes until no contamination is visible.
EThen rinse with water (drinking water quality as a
minimum) and dry with a soft, lint-free cloth.
Manual Disinfection (Intermediate Level Disinfection)
EAn intermediate level disinfection is possible only if
the light guide is covered with a protective sleeve
during use.
EDisinfect the light guide with ready-to-use disinfec-
tant wipes (e.g., CaviWipes™ based on the active
substances alcohols and quaternary compounds
(QAV)) or equivalent disinfection agents. Follow the
disinfection agent manufacturer’s directions for use,
observing in particular the contact times.
EThen rinse with water (drinking water quality as a
minimum) and dry with a soft, lint-free cloth.
Manual Cleaning and Disinfection the Light Guide
by Immersion Bath
Manual Cleaning
EA neutral enzymatic cleaning agent is recommend-
ed (e.g., Cidezyme/Enzol from Johnson & John-
son).
EPlace the light guide for the specified application
time into the solution, making sure that it is com-
pletely covered.
Cleaning
steps Parameters
Cleaning
Cleaning temperature: 45 ° ± 2 °C
Time: 5 min
Cleaning solution: Thermosept
RKN-zym
Concentration: 0.3% (3 ml/l)
Final rinse Temperature: 10 ° ± 2 °C
Time: 2 min
Thermal
disinfection
Temperature 90 ° ± 2 °C
Time: 5 min

SEITE 12 - 148 x 210 mm - 44000118149/02 - SCHWARZ - 20-113 (kn)
12
• Maximum sterilization temperature 135 °C (275 °F)
• The following cycles were validated for the light
guide:
tact pins cause an operating error (malfunction mes-
sage: the LED showing the operating status of the
charger glows red steadily).
*CaviWipes™, Metrex, were used for the validation of
the cleaning and disinfection procedure.
Storage of the Handpiece during Extended Periods
of Non-Use
EIf the handpiece will not be used for a number of
weeks
- e.g., during vacation - charge the battery
beforehand or connect the handpiece to the charger
for this time. A safety switch within the battery
prevents a total discharge.
Discharged or nearly discharged batteries must be
recharged as soon as possible.
Return of Old Electric and Electronic
Equipment for Disposal
1. Collection
Users of electric and electronic equipment are required
to collect their old equipment separately from other
waste in accordance with the regulations of the specific
country. Old electric and electronic equipment must not
be disposed of with unsorted household waste. This
separate collection is a prerequisite for recycling and
reprocessing as an important method for preserving
environmental resources.
2. Return and Collection Systems
When your Elipar DeepCure-L is no longer usable,
do not dispose of the device with household waste.
3M Deutschland GmbH has set up special disposal
facilities to handle the equipment. Details about the
procedure for the specific country can be obtained
from the pertinent 3M subsidiary.
3. Removing the Battery for Disposal
To dispose of the battery, disconnect the Elipar
DeepCure-L LED curing light from the charger, remove
the two screws on each side of the charging socket
and push the lower half of the housing towards the
back, away from the upper half of the housing. Use a
suitable tool to cut the connecting wires between the
battery and the circuit board and remove the battery
for disposal in accordance with 1. and 2.
Customer Information
No person is authorized to provide any information
that deviates from the information provided in this
instruction sheet.
Fractional
prevacuum Gravity displacement
Tempera-
ture 132 °C (270 °F) 134 °C (273 °F) 121 °C (250 °F)
Sterilization
time 4 min 3 min 20 min
Drying time 30 min 30 min 30 min
Check
Before using the light guide again, check it for dam-
aged surfaces, discoloration, and contamination; do
not use damaged light guides. If the light guide is still
contaminated, repeat all reprocessing steps.
Cleaning and Disinfecting Charger, Handpiece and
Glare Shield
• Cleaning and disinfecting solutions must not enter
the unit.
• Wipe the surfaces with ready-to-use disinfectant
wipes* (e.g., CaviWipes™ based on the active sub-
stances alcohols and quaternary compounds (QAV)
or equivalent disinfection agents). Subsequently in-
spect the surfaces for visible impurities. If any impu-
rities are visible, repeat the cleaning procedure.
• Do not use solvents or scouring agents, as they
may damage the device components.
• Wipe the device surfaces with a tuberculocidal dis-
infectant wipe* for disinfection and keep it wet ac-
cording to the disinfection agent manufacturer’s di-
rections for use, particularly observing the contact
time.
• Disinfectants must not be sprayed directly onto the
device surface.
• Wipe the device surfaces with a soft cloth moist-
ened with water (drinking water quality as a mini-
mum) and dry with a soft, lint-free cloth. If you do
not rinse well with water, the components will be
damaged.
• If necessary, ask the manufacturer of the disinfec-
tant if its constant use will damage plastic surfaces.
Clean the glare shield with a soft and fluff-free cloth.
Beware of scratches!
Ensure that the charge contact pins stay dry and are
not touched by any metallic or greasy parts. Dry up
necessarily damp contact pins. Do not bend the
charge contact pins during drying. Damp charge con-

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13
ENGLISH

en
Warranty
3M Deutschland GmbH warrants this product will
be free from defects in material and manufacture.
3M Deutschland GmbH MAKES NO OTHER
WARRANTIES INCLUDING ANY IMPLIED
WARRANTY OF MERCHANTABILITY OR FITNESS
FOR A PARTICULAR PURPOSE. User is responsible
for determining the suitability of the product for
user’s application. If this product is defective within
the warranty period, your exclusive remedy and
3M Deutschland GmbH’s sole obligation shall be
repair or replacement of the 3M Deutschland GmbH
product.
Limitation of Liability
Except where prohibited by law, 3M Deutschland GmbH
will not be liable for any loss or damage arising from
this product, whether direct, indirect, special, incidental
or consequential, regardless of the theory asserted,
including warranty, contract, negligence, or strict liability.
Symbol Glossary
Reference Number
and Symbol Title Symbol Description of Symbol
ISO 15223-1
5.1.1
Manufacturer
Indicates the medical device
manufacturer as defined in EU
Directives 90/385/EEC,
93/42/EEC and 98/79/EC.
ISO 15223-1
5.1.3
Date of Manufacture
Indicates the date when the
medical device was manufac-
tured.
ISO 15223-1
5.1.5
Batch code
Indicates the manufacturer's
batch code so that the batch or
lot can be identified.
ISO 15223-1
5.1.6
Catalogue number
Indicates the manufacturer's
catalogue number so that the
medical device can be identi-
fied.
ISO 15223-1
5.1.7
Serial number
Indicates the manufacturer's
serial number so that a specific
medical device can be identi-
fied.
ISO 15223-1
5.3.7
Temperature limit
Indicates the temperature limits
to which the medical device can
be safely exposed.
ISO 15223-1
5.3.8
Humidity limitation
Indicates the range of humidity
to which the medical device can
be safely exposed.
ISO 15223-1
5.3.9
Atmospheric
pressure limitation
Indicates the range of atmo-
spheric pressure to which the
medical device can be safely
exposed.
ISO 15223-1
5.4.4
Caution
Indicates the need for the user to
consult the instructions for use
for important cautionary informa-
tion such as warnings and pre-
cautions that cannot, for a vari-
ety of reasons, be presented on
the medical device itself.
CE Mark Indicates conformity to Euro-
pean Union Medical Device
Regulation or Directive.
Medical Device Indicates the item is a medical
device.
Follow instructions
for use
To signify that the instructions
for use must be followed.

SEITE 14 - 148 x 210 mm - 44000118149/02 - SCHWARZ - 20-113 (kn)
14
Information valid as of August 2020
Reference Number
and Symbol Title Symbol Description of Symbol
Rx Only Indicates that U.S. Federal Law
restricts this device to sale by or
on the order of a dental profes-
sional. 21 Code of Federal
Regulations (CFR) sec.
801.109(b)(1).
Type B applied part To identify a type B applied part
complying with IEC 60601-1.
Class II equipment To identify equipment meeting
the safety requirements for
Class II equipment per IEC
61140.
Use Indoors Indicates medical device be
used indoors
Battery Battery power level.
PAP 20/21 Indicates paper material is
recyclable.
Recycle electronic
equipment DO NOT throw this unit into a municipal trash bin when this
unit has reached the end of its
lifetime. Please recycle.
Green Dot Indicates a financial contribu-
tion to national packaging re-
covery company per European
Directive No. 94/62 and corre-
sponding national law. Packag-
ing Recovery Organization Eu-
rope.

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15


ru
РУССКИЙ
Elipar™DeepCure-L
Светодиодное устройство для
фотополимеризации
стоматологических материалов

ru
Безопасность
ВНИМАНИЕ!
Перед тем как начать использование устройства,
внимательно прочтите эту инструкцию!
Как илюбой другой электротехнический прибор,
это устройство будет работать надёжно и
безопасно только при соблюдении как общих
правил техники безопасности, так испецифических
инструкций по безопасности, представленных в
данной инструкции по эксплуатации.
1. Пользоваться устройством разрешается только
профессионалы всоответствии с
приведенной
ниже инструкцией. Производитель не несет
никакой ответственности за вред здоровью и
имуществу, возникший вследствие использования
данного устройства не по назначению.
2. Кблоку питания со встроенной вилкой должен
быть обеспечен постоянный хороший доступ.
Блок питания следует использовать
исключительно для зарядки ручного блока Elipar™
DeepCure-L. Перед использованием отсоедините
ручной блок от сети, отключив зарядное устрой-
ство от USB-разъема.
Вцелях безопасности лечение пациентов сис-
пользованием ручного блока, все еще подклю-
ченного кзарядному устройству, запрещено.
Облучение возможно только после отключения
зарядного устройства.
3. Используйте поставляемое вкомплекте
зарядное устройство фирмы-производителя 3M.
Использование какого-либо другого зарядного
устройства может привести кповреждению
аккумуляторной батареи.
4. ВНИМАНИЕ! Не смотреть непосредственно на
источник света. Существует опасность
причинения вреда глазам. Ограничить зону,
защитить пациента ипользователя от
отраженного иинтенсивного рассеянного света
путем принятия соответствующих мер (например,
антибликовый щиток, очки или покрытия).
5. ПРЕДУПРЕЖДЕНИЕ! Так же, как идля всех
высокоинтенсивных светополимеризирующих
устройств, высокая интенсивность света
сопровождается тепловыделением на
облучаемой поверхности. Это тепло вслучае
длительного воздействия вблизи пульпы или
мягких тканей может привести ких
необратимому поражению. Во избежание такого
поражения необходимо вточности соблюдать
время облучения, указанное винструкции по
эксплуатации производителя.
Содержание Страница
Безопасность 15
Описание изделия 17
Показания 18
Технические данные 18
Блок питания 18
Ручной блок 18
Блок питания со встроенной вилкой
иручной блок 19
Условия перевозки ихранения 19
Ввод устройства вэксплуатацию 19
Заводские настройки 19
Начальные шаги 19
Блок питания со встроенной вилкой 19
Световод / Ручной блок 20
Зарядка аккумулятора 20
Индикатор уровня мощности ручного
блока 20
Работа 21
Выбор времени полимеризации 21
Включение ивыключение излучения 21
Установка иизвлечение световода
вручном блоке 21
Позиционирование световода 22
Проверка интенсивности света 22
Дежурный режим 22
Рекомендуемая техника отверждения с
адгезивами фирмы 3M 22
Звуковые сигналы
- ручной блок 23
Поиск иустранение неисправностей 24
Техническое обслуживание иуход 25
Обращение сручным блоком 25
Обработка световода 25
Очистка идезинфекция зарядного устрой-
ства, ручного блока изащитного щитка 28
Хранение ручного блока во время
длительных нерабочих периодов 28
Возврат электрических иэлектронных
отслуживших свой срок приборов на
утилизацию 28
Информация для покупателя 29
Гарантийные обязательства 29
Ограничение ответственности 29
Пояснение условных обозначений 30

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16
циально опасному нарушению нормальной рабо-
ты.
11. Открывать ипроизводить ремонт устройства
может только сервисный центр, уполномоченный
компанией 3M Deutschland GmbH.
12. ВНИМАНИЕ: Запрещается внесение изменений
вданное устройство без получения на то разре-
шения производителя.
13. Лица судаленной катарактой могут проявлять
частичную чувствительность кизлучению света
и, поэтому, не должны допускаться клечению с
помощью Elipar DeepCure-L без
необходимых
мер безопасности, как, например,
защитные
очки для устранения голубого света.
14. Лица, имеющие ванамнезе болезни сетчатки,
перед началом лечения должны предоставить
заключение от своего офтальмолога. Используя
Elipar DeepCure-L на таких группах больных,
следует особо тщательно придерживаться всех
мер безопасности (вт.ч. пользоваться
соответствующими светофильтрирующими
защитными очками).
15. Это устройство было разработано ипроверено
всоответствии ссоответствующими
положениями истандартами по ЭМС.
Оно соответствует всем требованиям закона.
Если такие факторы как электропитание,
электропроводка иусловия окружающей
среды на месте работы могут повлиять на
характеристики ЭМС устройства, то, возможно,
что при неблагоприятных условиях невозможно
полностью исключить нарушения ЭМС. Вслучае
обнаружения неполадок вработе данного или
других устройств необходимо переставить
устройство вдругое место. Декларация про-
изводителя по ЭМС приведена вприложении.
16. ВНИМАНИЕ! Портативные высокочастотные
устройства связи, включая их принадлежности,
должны находиться на расстоянии не менее 30
см от Elipar DeepCure-L. Впротивном случае ра-
бочие характеристики устройства могут быть
занижены.
17. Перед каждым использованием устройства
убедитесь, что интенсивность излучаемого
света
достаточна для успешной полимеризации.
Для
этого проверьте чистоту световода икрепления
световода. Вслучае необходимости можно про-
извести очистку световода икрепления свето-
вода, как описано вглаве «Техническое обслу-
живание иуход» (смотрите
также раздел
«Проверка интенсивности света»).
Необходимо строго избегать превышение 20
секундного непрерывного времени облучения
на одной поверхности зуба и
непосредственного контакта со слизистой
оболочкой полости рта или кожей.
Работающие вэтой области ученые пришли к
выводу, что вызываемое во время
светоотверждения тепловыделением
раздражение можно свести кминимуму,
приняв две простые меры предосторожности:
Oполимеризация свнешним охлаждением
потоком воздуха
Oполимеризация спрерывистыми
временными интервалами (например, 2
облучения по
10 секунд каждое вместо 1 облучения
продолжительностью 20 секунд).
6. Устройство Elipar DeepCure-L разрешается
эксплуатировать только споставляемым в
комплекте световодом или соригинальным
световодом 3M из комплекта запчастей и
принадлежностей. Световод должен
рассматриваться как рабочая часть
устройства. Использование других световодов
может привести куменьшению или
увеличению интенсивности света. Вгарантию
изделия не входят какие-либо повреждения,
возникшие врезультате использования
световодов других производителей.
7. При замене поврежденных элементов
использовать исключительно оригинальные
части фирмы-производителя 3M согласно
данной инструкции по эксплуатации. В
гарантию изделия не входят какие-либо
повреждения, возникшие врезультате
использования запасных частей других
производителей.
8. Вслучае возникновения каких-либо
подозрений вбезопасности устройства
необходимо его выключить иустановить
табличку во избежание его эксплуатации
другими лицами. Безопасность может
оказаться под угрозой, если устройство,
например, функционирует неправильно или
имеет внешние признаки повреждений.
9. Держите вдали от прибора растворители,
воспламеняющиеся жидкости исильные
тепловые источники, так как они могут привести
кповреждениям пластмассового корпуса,
уплотнений икнопок управления прибора.
10. Не позволять моющим средствам проникать
вустройство, так как это может привести к
короткому замыканию устройства или
потен-

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ru
Осерьезных инцидентах сизделием сообщайте
компании 3Миместному компетентному органу
(ЕС) или местному органу государственного регу-
лирования иконтроля.
Описание изделия
Прибор Elipar DeepCure-L представляет собой
световое устройство СИД высокой мощности для
полимеризации фотоотверждаемых дентальных
материалов. Он состоит из ручного блока без
кабеля со встроенной батареей, которая может
быть заменена сервисной службой компании 3M, и
блока питания со встроенной вилкой. Устройство
представляет собой медицинское электрическое
устройство всоответствии сIEC 60601-1 и
доступно вкачестве устройства настольного типа.
Настенный монтаж невозможен.
По сравнению собычными светополимеризирующи-
ми
устройствами Elipar DeepCure-L отличается ве-
ликолепной коллимацией луча иоднородным про-
филем луча, направляющим больше световой
энергии на полимеризуемую реставрацию и
осуществляющим глубокое, однородное иполное
отверждение реставрации.
Источником света вустройстве служит
высокопроизводительный светоизлучающий диод
(СИД). Испускаемый устройством луч имеетдлину
волны вдиапазоне от 430 до 480 нм
(соответствующий диапазон, например, для
изделий из камфарахинона) инаиболее
эффективен для использования со
светоотверждаемыми стоматологическими
материалами, включая материалы для пломб,
виниров, надстроек культи, фиссурных
герметиков, временных реставраций ицементов
для непрямых реставраций.
Информацию онеобходимом времени
полимеризации
для определенного
стоматологического материала см. винструкции
по применению производителя.
Устанавливаемое время полимеризации:
O5, 10, 15, 20 сек
OНепрерывный режим (120 сек)
OФункция прерывистой полимеризации (tack cu-
re, 1 сек)
Вперерывах между применениями кладите ручной
блок на ровное основание. Между применениями
ручной блок можно соединять сблоком питания,
чтобы заряжать аккумулятор. Самое позднее, когда
индикатор зарядки начнет гореть постоянным
красным светом, (см. «Индикатор заряда на ручном
блоке»), нужно соединить ручной блок сблоком
питания, чтобы зарядить аккумулятор.
Устройство поставляется со световодом диаметром
10 мм. Запрещается использовать светодиоды
других устройств.
Уручного блока для уменьшения энергопотребления
имеется дежурный режим. Ручной блок переходит в
дежурный режим, если он втечение 5 минут не
использовался, или было
обнаружено недопустимое
напряжение ток зарядки.
Блок питания потребляет вготовом кработе
состоянии максимально 0,2 Вт.
+Данную инструкцию по применению следует
хранить на протяжении всего периода исполь-
зования продукта. Изделие разрешено кис-
пользованию только, если маркировка изделия
хорошо читаема. Вотношении всех других упо-
мянутых продуктов, пожалуйста, обращайтесь к
соответствующей инструкции по применению.
Предполагаемая область применения
Предполагаемая область применения: устройство
фотополимеризации для светоотверждаемых сто-
матологических материалов.
Предполагаемые пользователи: квалифицирован-
ные стоматологи, обладающие теоретическими и
практическими знаниями по использованию стома-
тологической продукции.
Целевая группа пациентов: все пациенты, нуждаю-
щиеся встоматологическом лечении, за исключени-
ем тех пациентов, для которых имеются ограниче-
ния на использование продукта.
Клиническая польза: вызывает реакцию полимери-
зации светоотверждаемых стоматологических ма-
териалов.
Световод
Ручной блок
Защитный щиток

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Показания
O Полимеризация стоматологических
материалов,
чувствительных кдиапазону
длины волны 430
- 480 нм.
- Большинство светоотверждаемых стомато-
логических материалов отвечают на этот
диапазон волн. Вслучае сомнений, пожалуй-
ста, свяжитесь ссоответствующим произво-
дителем.
Противопоказания
Не применяйте Elipar DeepCure-L на пациентах,
подверженных фотобиологическим реакциям
(включая тех, кто подвержен аллергии на солнце
или эритропоэтической протопорфирии), или тех,
кто внастоящий момент находится под действием
фотосенсибилизирующих медикаментов (включая
8-метоксипсорален или диметилхлоротетрацик-
лин).
Потенциальные нежелательные побочные
эффекты иосложнения
Выделение тепла может привести кповреждению
пульпы или тканей. Воздействие света при отсут-
ствии защиты может привести кповреждению
глаз.
Для обеспечения правильного обращения обрати-
тесь кразделу «Безопасность».
Технические данные
Модель зарядного устройства CPS008050100
Рабочее напряжение: 100 - 240 В50/60 Гц
Номинальная
потребляемая
мощность: 0,2 A макс.
Размеры без
специального
переходника для
разных стран: Длина: 65 мм
Ширина: 40 мм
Глубина 31 мм
Вес: 75 г
Классификация: степень защиты II,
Завод-изготовитель: Click Technology Co., Ltd.
Название модели: CPS008050100
Модель зарядного устройства GTM96060-0606-1.0
Рабочее напряжение: 100 - 240 В50/60 Гц
Номинальная
потребляемая
мощность: 0,6 A макс.
Размеры без
специального
переходника для
разных стран: Длина: 74 мм
Ширина: 44 мм
Глубина 37 мм
Вес: 107 г
Классификация: степень защиты II,
Завод-изготовитель: GlobTek, Inc.
Название модели: GTM96060-0606-1.0
Ручной блок
Электропитание: ионно-литиевая
аккумуляторная батарея,
номинальное напряжение
3,7 В, емкость 2300 мАч
Пригодный для
использования
диапазон длины волны: 430 - 480 нм
Пик длины волны: 444 - 452 нм
Интенсивность света
(между 400 и515 нм): 1470 мВт/см2
- 10% / +20%
(взависимости от уровня
мощности аккумуляторной
батареи)
Область светового
излучения: 60
- 65 мм2
(оптически активно)
Переменный режим
работы: Устройство было разработано
исключительно для
краткосрочной работы.
Обычное время работы при
комнатной температуре (23
°C): 7 мин, при температуре
окружающей среды 40 °C: 1
минута вкл., 15 минут выкл.
(время охлаждения)
Общее время облучения
сновой, полностью
заряженной аккумуляторной
батареей: обычно 120 мин.
Размеры: Диаметр: 28 мм
Длина: 270 мм
Вес: 180 г(включая световод)